ABLIM1 (actin binding LIM protein 1) - Rat Genome Database

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Gene: ABLIM1 (actin binding LIM protein 1) Homo sapiens
Analyze
Symbol: ABLIM1
Name: actin binding LIM protein 1
RGD ID: 1346152
HGNC Page HGNC:78
Description: Predicted to enable actin filament binding activity. Acts upstream of or within cilium assembly and lamellipodium assembly. Located in lamellipodium and stress fiber.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ABLIM; abLIM-1; actin-binding double zinc finger protein; actin-binding double-zinc-finger protein; actin-binding LIM protein 1; actin-binding LIM protein family member 1; DKFZp781D0148; FLJ14564; KIAA0059; LIM actin-binding protein 1; LIMAB1; LIMATIN; MGC1224
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
GRCh3810114,431,110 - 114,801,373 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl10114,431,112 - 114,768,061 (-)EnsemblGRCh38hg38GRCh38
GRCh3710116,190,869 - 116,528,063 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3610116,180,859 - 116,434,404 (-)NCBINCBI36Build 36hg18NCBI36
Build 3410116,180,859 - 116,276,675NCBI
Celera10109,920,119 - 110,173,614 (-)NCBICelera
Cytogenetic Map10q25.3NCBI
HuRef10109,817,609 - 110,070,887 (-)NCBIHuRef
CHM1_110116,474,653 - 116,728,179 (-)NCBICHM1_1
T2T-CHM13v2.010115,325,183 - 115,686,686 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-methylcholine  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (ISO)
8-Br-cAMP  (EXP)
acrolein  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP,ISO)
alpha-pinene  (EXP)
amphetamine  (ISO)
antirheumatic drug  (EXP)
Aroclor 1254  (ISO)
arsenite(3-)  (EXP,ISO)
arsenous acid  (EXP)
atrazine  (ISO)
Benoxacor  (ISO)
benzene  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
Benzo[k]fluoranthene  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
Brodifacoum  (ISO)
butan-1-ol  (EXP)
cadmium dichloride  (EXP)
caffeine  (EXP)
calcitriol  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
chrysene  (ISO)
cisplatin  (EXP)
coumarin  (EXP)
cyclosporin A  (EXP,ISO)
DDT  (ISO)
diarsenic trioxide  (EXP)
dibenz[a,h]anthracene  (ISO)
diuron  (ISO)
doxorubicin  (EXP)
enzyme inhibitor  (EXP)
epoxiconazole  (ISO)
ethanol  (EXP)
ethyl methanesulfonate  (EXP)
FR900359  (EXP)
hydrogen peroxide  (ISO)
lead(0)  (EXP)
methamphetamine  (ISO)
methoxychlor  (ISO)
methyl methanesulfonate  (EXP)
mifepristone  (EXP)
mitomycin C  (EXP)
nickel sulfate  (EXP)
ozone  (EXP,ISO)
paracetamol  (EXP)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenobarbital  (ISO)
phenytoin  (ISO)
pirinixic acid  (ISO)
poly(I:C)  (ISO)
potassium chromate  (EXP)
potassium dichromate  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
rotenone  (ISO)
silver atom  (EXP)
silver(0)  (EXP)
sodium arsenite  (EXP)
sodium fluoride  (ISO)
succimer  (EXP)
tamoxifen  (ISO)
temozolomide  (EXP)
tert-butyl hydroperoxide  (EXP)
tetrachloromethane  (ISO)
tetraphene  (ISO)
thioacetamide  (ISO)
thiram  (EXP)
titanium dioxide  (ISO)
triclosan  (EXP)
triphenyl phosphate  (EXP,ISO)
triptonide  (ISO)
troglitazone  (ISO)
tungsten  (ISO)
valproic acid  (ISO)
vincaleukoblastine  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7566098   PMID:7584044   PMID:8889548   PMID:9245787   PMID:9417918   PMID:12168954   PMID:12477932   PMID:14702039   PMID:15024025   PMID:15144186   PMID:15302935   PMID:15324660  
PMID:15489334   PMID:15570572   PMID:15592455   PMID:15778465   PMID:16094384   PMID:16189514   PMID:16344560   PMID:16385451   PMID:16712791   PMID:17081983   PMID:17194709   PMID:17979178  
PMID:20549515   PMID:20936779   PMID:20970119   PMID:21547531   PMID:21832049   PMID:21873635   PMID:22219177   PMID:22305495   PMID:22684256   PMID:23251661   PMID:23414517   PMID:24255178  
PMID:24337577   PMID:24457600   PMID:24613305   PMID:24711643   PMID:25403273   PMID:25416956   PMID:25468996   PMID:25659154   PMID:25662211   PMID:25852190   PMID:26186194   PMID:26209609  
PMID:26496610   PMID:26638075   PMID:26673895   PMID:26687681   PMID:27173435   PMID:27591049   PMID:27684187   PMID:28514442   PMID:28611215   PMID:28977470   PMID:29117863   PMID:29180619  
PMID:29507755   PMID:29509190   PMID:29513927   PMID:29540532   PMID:29778605   PMID:30196744   PMID:30833792   PMID:30884312   PMID:31527615   PMID:31586073   PMID:31980649   PMID:32203420  
PMID:32296183   PMID:32687490   PMID:32707033   PMID:33060197   PMID:33061800   PMID:33144569   PMID:33644029   PMID:33784440   PMID:33916271   PMID:33961781   PMID:34079125   PMID:34244482  
PMID:34315543   PMID:34597346   PMID:34672954   PMID:34702444   PMID:34709727   PMID:34795231   PMID:35013218   PMID:35013556   PMID:35063084   PMID:35256949   PMID:35271311   PMID:35337019  
PMID:35384245   PMID:35563538   PMID:35914814   PMID:35944360   PMID:36180527   PMID:36526897   PMID:36543142   PMID:36574265   PMID:36583064   PMID:36931259   PMID:36976175   PMID:37071682  
PMID:37167062   PMID:37381005   PMID:37536630   PMID:37616343   PMID:38113892   PMID:38228802   PMID:38280479  


Genomics

Comparative Map Data
ABLIM1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3810114,431,110 - 114,801,373 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl10114,431,112 - 114,768,061 (-)EnsemblGRCh38hg38GRCh38
GRCh3710116,190,869 - 116,528,063 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3610116,180,859 - 116,434,404 (-)NCBINCBI36Build 36hg18NCBI36
Build 3410116,180,859 - 116,276,675NCBI
Celera10109,920,119 - 110,173,614 (-)NCBICelera
Cytogenetic Map10q25.3NCBI
HuRef10109,817,609 - 110,070,887 (-)NCBIHuRef
CHM1_110116,474,653 - 116,728,179 (-)NCBICHM1_1
T2T-CHM13v2.010115,325,183 - 115,686,686 (-)NCBIT2T-CHM13v2.0
Ablim1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391957,021,165 - 57,303,776 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1957,021,165 - 57,303,351 (-)EnsemblGRCm39 Ensembl
GRCm381957,032,733 - 57,315,344 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1957,032,733 - 57,314,919 (-)EnsemblGRCm38mm10GRCm38
MGSCv371957,107,754 - 57,290,522 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361957,090,390 - 57,269,282 (-)NCBIMGSCv36mm8
Celera1959,226,385 - 59,408,337 (-)NCBICelera
Cytogenetic Map19D2NCBI
cM Map1952.09NCBI
Ablim1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81266,088,868 - 266,377,169 (-)NCBIGRCr8
mRatBN7.21256,083,747 - 256,372,075 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1256,084,297 - 256,371,969 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1264,293,977 - 264,485,616 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01271,000,027 - 271,191,663 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01263,645,117 - 263,836,899 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01277,853,877 - 278,043,096 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01285,233,699 - 285,420,807 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41263,380,818 - 263,465,905 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1251,779,866 - 252,069,514 (-)NCBICelera
Cytogenetic Map1q55NCBI
Ablim1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543119,402,023 - 19,683,589 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543119,397,136 - 19,684,574 (-)NCBIChiLan1.0ChiLan1.0
