MAPK10 (mitogen-activated protein kinase 10) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Gene: MAPK10 (mitogen-activated protein kinase 10) Homo sapiens
Analyze
Symbol: MAPK10
Name: mitogen-activated protein kinase 10
RGD ID: 733441
HGNC Page HGNC:6872
Description: Predicted to enable JUN kinase activity. Involved in protein phosphorylation. Located in nucleoplasm. Implicated in pancreatic adenocarcinoma. Biomarker of Alzheimer's disease.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: c-Jun N-terminal kinase 3; FLJ12099; FLJ33785; JNK3; JNK3 alpha protein kinase; JNK3A; MAP kinase 10; MAP kinase p49 3F12; MAPK 10; MGC50974; mitogen activated protein kinase 10; p493F12; p54bSAPK; PRKM10; RP13-514E23.1; SAPK1b; stress activated protein kinase beta; stress-activated protein kinase 1b; stress-activated protein kinase JNK3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38486,010,405 - 86,594,074 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl485,990,007 - 86,594,625 (-)Ensemblhg38GRCh38
GRCh37486,931,558 - 87,374,348 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36487,156,656 - 87,593,307 (-)NCBIBuild 36Build 36hg18NCBI36
Build 34487,294,810 - 87,632,922NCBI
Celera484,225,414 - 84,570,629 (-)NCBICelera
Cytogenetic Map4q21.3NCBI
HuRef482,680,152 - 83,118,708 (-)NCBIHuRef
CHM1_1486,912,970 - 87,350,773 (-)NCBICHM1_1
T2T-CHM13v2.0489,339,877 - 89,923,587 (-)NCBIT2T-CHM13v2.0
JBrowse:




Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-anisomycin  (EXP)
(R)-noradrenaline  (ISO)
1,2-dibromoethane  (ISO)
1,2-dichloroethane  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2-ethoxyethanol  (ISO)
2-methoxyethanol  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
8-Br-cAMP  (EXP)
acetohydrazide  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP,ISO)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenic trichloride  (EXP)
atrazine  (ISO)
Azoxymethane  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
bis(2-chloroethyl) sulfide  (ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
bortezomib  (EXP)
butanal  (EXP)
cadmium dichloride  (EXP,ISO)
cantharidin  (ISO)
carmustine  (EXP)
CGP 52608  (EXP)
chlordecone  (ISO)
chromium(6+)  (ISO)
cisplatin  (ISO)
cobalt dichloride  (EXP)
cocaine  (EXP)
curcumin  (ISO)
cypermethrin  (ISO)
D-glucitol  (EXP)
dextran sulfate  (ISO)
dichloroacetic acid  (ISO)
dicoumarol  (EXP)
dioxygen  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
emodin  (ISO)
endosulfan  (ISO)
entinostat  (EXP)
ethanol  (EXP,ISO)
flavonoids  (ISO)
flutamide  (ISO)
fulvestrant  (EXP)
genistein  (ISO)
glycidol  (ISO)
glyphosate  (ISO)
hydrogen peroxide  (ISO)
hypochlorous acid  (EXP)
ibuprofen  (ISO)
L-serine  (EXP)
lead diacetate  (ISO)
lipopolysaccharide  (EXP,ISO)
lithium chloride  (EXP)
luteolin  (EXP)
LY294002  (EXP)
mangiferin  (EXP)
menadione  (EXP,ISO)
mercury dibromide  (EXP)
metformin  (EXP)
methotrexate  (ISO)
methoxychlor  (ISO)
methylmercury chloride  (EXP)
N-acetyl-L-cysteine  (EXP)
N-methyl-4-phenylpyridinium  (EXP)
naringin  (ISO)
nickel atom  (EXP)
okadaic acid  (EXP)
ozone  (ISO)
p-menthan-3-ol  (EXP)
panobinostat  (EXP)
paracetamol  (ISO)
paraquat  (ISO)
pentanal  (EXP)
phenylephrine  (ISO)
phenylmercury acetate  (EXP)
pifithrin-alpha hydrobromide  (ISO)
potassium chloride  (ISO)
potassium dichromate  (ISO)
procymidone  (ISO)
quercetin  (ISO)
quinolin-8-ol  (ISO)
reactive oxygen species  (EXP)
rotenone  (EXP,ISO)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
S-nitrosoglutathione  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP,ISO)
sodium dichromate  (ISO)
streptozocin  (ISO)
sulfates  (EXP)
sulindac sulfide  (EXP)
sunitinib  (EXP)
tamoxifen  (ISO)
titanium dioxide  (ISO)
trichostatin A  (EXP)
valproic acid  (EXP)
vinclozolin  (ISO)
vorinostat  (EXP)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Stress- and cell type-dependent regulation of transfected c-Jun N-terminal kinase and mitogen-activated protein kinase kinase isoforms. Butterfield L, etal., Biochem J. 1999 Mar 15;338 ( Pt 3):681-6.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Relationship between SP1 polymorphism and osteoporosis in beta-thalassemia major patients. Guzeloglu-Kayisli O, etal., Pediatr Int. 2008 Aug;50(4):474-6. doi: 10.1111/j.1442-200X.2008.02609.x.
4. The c-jun kinase/stress-activated pathway: regulation, function and role in human disease. Johnson GL and Nakamura K, Biochim Biophys Acta. 2007 Aug;1773(8):1341-8. Epub 2007 Jan 4.
5. KEGG: Kyoto Encyclopedia of Genes and Genomes KEGG
6. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
7. The neuroprotective effects of K252a through inhibiting MLK3/MKK7/JNK3 signaling pathway on ischemic brain injury in rat hippocampal CA1 region. Pan J, etal., Neuroscience. 2005;131(1):147-59.
8. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
9. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
10. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
11. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
12. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
13. Activation and redistribution of c-jun N-terminal kinase/stress activated protein kinase in degenerating neurons in Alzheimer's disease. Zhu X, etal., J Neurochem. 2001 Jan;76(2):435-41.
Additional References at PubMed
PMID:1922387   PMID:7826642   PMID:8125298   PMID:8619474   PMID:8654373   PMID:9045910   PMID:9110174   PMID:9349820   PMID:9393873   PMID:9403476   PMID:9596579   PMID:9739089  
PMID:9847074   PMID:10101227   PMID:10383391   PMID:10471813   PMID:10523642   PMID:10629060   PMID:10715136   PMID:10756100   PMID:10878576   PMID:11090355   PMID:11185509   PMID:11231586  
PMID:11259409   PMID:11322657   PMID:11356842   PMID:11359773   PMID:11468147   PMID:11504923   PMID:11698270   PMID:11718727   PMID:11726686   PMID:11823425   PMID:11865055   PMID:12089333  
PMID:12167088   PMID:12189133   PMID:12239168   PMID:12436199   PMID:12477932   PMID:12714584   PMID:12775419   PMID:12788955   PMID:12818176   PMID:12857973   PMID:12960231   PMID:12963725  
PMID:14702039   PMID:15228592   PMID:15246824   PMID:15276183   PMID:15299005   PMID:15489334   PMID:15603708   PMID:15693750   PMID:16007099   PMID:16169070   PMID:16249883   PMID:16344560  
PMID:16481105   PMID:16611996   PMID:16737965   PMID:16824735   PMID:17670986   PMID:17680991   PMID:18408005   PMID:18624398   PMID:19001375   PMID:19204086   PMID:19294699   PMID:19525941  
PMID:19527717   PMID:19782076   PMID:19879840   PMID:20056178   PMID:20525557   PMID:20936779   PMID:21041242   PMID:21166945   PMID:21321401   PMID:21653829   PMID:21832049   PMID:21873635  
PMID:21988832   PMID:22001757   PMID:22047447   PMID:22327296   PMID:22441692   PMID:22523077   PMID:23142346   PMID:23329067   PMID:23602568   PMID:24412749   PMID:24483146   PMID:24767251  
PMID:25009551   PMID:25013167   PMID:25025079   PMID:25178256   PMID:25353672   PMID:25416956   PMID:25455349   PMID:25475894   PMID:26186194   PMID:26868142   PMID:27503909   PMID:28393229  
PMID:28514442   PMID:30585266   PMID:30591558   PMID:30655611   PMID:31080119   PMID:31432180   PMID:32040807   PMID:32066630   PMID:32296183   PMID:32468043   PMID:32572915   PMID:32707033  
PMID:32998477   PMID:33774030   PMID:33961781   PMID:34502556   PMID:34857952  


Genomics

Comparative Map Data
MAPK10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38486,010,405 - 86,594,074 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl485,990,007 - 86,594,625 (-)Ensemblhg38GRCh38
GRCh37486,931,558 - 87,374,348 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36487,156,656 - 87,593,307 (-)NCBIBuild 36Build 36hg18NCBI36
Build 34487,294,810 - 87,632,922NCBI
Celera484,225,414 - 84,570,629 (-)NCBICelera
Cytogenetic Map4q21.3NCBI
HuRef482,680,152 - 83,118,708 (-)NCBIHuRef
CHM1_1486,912,970 - 87,350,773 (-)NCBICHM1_1
T2T-CHM13v2.0489,339,877 - 89,923,587 (-)NCBIT2T-CHM13v2.0
Mapk10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395103,056,413 - 103,359,200 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl5103,055,814 - 103,359,200 (-)EnsemblGRCm39 EnsemblGRCm39
GRCm385102,908,547 - 103,212,604 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5102,907,948 - 103,211,334 (-)Ensemblmm10GRCm38
MGSCv375103,336,967 - 103,640,353 (-)NCBIMGSCv37MGSCv37mm9NCBIm37
MGSCv365103,152,671 - 103,451,379 (-)NCBIMGSCv36mm8
Celera5100,221,882 - 100,523,871 (-)NCBICelera
Cytogenetic Map5E5NCBI
cM Map549.61NCBI
Mapk10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8146,802,247 - 7,094,103 (+)NCBIGRCr8GRCr8GRCr8
GRCr8 Ensembl146,802,295 - 7,094,100 (+)EnsemblGRCr8
mRatBN7.2146,497,662 - 6,790,109 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl146,497,707 - 6,786,201 (+)EnsemblmRatBN7.2
UTH_Rnor_SHR_Utx146,475,683 - 6,751,915 (+)NCBIUTH_Rnor_SHR_UtxUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0147,775,937 - 8,052,130 (+)NCBIUTH_Rnor_SHRSP_BbbUtx_1.0UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0146,467,375 - 6,743,050 (+)NCBIUTH_Rnor_WKY_Bbb_1.0UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0148,079,955 - 8,371,508 (+)NCBIRnor_6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl148,080,275 - 8,368,254 (+)Ensemblrn6Rnor6.0
Rnor_5.0148,053,697 - 8,344,225 (+)NCBIRnor_5.0Rnor_5.0rn5
RGSC_v3.4147,719,595 - 8,010,694 (+)NCBIRGSC_v3.4RGSC_v3.4rn4
Celera146,636,411 - 6,919,118 (+)NCBICelera
RGSC_v3.1147,719,594 - 8,010,694 (+)NCBI
Cytogenetic Map14p22NCBI
Mapk10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554743,624,679 - 3,772,458 (+)Ensembl
ChiLan1.0NW_0049554743,451,656 - 3,772,405 (+)NCBIChiLan1.0ChiLan1.0
MAPK10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2384,040,153 - 84,470,878 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1484,304,836 - 84,732,991 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0478,326,129 - 78,756,794 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1489,056,754 - 89,392,980 (-)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl489,059,579 - 89,392,196 (-)EnsemblpanPan2panpan1.1
MAPK10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1329,584,437 - 9,889,118 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl329,575,492 - 9,884,325 (-)EnsemblcanFam3CanFam3.1
Dog10K_Boxer_Tasha3232,059,481 - 32,299,296 (+)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.0329,607,730 - 9,912,898 (-)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl329,597,455 - 9,907,345 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1329,698,411 - 10,025,887 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0329,545,360 - 9,851,058 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03230,098,318 - 30,403,778 (+)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
Mapk10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244052852,447,490 - 2,761,815 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936896230,494 - 540,071 (-)EnsemblSpeTri2.0 Ensembl
SpeTri2.0NW_004936896228,908 - 539,836 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MAPK10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl8132,298,299 - 132,776,820 (+)EnsemblsusScr11Sscrofa11.1
Sscrofa11.18132,445,818 - 132,751,575 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.28141,972,691 - 142,138,440 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MAPK10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1734,394,600 - 34,725,658 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl734,399,544 - 34,564,212 (-)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM
Vero_WHO_p1.0NW_02366603713,051,033 - 13,392,105 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mapk10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248722,461,362 - 2,825,161 (-)EnsemblHetGla_female_1.0 EnsemblhetGla2HetGla_female_1.0 Ensembl
HetGla 1.0NW_0046248722,460,308 - 2,830,569 (-)NCBIHetGla 1.0HetGla 1.0hetGla2

Variants

.