ABLIM1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v28126,315,945 - 126,645,544 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan110126,321,282 - 126,650,889 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v010111,030,953 - 111,360,527 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.110114,460,703 - 114,712,858 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl10114,465,838 - 114,712,561 (-)Ensemblpanpan1.1panPan2
ABLIM1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12825,260,323 - 25,543,369 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2825,260,873 - 25,545,304 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2825,412,116 - 25,695,587 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02825,794,442 - 26,078,835 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2825,793,574 - 26,078,829 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12825,349,757 - 25,633,749 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02825,364,845 - 25,649,366 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02825,558,277 - 25,842,977 (-)NCBIUU_Cfam_GSD_1.0
Ablim1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440721320,654,882 - 20,840,766 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364864,722,279 - 4,925,551 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364864,720,643 - 4,906,460 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ABLIM1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl14124,760,404 - 125,010,892 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.114124,759,811 - 125,108,722 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.214135,882,251 - 136,231,438 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ABLIM1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.19107,298,018 - 107,638,915 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl9107,302,821 - 107,524,945 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604868,532,262 - 68,873,635 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ablim1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473731,943,110 - 32,164,451 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473731,856,202 - 32,169,116 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ABLIM1
47 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10q25.3(chr10:114584882-117015907)x1 copy number loss See cases [RCV000050821] Chr10:114584882..117015907 [GRCh38]
Chr10:116344641..118775418 [GRCh37]
Chr10:116334631..118765408 [NCBI36]
Chr10:10q25.3
pathogenic
GRCh38/hg38 10q23.33-25.3(chr10:95112607-116776637)x3 copy number gain See cases [RCV000050747] Chr10:95112607..116776637 [GRCh38]
Chr10:96872364..118383651 [GRCh37]
Chr10:96862354..118526138 [NCBI36]
Chr10:10q23.33-25.3
pathogenic
GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3 copy number gain See cases [RCV000051218] Chr10:111313099..133620674 [GRCh38]
Chr10:113072857..135434178 [GRCh37]
Chr10:113062847..135284168 [NCBI36]
Chr10:10q25.2-26.3
pathogenic
GRCh38/hg38 10q25.1-26.11(chr10:107191100-118761489)x1 copy number loss See cases [RCV000052570] Chr10:107191100..118761489 [GRCh38]
Chr10:108950858..120521001 [GRCh37]
Chr10:108940848..120510991 [NCBI36]
Chr10:10q25.1-26.11
pathogenic
GRCh38/hg38 10q23.31-26.3(chr10:91048545-133620674)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]|See cases [RCV000053560] Chr10:91048545..133620674 [GRCh38]
Chr10:92808302..135434178 [GRCh37]
Chr10:92798282..135284168 [NCBI36]
Chr10:10q23.31-26.3
pathogenic
GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3 copy number gain See cases [RCV000053564] Chr10:100194215..132432797 [GRCh38]
Chr10:101953972..134246301 [GRCh37]
Chr10:101943962..134096291 [NCBI36]
Chr10:10q24.31-26.3
pathogenic
GRCh38/hg38 10q25.1-26.3(chr10:106925303-133620815)x3 copy number gain See cases [RCV000053588] Chr10:106925303..133620815 [GRCh38]
Chr10:108685061..135434319 [GRCh37]
Chr10:108675051..135284309 [NCBI36]
Chr10:10q25.1-26.3
pathogenic
NM_001003407.1(ABLIM1):c.1464C>T (p.Ser488=) single nucleotide variant Malignant melanoma [RCV000068811] Chr10:114447971 [GRCh38]
Chr10:116207730 [GRCh37]
Chr10:116197720 [NCBI36]
Chr10:10q25.3
not provided
NM_001003407.1(ABLIM1):c.973G>A (p.Asp325Asn) single nucleotide variant Malignant melanoma [RCV000068812] Chr10:114473099 [GRCh38]
Chr10:116232858 [GRCh37]
Chr10:116222848 [NCBI36]
Chr10:10q25.3
not provided
NM_001003407.1(ABLIM1):c.659T>G (p.Leu220Arg) single nucleotide variant Malignant melanoma [RCV000068813] Chr10:114545060 [GRCh38]
Chr10:116304819 [GRCh37]
Chr10:116294809 [NCBI36]
Chr10:10q25.3
not provided
NM_001003407.1(ABLIM1):c.199+24C>T single nucleotide variant Malignant melanoma [RCV000068814] Chr10:114601803 [GRCh38]
Chr10:116361562 [GRCh37]
Chr10:116351552 [NCBI36]
Chr10:10q25.3
not provided
GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3 copy number gain See cases [RCV000133688] Chr10:108102587..133620674 [GRCh38]
Chr10:109862345..135434178 [GRCh37]
Chr10:109852335..135284168 [NCBI36]
Chr10:10q25.1-26.3
pathogenic
GRCh38/hg38 10q25.3(chr10:114584882-115096595)x3 copy number gain See cases [RCV000135770] Chr10:114584882..115096595 [GRCh38]
Chr10:116344641..116856352 [GRCh37]
Chr10:116334631..116846342 [NCBI36]
Chr10:10q25.3
likely benign
GRCh38/hg38 10q25.2-25.3(chr10:112074094-115537174)x1 copy number loss See cases [RCV000135960] Chr10:112074094..115537174 [GRCh38]
Chr10:113833852..117032437 [GRCh37]
Chr10:113823842..117286674 [NCBI36]
Chr10:10q25.2-25.3
pathogenic
GRCh38/hg38 10q25.2-26.12(chr10:112701186-120970617)x3 copy number gain See cases [RCV000137511] Chr10:112701186..120970617 [GRCh38]
Chr10:114460945..122730130 [GRCh37]
Chr10:114450935..122720120 [NCBI36]
Chr10:10q25.2-26.12
likely pathogenic
GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3 copy number gain See cases [RCV000137747] Chr10:100600492..133622588 [GRCh38]
Chr10:102360249..135436092 [GRCh37]
Chr10:102350239..135286082 [NCBI36]
Chr10:10q24.31-26.3
pathogenic
GRCh38/hg38 10q25.2-25.3(chr10:110804735-114884010)x1 copy number loss See cases [RCV000139783] Chr10:110804735..114884010 [GRCh38]
Chr10:112564493..116643769 [GRCh37]
Chr10:112554483..116633759 [NCBI36]
Chr10:10q25.2-25.3
likely pathogenic
NR_120628.1(LOC101927692):n.206-3610T>C single nucleotide variant Lung cancer [RCV000108678] Chr10:114772332 [GRCh38]
Chr10:116532091 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3 copy number gain See cases [RCV000240457] Chr10:103288313..135512075 [GRCh37]
Chr10:10q24.32-26.3
pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:104633712-135427143)x3 copy number gain See cases [RCV000449386] Chr10:104633712..135427143 [GRCh37]
Chr10:10q24.32-26.3
pathogenic
GRCh37/hg19 10q24.2-26.3(chr10:100780957-135427143)x3 copy number gain See cases [RCV000446733] Chr10:100780957..135427143 [GRCh37]
Chr10:10q24.2-26.3
pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3
pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3
pathogenic|uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:106003533-135427143)x3 copy number gain See cases [RCV000510813] Chr10:106003533..135427143 [GRCh37]
Chr10:10q25.1-26.3
pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3
pathogenic
GRCh37/hg19 10q23.32-26.3(chr10:93283493-135427143)x3 copy number gain See cases [RCV000510972] Chr10:93283493..135427143 [GRCh37]
Chr10:10q23.32-26.3