Variants in MAPK10
102 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NC_000004.12:g.(?_86010404)_(86067956_86098523)del deletion Macrocephaly and epileptic encephalopathy [RCV000007138] Chr4:86010404..86067956 [GRCh38]
Chr4:4q21.3		 uncertain significance
NM_002753.3(MAPK10):c.-122+2698G>T single nucleotide variant Lung cancer [RCV000095061] Chr4:86450332 [GRCh38]
Chr4:87371485 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3 copy number gain See cases [RCV000051772] Chr4:51831622..97505618 [GRCh38]
Chr4:52697788..98426769 [GRCh37]
Chr4:52392545..98645792 [NCBI36]
Chr4:4q12-22.3		 pathogenic
GRCh38/hg38 4q13.3-22.1(chr4:74031395-90421127)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053296]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053296]|See cases [RCV000053296] Chr4:74031395..90421127 [GRCh38]
Chr4:74897112..91342278 [GRCh37]
Chr4:75115976..91561301 [NCBI36]
Chr4:4q13.3-22.1		 pathogenic
GRCh38/hg38 4q21.21-22.1(chr4:79575748-92412449)x1 copy number loss See cases [RCV000053297] Chr4:79575748..92412449 [GRCh38]
Chr4:80496902..93333600 [GRCh37]
Chr4:80715926..93552623 [NCBI36]
Chr4:4q21.21-22.1		 pathogenic
GRCh38/hg38 4q21.22-21.3(chr4:82248692-86778340)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053319]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053319]|See cases [RCV000053319] Chr4:82248692..86778340 [GRCh38]
Chr4:83169845..87699493 [GRCh37]
Chr4:83388869..87918517 [NCBI36]
Chr4:4q21.22-21.3		 pathogenic
NM_002753.3(MAPK10):c.802+9318C>T single nucleotide variant Malignant melanoma [RCV000066563] Chr4:86089206 [GRCh38]
Chr4:87010359 [GRCh37]
Chr4:87229383 [NCBI36]
Chr4:4q21.3		 not provided
NM_138982.4(MAPK10):c.1111-6C>T single nucleotide variant not provided [RCV004715688]|not specified [RCV000117594] Chr4:86031437 [GRCh38]
Chr4:86952590 [GRCh37]
Chr4:4q21.3		 benign|likely benign
NM_138982.4(MAPK10):c.960G>A (p.Ala320=) single nucleotide variant not provided [RCV000960845]|not specified [RCV000117595] Chr4:86067798 [GRCh38]
Chr4:86988951 [GRCh37]
Chr4:4q21.3		 benign|likely benign
NM_138982.4(MAPK10):c.1271G>A (p.Ser424Asn) single nucleotide variant Prostate cancer [RCV000149341] Chr4:86017352 [GRCh38]
Chr4:86938505 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh38/hg38 4q21.21-22.3(chr4:80879777-94809447)x1 copy number loss See cases [RCV000134977] Chr4:80879777..94809447 [GRCh38]
Chr4:81800931..95730598 [GRCh37]
Chr4:82019955..95949621 [NCBI36]
Chr4:4q21.21-22.3		 pathogenic
GRCh38/hg38 4q21.23-21.3(chr4:84577519-86077547)x3 copy number gain See cases [RCV000135441] Chr4:84577519..86077547 [GRCh38]
Chr4:85498672..86998700 [GRCh37]
Chr4:85717696..87217724 [NCBI36]
Chr4:4q21.23-21.3		 pathogenic
GRCh38/hg38 4q21.23-22.1(chr4:84329551-87679204)x1 copy number loss See cases [RCV000136623] Chr4:84329551..87679204 [GRCh38]
Chr4:85250704..88600356 [GRCh37]
Chr4:85469728..88819380 [NCBI36]
Chr4:4q21.23-22.1		 pathogenic
GRCh38/hg38 4q21.21-24(chr4:80427023-100855441)x1 copy number loss See cases [RCV000137269] Chr4:80427023..100855441 [GRCh38]
Chr4:81348177..101776598 [GRCh37]
Chr4:81567201..101995621 [NCBI36]
Chr4:4q21.21-24		 pathogenic
GRCh38/hg38 4q21.23-22.2(chr4:84329551-93654474)x1 copy number loss See cases [RCV000139231] Chr4:84329551..93654474 [GRCh38]
Chr4:85250704..94575625 [GRCh37]
Chr4:85469728..94794648 [NCBI36]
Chr4:4q21.23-22.2		 likely benign
GRCh38/hg38 4q21.21-21.3(chr4:80043949-86948317)x1 copy number loss See cases [RCV000140416] Chr4:80043949..86948317 [GRCh38]
Chr4:80965103..87869469 [GRCh37]
Chr4:81184127..88088493 [NCBI36]
Chr4:4q21.21-21.3		 pathogenic
GRCh38/hg38 4q21.3(chr4:86276186-86884105)x1 copy number loss See cases [RCV000141394] Chr4:86276186..86884105 [GRCh38]
Chr4:87197339..87805258 [GRCh37]
Chr4:87416363..88024282 [NCBI36]
Chr4:4q21.3		 uncertain significance
GRCh38/hg38 4q21.23-21.3(chr4:85972086-87031375)x1 copy number loss See cases [RCV000141421] Chr4:85972086..87031375 [GRCh38]
Chr4:86893239..87952527 [GRCh37]
Chr4:87112263..88171551 [NCBI36]
Chr4:4q21.23-21.3		 pathogenic
GRCh38/hg38 4q21.23-22.2(chr4:85449365-93973194)x1 copy number loss See cases [RCV000141424] Chr4:85449365..93973194 [GRCh38]
Chr4:86370518..94894345 [GRCh37]
Chr4:86589542..95113368 [NCBI36]
Chr4:4q21.23-22.2		 pathogenic
GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3 copy number gain See cases [RCV000143458] Chr4:68686088..95294456 [GRCh38]
Chr4:69551806..96215607 [GRCh37]
Chr4:69234401..96434630 [NCBI36]
Chr4:4q13.2-22.3		 pathogenic
NC_000004.12:g.86551290C>T single nucleotide variant Lung cancer [RCV000095062] Chr4:86551290 [GRCh38]
Chr4:87472443 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*47A>G single nucleotide variant Epileptic encephalopathy [RCV000259907] Chr4:86017181 [GRCh38]
Chr4:86938334 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.21C>A (p.Tyr7Ter) single nucleotide variant not specified [RCV000193982] Chr4:86194381 [GRCh38]
Chr4:87115534 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.339C>T (p.Val113=) single nucleotide variant not provided [RCV000968579]|not specified [RCV000195174] Chr4:86107250 [GRCh38]
Chr4:87028403 [GRCh37]
Chr4:4q21.3		 benign|likely benign
NM_138982.4(MAPK10):c.*1146_*1150del deletion Epileptic encephalopathy [RCV000280468]|not provided [RCV004695814] Chr4:86016078..86016082 [GRCh38]
Chr4:86937231..86937235 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.1223G>T (p.Gly408Val) single nucleotide variant MAPK10-related disorder [RCV003919824] Chr4:86029226 [GRCh38]
Chr4:86950379 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1489C>T single nucleotide variant Epileptic encephalopathy [RCV000274440] Chr4:86015739 [GRCh38]
Chr4:86936892 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1647C>T single nucleotide variant Epileptic encephalopathy [RCV000270495] Chr4:86015581 [GRCh38]
Chr4:86936734 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1913T>C single nucleotide variant Epileptic encephalopathy [RCV000266962] Chr4:86015315 [GRCh38]
Chr4:86936468 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.*265T>G single nucleotide variant Epileptic encephalopathy [RCV000332596] Chr4:86016963 [GRCh38]
Chr4:86938116 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*1224C>T single nucleotide variant Epileptic encephalopathy [RCV000373592] Chr4:86016004 [GRCh38]
Chr4:86937157 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*2071T>G single nucleotide variant Epileptic encephalopathy [RCV000396903] Chr4:86015157 [GRCh38]
Chr4:86936310 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.1323C>T (p.Thr441=) single nucleotide variant Epileptic encephalopathy [RCV000375350] Chr4:86017300 [GRCh38]
Chr4:86938453 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.367-12A>G single nucleotide variant Epileptic encephalopathy [RCV000398149] Chr4:86103256 [GRCh38]
Chr4:87024409 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.*1273T>A single nucleotide variant Epileptic encephalopathy [RCV000335326] Chr4:86015955 [GRCh38]
Chr4:86937108 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.*507G>A single nucleotide variant Epileptic encephalopathy [RCV000399494] Chr4:86016721 [GRCh38]
Chr4:86937874 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.*2039A>C single nucleotide variant Epileptic encephalopathy [RCV000302340] Chr4:86015189 [GRCh38]
Chr4:86936342 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.1080C>T (p.Asn360=) single nucleotide variant not provided [RCV000898693] Chr4:86064296 [GRCh38]
Chr4:86985449 [GRCh37]
Chr4:4q21.3		 benign|likely benign
NM_138982.4(MAPK10):c.*649G>C single nucleotide variant Epileptic encephalopathy [RCV000302801] Chr4:86016579 [GRCh38]
Chr4:86937732 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*27G>A single nucleotide variant Epileptic encephalopathy [RCV000317440] Chr4:86017201 [GRCh38]
Chr4:86938354 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*2087A>G single nucleotide variant Epileptic encephalopathy [RCV000337513] Chr4:86015141 [GRCh38]
Chr4:86936294 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_002753.5(MAPK10):c.-121-5540G>T single nucleotide variant Epileptic encephalopathy [RCV000380169] Chr4:86360184 [GRCh38]
Chr4:87281337 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.1053C>T (p.Asp351=) single nucleotide variant not provided [RCV000901577] Chr4:86064323 [GRCh38]
Chr4:86985476 [GRCh37]
Chr4:4q21.3		 benign|likely benign
NM_138982.4(MAPK10):c.-378T>C single nucleotide variant Epileptic encephalopathy [RCV000319898] Chr4:86359914 [GRCh38]
Chr4:87281067 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.-450C>T single nucleotide variant Epileptic encephalopathy [RCV000358304] Chr4:86359986 [GRCh38]
Chr4:87281139 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*1973G>A single nucleotide variant Epileptic encephalopathy [RCV000359368] Chr4:86015255 [GRCh38]
Chr4:86936408 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.425+11A>C single nucleotide variant Epileptic encephalopathy [RCV000290260] Chr4:86103175 [GRCh38]
Chr4:87024328 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*1784AAG[1] microsatellite Epileptic encephalopathy [RCV000305749] Chr4:86015439..86015441 [GRCh38]
Chr4:86936592..86936594 [GRCh37]
Chr4:4q21.3		 likely benign
NM_002753.5(MAPK10):c.-121-5573C>T single nucleotide variant Epileptic encephalopathy [RCV000383644] Chr4:86360217 [GRCh38]
Chr4:87281370 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1714C>T single nucleotide variant Epileptic encephalopathy [RCV000362688] Chr4:86015514 [GRCh38]
Chr4:86936667 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1346C>T single nucleotide variant Epileptic encephalopathy [RCV000388510] Chr4:86015882 [GRCh38]
Chr4:86937035 [GRCh37]
Chr4:4q21.3		 likely benign
NM_002753.5(MAPK10):c.-121-5566C>T single nucleotide variant Epileptic encephalopathy [RCV000326772] Chr4:86360210 [GRCh38]
Chr4:87281363 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*441C>T single nucleotide variant Epileptic encephalopathy [RCV000367505] Chr4:86016787 [GRCh38]
Chr4:86937940 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1623A>G single nucleotide variant Epileptic encephalopathy [RCV000328351] Chr4:86015605 [GRCh38]
Chr4:86936758 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.236+7G>A single nucleotide variant Epileptic encephalopathy [RCV000312210] Chr4:86159291 [GRCh38]
Chr4:87080444 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*201A>G single nucleotide variant Epileptic encephalopathy [RCV000370924] Chr4:86017027 [GRCh38]
Chr4:86938180 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*622T>C single nucleotide variant Epileptic encephalopathy [RCV000394451] Chr4:86016606 [GRCh38]
Chr4:86937759 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*1360A>C single nucleotide variant Epileptic encephalopathy [RCV000331896] Chr4:86015868 [GRCh38]
Chr4:86937021 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*1285T>G single nucleotide variant Epileptic encephalopathy [RCV000296746] Chr4:86015943 [GRCh38]
Chr4:86937096 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.-199G>A single nucleotide variant Epileptic encephalopathy [RCV000261853] Chr4:86359735 [GRCh38]
Chr4:87280888 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*835T>A single nucleotide variant Epileptic encephalopathy [RCV000337878] Chr4:86016393 [GRCh38]
Chr4:86937546 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.*373C>T single nucleotide variant Epileptic encephalopathy [RCV000275282] Chr4:86016855 [GRCh38]
Chr4:86938008 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.-514A>G single nucleotide variant Epileptic encephalopathy [RCV000265870] Chr4:86360050 [GRCh38]
Chr4:87281203 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.426-5_426-3dup duplication Epileptic encephalopathy [RCV000403139]|MAPK10-related disorder [RCV003932436] Chr4:86102034..86102035 [GRCh38]
Chr4:87023187..87023188 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.*793C>G single nucleotide variant Epileptic encephalopathy [RCV000405784] Chr4:86016435 [GRCh38]
Chr4:86937588 [GRCh37]
Chr4:4q21.3		 benign
NM_138982.4(MAPK10):c.385G>A (p.Val129Ile) single nucleotide variant Epileptic encephalopathy [RCV000347170] Chr4:86103226 [GRCh38]
Chr4:87024379 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*556G>A single nucleotide variant Epileptic encephalopathy [RCV000363517] Chr4:86016672 [GRCh38]
Chr4:86937825 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*1573A>G single nucleotide variant Epileptic encephalopathy [RCV000385139] Chr4:86015655 [GRCh38]
Chr4:86936808 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*611G>C single nucleotide variant Epileptic encephalopathy [RCV000306465] Chr4:86016617 [GRCh38]
Chr4:86937770 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.-55C>A single nucleotide variant Epileptic encephalopathy [RCV000369190] Chr4:86354578 [GRCh38]