pathogenic
NM_002313.7(ABLIM1):c.1742A>G (p.Asp581Gly) single nucleotide variant not specified [RCV004298910] Chr10:114445397 [GRCh38]
Chr10:116205156 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1883G>A (p.Arg628Gln) single nucleotide variant not specified [RCV004291788] Chr10:114444079 [GRCh38]
Chr10:116203838 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1997G>C (p.Arg666Pro) single nucleotide variant not specified [RCV004319380] Chr10:114441723 [GRCh38]
Chr10:116201482 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438] Chr10:42347406..135534747 [GRCh37]
Chr10:10q11.21-26.3
drug response
NM_002313.7(ABLIM1):c.1343A>T (p.His448Leu) single nucleotide variant not specified [RCV004308899] Chr10:114465796 [GRCh38]
Chr10:116225555 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10q25.3(chr10:116322646-116572153)x3 copy number gain not provided [RCV000683211] Chr10:116322646..116572153 [GRCh37]
Chr10:10q25.3
likely benign
GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3 copy number gain not provided [RCV000683291] Chr10:94346520..135427143 [GRCh37]
Chr10:10q23.33-26.3
pathogenic
GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3 copy number gain not provided [RCV000683290] Chr10:105613040..135427143 [GRCh37]
Chr10:10q24.33-26.3
pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3
pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3
pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095) copy number gain not provided [RCV000767665] Chr10:110022170..135439095 [GRCh37]
Chr10:10q25.1-26.3
pathogenic
GRCh37/hg19 10q25.3(chr10:116139681-116522804)x3 copy number gain not provided [RCV000848644] Chr10:116139681..116522804 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3 copy number gain not provided [RCV000847820] Chr10:114544537..135427143 [GRCh37]
Chr10:10q25.2-26.3
pathogenic
GRCh37/hg19 10q25.3(chr10:116322646-116572153)x3 copy number gain not provided [RCV000847499] Chr10:116322646..116572153 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.314C>G (p.Pro105Arg) single nucleotide variant not specified [RCV004684130] Chr10:114601892 [GRCh38]
Chr10:116361651 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.250C>T (p.His84Tyr) single nucleotide variant not specified [RCV004684219] Chr10:114601956 [GRCh38]
Chr10:116361715 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1771G>A (p.Glu591Lys) single nucleotide variant not specified [RCV004684293] Chr10:114445368 [GRCh38]
Chr10:116205127 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.580G>A (p.Gly194Arg) single nucleotide variant not specified [RCV004684379] Chr10:114571390 [GRCh38]
Chr10:116331149 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143) copy number gain not specified [RCV002052891] Chr10:108455687..135427143 [GRCh37]
Chr10:10q25.1-26.3
pathogenic
GRCh37/hg19 10q25.1-25.3(chr10:107092654-117852548)x1 copy number loss not provided [RCV001827678] Chr10:107092654..117852548 [GRCh37]
Chr10:10q25.1-25.3
uncertain significance
NM_002313.7(ABLIM1):c.671G>A (p.Ser224Asn) single nucleotide variant not specified [RCV004323155] Chr10:114571299 [GRCh38]
Chr10:116331058 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.164C>G (p.Ala55Gly) single nucleotide variant not specified [RCV004202588] Chr10:114658037 [GRCh38]
Chr10:116417796 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.566G>A (p.Arg189His) single nucleotide variant not specified [RCV004230966] Chr10:114571404 [GRCh38]
Chr10:116331163 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1459G>A (p.Gly487Ser) single nucleotide variant not specified [RCV004200331] Chr10:114453466 [GRCh38]
Chr10:116213225 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1471C>A (p.Pro491Thr) single nucleotide variant not specified [RCV004198884] Chr10:114453454 [GRCh38]
Chr10:116213213 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1415G>A (p.Arg472His) single nucleotide variant not specified [RCV004215206] Chr10:114465724 [GRCh38]
Chr10:116225483 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.901G>A (p.Asp301Asn) single nucleotide variant not specified [RCV004149601] Chr10:114491872 [GRCh38]
Chr10:116251631 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.695A>G (p.Asp232Gly) single nucleotide variant not specified [RCV004106196] Chr10:114547755 [GRCh38]
Chr10:116307514 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.478G>A (p.Gly160Ser) single nucleotide variant not specified [RCV004231111] Chr10:114575501 [GRCh38]
Chr10:116335260 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.991G>A (p.Val331Ile) single nucleotide variant not specified [RCV004206579] Chr10:114488008 [GRCh38]
Chr10:116247767 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.812C>T (p.Pro271Leu) single nucleotide variant not specified [RCV004226832] Chr10:114545087 [GRCh38]
Chr10:116304846 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.948G>C (p.Gln316His) single nucleotide variant not specified [RCV004102777] Chr10:114491825 [GRCh38]
Chr10:116251584 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1516G>A (p.Ala506Thr) single nucleotide variant not provided [RCV004695424]|not specified [RCV004113451] Chr10:114453409 [GRCh38]
Chr10:116213168 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1882C>T (p.Arg628Trp) single nucleotide variant not specified [RCV004218015] Chr10:114444080 [GRCh38]
Chr10:116203839 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.223T>C (p.Cys75Arg) single nucleotide variant not specified [RCV004130549] Chr10:114657978 [GRCh38]
Chr10:116417737 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2081G>T (p.Gly694Val) single nucleotide variant not specified [RCV004089595] Chr10:114439237 [GRCh38]
Chr10:116198996 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2251G>A (p.Glu751Lys) single nucleotide variant not specified [RCV004214023] Chr10:114436346 [GRCh38]
Chr10:116196105 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.253C>G (p.Pro85Ala) single nucleotide variant not specified [RCV004106410] Chr10:114601953 [GRCh38]
Chr10:116361712 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1100C>T (p.Ser367Leu) single nucleotide variant not specified [RCV004133970] Chr10:114473898 [GRCh38]
Chr10:116233657 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2033A>G (p.Tyr678Cys) single nucleotide variant not specified [RCV004122417] Chr10:114441043 [GRCh38]
Chr10:116200802 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1409C>T (p.Thr470Met) single nucleotide variant not specified [RCV004096996] Chr10:114465730 [GRCh38]
Chr10:116225489 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.217C>T (p.Arg73Cys) single nucleotide variant not specified [RCV004214780] Chr10:114657984 [GRCh38]
Chr10:116417743 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2170A>G (p.Thr724Ala) single nucleotide variant not specified [RCV004130940] Chr10:114437897 [GRCh38]
Chr10:116197656 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1381T>G (p.Tyr461Asp) single nucleotide variant not specified [RCV004211594] Chr10:114465758 [GRCh38]
Chr10:116225517 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.409T>C (p.Phe137Leu) single nucleotide variant not specified [RCV004084238] Chr10:114575570 [GRCh38]