Chr4:87275731 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.-101C>G single nucleotide variant Epileptic encephalopathy [RCV000297020] Chr4:86354624 [GRCh38]
Chr4:87275777 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_002753.5(MAPK10):c.-121-5480T>C single nucleotide variant Epileptic encephalopathy [RCV000323338] Chr4:86360124 [GRCh38]
Chr4:87281277 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.-102A>G single nucleotide variant Epileptic encephalopathy [RCV000354273] Chr4:86354625 [GRCh38]
Chr4:87275778 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_002753.5(MAPK10):c.-121-5552C>T single nucleotide variant Epileptic encephalopathy [RCV000288023] Chr4:86360196 [GRCh38]
Chr4:87281349 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*473T>C single nucleotide variant Epileptic encephalopathy [RCV000310531] Chr4:86016755 [GRCh38]
Chr4:86937908 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.*625T>G single nucleotide variant Epileptic encephalopathy [RCV000341447] Chr4:86016603 [GRCh38]
Chr4:86937756 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.-67T>G single nucleotide variant Epileptic encephalopathy [RCV000398161] Chr4:86354590 [GRCh38]
Chr4:87275743 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.3(chr4:87165664-87259133)x1 copy number loss not specified [RCV000452787] Chr4:87165664..87259133 [GRCh37]
Chr4:4q21.3		 likely benign
GRCh37/hg19 4q21.23-22.1(chr4:85839771-93071150)x1 copy number loss See cases [RCV000446648] Chr4:85839771..93071150 [GRCh37]
Chr4:4q21.23-22.1		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3 copy number gain See cases [RCV000446653] Chr4:12440..190904441 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4q21.23-24(chr4:85805268-103678797)x1 copy number loss See cases [RCV000445741] Chr4:85805268..103678797 [GRCh37]
Chr4:4q21.23-24		 pathogenic
GRCh37/hg19 4q21.21-22.1(chr4:82283358-90341831)x1 copy number loss See cases [RCV000447691] Chr4:82283358..90341831 [GRCh37]
Chr4:4q21.21-22.1		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473) copy number gain See cases [RCV000510453] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3 copy number gain See cases [RCV000512241] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4q21.21-22.3(chr4:81314915-96636651)x1 copy number loss not provided [RCV000682426] Chr4:81314915..96636651 [GRCh37]
Chr4:4q21.21-22.3		 pathogenic
GRCh37/hg19 4q21.3(chr4:86976413-87010825)x1 copy number loss not provided [RCV000743756] Chr4:86976413..87010825 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87007954-87027857)x3 copy number gain not provided [RCV000743757] Chr4:87007954..87027857 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87007954-87028072)x3 copy number gain not provided [RCV000743758] Chr4:87007954..87028072 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87014729-87028072)x4 copy number gain not provided [RCV000743759] Chr4:87014729..87028072 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87039732-87104170)x3 copy number gain not provided [RCV000743760] Chr4:87039732..87104170 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87118081-87142271)x3 copy number gain not provided [RCV000743761] Chr4:87118081..87142271 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87118930-87156742)x3 copy number gain not provided [RCV000743762] Chr4:87118930..87156742 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87139772)x3 copy number gain not provided [RCV000743763] Chr4:87119830..87139772 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87141106)x3 copy number gain not provided [RCV000743764] Chr4:87119830..87141106 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87141384)x3 copy number gain not provided [RCV000743765] Chr4:87119830..87141384 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87141521)x3 copy number gain not provided [RCV000743766] Chr4:87119830..87141521 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87142271)x3 copy number gain not provided [RCV000743767] Chr4:87119830..87142271 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87153443)x3 copy number gain not provided [RCV000743768] Chr4:87119830..87153443 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87156742)x3 copy number gain not provided [RCV000743769] Chr4:87119830..87156742 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4q21.3(chr4:87119830-87159318)x3 copy number gain not provided [RCV000743770] Chr4:87119830..87159318 [GRCh37]
Chr4:4q21.3		 benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3 copy number gain not provided [RCV000743155] Chr4:49450..190915650 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3 copy number gain not provided [RCV000743156] Chr4:49450..190963766 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3 copy number gain not provided [RCV000743147] Chr4:11525..191028879 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
NM_138982.4(MAPK10):c.930C>G (p.Pro310=) single nucleotide variant not provided [RCV000923989] Chr4:86067828 [GRCh38]
Chr4:86988981 [GRCh37]
Chr4:4q21.3		 likely benign
GRCh37/hg19 4q21.21-22.1(chr4:82043901-88334228) copy number loss not provided [RCV000767792] Chr4:82043901..88334228 [GRCh37]
Chr4:4q21.21-22.1		 pathogenic
NM_138982.4(MAPK10):c.348G>A (p.Lys116=) single nucleotide variant not provided [RCV000942198] Chr4:86107241 [GRCh38]
Chr4:87028394 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.24C>T (p.Tyr8=) single nucleotide variant not provided [RCV000976170] Chr4:86194378 [GRCh38]
Chr4:87115531 [GRCh37]
Chr4:4q21.3		 likely benign
GRCh37/hg19 4q21.3(chr4:87306927-87496888)x3 copy number gain not provided [RCV000849798] Chr4:87306927..87496888 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.21-22.1(chr4:80482400-92572499)x1 copy number loss See cases [RCV000790579] Chr4:80482400..92572499 [GRCh37]
Chr4:4q21.21-22.1		 pathogenic
GRCh37/hg19 4q21.3(chr4:86911035-86983232)x3 copy number gain not provided [RCV000847244] Chr4:86911035..86983232 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.3(chr4:86913748-86983232)x3 copy number gain not provided [RCV000847528] Chr4:86913748..86983232 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.606A>G (p.Thr202=) single nucleotide variant not provided [RCV000942885] Chr4:86101176 [GRCh38]
Chr4:87022329 [GRCh37]
Chr4:4q21.3		 likely benign
GRCh37/hg19 4q21.23-21.3(chr4:85703330-87825978)x1 copy number loss not provided [RCV001005568] Chr4:85703330..87825978 [GRCh37]
Chr4:4q21.23-21.3		 uncertain significance
GRCh37/hg19 4q13.3-21.3(chr4:71412409-87920784)x1 copy number loss See cases [RCV001263040] Chr4:71412409..87920784 [GRCh37]
Chr4:4q13.3-21.3		 pathogenic
NC_000004.12:g.86457483C>A single nucleotide variant not provided [RCV001356336] Chr4:86457483 [GRCh38]
Chr4:87378636 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3 copy number gain not provided [RCV001827738] Chr4:52866944..143582507 [GRCh37]
Chr4:4q12-31.21		 pathogenic
GRCh37/hg19 4q21.21-22.1(chr4:80467886-93362064)x1 copy number loss not provided [RCV001829208] Chr4:80467886..93362064 [GRCh37]
Chr4:4q21.21-22.1		 pathogenic
GRCh37/hg19 4q21.23-22.1(chr4:85839771-93071150) copy number loss not specified [RCV002053440] Chr4:85839771..93071150 [GRCh37]
Chr4:4q21.23-22.1		 pathogenic
GRCh37/hg19 4q13.3-22.1(chr4:75737340-91131156) copy number gain not specified [RCV002053429] Chr4:75737340..91131156 [GRCh37]
Chr4:4q13.3-22.1		 pathogenic
GRCh37/hg19 4q21.21-22.1(chr4:81054789-90667421) copy number loss not specified [RCV002053435] Chr4:81054789..90667421 [GRCh37]
Chr4:4q21.21-22.1		 pathogenic
GRCh37/hg19 4q21.21-22.2(chr4:79780152-94873225) copy number loss not specified [RCV002053432] Chr4:79780152..94873225 [GRCh37]
Chr4:4q21.21-22.2		 pathogenic
NM_138982.4(MAPK10):c.1375C>T (p.Pro459Ser) single nucleotide variant not specified [RCV004273066] Chr4:86017248 [GRCh38]
Chr4:86938401 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.1057G>A (p.Ala353Thr) single nucleotide variant Epileptic encephalopathy with cognitive deficit [RCV003225262] Chr4:86064319 [GRCh38]
Chr4:86985472 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.23-21.3(chr4:86788719-87014832)x3 copy number gain not provided [RCV003484189] Chr4:86788719..87014832 [GRCh37]
Chr4:4q21.23-21.3		 uncertain significance
GRCh37/hg19 4q21.3(chr4:87027204-87536353)x3 copy number gain not provided [RCV003484190] Chr4:87027204..87536353 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.3(chr4:87265364-87934081)x3 copy number gain not provided [RCV003484191] Chr4:87265364..87934081 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.21-22.3(chr4:81558759-95965995)x1 copy number loss not specified [RCV003986493] Chr4:81558759..95965995 [GRCh37]
Chr4:4q21.21-22.3		 pathogenic
NM_138982.4(MAPK10):c.237-10A>G single nucleotide variant MAPK10-related disorder [RCV003977064] Chr4:86107362 [GRCh38]
Chr4:87028515 [GRCh37]
Chr4:4q21.3		 likely benign
GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3 copy number gain not provided [RCV003885507] Chr4:45455621..191003541 [GRCh37]
Chr4:4p12-q35.2		 pathogenic
NM_138982.4(MAPK10):c.1293G>A (p.Ser431=) single nucleotide variant MAPK10-related disorder [RCV003933848] Chr4:86017330 [GRCh38]
Chr4:86938483 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.731-2A>G single nucleotide variant MAPK10-related disorder [RCV004758556] Chr4:86098597 [GRCh38]
Chr4:87019750 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.107A>G (p.His36Arg) single nucleotide variant not specified [RCV005371423] Chr4:86159427 [GRCh38]
Chr4:87080580 [GRCh37]
Chr4:4q21.3		 uncertain significance
NC_000004.12:g.85992138T>G single nucleotide variant not provided [RCV005257386] Chr4:85992138 [GRCh38]
Chr4:86913291 [GRCh37]
Chr4:4q21.23		 likely benign
NM_138982.4(MAPK10):c.404C>T (p.Thr135Met) single nucleotide variant not specified [RCV005375507] Chr4:86103207 [GRCh38]
Chr4:87024360 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.23-22.1(chr4:84418529-88078532)x1 copy number loss not provided [RCV005430878] Chr4:84418529..88078532 [GRCh37]
Chr4:4q21.23-22.1		 pathogenic
GRCh37/hg19 4q21.23-21.3(chr4:86871598-87102069)x3 copy number gain not provided [RCV004819480] Chr4:86871598..87102069 [GRCh37]
Chr4:4q21.23-21.3		 uncertain significance
GRCh38/hg38 4q21.3(chr4:86002088-86051292)x3 copy number gain See cases [RCV000140385] Chr4:86002088..86051292 [GRCh38]
Chr4:86923241..86972445 [GRCh37]
Chr4:87142265..87191469 [NCBI36]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.3(chr4:87126778-87764431)x3 copy number gain not provided [RCV001827820] Chr4:87126778..87764431 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.943G>A (p.Asp315Asn) single nucleotide variant not specified [RCV004939073] Chr4:86067815 [GRCh38]
Chr4:86988968 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.1105G>A (p.Glu369Lys) single nucleotide variant not specified [RCV004267517] Chr4:86064271 [GRCh38]
Chr4:86985424 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh38/hg38 4q21.21-23(chr4:79123548-99457773)x1 copy number loss Chromosome 4q21 deletion syndrome [RCV003327709] Chr4:79123548..99457773 [GRCh38]
Chr4:4q21.21-23		 pathogenic
GRCh37/hg19 4q21.23-21.3(chr4:85721709-86937764)x1 copy number loss not provided [RCV003485426] Chr4:85721709..86937764 [GRCh37]
Chr4:4q21.23-21.3		 pathogenic
GRCh37/hg19 4q21.3(chr4:87162492-87321894)x1 copy number loss not provided [RCV003485427] Chr4:87162492..87321894 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.23-22.3(chr4:85139670-96295033)x3 copy number gain not specified [RCV003986489] Chr4:85139670..96295033 [GRCh37]
Chr4:4q21.23-22.3		 likely pathogenic
NM_138982.4(MAPK10):c.1252+4C>T single nucleotide variant MAPK10-related disorder [RCV003981746] Chr4:86029193 [GRCh38]
Chr4:86950346 [GRCh37]
Chr4:4q21.3		 likely benign
NM_138982.4(MAPK10):c.121A>C (p.Lys41Gln) single nucleotide variant not specified [RCV004408584] Chr4:86159413 [GRCh38]
Chr4:87080566 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.1321A>G (p.Thr441Ala) single nucleotide variant not specified [RCV004408585] Chr4:86017302 [GRCh38]
Chr4:86938455 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.20A>G (p.Tyr7Cys) single nucleotide variant not specified [RCV004408586] Chr4:86194382 [GRCh38]
Chr4:87115535 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.506T>C (p.Leu169Pro) single nucleotide variant not specified [RCV004408587] Chr4:86101952 [GRCh38]
Chr4:87023105 [GRCh37]
Chr4:4q21.3		 uncertain significance
NM_138982.4(MAPK10):c.95A>T (p.Tyr32Phe) single nucleotide variant not specified [RCV004408588] Chr4:86159439 [GRCh38]
Chr4:87080592 [GRCh37]
Chr4:4q21.3		 uncertain significance
GRCh37/hg19 4q21.3(chr4:87162492-87927501)x3 copy number gain not provided [RCV004819481] Chr4:87162492..87927501 [GRCh37]
Chr4:4q21.3		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:6820