Chr10:116335329 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1997G>A (p.Arg666Gln) single nucleotide variant not specified [RCV004079806] Chr10:114441723 [GRCh38]
Chr10:116201482 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1387C>T (p.Arg463Cys) single nucleotide variant not specified [RCV004255031] Chr10:114465752 [GRCh38]
Chr10:116225511 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1079C>G (p.Pro360Arg) single nucleotide variant not specified [RCV004260303] Chr10:114473919 [GRCh38]
Chr10:116233678 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1334G>A (p.Arg445Gln) single nucleotide variant not specified [RCV004278429] Chr10:114465805 [GRCh38]
Chr10:116225564 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.916C>T (p.Pro306Ser) single nucleotide variant not specified [RCV004254348] Chr10:114491857 [GRCh38]
Chr10:116251616 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2269A>G (p.Ile757Val) single nucleotide variant not specified [RCV004684434] Chr10:114436328 [GRCh38]
Chr10:116196087 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3
pathogenic
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3
pathogenic
NM_002313.7(ABLIM1):c.1082G>C (p.Gly361Ala) single nucleotide variant not specified [RCV004340848] Chr10:114473916 [GRCh38]
Chr10:116233675 [GRCh37]
Chr10:10q25.3
uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3 copy number gain Distal trisomy 10q [RCV003458955] Chr10:111378692..135427143 [GRCh37]
Chr10:10q25.1-26.3
pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:111447991-133435388)x3 copy number gain not provided [RCV003484817] Chr10:111447991..133435388 [GRCh37]
Chr10:10q25.1-26.3
pathogenic
NC_000010.11:g.114571296CTG[3] microsatellite not provided [RCV003422912] Chr10:114571295..114571296 [GRCh38]
Chr10:116331054..116331055 [GRCh37]
Chr10:10q25.3
likely benign
GRCh37/hg19 10q25.1-26.13(chr10:107129993-123817654)x3 copy number gain not specified [RCV003986891] Chr10:107129993..123817654 [GRCh37]
Chr10:10q25.1-26.13
likely pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3 copy number gain not specified [RCV003986893] Chr10:95078198..135427143 [GRCh37]
Chr10:10q23.33-26.3
pathogenic
NM_002313.7(ABLIM1):c.463G>A (p.Gly155Arg) single nucleotide variant not specified [RCV004420948] Chr10:114575516 [GRCh38]
Chr10:116335275 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2197A>G (p.Arg733Gly) single nucleotide variant not specified [RCV004420924] Chr10:114437870 [GRCh38]
Chr10:116197629 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.489G>C (p.Glu163Asp) single nucleotide variant not specified [RCV004420955] Chr10:114575490 [GRCh38]
Chr10:116335249 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2024A>G (p.Tyr675Cys) single nucleotide variant not specified [RCV004418838] Chr10:114441052 [GRCh38]
Chr10:116200811 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.457A>G (p.Met153Val) single nucleotide variant not specified [RCV004420946] Chr10:114575522 [GRCh38]
Chr10:116335281 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.95C>T (p.Ser32Leu) single nucleotide variant not specified [RCV004420986] Chr10:114658106 [GRCh38]
Chr10:116417865 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1690A>T (p.Ile564Phe) single nucleotide variant not specified [RCV004418822] Chr10:114447925 [GRCh38]
Chr10:116207684 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1894T>C (p.Ser632Pro) single nucleotide variant not specified [RCV004418835] Chr10:114444068 [GRCh38]
Chr10:116203827 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.2249G>T (p.Arg750Leu) single nucleotide variant not specified [RCV004420929] Chr10:114436348 [GRCh38]
Chr10:116196107 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.455G>A (p.Arg152Gln) single nucleotide variant not specified [RCV004420941] Chr10:114575524 [GRCh38]
Chr10:116335283 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1474C>G (p.Leu492Val) single nucleotide variant not specified [RCV004668697] Chr10:114453451 [GRCh38]
Chr10:116213210 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.159G>T (p.Arg53Ser) single nucleotide variant not specified [RCV004668551] Chr10:114658042 [GRCh38]
Chr10:116417801 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1328G>A (p.Arg443Gln) single nucleotide variant not specified [RCV004676869] Chr10:114465811 [GRCh38]
Chr10:116225570 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.469C>T (p.Arg157Cys) single nucleotide variant not specified [RCV004677055] Chr10:114575510 [GRCh38]
Chr10:116335269 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1483C>T (p.Arg495Trp) single nucleotide variant not specified [RCV004676976] Chr10:114453442 [GRCh38]
Chr10:116213201 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.176A>G (p.His59Arg) single nucleotide variant not specified [RCV004360030] Chr10:114658025 [GRCh38]
Chr10:116417784 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1216T>C (p.Tyr406His) single nucleotide variant not specified [RCV004418797] Chr10:114473036 [GRCh38]
Chr10:116232795 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1621T>G (p.Ser541Ala) single nucleotide variant not specified [RCV004418815] Chr10:114447994 [GRCh38]
Chr10:116207753 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1681A>T (p.Thr561Ser) single nucleotide variant not specified [RCV004418819] Chr10:114447934 [GRCh38]
Chr10:116207693 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1283G>A (p.Arg428Lys) single nucleotide variant not specified [RCV004418800] Chr10:114468209 [GRCh38]
Chr10:116227968 [GRCh37]
Chr10:10q25.3
uncertain significance
NM_002313.7(ABLIM1):c.1285A>T (p.Thr429Ser) single nucleotide variant not specified [RCV004418802] Chr10:114468207 [GRCh38]
Chr10:116227966 [GRCh37]
Chr10:10q25.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:10656
Count of miRNA genes:1251
Interacting mature miRNAs:1593
Transcripts:ENST00000277895, ENST00000369252, ENST00000369253, ENST00000369256, ENST00000369266, ENST00000392952, ENST00000392955, ENST00000428430, ENST00000440467, ENST00000466400, ENST00000477638, ENST00000481974, ENST00000485570, ENST00000533213
Prediction methods: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
407283719GWAS932695_Hskin hydration measurement QTL GWAS932695 (human)0.000003skin hydration measurementskin water level (CMO:0002766)10114511206114511207Human
407148771GWAS797747_Hresponse to norepinephrine-dopamine reuptake inhibitor QTL GWAS797747 (human)0.000006response to norepinephrine-dopamine reuptake inhibitor10114593515114593516Human
406963657GWAS612633_Hsevere acute respiratory syndrome, COVID-19 QTL GWAS612633 (human)0.0000005severe acute respiratory syndrome, COVID-1910114444215114444216Human
407049839GWAS698815_Hsalicylurate measurement QTL GWAS698815 (human)0.000005salicylurate measurement10114557021114557022Human
406909837GWAS558813_Hcoffee consumption measurement QTL GWAS558813 (human)4e-08coffee consumption measurement10114511206114511207Human
407046316GWAS695292_Hbody mass index QTL GWAS695292 (human)0.000006body mass indexbody mass index (BMI) (CMO:0000105)10114439416114439417Human
407115381GWAS764357_Hcognitive decline measurement QTL GWAS764357 (human)0.000005cognitive behavior trait (VT:0010450)10114435021114435022Human
407210487GWAS859463_Hblood protein measurement QTL GWAS859463 (human)2e-10blood protein measurementblood protein measurement (CMO:0000028)10114634467114634468Human
407093488GWAS742464_Hsensory perception of taste QTL GWAS742464 (human)0.000009sensory perception of taste10114498625114498626Human
407091415GWAS740391_Huracil measurement QTL GWAS740391 (human)0.000002uracil measurement10114457904114457905Human
406951705GWAS600681_Htrait in response to paclitaxel QTL GWAS600681 (human)0.000002trait in response to paclitaxel10114642349114642350Human
406963768GWAS612744_Hsevere acute respiratory syndrome, COVID-19 QTL GWAS612744 (human)7e-09severe acute respiratory syndrome, COVID-1910114456946114456947Human
406901276GWAS550252_Hneuroimaging measurement QTL GWAS550252 (human)5e-16neuroimaging measurement10114478001114478002Human
406901724GWAS550700_Hneuroimaging measurement QTL GWAS550700 (human)3e-12neuroimaging measurement10114478001114478002Human

Markers in Region
D10S1158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,272,547 - 116,272,846UniSTSGRCh37
Build 3610116,262,537 - 116,262,836RGDNCBI36
Celera10110,001,780 - 110,002,079RGD
Cytogenetic Map10q25UniSTS
HuRef10109,899,298 - 109,899,597UniSTS
Marshfield Genetic Map10135.24UniSTS
Marshfield Genetic Map10135.24RGD
G15970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,193,887 - 116,194,117UniSTSGRCh37
Build 3610116,183,877 - 116,184,107RGDNCBI36
Celera10109,923,136 - 109,923,355RGD
Cytogenetic Map10q25UniSTS
HuRef10109,820,626 - 109,820,860UniSTS
RH25292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,192,389 - 116,192,669UniSTSGRCh37
Build 3610116,182,379 - 116,182,659RGDNCBI36
Celera10109,921,638 - 109,921,918RGD
Cytogenetic Map10q25UniSTS
HuRef10109,819,128 - 109,819,408UniSTS
GeneMap99-GB4 RH Map10521.27UniSTS
D10S1336E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,190,894 - 116,191,045UniSTSGRCh37
Build 3610116,180,884 - 116,181,035RGDNCBI36
Celera10109,920,144 - 109,920,295RGD
Cytogenetic Map10q25UniSTS
HuRef10109,817,634 - 109,817,785UniSTS
GeneMap99-GB4 RH Map10519.15UniSTS
NCBI RH Map101247.5UniSTS
RH66528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,409,949 - 116,410,143UniSTSGRCh37
Build 3610116,399,939 - 116,400,133RGDNCBI36
Celera10110,139,142 - 110,139,336RGD
Cytogenetic Map10q25UniSTS
HuRef10110,036,413 - 110,036,607UniSTS
GeneMap99-GB4 RH Map10517.81UniSTS
NCBI RH Map101266.9UniSTS
RH91180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,190,946 - 116,191,078UniSTSGRCh37
Build 3610116,180,936 - 116,181,068RGDNCBI36
Celera10109,920,196 - 109,920,328RGD
Cytogenetic Map10q25UniSTS
HuRef10109,817,686 - 109,817,818UniSTS
GeneMap99-GB4 RH Map10519.86UniSTS
RH119261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,346,564 - 116,346,883UniSTSGRCh37
Build 3610116,336,554 - 116,336,873RGDNCBI36
Celera10110,075,755 - 110,076,074RGD
Cytogenetic Map10q25UniSTS
HuRef10109,973,033 - 109,973,352UniSTS
TNG Radiation Hybrid Map1056535.0UniSTS
RH122579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,190,666 - 116,190,953UniSTSGRCh37
Build 3610116,180,656 - 116,180,943RGDNCBI36
Cytogenetic Map10q25UniSTS
D10S1298E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,243,893 - 116,244,018UniSTSGRCh37
Build 3610116,233,883 - 116,234,008RGDNCBI36
Celera10109,973,131 - 109,973,256RGD
Cytogenetic Map10q25UniSTS
HuRef10109,870,631 - 109,870,756UniSTS
SHGC-146082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,300,321 - 116,300,645UniSTSGRCh37
Build 3610116,290,311 - 116,290,635RGDNCBI36
Celera10110,029,543 - 110,029,867RGD
Cytogenetic Map10q25UniSTS
HuRef10109,926,805 - 109,927,129UniSTS
TNG Radiation Hybrid Map1056519.0UniSTS
SHGC-146643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,300,596 - 116,300,867UniSTSGRCh37
Build 3610116,290,586 - 116,290,857RGDNCBI36
Celera10110,029,818 - 110,030,089RGD
Cytogenetic Map10q25UniSTS
HuRef10109,927,080 - 109,927,351UniSTS
TNG Radiation Hybrid Map1056523.0UniSTS
SHGC-53066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,239,766 - 116,239,999UniSTSGRCh37
Build 3610116,229,756 - 116,229,989RGDNCBI36
Celera10109,969,004 - 109,969,237RGD
Cytogenetic Map10q25UniSTS
HuRef10109,866,504 - 109,866,737UniSTS
TNG Radiation Hybrid Map1056512.0UniSTS
D10S2292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,194,377 - 116,194,711UniSTSGRCh37
Build 3610116,184,367 - 116,184,701RGDNCBI36
Celera10109,923,615 - 109,923,949RGD
Cytogenetic Map10q25UniSTS
HuRef10109,821,120 - 109,821,454UniSTS
Whitehead-YAC Contig Map10 UniSTS
SGC30280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,190,899 - 116,191,000UniSTSGRCh37
Build 3610116,180,889 - 116,180,990RGDNCBI36
Celera10109,920,149 - 109,920,250RGD
Cytogenetic Map10q25UniSTS
HuRef10109,817,639 - 109,817,740UniSTS
GeneMap99-GB4 RH Map10517.71UniSTS
Whitehead-RH Map10622.9UniSTS
RH44627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,222,581 - 116,222,749UniSTSGRCh37
Build 3610116,212,571 - 116,212,739RGDNCBI36
Celera10109,951,818 - 109,951,986RGD
Cytogenetic Map10q25UniSTS
HuRef10109,849,318 - 109,849,486UniSTS
GeneMap99-GB4 RH Map10519.86UniSTS
SHGC-35224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710116,222,581 - 116,222,714UniSTSGRCh37
Build 3610116,212,571 - 116,212,704RGDNCBI36
Celera10109,951,818 - 109,951,951RGD
Cytogenetic Map10q25UniSTS
HuRef10109,849,318 - 109,849,451UniSTS
Stanford-G3 RH Map105333.0UniSTS
GeneMap99-GB4 RH Map10521.27UniSTS
Whitehead-RH Map10622.0UniSTS
GeneMap99-G3 RH Map105569.0UniSTS
D15S1477  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q32-q35UniSTS
Cytogenetic Map5q11UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map2q31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map1q31.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map3p25-p24UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map3p12UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map14q11.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p22.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map15q21-q23UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map17qUniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map6p24.2UniSTS


Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029872 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001003407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322891 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001352440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001352441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001352442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001352443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006720 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011539801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011539802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011539805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365914 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054365940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA314019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF005654 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI680726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