Count of miRNA genes:1313
Interacting mature miRNAs:1734
Transcripts:ENST00000310816, ENST00000359221, ENST00000361569, ENST00000395157, ENST00000395160, ENST00000395161, ENST00000395166, ENST00000395169, ENST00000430389, ENST00000449047, ENST00000468020, ENST00000472236, ENST00000475679, ENST00000479377, ENST00000486985, ENST00000489368, ENST00000502302, ENST00000503911, ENST00000504397, ENST00000505356, ENST00000506385, ENST00000506773, ENST00000508262, ENST00000509464, ENST00000511167, ENST00000511328, ENST00000512017, ENST00000512046, ENST00000512564, ENST00000512689, ENST00000513186, ENST00000513839, ENST00000514856, ENST00000515400, ENST00000515650
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597096918GWAS1192992_Hsex hormone-binding globulin measurement QTL GWAS1192992 (human)2e-13sex hormone-binding globulin measurement48626411886264119Human
597142806GWAS1238880_Htriglyceride measurement QTL GWAS1238880 (human)8e-12triglyceride amount (VT:0000187)blood triglyceride level (CMO:0000118)48629825286298253Human
596986132GWAS1105651_Hmean corpuscular hemoglobin concentration QTL GWAS1105651 (human)5e-10mean corpuscular hemoglobin concentration48650359286503593Human
597096593GWAS1192667_Hsex hormone-binding globulin measurement QTL GWAS1192667 (human)6e-12sex hormone-binding globulin measurement48626411886264119Human
597514458GWAS1610532_Hmitogen-activated protein kinase 8 measurement QTL GWAS1610532 (human)0.0000002mitogen-activated protein kinase 8 measurement48632607486326075Human
597437716GWAS1533790_Hnucleotide measurement QTL GWAS1533790 (human)0.000005nucleotide metabolism trait (VT:0003806)48619807186198072Human
406965769GWAS614745_Hperipheral arterial disease QTL GWAS614745 (human)0.000002artery integrity trait (VT:0010639)48631183186311832Human
597607639GWAS1664499_Hgout QTL GWAS1664499 (human)4e-14joint integrity trait (VT:0010548)48632455486324555Human
597344208GWAS1440282_Hcolor vision disorder QTL GWAS1440282 (human)2e-09color vision disorder48623863086238631Human
597054594GWAS1150668_Hmultiple sclerosis QTL GWAS1150668 (human)0.000008multiple sclerosis48659242686592427Human
597097603GWAS1193677_Hsex hormone-binding globulin measurement QTL GWAS1193677 (human)6e-11sex hormone-binding globulin measurement48626411886264119Human
407056022GWAS704998_Hresponse to trauma exposure QTL GWAS704998 (human)0.000004stress-related behavior trait (VT:0010451)48646212386462124Human
597267139GWAS1363213_Htriglyceride measurement QTL GWAS1363213 (human)6e-20triglyceride amount (VT:0000187)blood triglyceride level (CMO:0000118)48631900486319005Human
597057160GWAS1153234_HCleft palate, tobacco smoke exposure measurement, cleft lip, parental genotype effect measurement QTL GWAS1153234 (human)0.000006Cleft palate, tobacco smoke exposure measurement, cleft lip, parental genotype effect measurement48633110686331107Human
597161928GWAS1258002_Hcarbohydrate measurement QTL GWAS1258002 (human)0.00001blood carbohydrate or carbohydrate derivative amount (VT:0010903)48618675586186756Human
597265798GWAS1361872_Htriglyceride measurement QTL GWAS1361872 (human)6e-25triglyceride amount (VT:0000187)blood triglyceride level (CMO:0000118)48637314086373141Human
597097270GWAS1193344_Hsex hormone-binding globulin measurement QTL GWAS1193344 (human)1e-11sex hormone-binding globulin measurement48626411886264119Human
406993635GWAS642611_Hintelligence QTL GWAS642611 (human)0.000007intelligence48635592086355921Human
597265016GWAS1361090_Hhigh density lipoprotein cholesterol measurement QTL GWAS1361090 (human)2e-08blood HDL cholesterol amount (VT:0000184)blood high density lipoprotein cholesterol level (CMO:0000052)48637314086373141Human
597161206GWAS1257280_Hleucine measurement QTL GWAS1257280 (human)2e-10blood amino acid amount (VT:0005311)blood amino acid measurement (CMO:0003730)48655116286551163Human
407148005GWAS796981_Hmigraine disorder QTL GWAS796981 (human)0.000002migraine disorder48655262386552624Human
597332792GWAS1428866_Hurate measurement QTL GWAS1428866 (human)2e-10urate measurementblood uric acid level (CMO:0000501)48632455486324555Human
597242427GWAS1338501_Htriglyceride measurement QTL GWAS1338501 (human)6e-13triglyceride amount (VT:0000187)blood triglyceride level (CMO:0000118)48649227186492272Human
597345788GWAS1441862_Hurate measurement QTL GWAS1441862 (human)6e-10urate measurementblood uric acid level (CMO:0000501)48632455486324555Human
597097724GWAS1193798_Htestosterone measurement QTL GWAS1193798 (human)8e-10blood testosterone amount (VT:0005180)serum testosterone level (CMO:0000568)48630154386301544Human
597202355GWAS1298429_Hlean body mass QTL GWAS1298429 (human)1e-09body lean mass (VT:0010483)total body lean mass (CMO:0003950)48639248186392482Human
597107707GWAS1203781_Hnucleus accumbens volume change measurement QTL GWAS1203781 (human)0.000002nucleus accumbens volume change measurement48626967786269678Human
597614514GWAS1671374_Hgout QTL GWAS1671374 (human)7e-12joint integrity trait (VT:0010548)48632455486324555Human
406958380GWAS607356_Hresponse to gemcitabine QTL GWAS607356 (human)0.000003response to gemcitabine48605843086058431Human
597161465GWAS1257539_Hgut microbiome measurement QTL GWAS1257539 (human)3e-08gut microbiome measurement48615584386155844Human
597175990GWAS1272064_Hmitogen-activated protein kinase 8 measurement QTL GWAS1272064 (human)3e-25mitogen-activated protein kinase 8 measurement48633584086335841Human
597291574GWAS1387648_Hmean corpuscular hemoglobin concentration QTL GWAS1387648 (human)5e-10erythrocyte hemoglobin amount (VT:0010953)mean corpuscular hemoglobin concentration (CMO:0000291)48650359286503593Human
407368561GWAS1017537_Hmammographic density measurement QTL GWAS1017537 (human)0.000008mammary gland morphology trait (VT:0000627)48621161886211619Human
597066016GWAS1162090_Hbreast carcinoma QTL GWAS1162090 (human)0.000004mammary gland integrity trait (VT:0010552)48630203286302033Human
597620520GWAS1677380_Hmental or behavioural disorder QTL GWAS1677380 (human)4e-11behavior trait (VT:0010442)48632320986323210Human
407387263GWAS1036239_Hacute myeloid leukemia QTL GWAS1036239 (human)2e-10leukocyte integrity trait (VT:0010898)48649613886496139Human
597267300GWAS1363374_Hmitogen-activated protein kinase 8 measurement QTL GWAS1363374 (human)1e-14mitogen-activated protein kinase 8 measurement48633537686335377Human

Markers in Region
G01820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,037,731 - 87,037,894UniSTSGRCh37
Build 36487,256,755 - 87,256,918RGDNCBI36
Celera484,326,865 - 84,327,028RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,781,756 - 82,781,919UniSTS
G34449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,123,704 - 87,123,885UniSTSGRCh37
Build 36487,342,728 - 87,342,909RGDNCBI36
Celera484,412,965 - 84,413,146RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,868,100 - 82,868,281UniSTS
SHGC-59777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,936,295 - 86,936,528UniSTSGRCh37
Build 36487,155,319 - 87,155,552RGDNCBI36
Celera484,225,433 - 84,225,666RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,680,171 - 82,680,404UniSTS
GeneMap99-GB4 RH Map4467.36UniSTS
NCBI RH Map41106.7UniSTS
AFMa059xc9  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,277,063 - 87,277,277UniSTSGRCh37
Build 36487,496,087 - 87,496,301RGDNCBI36
Celera484,566,317 - 84,566,531RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef483,021,453 - 83,021,667UniSTS
Whitehead-RH Map4498.5UniSTS
Whitehead-YAC Contig Map4 UniSTS
NCBI RH Map41031.9UniSTS
SHGC-79840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,950,014 - 86,950,295UniSTSGRCh37
Build 36487,169,038 - 87,169,319RGDNCBI36
Celera484,239,151 - 84,239,432RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,694,043 - 82,694,324UniSTS
TNG Radiation Hybrid Map451644.0UniSTS
RH102171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,250,702 - 87,250,843UniSTSGRCh37
Build 36487,469,726 - 87,469,867RGDNCBI36
Celera484,539,956 - 84,540,097RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,995,086 - 82,995,227UniSTS
GeneMap99-GB4 RH Map4453.53UniSTS
SHGC-81500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,976,254 - 86,976,590UniSTSGRCh37
Build 36487,195,278 - 87,195,614RGDNCBI36
Celera484,265,390 - 84,265,726RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,720,284 - 82,720,620UniSTS
TNG Radiation Hybrid Map451644.0UniSTS
RH123938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,020,007 - 87,020,312UniSTSGRCh37
Build 36487,239,031 - 87,239,336RGDNCBI36
Celera484,309,143 - 84,309,448RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,764,029 - 82,764,334UniSTS
TNG Radiation Hybrid Map451744.0UniSTS
D4S2898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,937,828 - 86,937,942UniSTSGRCh37
Build 36487,156,852 - 87,156,966RGDNCBI36
Celera484,226,966 - 84,227,080RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,681,704 - 82,681,818UniSTS
G66840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,239,603 - 87,239,911UniSTSGRCh37
Build 36487,458,627 - 87,458,935RGDNCBI36
Celera484,528,857 - 84,529,165RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,983,986 - 82,984,294UniSTS
D4S1055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,280,355 - 87,280,688UniSTSGRCh37
Build 36487,499,379 - 87,499,712RGDNCBI36
Celera484,569,609 - 84,569,942RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef483,024,745 - 83,025,092UniSTS
Stanford-G3 RH Map44802.0UniSTS
NCBI RH Map41028.0UniSTS
D4S2785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,937,640 - 86,937,941UniSTSGRCh37
Build 36487,156,664 - 87,156,965RGDNCBI36
Celera484,226,778 - 84,227,079RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,681,516 - 82,681,817UniSTS
GeneMap99-GB4 RH Map4456.9UniSTS
Whitehead-RH Map4498.4UniSTS
Whitehead-YAC Contig Map4 UniSTS
SHGC4-1855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,252,281 - 87,252,385UniSTSGRCh37
Build 36487,471,305 - 87,471,409RGDNCBI36
Celera484,541,535 - 84,541,639RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,996,665 - 82,996,769UniSTS
MAPK10_182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,937,577 - 86,938,361UniSTSGRCh37
Build 36487,156,601 - 87,157,385RGDNCBI36
Celera484,226,715 - 84,227,499RGD
HuRef482,681,453 - 82,682,237UniSTS
MARC_31431-31432:1049827311:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,936,824 - 86,937,630UniSTSGRCh37
Build 36487,155,848 - 87,156,654RGDNCBI36
Celera484,225,962 - 84,226,768RGD
HuRef482,680,700 - 82,681,506UniSTS
D4S2469E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,252,250 - 87,252,355UniSTSGRCh37
Build 36487,471,274 - 87,471,379RGDNCBI36
Celera484,541,504 - 84,541,609RGD
HuRef482,996,634 - 82,996,739UniSTS
D4S1153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,123,735 - 87,123,950UniSTSGRCh37
Build 36487,342,759 - 87,342,974RGDNCBI36
Celera484,412,996 - 84,413,211RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,868,131 - 82,868,346UniSTS
SHGC-50852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,985,831 - 86,985,940UniSTSGRCh37
Build 36487,204,855 - 87,204,964RGDNCBI36
Celera484,274,967 - 84,275,076RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,729,860 - 82,729,969UniSTS
TNG Radiation Hybrid Map451644.0UniSTS
G10714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,938,193 - 86,938,440UniSTSGRCh37
Build 36487,157,217 - 87,157,464RGDNCBI36
Celera484,227,331 - 84,227,578RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,682,069 - 82,682,316UniSTS
D4S1019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,982,330 - 86,982,506UniSTSGRCh37
Build 36487,201,354 - 87,201,530RGDNCBI36
Celera484,271,466 - 84,271,642RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,726,359 - 82,726,535UniSTS
TNG Radiation Hybrid Map451644.0UniSTS
Stanford-G3 RH Map44772.0UniSTS
NCBI RH Map41028.0UniSTS
SHGC-7527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,985,805 - 86,985,937UniSTSGRCh37
Build 36487,204,829 - 87,204,961RGDNCBI36
Celera484,274,941 - 84,275,073RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,729,834 - 82,729,966UniSTS
SHGC-24232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37487,280,674 - 87,280,809UniSTSGRCh37
Build 36487,499,698 - 87,499,833RGDNCBI36
Celera484,569,928 - 84,570,063RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef483,025,078 - 83,025,213UniSTS
D4S3161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37486,938,129 - 86,938,474UniSTSGRCh37
Build 36487,157,153 - 87,157,498RGDNCBI36
Celera484,227,267 - 84,227,612RGD
Cytogenetic Map4q22.1-q23UniSTS
HuRef482,682,005 - 82,682,350UniSTS
TNG Radiation Hybrid Map451544.0UniSTS
Whitehead-YAC Contig Map4 UniSTS
GeneMap99-G3 RH Map44756.0UniSTS