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  AK058007 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK098277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK122891 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL133384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL600892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL710059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL712271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW627433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE395092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE672277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG426037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ721521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA450184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB128609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD558045 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
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  DB039901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC376979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF597763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000277895   ⟹   ENSP00000277895
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,436,038 - 114,658,298 (-)Ensembl
Ensembl Acc Id: ENST00000369252   ⟹   ENSP00000358256
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,431,113 - 114,684,655 (-)Ensembl
Ensembl Acc Id: ENST00000369253   ⟹   ENSP00000358257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,435,441 - 114,526,835 (-)Ensembl
Ensembl Acc Id: ENST00000369256   ⟹   ENSP00000358260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,435,954 - 114,685,003 (-)Ensembl
Ensembl Acc Id: ENST00000369266   ⟹   ENSP00000358270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,435,461 - 114,526,830 (-)Ensembl
Ensembl Acc Id: ENST00000392952   ⟹   ENSP00000376679
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,431,113 - 114,526,931 (-)Ensembl
Ensembl Acc Id: ENST00000392955   ⟹   ENSP00000376682
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,431,113 - 114,684,457 (-)Ensembl
Ensembl Acc Id: ENST00000428430   ⟹   ENSP00000400934
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,451,645 - 114,526,918 (-)Ensembl
Ensembl Acc Id: ENST00000440467   ⟹   ENSP00000414154
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,450,079 - 114,487,993 (-)Ensembl
Ensembl Acc Id: ENST00000466400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,465,465 - 114,468,265 (-)Ensembl
Ensembl Acc Id: ENST00000477638
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,595,002 - 114,610,717 (-)Ensembl
Ensembl Acc Id: ENST00000481974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,547,491 - 114,575,537 (-)Ensembl
Ensembl Acc Id: ENST00000485570
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,439,617 - 114,441,041 (-)Ensembl
Ensembl Acc Id: ENST00000533213   ⟹   ENSP00000433629
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,431,112 - 114,658,275 (-)Ensembl
Ensembl Acc Id: ENST00000649363   ⟹   ENSP00000497150
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,436,178 - 114,658,283 (-)Ensembl
Ensembl Acc Id: ENST00000651023   ⟹   ENSP00000499023
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,435,459 - 114,632,092 (-)Ensembl
Ensembl Acc Id: ENST00000651092   ⟹   ENSP00000499163
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,444,086 - 114,768,061 (-)Ensembl
Ensembl Acc Id: ENST00000707119   ⟹   ENSP00000516747
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10114,431,125 - 114,632,044 (-)Ensembl
RefSeq Acc Id: NM_001003407   ⟹   NP_001003407
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,684,443 (-)NCBI
GRCh3710116,190,869 - 116,444,762 (-)NCBI
Build 3610116,180,859 - 116,434,404 (-)NCBI Archive
Celera10109,920,119 - 110,173,614 (-)RGD
HuRef10109,817,609 - 110,070,887 (-)ENTREZGENE
CHM1_110116,474,653 - 116,728,179 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,578,497 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322882   ⟹   NP_001309811
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,685,003 (-)NCBI
CHM1_110116,474,653 - 116,728,179 (-)NCBI
T2T-CHM13v2.010115,325,183 - 115,579,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322883   ⟹   NP_001309812
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,684,443 (-)NCBI
CHM1_110116,474,653 - 116,728,179 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,578,497 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322884   ⟹   NP_001309813
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,768,304 (-)NCBI
CHM1_110116,474,653 - 116,811,735 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,662,414 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322885   ⟹   NP_001309814
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,768,304 (-)NCBI
CHM1_110116,474,653 - 116,811,735 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,662,414 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322886   ⟹   NP_001309815
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,768,304 (-)NCBI
CHM1_110116,474,653 - 116,811,735 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,662,414 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322887   ⟹   NP_001309816
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,684,443 (-)NCBI
CHM1_110116,474,653 - 116,728,179 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,578,497 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322888   ⟹   NP_001309817
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322889   ⟹   NP_001309818
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322890   ⟹   NP_001309819
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322891   ⟹   NP_001309820
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322892   ⟹   NP_001309821
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322893   ⟹   NP_001309822
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322894   ⟹   NP_001309823
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322895   ⟹   NP_001309824
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322896   ⟹   NP_001309825
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322897   ⟹   NP_001309826
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322898   ⟹   NP_001309827
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322899   ⟹   NP_001309828
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322900   ⟹   NP_001309829
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001352440   ⟹   NP_001339369
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,632,397 (-)NCBI
T2T-CHM13v2.010115,325,183 - 115,526,451 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001352441   ⟹   NP_001339370
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,632,397 (-)NCBI
T2T-CHM13v2.010115,325,183 - 115,526,451 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001352442   ⟹   NP_001339371
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,613,736 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,507,789 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001352443   ⟹   NP_001339372
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: NM_002313   ⟹   NP_002304
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,658,275 (-)NCBI
GRCh3710116,190,869 - 116,444,762 (-)NCBI
Build 3610116,180,859 - 116,408,048 (-)NCBI Archive
Celera10109,920,119 - 110,173,614 (-)RGD
HuRef10109,817,609 - 110,070,887 (-)ENTREZGENE
CHM1_110116,474,653 - 116,701,823 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,552,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_006720   ⟹   NP_006711
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,112 - 114,526,913 (-)NCBI
GRCh3710116,190,869 - 116,444,762 (-)NCBI
Build 3610116,180,859 - 116,276,675 (-)NCBI Archive
Celera10109,920,119 - 110,173,614 (-)RGD
HuRef10109,817,609 - 110,070,887 (-)ENTREZGENE
CHM1_110116,474,653 - 116,570,463 (-)NCBI
T2T-CHM13v2.010115,325,185 - 115,420,991 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717837   ⟹   XP_006717900
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,685,003 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717846   ⟹   XP_006717909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,526,913 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011539801   ⟹   XP_011538103
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,613,736 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011539802   ⟹   XP_011538104
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,633,184 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017016245   ⟹   XP_016871734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,768,304 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017016247   ⟹   XP_016871736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017016250   ⟹   XP_016871739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,768,304 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017016255   ⟹   XP_016871744
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,768,304 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017016256   ⟹   XP_016871745
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,632,397 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448010   ⟹   XP_024303778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448011   ⟹   XP_024303779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448013   ⟹   XP_024303781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,613,736 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448014   ⟹   XP_024303782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,632,397 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448016   ⟹   XP_024303784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,632,397 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448018   ⟹   XP_024303786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,632,397 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047425229   ⟹   XP_047281185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425231   ⟹   XP_047281187
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425232   ⟹   XP_047281188
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425233   ⟹   XP_047281189
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,685,003 (-)NCBI
RefSeq Acc Id: XM_047425234   ⟹   XP_047281190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425236   ⟹   XP_047281192
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425237   ⟹   XP_047281193
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425238   ⟹   XP_047281194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425239   ⟹   XP_047281195
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425240   ⟹   XP_047281196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425242   ⟹   XP_047281198
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425243   ⟹   XP_047281199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,431,110 - 114,685,003 (-)NCBI
RefSeq Acc Id: XM_047425244   ⟹   XP_047281200
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,449,980 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425245   ⟹   XP_047281201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,449,980 - 114,801,373 (-)NCBI
RefSeq Acc Id: XM_047425246   ⟹   XP_047281202
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810114,449,980 - 114,632,397 (-)NCBI
RefSeq Acc Id: XM_054365907   ⟹   XP_054221882
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,686 (-)NCBI
RefSeq Acc Id: XM_054365908   ⟹   XP_054221883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365909   ⟹   XP_054221884
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,507,789 (-)NCBI
RefSeq Acc Id: XM_054365910   ⟹   XP_054221885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365911   ⟹   XP_054221886
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365912   ⟹   XP_054221887
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,579,057 (-)NCBI
RefSeq Acc Id: XM_054365913   ⟹   XP_054221888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,686 (-)NCBI
RefSeq Acc Id: XM_054365914   ⟹   XP_054221889
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,527,219 (-)NCBI
RefSeq Acc Id: XM_054365915   ⟹   XP_054221890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,507,789 (-)NCBI
RefSeq Acc Id: XM_054365916   ⟹   XP_054221891
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,526,451 (-)NCBI
RefSeq Acc Id: XM_054365917   ⟹   XP_054221892
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,662,414 (-)NCBI
RefSeq Acc Id: XM_054365918   ⟹   XP_054221893
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365919   ⟹   XP_054221894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365920   ⟹   XP_054221895
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,579,057 (-)NCBI
RefSeq Acc Id: XM_054365921   ⟹   XP_054221896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365922   ⟹   XP_054221897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365923   ⟹   XP_054221898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,686 (-)NCBI
RefSeq Acc Id: XM_054365924   ⟹   XP_054221899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,686 (-)NCBI
RefSeq Acc Id: XM_054365925   ⟹   XP_054221900
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,526,451 (-)NCBI
RefSeq Acc Id: XM_054365926   ⟹   XP_054221901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,662,414 (-)NCBI
RefSeq Acc Id: XM_054365927   ⟹   XP_054221902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365928   ⟹   XP_054221903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365929   ⟹   XP_054221904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365930   ⟹   XP_054221905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365931   ⟹   XP_054221906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,662,414 (-)NCBI
RefSeq Acc Id: XM_054365932   ⟹   XP_054221907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,526,451 (-)NCBI
RefSeq Acc Id: XM_054365933   ⟹   XP_054221908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,686,685 (-)NCBI
RefSeq Acc Id: XM_054365934   ⟹   XP_054221909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,579,057 (-)NCBI
RefSeq Acc Id: XM_054365935   ⟹   XP_054221910
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,526,451 (-)NCBI
RefSeq Acc Id: XM_054365936   ⟹   XP_054221911
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,523,952 (-)NCBI
RefSeq Acc Id: XM_054365937   ⟹   XP_054221912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,325,183 - 115,420,991 (-)NCBI
RefSeq Acc Id: XM_054365938   ⟹   XP_054221913
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,344,138 - 115,686,686 (-)NCBI