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2358 2788 2241 4935 1708 2287 4 607 1563 448 2240 6832 6073 44 3728 845 1708 1571 172 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_013325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005263129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005263130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005263131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005263135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006714268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006714269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017008454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024454149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047415964 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047415965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047415966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047415967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047415968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054350507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054350508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054350509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054350510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001741289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC096953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC108054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC110076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF052141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK124791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX027293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX027295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI549234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB069160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS693282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS693286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS693290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA192997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT585173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U07620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U34819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U34820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000310816   ⟹   ENSP00000309857
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,478 - 86,453,145 (-)Ensembl
Ensembl Acc Id: ENST00000359221   ⟹   ENSP00000352157
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,478 - 86,360,027 (-)Ensembl
Ensembl Acc Id: ENST00000361569   ⟹   ENSP00000355297
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,453,192 (-)Ensembl
Ensembl Acc Id: ENST00000395157   ⟹   ENSP00000378586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,478 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000395160   ⟹   ENSP00000378589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,453,219 (-)Ensembl
Ensembl Acc Id: ENST00000395166   ⟹   ENSP00000378595
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,480 - 86,358,874 (-)Ensembl
Ensembl Acc Id: ENST00000395169   ⟹   ENSP00000378598
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,135 - 86,360,092 (-)Ensembl
Ensembl Acc Id: ENST00000430389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,102,869 - 86,159,334 (-)Ensembl
Ensembl Acc Id: ENST00000449047   ⟹   ENSP00000414469
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,013,874 - 86,194,407 (-)Ensembl
Ensembl Acc Id: ENST00000472236   ⟹   ENSP00000491686
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,095,135 - 86,101,922 (-)Ensembl
Ensembl Acc Id: ENST00000475679
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,106,807 - 86,117,766 (-)Ensembl
Ensembl Acc Id: ENST00000479377   ⟹   ENSP00000492213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,067,849 - 86,107,243 (-)Ensembl
Ensembl Acc Id: ENST00000486985
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,067,836 - 86,117,853 (-)Ensembl
Ensembl Acc Id: ENST00000489368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,067,824 - 86,089,549 (-)Ensembl
Ensembl Acc Id: ENST00000502302   ⟹   ENSP00000423918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,107,288 - 86,594,110 (-)Ensembl
Ensembl Acc Id: ENST00000503911   ⟹   ENSP00000421409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,382 - 86,453,183 (-)Ensembl
Ensembl Acc Id: ENST00000504397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,300,584 - 86,453,046 (-)Ensembl
Ensembl Acc Id: ENST00000505356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,164,446 - 86,359,671 (-)Ensembl
Ensembl Acc Id: ENST00000506773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,050 - 86,594,074 (-)Ensembl
Ensembl Acc Id: ENST00000508262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,480 - 86,101,434 (-)Ensembl
Ensembl Acc Id: ENST00000509464   ⟹   ENSP00000424128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,404 - 86,453,212 (-)Ensembl
Ensembl Acc Id: ENST00000511167   ⟹   ENSP00000422277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,095,331 - 86,354,644 (-)Ensembl
Ensembl Acc Id: ENST00000511328   ⟹   ENSP00000421762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,107,237 - 86,453,180 (-)Ensembl
Ensembl Acc Id: ENST00000512017   ⟹   ENSP00000424755
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,103,220 - 86,453,219 (-)Ensembl
Ensembl Acc Id: ENST00000512046   ⟹   ENSP00000492508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,413 - 86,594,119 (-)Ensembl
Ensembl Acc Id: ENST00000512564   ⟹   ENSP00000422985
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,101,194 - 86,359,694 (-)Ensembl
Ensembl Acc Id: ENST00000512689   ⟹   ENSP00000425654
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,498 - 86,358,512 (-)Ensembl
Ensembl Acc Id: ENST00000513186   ⟹   ENSP00000420987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,604 - 86,594,131 (-)Ensembl
Ensembl Acc Id: ENST00000513839   ⟹   ENSP00000492266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,101,942 - 86,594,110 (-)Ensembl
Ensembl Acc Id: ENST00000514856
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,277,204 - 86,360,224 (-)Ensembl
Ensembl Acc Id: ENST00000515400   ⟹   ENSP00000424154
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,870 - 86,594,074 (-)Ensembl
Ensembl Acc Id: ENST00000515650   ⟹   ENSP00000492204
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,017,177 - 86,360,039 (-)Ensembl
Ensembl Acc Id: ENST00000564854   ⟹   ENSP00000491938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,012,322 - 86,360,064 (-)Ensembl
Ensembl Acc Id: ENST00000638225   ⟹   ENSP00000491866
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,010,395 - 86,360,222 (-)Ensembl
Ensembl Acc Id: ENST00000638313   ⟹   ENSP00000492292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,031 - 86,357,895 (-)Ensembl
Ensembl Acc Id: ENST00000638499   ⟹   ENSP00000491626
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,478 - 86,453,360 (-)Ensembl
Ensembl Acc Id: ENST00000638867   ⟹   ENSP00000490974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,194,394 - 86,453,278 (-)Ensembl
Ensembl Acc Id: ENST00000638946   ⟹   ENSP00000492593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,361 - 86,453,214 (-)Ensembl
Ensembl Acc Id: ENST00000639175   ⟹   ENSP00000491160
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,629 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000639234   ⟹   ENSP00000491306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,628 - 86,360,076 (-)Ensembl
Ensembl Acc Id: ENST00000639242   ⟹   ENSP00000491089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,935 - 86,357,889 (-)Ensembl
Ensembl Acc Id: ENST00000639930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,480 - 86,107,653 (-)Ensembl
Ensembl Acc Id: ENST00000639972   ⟹   ENSP00000492809
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,154 - 86,453,225 (-)Ensembl
Ensembl Acc Id: ENST00000639989   ⟹   ENSP00000491462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,107,318 - 86,453,194 (-)Ensembl
Ensembl Acc Id: ENST00000640064   ⟹   ENSP00000491414
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,757 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000640445   ⟹   ENSP00000491304
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,298 - 86,453,185 (-)Ensembl
Ensembl Acc Id: ENST00000640490   ⟹   ENSP00000492484
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,490 - 86,360,028 (-)Ensembl
Ensembl Acc Id: ENST00000640527   ⟹   ENSP00000491389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,401 - 86,594,110 (-)Ensembl
Ensembl Acc Id: ENST00000640544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,277,090 - 86,453,360 (-)Ensembl
Ensembl Acc Id: ENST00000640858   ⟹   ENSP00000491122
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,358,874 (-)Ensembl
Ensembl Acc Id: ENST00000640970   ⟹   ENSP00000492231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,358,566 (-)Ensembl
Ensembl Acc Id: ENST00000641010   ⟹   ENSP00000493178
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl485,990,007 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641016   ⟹   ENSP00000493210
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,382 - 86,453,203 (-)Ensembl
Ensembl Acc Id: ENST00000641020   ⟹   ENSP00000493377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641022
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,191,598 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641032   ⟹   ENSP00000493356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,629 - 86,277,129 (-)Ensembl
Ensembl Acc Id: ENST00000641037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,326,329 - 86,457,985 (-)Ensembl
Ensembl Acc Id: ENST00000641041   ⟹   ENSP00000493339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,453,138 (-)Ensembl
Ensembl Acc Id: ENST00000641047   ⟹   ENSP00000493455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,436 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641050   ⟹   ENSP00000493270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,945 - 86,594,062 (-)Ensembl
Ensembl Acc Id: ENST00000641051   ⟹   ENSP00000493275
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,013,874 - 86,594,625 (-)Ensembl
Ensembl Acc Id: ENST00000641052   ⟹   ENSP00000493407
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,042 - 86,360,222 (-)Ensembl
Ensembl Acc Id: ENST00000641058
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,480 - 86,065,603 (-)Ensembl
Ensembl Acc Id: ENST00000641061   ⟹   ENSP00000493274
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,358 - 86,354,628 (-)Ensembl
Ensembl Acc Id: ENST00000641066   ⟹   ENSP00000493072
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,012,491 - 86,358,509 (-)Ensembl
Ensembl Acc Id: ENST00000641072   ⟹   ENSP00000493080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,029,212 - 86,360,025 (-)Ensembl
Ensembl Acc Id: ENST00000641080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,191,641 - 86,453,212 (-)Ensembl
Ensembl Acc Id: ENST00000641101
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,067,844 - 86,082,344 (-)Ensembl
Ensembl Acc Id: ENST00000641102   ⟹   ENSP00000493048
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl485,999,848 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641108
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,064,355 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641110   ⟹   ENSP00000493163
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,503 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641116   ⟹   ENSP00000492976
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,428 - 86,357,740 (-)Ensembl
Ensembl Acc Id: ENST00000641120   ⟹   ENSP00000493259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,453,197 (-)Ensembl
Ensembl Acc Id: ENST00000641126
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,123,693 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000641130
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,534 - 86,031,972 (-)Ensembl
Ensembl Acc Id: ENST00000641142
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,102,013 - 86,107,564 (-)Ensembl
Ensembl Acc Id: ENST00000641148   ⟹   ENSP00000493022
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,629 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641157   ⟹   ENSP00000493363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,534 - 86,594,088 (-)Ensembl
Ensembl Acc Id: ENST00000641166   ⟹   ENSP00000493350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,490 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641170   ⟹   ENSP00000493237
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,086 - 86,453,436 (-)Ensembl
Ensembl Acc Id: ENST00000641184
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,017,065 - 86,117,846 (-)Ensembl
Ensembl Acc Id: ENST00000641195
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,644 - 86,171,072 (-)Ensembl
Ensembl Acc Id: ENST00000641203   ⟹   ENSP00000493409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,067,812 - 86,453,219 (-)Ensembl
Ensembl Acc Id: ENST00000641207   ⟹   ENSP00000493450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,360,062 (-)Ensembl
Ensembl Acc Id: ENST00000641208   ⟹   ENSP00000492922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,010,431 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000641217   ⟹   ENSP00000493313
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,960 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641221   ⟹   ENSP00000492956
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,490 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641227   ⟹   ENSP00000493078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,107,283 - 86,268,569 (-)Ensembl
Ensembl Acc Id: ENST00000641237   ⟹   ENSP00000493215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,326,557 (-)Ensembl
Ensembl Acc Id: ENST00000641253   ⟹   ENSP00000493361
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,360,038 (-)Ensembl
Ensembl Acc Id: ENST00000641255
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,352,172 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641265   ⟹   ENSP00000493306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000641273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,124,359 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641274   ⟹   ENSP00000492929
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,604 - 86,453,130 (-)Ensembl
Ensembl Acc Id: ENST00000641283   ⟹   ENSP00000493444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,075 - 86,384,229 (-)Ensembl
Ensembl Acc Id: ENST00000641287   ⟹   ENSP00000493100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,212 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641297   ⟹   ENSP00000493092
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,132 - 86,453,370 (-)Ensembl
Ensembl Acc Id: ENST00000641300
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,459 - 86,453,216 (-)Ensembl
Ensembl Acc Id: ENST00000641306   ⟹   ENSP00000493125
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,799 - 86,359,997 (-)Ensembl
Ensembl Acc Id: ENST00000641313   ⟹   ENSP00000493204
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,453,325 (-)Ensembl
Ensembl Acc Id: ENST00000641317   ⟹   ENSP00000493336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,478 - 86,360,014 (-)Ensembl
Ensembl Acc Id: ENST00000641324   ⟹   ENSP00000492888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl485,990,138 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641341   ⟹   ENSP00000493290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,031 - 86,357,722 (-)Ensembl
Ensembl Acc Id: ENST00000641345
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,067,886 - 86,091,470 (-)Ensembl
Ensembl Acc Id: ENST00000641347
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,095,426 - 86,119,538 (-)Ensembl
Ensembl Acc Id: ENST00000641358   ⟹   ENSP00000493394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,490 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl485,991,108 - 86,003,704 (-)Ensembl
Ensembl Acc Id: ENST00000641379   ⟹   ENSP00000492996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,360,055 (-)Ensembl
Ensembl Acc Id: ENST00000641384   ⟹   ENSP00000492898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,532 - 86,453,075 (-)Ensembl
Ensembl Acc Id: ENST00000641385   ⟹   ENSP00000493169
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,221 - 86,453,196 (-)Ensembl
Ensembl Acc Id: ENST00000641391   ⟹   ENSP00000493008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,499 - 86,594,088 (-)Ensembl
Ensembl Acc Id: ENST00000641405   ⟹   ENSP00000493009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,367 - 86,359,731 (-)Ensembl
Ensembl Acc Id: ENST00000641408   ⟹   ENSP00000492998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,422 - 86,360,092 (-)Ensembl
Ensembl Acc Id: ENST00000641410   ⟹   ENSP00000493208
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,012,501 - 86,360,014 (-)Ensembl
Ensembl Acc Id: ENST00000641430   ⟹   ENSP00000492972
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,340,450 (-)Ensembl
Ensembl Acc Id: ENST00000641435   ⟹   ENSP00000493067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,478 - 86,453,138 (-)Ensembl
Ensembl Acc Id: ENST00000641452   ⟹   ENSP00000493403
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641459   ⟹   ENSP00000493360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,360,058 (-)Ensembl
Ensembl Acc Id: ENST00000641462   ⟹   ENSP00000493435
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,010,405 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641467   ⟹   ENSP00000493381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,734 - 86,359,911 (-)Ensembl
Ensembl Acc Id: ENST00000641485   ⟹   ENSP00000493378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,026,436 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641493   ⟹   ENSP00000493094
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,952 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000641531   ⟹   ENSP00000493214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,017,082 - 86,359,849 (-)Ensembl
Ensembl Acc Id: ENST00000641537   ⟹   ENSP00000493329
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,486 - 86,360,089 (-)Ensembl
Ensembl Acc Id: ENST00000641543
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,095,602 - 86,117,827 (-)Ensembl
Ensembl Acc Id: ENST00000641550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,300,592 - 86,359,984 (-)Ensembl
Ensembl Acc Id: ENST00000641553   ⟹   ENSP00000492913
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,161 - 86,360,083 (-)Ensembl
Ensembl Acc Id: ENST00000641555   ⟹   ENSP00000493395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,359,842 (-)Ensembl
Ensembl Acc Id: ENST00000641561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,158 - 86,360,103 (-)Ensembl
Ensembl Acc Id: ENST00000641563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,095,177 - 86,359,822 (-)Ensembl
Ensembl Acc Id: ENST00000641595   ⟹   ENSP00000493413
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,017,225 - 86,359,665 (-)Ensembl
Ensembl Acc Id: ENST00000641607   ⟹   ENSP00000492920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,486 - 86,360,050 (-)Ensembl
Ensembl Acc Id: ENST00000641609   ⟹   ENSP00000493400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,533 - 86,358,586 (-)Ensembl
Ensembl Acc Id: ENST00000641620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,193,776 - 86,360,092 (-)Ensembl
Ensembl Acc Id: ENST00000641629   ⟹   ENSP00000493165
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,103,213 - 86,453,165 (-)Ensembl
Ensembl Acc Id: ENST00000641634   ⟹   ENSP00000493428
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,015 - 86,453,185 (-)Ensembl
Ensembl Acc Id: ENST00000641647   ⟹   ENSP00000493375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,969 - 86,360,058 (-)Ensembl
Ensembl Acc Id: ENST00000641653   ⟹   ENSP00000493225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,618 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641656   ⟹   ENSP00000493414
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,629 - 86,159,466 (-)Ensembl
Ensembl Acc Id: ENST00000641657   ⟹   ENSP00000493105
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,269 - 86,453,387 (-)Ensembl
Ensembl Acc Id: ENST00000641675   ⟹   ENSP00000493358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,446 - 86,453,185 (-)Ensembl
Ensembl Acc Id: ENST00000641677   ⟹   ENSP00000493368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,503 - 86,360,072 (-)Ensembl
Ensembl Acc Id: ENST00000641718   ⟹   ENSP00000493344
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,143 - 86,453,174 (-)Ensembl
Ensembl Acc Id: ENST00000641724   ⟹   ENSP00000493038
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,368 - 86,360,048 (-)Ensembl
Ensembl Acc Id: ENST00000641737   ⟹   ENSP00000493177
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,594,110 (-)Ensembl
Ensembl Acc Id: ENST00000641762   ⟹   ENSP00000492926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,360,058 (-)Ensembl
Ensembl Acc Id: ENST00000641763
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,124,333 - 86,453,142 (-)Ensembl
Ensembl Acc Id: ENST00000641767   ⟹   ENSP00000493309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,269 - 86,357,791 (-)Ensembl
Ensembl Acc Id: ENST00000641777   ⟹   ENSP00000493032
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,091 - 86,360,058 (-)Ensembl
Ensembl Acc Id: ENST00000641782   ⟹   ENSP00000493117
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,194,380 - 86,453,174 (-)Ensembl
Ensembl Acc Id: ENST00000641798   ⟹   ENSP00000493258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,125,122 - 86,360,028 (-)Ensembl
Ensembl Acc Id: ENST00000641803   ⟹   ENSP00000493049
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,010,608 - 86,358,527 (-)Ensembl
Ensembl Acc Id: ENST00000641823   ⟹   ENSP00000493408
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,487 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641824
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,002 - 86,032,578 (-)Ensembl
Ensembl Acc Id: ENST00000641826   ⟹   ENSP00000493294
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,101,986 - 86,360,083 (-)Ensembl
Ensembl Acc Id: ENST00000641831   ⟹   ENSP00000492886
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,522 - 86,594,062 (-)Ensembl
Ensembl Acc Id: ENST00000641854   ⟹   ENSP00000493030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,075 - 86,453,196 (-)Ensembl
Ensembl Acc Id: ENST00000641855   ⟹   ENSP00000493426
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,107,343 - 86,359,834 (-)Ensembl
Ensembl Acc Id: ENST00000641858   ⟹   ENSP00000492938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,020,222 - 86,031,431 (-)Ensembl
Ensembl Acc Id: ENST00000641862   ⟹   ENSP00000493396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,502 - 86,453,185 (-)Ensembl
Ensembl Acc Id: ENST00000641864   ⟹   ENSP00000493451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,026,509 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641873   ⟹   ENSP00000492967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,064,337 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641881   ⟹   ENSP00000492912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,119 - 86,101,992 (-)Ensembl
Ensembl Acc Id: ENST00000641902   ⟹   ENSP00000492903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,153 - 86,453,203 (-)Ensembl
Ensembl Acc Id: ENST00000641903   ⟹   ENSP00000492988
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,010,453 - 86,360,051 (-)Ensembl
Ensembl Acc Id: ENST00000641907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,158 - 86,453,144 (-)Ensembl
Ensembl Acc Id: ENST00000641911   ⟹   ENSP00000493374
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,771 - 86,360,010 (-)Ensembl
Ensembl Acc Id: ENST00000641917   ⟹   ENSP00000493051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,488 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000641943   ⟹   ENSP00000492941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,231 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000641952   ⟹   ENSP00000493013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,013,880 - 86,453,374 (-)Ensembl
Ensembl Acc Id: ENST00000641954   ⟹   ENSP00000493310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,023,931 - 86,360,055 (-)Ensembl
Ensembl Acc Id: ENST00000641983   ⟹   ENSP00000493045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,012,478 - 86,358,586 (-)Ensembl
Ensembl Acc Id: ENST00000641985
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,445 - 86,357,740 (-)Ensembl
Ensembl Acc Id: ENST00000641989   ⟹   ENSP00000493206
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,493 - 86,358,128 (-)Ensembl
Ensembl Acc Id: ENST00000641997   ⟹   ENSP00000493064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,979 - 86,360,043 (-)Ensembl
Ensembl Acc Id: ENST00000642006   ⟹   ENSP00000493199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,250 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000642009   ⟹   ENSP00000493168
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,536 - 86,453,103 (-)Ensembl
Ensembl Acc Id: ENST00000642013   ⟹   ENSP00000492904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,044,540 - 86,354,582 (-)Ensembl
Ensembl Acc Id: ENST00000642015   ⟹   ENSP00000493040
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,937 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000642019   ⟹   ENSP00000493239
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,064,337 - 86,453,319 (-)Ensembl
Ensembl Acc Id: ENST00000642023   ⟹   ENSP00000493447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,503 - 86,453,197 (-)Ensembl
Ensembl Acc Id: ENST00000642032   ⟹   ENSP00000493373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,962 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000642033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,491 - 86,160,519 (-)Ensembl
Ensembl Acc Id: ENST00000642035   ⟹   ENSP00000493176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,012,491 - 86,453,174 (-)Ensembl
Ensembl Acc Id: ENST00000642038   ⟹   ENSP00000492942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,016,490 - 86,357,732 (-)Ensembl
Ensembl Acc Id: ENST00000642048   ⟹   ENSP00000492980
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,366 - 86,453,399 (-)Ensembl
Ensembl Acc Id: ENST00000642049
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,159,298 - 86,453,162 (-)Ensembl
Ensembl Acc Id: ENST00000642060   ⟹   ENSP00000493282
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,010,431 - 86,360,053 (-)Ensembl
Ensembl Acc Id: ENST00000642081   ⟹   ENSP00000493249
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,107,243 - 86,358,488 (-)Ensembl
Ensembl Acc Id: ENST00000642098
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,100,479 - 86,360,059 (-)Ensembl
Ensembl Acc Id: ENST00000642103   ⟹   ENSP00000493001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,015,976 - 86,360,060 (-)Ensembl
Ensembl Acc Id: ENST00000642136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl486,191,608 - 86,357,695 (-)Ensembl
RefSeq Acc Id: NM_001318067   ⟹   NP_001304996
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,012,296 - 86,354,644 (-)NCBI
CHM1_1486,910,143 - 87,252,290 (-)NCBI
T2T-CHM13v2.0489,341,768 - 89,684,122 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001318068   ⟹   NP_001304997
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,012,296 - 86,370,867 (-)NCBI
CHM1_1486,910,143 - 87,268,515 (-)NCBI
T2T-CHM13v2.0489,341,768 - 89,700,340 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001318069   ⟹   NP_001304998
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,360,053 (-)NCBI
CHM1_1486,910,143 - 87,257,866 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,689,527 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351624   ⟹   NP_001338553
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,360,053 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,689,527 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351625   ⟹   NP_001338554
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,360,053 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,689,527 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363657   ⟹   NP_001350586
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,360,053 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,689,527 (-)NCBI
Sequence:
RefSeq Acc Id: NM_002753   ⟹   NP_002744
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,453,195 (-)NCBI
GRCh37486,933,452 - 87,374,283 (-)NCBI
Build 36487,156,656 - 87,593,307 (-)NCBI Archive
HuRef482,680,152 - 83,118,708 (-)NCBI
CHM1_1486,910,143 - 87,350,773 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,782,667 (-)NCBI
Sequence:
RefSeq Acc Id: NM_138980   ⟹   NP_620446
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,360,053 (-)NCBI
GRCh37486,933,452 - 87,374,283 (-)NCBI
Build 36487,156,656 - 87,500,240 (-)NCBI Archive
HuRef482,680,152 - 83,118,708 (-)NCBI
CHM1_1486,910,143 - 87,257,866 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,689,527 (-)NCBI
Sequence:
RefSeq Acc Id: NM_138982   ⟹   NP_620448
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,360,053 (-)NCBI
GRCh37486,933,452 - 87,374,283 (-)NCBI
Build 36487,156,656 - 87,494,767 (-)NCBI Archive
HuRef482,680,152 - 83,118,708 (-)NCBI
CHM1_1486,910,143 - 87,257,866 (-)NCBI
T2T-CHM13v2.0489,339,877 - 89,689,527 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047415964   ⟹   XP_047271920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,010,405 - 86,594,074 (-)NCBI
RefSeq Acc Id: XM_047415965   ⟹   XP_047271921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,098,602 - 86,594,074 (-)NCBI
RefSeq Acc Id: XM_047415966   ⟹   XP_047271922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,093,364 - 86,594,074 (-)NCBI
RefSeq Acc Id: XM_047415967   ⟹   XP_047271923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,093,364 - 86,594,074 (-)NCBI
RefSeq Acc Id: XM_047415968   ⟹   XP_047271924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,097,107 - 86,594,074 (-)NCBI
RefSeq Acc Id: XM_054350507   ⟹   XP_054206482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0489,339,877 - 89,923,582 (-)NCBI
RefSeq Acc Id: XM_054350508   ⟹   XP_054206483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0489,428,049 - 89,923,587 (-)NCBI
RefSeq Acc Id: XM_054350509   ⟹   XP_054206484
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0489,424,800 - 89,923,585 (-)NCBI
RefSeq Acc Id: XM_054350510   ⟹   XP_054206485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0489,424,800 - 89,923,584 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001304996 (Get FASTA)   NCBI Sequence Viewer  
  NP_001304997 (Get FASTA)   NCBI Sequence Viewer  
  NP_001304998 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338553 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338554 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350586 (Get FASTA)   NCBI Sequence Viewer  
  NP_002744 (Get FASTA)   NCBI Sequence Viewer  
  NP_620446 (Get FASTA)   NCBI Sequence Viewer  
  NP_620448 (Get FASTA)   NCBI Sequence Viewer  
  XP_047271920 (Get FASTA)   NCBI Sequence Viewer  
  XP_047271921 (Get FASTA)   NCBI Sequence Viewer  
  XP_047271922 (Get FASTA)   NCBI Sequence Viewer  
  XP_047271923 (Get FASTA)   NCBI Sequence Viewer  
  XP_047271924 (Get FASTA)   NCBI Sequence Viewer  
  XP_054206482 (Get FASTA)   NCBI Sequence Viewer  
  XP_054206483 (Get FASTA)   NCBI Sequence Viewer  
  XP_054206484 (Get FASTA)   NCBI Sequence Viewer  
  XP_054206485 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC50101 (Get FASTA)   NCBI Sequence Viewer  
  AAC50604 (Get FASTA)   NCBI Sequence Viewer  
  AAC50605 (Get FASTA)   NCBI Sequence Viewer  
  AAH35057 (Get FASTA)   NCBI Sequence Viewer  
  AAH51731 (Get FASTA)   NCBI Sequence Viewer  
  AAH65516 (Get FASTA)   NCBI Sequence Viewer  
  BAG51956 (Get FASTA)   NCBI Sequence Viewer  
  BAG52284 (Get FASTA)   NCBI Sequence Viewer  
  BAG54096 (Get FASTA)   NCBI Sequence Viewer  
  BAH11677 (Get FASTA)   NCBI Sequence Viewer  
  CAC09125 (Get FASTA)   NCBI Sequence Viewer  
  CAC09126 (Get FASTA)   NCBI Sequence Viewer  
  CAP12256 (Get FASTA)   NCBI Sequence Viewer  
  CAP12257 (Get FASTA)   NCBI Sequence Viewer  
  CAP12259 (Get FASTA)   NCBI Sequence Viewer  
  EAX05962 (Get FASTA)   NCBI Sequence Viewer  
  EAX05963 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000352157
  ENSP00000378586.4
  ENSP00000378595.1
  ENSP00000414469
  ENSP00000422277
  ENSP00000424154.3
  ENSP00000491089.1
  ENSP00000491122.1
  ENSP00000491160.1
  ENSP00000491306.1
  ENSP00000491866
  ENSP00000491866.1
  ENSP00000492204.1
  ENSP00000492231.1
  ENSP00000492292.1
  ENSP00000492903.1
  ENSP00000492922
  ENSP00000492929.1
  ENSP00000492941.1
  ENSP00000492942.1
  ENSP00000493001.1
  ENSP00000493008.1
  ENSP00000493013.1
  ENSP00000493038.1
  ENSP00000493040
  ENSP00000493040.1
  ENSP00000493045.1
  ENSP00000493049.1
  ENSP00000493072.1
  ENSP00000493092.1
  ENSP00000493100.1
  ENSP00000493105.1
  ENSP00000493163.1
  ENSP00000493168.1
  ENSP00000493177.1
  ENSP00000493208.1
  ENSP00000493237
  ENSP00000493237.1
  ENSP00000493270.1
  ENSP00000493275.1
  ENSP00000493290.1
  ENSP00000493344
  ENSP00000493363.1
  ENSP00000493374.1
  ENSP00000493375.1
  ENSP00000493396.1
  ENSP00000493408.1
  ENSP00000493435
  ENSP00000493435.1
  ENSP00000493444.1
  ENSP00000493450.1
GenBank Protein P53779 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_620448   ⟸   NM_138982
- Peptide Label: isoform 1
- UniProtKB: Q15707 (UniProtKB/Swiss-Prot),   B3KQ94 (UniProtKB/Swiss-Prot),   A6NG28 (UniProtKB/Swiss-Prot),   A6NFS3 (UniProtKB/Swiss-Prot),   Q49AP1 (UniProtKB/Swiss-Prot),   P53779 (UniProtKB/Swiss-Prot),   A0A286YFA6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_620446   ⟸   NM_138980
- Peptide Label: isoform 3
- UniProtKB: A0A286YEN5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_002744   ⟸   NM_002753
- Peptide Label: isoform 2
- UniProtKB: A0A286YFJ4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001304997   ⟸   NM_001318068
- Peptide Label: isoform 6
- UniProtKB: Q499Y8 (UniProtKB/TrEMBL),   B7Z1Z1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001304998   ⟸   NM_001318069
- Peptide Label: isoform 1x
- UniProtKB: F8W9R5 (UniProtKB/TrEMBL),   A0A286YFA6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001304996   ⟸   NM_001318067
- Peptide Label: isoform 5
- UniProtKB: A0A286YF97 (UniProtKB/TrEMBL),   A0A286YFA6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001338553   ⟸   NM_001351624
- Peptide Label: isoform 3
- UniProtKB: A0A286YEN5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001338554   ⟸   NM_001351625
- Peptide Label: isoform 7
- UniProtKB: D6RJF9 (UniProtKB/TrEMBL),   A0A286YFI3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001350586   ⟸   NM_001363657
- Peptide Label: isoform 8
- UniProtKB: A0A286YEQ0 (UniProtKB/TrEMBL),   A0A286YFI3 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000352157   ⟸   ENST00000359221
Ensembl Acc Id: ENSP00000423918   ⟸   ENST00000502302
Ensembl Acc Id: ENSP00000421409   ⟸   ENST00000503911
Ensembl Acc Id: ENSP00000492213   ⟸   ENST00000479377
Ensembl Acc Id: ENSP00000490974   ⟸   ENST00000638867
Ensembl Acc Id: ENSP00000491626   ⟸   ENST00000638499
Ensembl Acc Id: ENSP00000492593   ⟸   ENST00000638946
Ensembl Acc Id: ENSP00000492292   ⟸   ENST00000638313
Ensembl Acc Id: ENSP00000491866   ⟸   ENST00000638225
Ensembl Acc Id: ENSP00000492809   ⟸   ENST00000639972
Ensembl Acc Id: ENSP00000491462   ⟸   ENST00000639989
Ensembl Acc Id: ENSP00000355297   ⟸   ENST00000361569
Ensembl Acc Id: ENSP00000491089   ⟸   ENST00000639242
Ensembl Acc Id: ENSP00000491306   ⟸   ENST00000639234
Ensembl Acc Id: ENSP00000491160   ⟸   ENST00000639175
Ensembl Acc Id: ENSP00000424128   ⟸   ENST00000509464
Ensembl Acc Id: ENSP00000309857   ⟸   ENST00000310816
Ensembl Acc Id: ENSP00000492231   ⟸   ENST00000640970
Ensembl Acc Id: ENSP00000491122   ⟸   ENST00000640858
Ensembl Acc Id: ENSP00000491414   ⟸   ENST00000640064
Ensembl Acc Id: ENSP00000491389   ⟸   ENST00000640527
Ensembl Acc Id: ENSP00000491304   ⟸   ENST00000640445
Ensembl Acc Id: ENSP00000492484   ⟸   ENST00000640490
Ensembl Acc Id: ENSP00000493259   ⟸   ENST00000641120
Ensembl Acc Id: ENSP00000493163   ⟸   ENST00000641110
Ensembl Acc Id: ENSP00000492976   ⟸   ENST00000641116
Ensembl Acc Id: ENSP00000493048   ⟸   ENST00000641102
Ensembl Acc Id: ENSP00000493237   ⟸   ENST00000641170
Ensembl Acc Id: ENSP00000493350   ⟸   ENST00000641166
Ensembl Acc Id: ENSP00000493363   ⟸   ENST00000641157
Ensembl Acc Id: ENSP00000493022   ⟸   ENST00000641148
Ensembl Acc Id: ENSP00000493080   ⟸   ENST00000641072
Ensembl Acc Id: ENSP00000493072   ⟸   ENST00000641066
Ensembl Acc Id: ENSP00000493178   ⟸   ENST00000641010
Ensembl Acc Id: ENSP00000493210   ⟸   ENST00000641016
Ensembl Acc Id: ENSP00000493274   ⟸   ENST00000641061
Ensembl Acc Id: ENSP00000493407   ⟸   ENST00000641052
Ensembl Acc Id: ENSP00000493270   ⟸   ENST00000641050
Ensembl Acc Id: ENSP00000493275   ⟸   ENST00000641051
Ensembl Acc Id: ENSP00000493455   ⟸   ENST00000641047
Ensembl Acc Id: ENSP00000493339   ⟸   ENST00000641041
Ensembl Acc Id: ENSP00000493356   ⟸   ENST00000641032
Ensembl Acc Id: ENSP00000493377   ⟸   ENST00000641020
Ensembl Acc Id: ENSP00000492920   ⟸   ENST00000641607
Ensembl Acc Id: ENSP00000493400   ⟸   ENST00000641609
Ensembl Acc Id: ENSP00000493214   ⟸   ENST00000641531
Ensembl Acc Id: ENSP00000493329   ⟸   ENST00000641537
Ensembl Acc Id: ENSP00000492913   ⟸   ENST00000641553
Ensembl Acc Id: ENSP00000493395   ⟸   ENST00000641555
Ensembl Acc Id: ENSP00000493413   ⟸   ENST00000641595
Ensembl Acc Id: ENSP00000493208   ⟸   ENST00000641410
Ensembl Acc Id: ENSP00000493009   ⟸   ENST00000641405
Ensembl Acc Id: ENSP00000492998   ⟸   ENST00000641408
Ensembl Acc Id: ENSP00000493403   ⟸   ENST00000641452
Ensembl Acc Id: ENSP00000493360   ⟸   ENST00000641459
Ensembl Acc Id: ENSP00000492972   ⟸   ENST00000641430
Ensembl Acc Id: ENSP00000493067   ⟸   ENST00000641435
Ensembl Acc Id: ENSP00000493094   ⟸   ENST00000641493
Ensembl Acc Id: ENSP00000493378   ⟸   ENST00000641485
Ensembl Acc Id: ENSP00000493435   ⟸   ENST00000641462
Ensembl Acc Id: ENSP00000493381   ⟸   ENST00000641467
Ensembl Acc Id: ENSP00000492888   ⟸   ENST00000641324
Ensembl Acc Id: ENSP00000493336   ⟸   ENST00000641317
Ensembl Acc Id: ENSP00000493204   ⟸   ENST00000641313
Ensembl Acc Id: ENSP00000493125   ⟸   ENST00000641306
Ensembl Acc Id: ENSP00000492996   ⟸   ENST00000641379
Ensembl Acc Id: ENSP00000493394   ⟸   ENST00000641358
Ensembl Acc Id: ENSP00000493290   ⟸   ENST00000641341
Ensembl Acc Id: ENSP00000493008   ⟸   ENST00000641391
Ensembl Acc Id: ENSP00000493169   ⟸   ENST00000641385
Ensembl Acc Id: ENSP00000492898   ⟸   ENST00000641384
Ensembl Acc Id: ENSP00000493313   ⟸   ENST00000641217
Ensembl Acc Id: ENSP00000492922   ⟸   ENST00000641208
Ensembl Acc Id: ENSP00000493450   ⟸   ENST00000641207
Ensembl Acc Id: ENSP00000493409   ⟸   ENST00000641203
Ensembl Acc Id: ENSP00000493361   ⟸   ENST00000641253
Ensembl Acc Id: ENSP00000493215   ⟸   ENST00000641237
Ensembl Acc Id: ENSP00000492956   ⟸   ENST00000641221
Ensembl Acc Id: ENSP00000493078   ⟸   ENST00000641227
Ensembl Acc Id: ENSP00000493092   ⟸   ENST00000641297
Ensembl Acc Id: ENSP00000493100   ⟸   ENST00000641287
Ensembl Acc Id: ENSP00000493444   ⟸   ENST00000641283
Ensembl Acc Id: ENSP00000492929   ⟸   ENST00000641274
Ensembl Acc Id: ENSP00000493306   ⟸   ENST00000641265
Ensembl Acc Id: ENSP00000493064   ⟸   ENST00000641997
Ensembl Acc Id: ENSP00000493045   ⟸   ENST00000641983
Ensembl Acc Id: ENSP00000493206   ⟸   ENST00000641989
Ensembl Acc Id: ENSP00000493051   ⟸   ENST00000641917
Ensembl Acc Id: ENSP00000493374   ⟸   ENST00000641911
Ensembl Acc Id: ENSP00000492988   ⟸   ENST00000641903
Ensembl Acc Id: ENSP00000492903   ⟸   ENST00000641902
Ensembl Acc Id: ENSP00000493013   ⟸   ENST00000641952
Ensembl Acc Id: ENSP00000493310   ⟸   ENST00000641954
Ensembl Acc Id: ENSP00000492941   ⟸   ENST00000641943
Ensembl Acc Id: ENSP00000492912   ⟸   ENST00000641881
Ensembl Acc Id: ENSP00000492967   ⟸   ENST00000641873
Ensembl Acc Id: ENSP00000493396   ⟸   ENST00000641862
Ensembl Acc Id: ENSP00000493451   ⟸   ENST00000641864
Ensembl Acc Id: ENSP00000493049   ⟸   ENST00000641803
Ensembl Acc Id: ENSP00000492938   ⟸   ENST00000641858
Ensembl Acc Id: ENSP00000493426   ⟸   ENST00000641855
Ensembl Acc Id: ENSP00000493030   ⟸   ENST00000641854
Ensembl Acc Id: ENSP00000492886   ⟸   ENST00000641831
Ensembl Acc Id: ENSP00000493408   ⟸   ENST00000641823
Ensembl Acc Id: ENSP00000493294   ⟸   ENST00000641826
Ensembl Acc Id: ENSP00000493032   ⟸   ENST00000641777
Ensembl Acc Id: ENSP00000492926   ⟸   ENST00000641762
Ensembl Acc Id: ENSP00000493309   ⟸   ENST00000641767
Ensembl Acc Id: ENSP00000493258   ⟸   ENST00000641798
Ensembl Acc Id: ENSP00000493117   ⟸   ENST00000641782
Ensembl Acc Id: ENSP00000493177   ⟸   ENST00000641737
Ensembl Acc Id: ENSP00000493038   ⟸   ENST00000641724
Ensembl Acc Id: ENSP00000493344   ⟸   ENST00000641718
Ensembl Acc Id: ENSP00000493225   ⟸   ENST00000641653
Ensembl Acc Id: ENSP00000493105   ⟸   ENST00000641657
Ensembl Acc Id: ENSP00000493414   ⟸   ENST00000641656
Ensembl Acc Id: ENSP00000493375   ⟸   ENST00000641647
Ensembl Acc Id: ENSP00000493428   ⟸   ENST00000641634
Ensembl Acc Id: ENSP00000493165   ⟸   ENST00000641629
Ensembl Acc Id: ENSP00000493358   ⟸   ENST00000641675
Ensembl Acc Id: ENSP00000493368   ⟸   ENST00000641677
Ensembl Acc Id: ENSP00000493282   ⟸   ENST00000642060
Ensembl Acc Id: ENSP00000492980   ⟸   ENST00000642048
Ensembl Acc Id: ENSP00000493176   ⟸   ENST00000642035
Ensembl Acc Id: ENSP00000492942   ⟸   ENST00000642038
Ensembl Acc Id: ENSP00000493373   ⟸   ENST00000642032
Ensembl Acc Id: ENSP00000493249   ⟸   ENST00000642081
Ensembl Acc Id: ENSP00000493447   ⟸   ENST00000642023
Ensembl Acc Id: ENSP00000492904   ⟸   ENST00000642013
Ensembl Acc Id: ENSP00000493040   ⟸   ENST00000642015
Ensembl Acc Id: ENSP00000493239   ⟸   ENST00000642019
Ensembl Acc Id: ENSP00000493199   ⟸   ENST00000642006
Ensembl Acc Id: ENSP00000493168   ⟸   ENST00000642009
Ensembl Acc Id: ENSP00000493001   ⟸   ENST00000642103
Ensembl Acc Id: ENSP00000421762   ⟸   ENST00000511328
Ensembl Acc Id: ENSP00000491938   ⟸   ENST00000564854
Ensembl Acc Id: ENSP00000422277   ⟸   ENST00000511167
Ensembl Acc Id: ENSP00000491686   ⟸   ENST00000472236
Ensembl Acc Id: ENSP00000425654   ⟸   ENST00000512689
Ensembl Acc Id: ENSP00000422985   ⟸   ENST00000512564
Ensembl Acc Id: ENSP00000424755   ⟸   ENST00000512017
Ensembl Acc Id: ENSP00000492508   ⟸   ENST00000512046
Ensembl Acc Id: ENSP00000378586   ⟸   ENST00000395157
Ensembl Acc Id: ENSP00000378598   ⟸   ENST00000395169
Ensembl Acc Id: ENSP00000378595   ⟸   ENST00000395166
Ensembl Acc Id: ENSP00000378589   ⟸   ENST00000395160
Ensembl Acc Id: ENSP00000414469   ⟸   ENST00000449047
Ensembl Acc Id: ENSP00000492266   ⟸   ENST00000513839
Ensembl Acc Id: ENSP00000420987   ⟸   ENST00000513186
Ensembl Acc Id: ENSP00000424154   ⟸   ENST00000515400
Ensembl Acc Id: ENSP00000492204   ⟸   ENST00000515650
RefSeq Acc Id: XP_047271920   ⟸   XM_047415964
- Peptide Label: isoform X1
- UniProtKB: A0A286YFA6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047271922   ⟸   XM_047415966
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047271923   ⟸   XM_047415967
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047271924   ⟸   XM_047415968
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047271921   ⟸   XM_047415965
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054206482   ⟸   XM_054350507
- Peptide Label: isoform X1
- UniProtKB: A0A286YFA6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054206484   ⟸   XM_054350509
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054206485   ⟸   XM_054350510
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054206483   ⟸   XM_054350508
- Peptide Label: isoform X2
Protein Domains
Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P53779-F1-model_v2 AlphaFold P53779 1-464 view protein structure

Promoters
RGD ID:6867926
Promoter ID:EPDNEW_H7128
Type:multiple initiation site
Name:MAPK10_4
Description:mitogen-activated protein kinase 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7129  EPDNEW_H7130  EPDNEW_H7131  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,221,200 - 86,221,260EPDNEW
RGD ID:6867928
Promoter ID:EPDNEW_H7129
Type:initiation region
Name:MAPK10_1
Description:mitogen-activated protein kinase 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7128  EPDNEW_H7130  EPDNEW_H7131  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,360,053 - 86,360,113EPDNEW
RGD ID:6867930
Promoter ID:EPDNEW_H7130
Type:initiation region
Name:MAPK10_2
Description:mitogen-activated protein kinase 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7128  EPDNEW_H7129  EPDNEW_H7131  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,453,195 - 86,453,255EPDNEW
RGD ID:6867932
Promoter ID:EPDNEW_H7131
Type:initiation region
Name:MAPK10_3
Description:mitogen-activated protein kinase 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7128  EPDNEW_H7129  EPDNEW_H7130  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38486,594,074 - 86,594,134EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6872 AgrOrtholog
COSMIC MAPK10 COSMIC
Ensembl Genes ENSG00000109339 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000359221 ENTREZGENE
  ENST00000395157.9 UniProtKB/Swiss-Prot
  ENST00000395166.6 UniProtKB/Swiss-Prot
  ENST00000449047 ENTREZGENE
  ENST00000511167 ENTREZGENE
  ENST00000515400.3 UniProtKB/Swiss-Prot
  ENST00000515650.2 UniProtKB/Swiss-Prot
  ENST00000638225 ENTREZGENE
  ENST00000638225.1 UniProtKB/Swiss-Prot
  ENST00000638313.1 UniProtKB/Swiss-Prot
  ENST00000639175.1 UniProtKB/Swiss-Prot
  ENST00000639234.1 UniProtKB/Swiss-Prot
  ENST00000639242.1 UniProtKB/Swiss-Prot
  ENST00000640858.1 UniProtKB/Swiss-Prot
  ENST00000640970.1 UniProtKB/Swiss-Prot
  ENST00000641050.1 UniProtKB/Swiss-Prot
  ENST00000641051.1 UniProtKB/Swiss-Prot
  ENST00000641066.1 UniProtKB/Swiss-Prot
  ENST00000641110.1 UniProtKB/Swiss-Prot
  ENST00000641157.1 UniProtKB/Swiss-Prot
  ENST00000641170 ENTREZGENE
  ENST00000641170.1 UniProtKB/Swiss-Prot
  ENST00000641207.1 UniProtKB/Swiss-Prot
  ENST00000641208 ENTREZGENE
  ENST00000641274.1 UniProtKB/Swiss-Prot
  ENST00000641283.1 UniProtKB/Swiss-Prot
  ENST00000641287.1 UniProtKB/Swiss-Prot
  ENST00000641297.1 UniProtKB/Swiss-Prot
  ENST00000641341.1 UniProtKB/Swiss-Prot
  ENST00000641391.1 UniProtKB/Swiss-Prot
  ENST00000641410.1 UniProtKB/Swiss-Prot
  ENST00000641462 ENTREZGENE
  ENST00000641462.2 UniProtKB/Swiss-Prot
  ENST00000641647.1 UniProtKB/Swiss-Prot
  ENST00000641657.1 UniProtKB/Swiss-Prot
  ENST00000641718 ENTREZGENE
  ENST00000641724.1 UniProtKB/Swiss-Prot
  ENST00000641737.1 UniProtKB/Swiss-Prot
  ENST00000641803.1 UniProtKB/Swiss-Prot
  ENST00000641823.1 UniProtKB/Swiss-Prot
  ENST00000641862.1 UniProtKB/Swiss-Prot
  ENST00000641902.1 UniProtKB/Swiss-Prot
  ENST00000641911.1 UniProtKB/Swiss-Prot
  ENST00000641943.1 UniProtKB/Swiss-Prot
  ENST00000641952.1 UniProtKB/Swiss-Prot
  ENST00000641983.1 UniProtKB/Swiss-Prot
  ENST00000642009.1 UniProtKB/Swiss-Prot
  ENST00000642015 ENTREZGENE
  ENST00000642015.1 UniProtKB/Swiss-Prot
  ENST00000642038.1 UniProtKB/Swiss-Prot
  ENST00000642103.1 UniProtKB/Swiss-Prot
Gene3D-CATH Phosphorylase Kinase, domain 1 UniProtKB/Swiss-Prot
  Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot
GTEx ENSG00000109339 GTEx
HGNC ID HGNC:6872 ENTREZGENE
Human Proteome Map MAPK10 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot
  MAP_kinase UniProtKB/Swiss-Prot
  MAP_kinase_CS UniProtKB/Swiss-Prot
  MAPK_JNK UniProtKB/Swiss-Prot
  Prot_kinase_dom UniProtKB/Swiss-Prot
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot
KEGG Report hsa:5602 UniProtKB/Swiss-Prot
NCBI Gene 5602 ENTREZGENE
OMIM 602897 OMIM
PANTHER MITOGEN-ACTIVATED PROTEIN KINASE UniProtKB/Swiss-Prot
Pfam Pkinase UniProtKB/Swiss-Prot
PharmGKB PA30617 PharmGKB
PRINTS JNKMAPKINASE UniProtKB/Swiss-Prot
PROSITE MAPK UniProtKB/Swiss-Prot
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot
SMART S_TKc UniProtKB/Swiss-Prot
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot
UniProt A0A1P0B7D2_HUMAN UniProtKB/TrEMBL
  A0A1W2PNF5_HUMAN UniProtKB/TrEMBL
  A0A1W2PPM4_HUMAN UniProtKB/TrEMBL
  A0A1W2PPW1_HUMAN UniProtKB/TrEMBL
  A0A1W2PPZ3_HUMAN UniProtKB/TrEMBL
  A0A1W2PQ03_HUMAN UniProtKB/TrEMBL
  A0A1W2PQX4_HUMAN UniProtKB/TrEMBL
  A0A1W2PRF2_HUMAN UniProtKB/TrEMBL
  A0A1W2PRG9_HUMAN UniProtKB/TrEMBL
  A0A1W2PRZ2_HUMAN UniProtKB/TrEMBL
  A0A286YEN5 ENTREZGENE, UniProtKB/TrEMBL
  A0A286YEQ0 ENTREZGENE, UniProtKB/TrEMBL
  A0A286YEQ7_HUMAN UniProtKB/TrEMBL
  A0A286YES0_HUMAN UniProtKB/TrEMBL
  A0A286YES8_HUMAN UniProtKB/TrEMBL
  A0A286YES9_HUMAN UniProtKB/TrEMBL
  A0A286YEV3_HUMAN UniProtKB/TrEMBL
  A0A286YEV5_HUMAN UniProtKB/TrEMBL
  A0A286YEV8_HUMAN UniProtKB/TrEMBL
  A0A286YEW4_HUMAN UniProtKB/TrEMBL
  A0A286YEW9_HUMAN UniProtKB/TrEMBL
  A0A286YEX7_HUMAN UniProtKB/TrEMBL
  A0A286YEY0_HUMAN UniProtKB/TrEMBL
  A0A286YEY2_HUMAN UniProtKB/TrEMBL
  A0A286YEZ1_HUMAN UniProtKB/TrEMBL
  A0A286YF02_HUMAN UniProtKB/TrEMBL
  A0A286YF04_HUMAN UniProtKB/TrEMBL
  A0A286YF19_HUMAN UniProtKB/TrEMBL
  A0A286YF35_HUMAN UniProtKB/TrEMBL
  A0A286YF43_HUMAN UniProtKB/TrEMBL
  A0A286YF53_HUMAN UniProtKB/TrEMBL
  A0A286YF62_HUMAN UniProtKB/TrEMBL
  A0A286YF80_HUMAN UniProtKB/TrEMBL
  A0A286YF83_HUMAN UniProtKB/TrEMBL
  A0A286YF85_HUMAN UniProtKB/TrEMBL
  A0A286YF95_HUMAN UniProtKB/TrEMBL
  A0A286YF97 ENTREZGENE, UniProtKB/TrEMBL
  A0A286YFA3_HUMAN UniProtKB/TrEMBL
  A0A286YFA6 ENTREZGENE, UniProtKB/TrEMBL
  A0A286YFA7_HUMAN UniProtKB/TrEMBL
  A0A286YFB6_HUMAN UniProtKB/TrEMBL
  A0A286YFB7_HUMAN UniProtKB/TrEMBL
  A0A286YFC0_HUMAN UniProtKB/TrEMBL
  A0A286YFC3_HUMAN UniProtKB/TrEMBL
  A0A286YFD7_HUMAN UniProtKB/TrEMBL
  A0A286YFD9_HUMAN UniProtKB/TrEMBL
  A0A286YFE2_HUMAN UniProtKB/TrEMBL
  A0A286YFE9_HUMAN UniProtKB/TrEMBL
  A0A286YFH4_HUMAN UniProtKB/TrEMBL
  A0A286YFI3 ENTREZGENE, UniProtKB/TrEMBL
  A0A286YFJ0_HUMAN UniProtKB/TrEMBL
  A0A286YFJ4 ENTREZGENE, UniProtKB/TrEMBL
  A0A286YFJ6_HUMAN UniProtKB/TrEMBL
  A0A286YFK3_HUMAN UniProtKB/TrEMBL
  A0A286YFM6_HUMAN UniProtKB/TrEMBL
  A0A286YFN2_HUMAN UniProtKB/TrEMBL
  A6NFS3 ENTREZGENE
  A6NG28 ENTREZGENE
  A8MPV1_HUMAN UniProtKB/TrEMBL
  B3KQ94 ENTREZGENE
  B7Z1Z1 ENTREZGENE, UniProtKB/TrEMBL
  D6R9C1_HUMAN UniProtKB/TrEMBL
  D6RAJ0_HUMAN UniProtKB/TrEMBL
  D6RAU3_HUMAN UniProtKB/TrEMBL
  D6RBH2_HUMAN UniProtKB/TrEMBL
  D6RC26_HUMAN UniProtKB/TrEMBL
  D6RCB1_HUMAN UniProtKB/TrEMBL
  D6RDG1_HUMAN UniProtKB/TrEMBL
  D6RFX8_HUMAN UniProtKB/TrEMBL
  D6RFZ7_HUMAN UniProtKB/TrEMBL
  D6RJF9 ENTREZGENE, UniProtKB/TrEMBL
  F8W9R5 ENTREZGENE, UniProtKB/TrEMBL
  I6L9F3_HUMAN UniProtKB/TrEMBL
  MK10_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q15707 ENTREZGENE
  Q499Y8 ENTREZGENE, UniProtKB/TrEMBL
  Q49AP1 ENTREZGENE
UniProt Secondary A6NFS3 UniProtKB/Swiss-Prot
  A6NG28 UniProtKB/Swiss-Prot
  B3KQ94 UniProtKB/Swiss-Prot
  Q15707 UniProtKB/Swiss-Prot
  Q49AP1 UniProtKB/Swiss-Prot