RefSeq Acc Id: XM_054365939   ⟹   XP_054221914
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,344,138 - 115,686,686 (-)NCBI
RefSeq Acc Id: XM_054365940   ⟹   XP_054221915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010115,344,138 - 115,526,451 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001003407 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309811 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309812 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309813 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309814 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309815 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309816 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309817 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309818 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309819 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309820 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309821 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309822 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309823 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309824 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309825 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309826 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309827 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309828 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309829 (Get FASTA)   NCBI Sequence Viewer  
  NP_001339369 (Get FASTA)   NCBI Sequence Viewer  
  NP_001339370 (Get FASTA)   NCBI Sequence Viewer  
  NP_001339371 (Get FASTA)   NCBI Sequence Viewer  
  NP_001339372 (Get FASTA)   NCBI Sequence Viewer  
  NP_002304 (Get FASTA)   NCBI Sequence Viewer  
  NP_006711 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717900 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717909 (Get FASTA)   NCBI Sequence Viewer  
  XP_011538103 (Get FASTA)   NCBI Sequence Viewer  
  XP_011538104 (Get FASTA)   NCBI Sequence Viewer  
  XP_016871734 (Get FASTA)   NCBI Sequence Viewer  
  XP_016871736 (Get FASTA)   NCBI Sequence Viewer  
  XP_016871739 (Get FASTA)   NCBI Sequence Viewer  
  XP_016871744 (Get FASTA)   NCBI Sequence Viewer  
  XP_016871745 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303778 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303779 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303781 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303782 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303784 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303786 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281185 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281187 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281188 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281189 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281190 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281192 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281193 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281194 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281195 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281196 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281198 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281199 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281200 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281201 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281202 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221882 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221883 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221884 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221885 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221886 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221887 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221888 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221889 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221890 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221891 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221892 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221893 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221894 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221895 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221896 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221897 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221898 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221899 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221900 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221901 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221902 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221903 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221904 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221905 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221906 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221907 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221908 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221909 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221910 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221911 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221912 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221913 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221914 (Get FASTA)   NCBI Sequence Viewer  
  XP_054221915 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC51676 (Get FASTA)   NCBI Sequence Viewer  
  AAH02448 (Get FASTA)   NCBI Sequence Viewer  
  AWX65651 (Get FASTA)   NCBI Sequence Viewer  
  BAA06681 (Get FASTA)   NCBI Sequence Viewer  
  BAG52725 (Get FASTA)   NCBI Sequence Viewer  
  BAG53605 (Get FASTA)   NCBI Sequence Viewer  
  BAG53784 (Get FASTA)   NCBI Sequence Viewer  
  BAG60865 (Get FASTA)   NCBI Sequence Viewer  
  BAH12557 (Get FASTA)   NCBI Sequence Viewer  
  CAH18679 (Get FASTA)   NCBI Sequence Viewer  
  EAW49467 (Get FASTA)   NCBI Sequence Viewer  
  EAW49468 (Get FASTA)   NCBI Sequence Viewer  
  EAW49469 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000358257
  ENSP00000358257.2
  ENSP00000358260
  ENSP00000358260.3
  ENSP00000376679
  ENSP00000376679.3
  ENSP00000376682
  ENSP00000376682.4
  ENSP00000400934.1
  ENSP00000414154.1
  ENSP00000433629
  ENSP00000433629.3
  ENSP00000497150.1
  ENSP00000499023
  ENSP00000499023.2
  ENSP00000499163.1
  ENSP00000516747
  ENSP00000516747.1
GenBank Protein O14639 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001003407   ⟸   NM_001003407
- Peptide Label: isoform b
- UniProtKB: F8W8M4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_002304   ⟸   NM_002313
- Peptide Label: isoform a
- UniProtKB: Q68CQ9 (UniProtKB/Swiss-Prot),   Q5T6N5 (UniProtKB/Swiss-Prot),   Q5T6N3 (UniProtKB/Swiss-Prot),   Q5T6N2 (UniProtKB/Swiss-Prot),   Q5JVV2 (UniProtKB/Swiss-Prot),   Q5JVV1 (UniProtKB/Swiss-Prot),   Q15039 (UniProtKB/Swiss-Prot),   B3KVH2 (UniProtKB/Swiss-Prot),   A8MXA9 (UniProtKB/Swiss-Prot),   A6NJ06 (UniProtKB/Swiss-Prot),   A6NI16 (UniProtKB/Swiss-Prot),   Q9BUP1 (UniProtKB/Swiss-Prot),   O14639 (UniProtKB/Swiss-Prot),   A0A2Z4N5U1 (UniProtKB/TrEMBL)
- Sequence: