ERC1 (ELKS/RAB6-interacting/CAST family member 1) - Rat Genome Database

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Gene: ERC1 (ELKS/RAB6-interacting/CAST family member 1) Homo sapiens
Analyze
Symbol: ERC1
Name: ELKS/RAB6-interacting/CAST family member 1
RGD ID: 1604628
HGNC Page HGNC:17072
Description: Enables cadherin binding activity. Involved in I-kappaB phosphorylation and positive regulation of NF-kappaB transcription factor activity. Located in centrosome; ciliary basal body; and cytoplasm. Part of IkappaB kinase complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: Cast2; ELKS; ERC-1; FLJ31750; KIAA1081; MGC12974; RAB6 interacting protein 2; Rab6-interacting protein 2; RAB6IP2
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
GRCh3812989,959 - 1,495,933 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl12990,509 - 1,495,933 (+)EnsemblGRCh38hg38GRCh38
GRCh37121,100,389 - 1,605,099 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3612970,665 - 1,472,958 (+)NCBINCBI36Build 36hg18NCBI36
Celera122,707,077 - 3,211,656 (+)NCBICelera
Cytogenetic Map12p13.33NCBI
HuRef12952,225 - 1,457,980 (+)NCBIHuRef
CHM1_1121,099,408 - 1,604,090 (+)NCBICHM1_1
T2T-CHM13v2.012985,850 - 1,490,194 (+)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
(-)-epigallocatechin 3-gallate  (EXP)
(1->4)-beta-D-glucan  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,5-hexanedione  (ISO)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
acetamide  (ISO)
acrolein  (EXP)
aflatoxin B1  (EXP)
Aflatoxin B2 alpha  (EXP)
alpha-pinene  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
beta-lapachone  (EXP)
bisphenol A  (EXP,ISO)
bisphenol AF  (EXP)
Bisphenol B  (EXP)
bisphenol F  (EXP,ISO)
cadmium dichloride  (EXP)
caffeine  (EXP)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
diarsenic trioxide  (EXP)
Dibutyl phosphate  (EXP)
dicrotophos  (EXP)
endosulfan  (ISO)
entinostat  (EXP)
epoxiconazole  (ISO)
ethanol  (ISO)
folic acid  (ISO)
FR900359  (EXP)
fulvestrant  (EXP)
genistein  (ISO)
geraniol  (EXP)
glycidol  (ISO)
hydroquinone O-beta-D-glucopyranoside  (EXP)
irinotecan  (EXP)
ivermectin  (EXP)
ketoconazole  (EXP)
methapyrilene  (EXP)
methoxychlor  (ISO)
N,N-diethyl-m-toluamide  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
ozone  (EXP)
paracetamol  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
permethrin  (ISO)
pinostrobin  (EXP)
pirinixic acid  (ISO)
potassium chromate  (EXP)
sodium arsenite  (EXP)
sunitinib  (EXP)
testosterone enanthate  (EXP)
thimerosal  (EXP)
thiram  (EXP)
titanium dioxide  (ISO)
torcetrapib  (EXP)
triphenyl phosphate  (EXP)
triptonide  (ISO)
valproic acid  (EXP,ISO)

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
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:1733848   PMID:8889548   PMID:10337992   PMID:10470851   PMID:10697956   PMID:11929610   PMID:12168954   PMID:12203787   PMID:12391317   PMID:12477932   PMID:12923177   PMID:14702039  
PMID:14723704   PMID:15218148   PMID:15324660   PMID:15489334   PMID:16033967   PMID:16964243   PMID:17353931   PMID:17690697   PMID:19013454   PMID:19531213   PMID:20201926   PMID:20379614  
PMID:20533395   PMID:20562859   PMID:20932476   PMID:21144913   PMID:21145461   PMID:21150319   PMID:21832049   PMID:21873635   PMID:21911577   PMID:21917424   PMID:22107844   PMID:22504420  
PMID:22558309   PMID:22713806   PMID:22939629   PMID:23398456   PMID:23455922   PMID:23583364   PMID:23602568   PMID:24152084   PMID:24255178   PMID:24613754   PMID:24982445   PMID:24999758  
PMID:25281560   PMID:25468996   PMID:25735744   PMID:26167880   PMID:26186194   PMID:26344197   PMID:26472760   PMID:26496610   PMID:26638075   PMID:26687479   PMID:26831064   PMID:27173435  
PMID:27224062   PMID:27253063   PMID:27880917   PMID:28514442   PMID:28515276   PMID:28656962   PMID:28718761   PMID:28986522   PMID:29117863   PMID:29121065   PMID:29348417   PMID:29467281  
PMID:29491150   PMID:29507755   PMID:29778605   PMID:29946045   PMID:29997244   PMID:30021884   PMID:30575818   PMID:31024071   PMID:31073040   PMID:31091453   PMID:31500835   PMID:31519766  
PMID:31586073   PMID:31753913   PMID:31762063   PMID:31980649   PMID:32060556   PMID:32353859   PMID:32460013   PMID:32707033   PMID:32768867   PMID:32788342   PMID:32838362   PMID:33060197  
PMID:33111431   PMID:33761347   PMID:33916271   PMID:33961781   PMID:34011540   PMID:34079125   PMID:34162889   PMID:34299191   PMID:34349018   PMID:34662580   PMID:34709266   PMID:34709727  
PMID:34901782   PMID:35063084   PMID:35235311   PMID:35271311   PMID:35384245   PMID:35446349   PMID:35575683   PMID:35831314   PMID:35906200   PMID:35914814   PMID:35944360   PMID:35987950  
PMID:36215168   PMID:36232890   PMID:36526897   PMID:36779422   PMID:36931259   PMID:37071682   PMID:37437062   PMID:37774976   PMID:38280479   PMID:38334954   PMID:38580884   PMID:38803224  
PMID:39231216  


Genomics

Comparative Map Data
ERC1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3812989,959 - 1,495,933 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl12990,509 - 1,495,933 (+)EnsemblGRCh38hg38GRCh38
GRCh37121,100,389 - 1,605,099 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3612970,665 - 1,472,958 (+)NCBINCBI36Build 36hg18NCBI36
Celera122,707,077 - 3,211,656 (+)NCBICelera
Cytogenetic Map12p13.33NCBI
HuRef12952,225 - 1,457,980 (+)NCBIHuRef
CHM1_1121,099,408 - 1,604,090 (+)NCBICHM1_1
T2T-CHM13v2.012985,850 - 1,490,194 (+)NCBIT2T-CHM13v2.0
Erc1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm396119,547,757 - 119,830,985 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl6119,547,757 - 119,825,128 (-)EnsemblGRCm39 Ensembl
GRCm386119,570,796 - 119,848,184 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl6119,570,796 - 119,848,167 (-)EnsemblGRCm38mm10GRCm38
MGSCv376119,520,814 - 119,798,168 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv366119,540,864 - 119,813,753 (-)NCBIMGSCv36mm8
Celera6121,405,104 - 121,685,429 (-)NCBICelera
Cytogenetic Map6F1NCBI
cM Map656.86NCBI
Erc1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84154,435,936 - 154,727,987 (-)NCBIGRCr8
mRatBN7.24152,763,664 - 153,055,724 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4152,767,419 - 153,055,639 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4159,025,966 - 159,332,211 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04154,809,683 - 155,115,934 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04153,433,030 - 153,739,286 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04152,087,393 - 152,380,023 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4152,087,379 - 152,380,184 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04219,174,705 - 219,465,108 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44155,931,377 - 156,221,104 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.14156,234,169 - 156,465,945 (-)NCBI
Celera4141,623,820 - 141,910,539 (-)NCBICelera
Cytogenetic Map4q42NCBI
Erc1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554543,586,667 - 4,031,130 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554543,584,910 - 4,036,276 (+)NCBIChiLan1.0ChiLan1.0
ERC1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2106,489,987 - 7,025,406 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1126,486,819 - 7,022,165 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0121,066,034 - 1,597,562 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1121,027,967 - 1,550,182 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl121,027,967 - 1,545,431 (+)Ensemblpanpan1.1panPan2
ERC1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12743,004,243 - 43,544,260 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2743,038,544 - 43,678,843 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha273,140,420 - 3,679,170 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02743,365,560 - 43,911,683 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2743,365,538 - 43,911,649 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12743,303,937 - 43,842,830 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02743,275,814 - 43,815,242 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0272,498,548 - 3,038,339 (-)NCBIUU_Cfam_GSD_1.0
Erc1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404945107,470,207 - 107,982,754 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366061,201,657 - 1,708,551 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366061,201,420 - 1,713,894 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ERC1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl568,223,729 - 68,608,703 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1568,223,722 - 68,608,705 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2570,490,274 - 70,873,482 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ERC1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.111989,376 - 1,530,470 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl111,030,294 - 1,524,817 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660636,812,077 - 7,356,786 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Erc1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473511,400,159 - 11,841,920 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473511,398,603 - 11,907,553 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ERC1
88 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12p13.33(chr12:832749-1632145)x3 copy number gain See cases [RCV000050805] Chr12:832749..1632145 [GRCh38]
Chr12:941915..1741311 [GRCh37]
Chr12:812176..1611572 [NCBI36]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33-13.32(chr12:121255-3968447)x1 copy number loss See cases [RCV000050637] Chr12:121255..3968447 [GRCh38]
Chr12:282465..4077613 [GRCh37]
Chr12:100682..3947874 [NCBI36]
Chr12:12p13.33-13.32
pathogenic
GRCh38/hg38 12p13.33(chr12:1453550-2575642)x3 copy number gain See cases [RCV000051953] Chr12:1453550..2575642 [GRCh38]
Chr12:1562716..2684808 [GRCh37]
Chr12:1432977..2555069 [NCBI36]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33-11.22(chr12:121055-28415184)x1 copy number loss See cases [RCV000052776] Chr12:121055..28415184 [GRCh38]
Chr12:282465..28568117 [GRCh37]
Chr12:100482..28459384 [NCBI36]
Chr12:12p13.33-11.22
pathogenic
GRCh38/hg38 12p13.33(chr12:99592-1786491)x1 copy number loss See cases [RCV000052745] Chr12:99592..1786491 [GRCh38]
Chr12:282465..1895657 [GRCh37]
Chr12:79019..1765918 [NCBI36]
Chr12:12p13.33
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3 copy number gain See cases [RCV000053660] Chr12:77187..34380176 [GRCh38]
Chr12:282465..34533111 [GRCh37]
Chr12:56614..34424378 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3 copy number gain See cases [RCV000053662] Chr12:80412..25470329 [GRCh38]
Chr12:282465..25623263 [GRCh37]
Chr12:59839..25514530 [NCBI36]
Chr12:12p13.33-12.1
pathogenic
GRCh38/hg38 12p13.33-13.31(chr12:121055-7272606)x3 copy number gain See cases [RCV000053663] Chr12:121055..7272606 [GRCh38]
Chr12:282465..7425202 [GRCh37]
Chr12:100482..7316469 [NCBI36]
Chr12:12p13.33-13.31
pathogenic
GRCh38/hg38 12p13.33-13.31(chr12:121255-8361746)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053664]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053664]|See cases [RCV000053664] Chr12:121255..8361746 [GRCh38]
Chr12:282465..8514342 [GRCh37]
Chr12:100682..8405609 [NCBI36]
Chr12:12p13.33-13.31
pathogenic
GRCh38/hg38 12p13.33-13.32(chr12:199896-3284963)x3 copy number gain See cases [RCV000053665] Chr12:199896..3284963 [GRCh38]
Chr12:309062..3394129 [GRCh37]
Chr12:179323..3264390 [NCBI36]
Chr12:12p13.33-13.32
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4 copy number gain See cases [RCV000053666] Chr12:212976..33926913 [GRCh38]
Chr12:322142..34079848 [GRCh37]
Chr12:192403..33971115 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
NM_178039.3(ERC1):c.1653+2762A>T single nucleotide variant Lung cancer [RCV000110674] Chr12:1144549 [GRCh38]
Chr12:1253715 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33(chr12:902526-1279346)x3 copy number gain See cases [RCV000134186] Chr12:902526..1279346 [GRCh38]
Chr12:1011692..1388512 [GRCh37]
Chr12:881953..1258773 [NCBI36]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33-13.31(chr12:45740-6945196)x3 copy number gain See cases [RCV000135350] Chr12:45740..6945196 [GRCh38]
Chr12:147099..7054359 [GRCh37]
Chr12:17360..6924620 [NCBI36]
Chr12:12p13.33-13.31
pathogenic
GRCh38/hg38 12p13.33(chr12:54452-2558097)x1 copy number loss See cases [RCV000136313] Chr12:54452..2558097 [GRCh38]
Chr12:282465..2667263 [GRCh37]
Chr12:33879..2537524 [NCBI36]
Chr12:12p13.33
pathogenic
GRCh38/hg38 12p13.33-13.31(chr12:199896-5807366)x1 copy number loss See cases [RCV000136848] Chr12:199896..5807366 [GRCh38]
Chr12:309062..5916532 [GRCh37]
Chr12:179323..5786793 [NCBI36]
Chr12:12p13.33-13.31
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3 copy number gain See cases [RCV000136611] Chr12:121255..34603274 [GRCh38]
Chr12:282465..34756209 [GRCh37]
Chr12:100682..34647476 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33(chr12:936769-1244917)x1 copy number loss See cases [RCV000137681] Chr12:936769..1244917 [GRCh38]
Chr12:1045935..1354083 [GRCh37]
Chr12:916196..1224344 [NCBI36]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33(chr12:80412-2850599)x1 copy number loss See cases [RCV000137693] Chr12:80412..2850599 [GRCh38]
Chr12:282465..2959765 [GRCh37]
Chr12:59839..2830026 [NCBI36]
Chr12:12p13.33
pathogenic|uncertain significance
GRCh38/hg38 12p13.33-13.32(chr12:80412-4420585)x1 copy number loss See cases [RCV000138558] Chr12:80412..4420585 [GRCh38]
Chr12:282465..4529751 [GRCh37]
Chr12:59839..4400012 [NCBI36]
Chr12:12p13.33-13.32
pathogenic
GRCh38/hg38 12p13.33(chr12:431903-1521472)x3 copy number gain See cases [RCV000138907] Chr12:431903..1521472 [GRCh38]
Chr12:541069..1630638 [GRCh37]
Chr12:411330..1500899 [NCBI36]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3 copy number gain See cases [RCV000139052] Chr12:121271..34603261 [GRCh38]
Chr12:282465..34756196 [GRCh37]
Chr12:100698..34647463 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33(chr12:1160947-1364162)x1 copy number loss See cases [RCV000139878] Chr12:1160947..1364162 [GRCh38]
Chr12:1270113..1473328 [GRCh37]
Chr12:1140374..1343589 [NCBI36]
Chr12:12p13.33
uncertain significance
GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4 copy number gain See cases [RCV000139787] Chr12:54427..34608071 [GRCh38]
Chr12:282465..34761006 [GRCh37]
Chr12:33854..34652273 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33
pathogenic
GRCh38/hg38 12p13.33-13.32(chr12:54427-3639603)x1 copy number loss See cases [RCV000141250] Chr12:54427..3639603 [GRCh38]
Chr12:282465..3748769 [GRCh37]
Chr12:33854..3619030 [NCBI36]
Chr12:12p13.33-13.32
pathogenic
GRCh38/hg38 12p13.33-13.32(chr12:54427-4004912)x1 copy number loss See cases [RCV000140991] Chr12:54427..4004912 [GRCh38]
Chr12:282465..4114078 [GRCh37]
Chr12:33854..3984339 [NCBI36]
Chr12:12p13.33-13.32
pathogenic
GRCh38/hg38 12p13.33-12.2(chr12:1258274-20657577)x3 copy number gain See cases [RCV000141905] Chr12:1258274..20657577 [GRCh38]
Chr12:1367440..20810511 [GRCh37]
Chr12:1237701..20701778 [NCBI36]
Chr12:12p13.33-12.2
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4 copy number gain See cases [RCV000142149] Chr12:64620..34682902 [GRCh38]
Chr12:173786..34835837 [GRCh37]
Chr12:44047..34727104 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33(chr12:121255-3003320)x1 copy number loss See cases [RCV000142595] Chr12:121255..3003320 [GRCh38]
Chr12:282465..3112486 [GRCh37]
Chr12:100682..2982747 [NCBI36]
Chr12:12p13.33
pathogenic
GRCh38/hg38 12p13.33-13.31(chr12:418421-6235914)x3 copy number gain See cases [RCV000143357] Chr12:418421..6235914 [GRCh38]
Chr12:527587..6345080 [GRCh37]
Chr12:397848..6215341 [NCBI36]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:148034-34178799)x4 copy number gain See cases [RCV000240164] Chr12:148034..34178799 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic|likely pathogenic
GRCh37/hg19 12p13.33(chr12:1555573-2655985)x3 copy number gain See cases [RCV000240005] Chr12:1555573..2655985 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-13.32(chr12:222888-3931052)x1 copy number loss See cases [RCV000239873] Chr12:222888..3931052 [GRCh37]
Chr12:12p13.33-13.32
pathogenic
GRCh37/hg19 12p13.33(chr12:915106-1577381)x3 copy number gain See cases [RCV000240010] Chr12:915106..1577381 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-11.1(chr12:89061-34178799)x3 copy number gain See cases [RCV000240487] Chr12:89061..34178799 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)x3 copy number gain See cases [RCV000449191] Chr12:173786..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33-12.1(chr12:173786-25286865)x3 copy number gain See cases [RCV000449287] Chr12:173786..25286865 [GRCh37]
Chr12:12p13.33-12.1
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3 copy number gain See cases [RCV000447551] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33(chr12:1122611-1577322)x3 copy number gain See cases [RCV000446853] Chr12:1122611..1577322 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33-13.31(chr12:173786-6378954)x1 copy number loss See cases [RCV000447106] Chr12:173786..6378954 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:173786-5737510)x1 copy number loss See cases [RCV000446628] Chr12:173786..5737510 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33(chr12:1120083-1430236)x1 copy number loss See cases [RCV000447401] Chr12:1120083..1430236 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-12.2(chr12:173786-20026080)x3 copy number gain See cases [RCV000446050] Chr12:173786..20026080 [GRCh37]
Chr12:12p13.33-12.2
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:173786-8257049)x3 copy number gain See cases [RCV000446749] Chr12:173786..8257049 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:189578-34756150) copy number gain See cases [RCV000446017] Chr12:189578..34756150 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33(chr12:173786-2865649)x1 copy number loss See cases [RCV000447876] Chr12:173786..2865649 [GRCh37]
Chr12:12p13.33
pathogenic
GRCh37/hg19 12p13.33(chr12:706022-1125143) copy number gain Abnormal esophagus morphology [RCV000416808] Chr12:706022..1125143 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33(chr12:173786-2108237)x3 copy number gain See cases [RCV000510561] Chr12:173786..2108237 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-11.1(chr12:565369-34835837)x3 copy number gain See cases [RCV000511580] Chr12:565369..34835837 [GRCh37]
Chr12:12p13.33-11.1
likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-13.2(chr12:173786-11677456)x3 copy number gain See cases [RCV000510853] Chr12:173786..11677456 [GRCh37]
Chr12:12p13.33-13.2
pathogenic
GRCh37/hg19 12p13.33-11.22(chr12:173786-28219229)x3 copy number gain See cases [RCV000510961] Chr12:173786..28219229 [GRCh37]
Chr12:12p13.33-11.22
pathogenic
NM_178040.4(ERC1):c.3163G>A (p.Asp1055Asn) single nucleotide variant not specified [RCV004295959] Chr12:1444700 [GRCh38]
Chr12:1553866 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.17G>A (p.Arg6His) single nucleotide variant not specified [RCV004295174] Chr12:1027920 [GRCh38]
Chr12:1137086 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.809T>A (p.Leu270His) single nucleotide variant not specified [RCV004309587] Chr12:1083303 [GRCh38]
Chr12:1192469 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:173786-2793493)x1 copy number loss not provided [RCV000683468] Chr12:173786..2793493 [GRCh37]
Chr12:12p13.33
pathogenic
GRCh37/hg19 12p13.33-q11(chr12:173786-37869107)x3 copy number gain not provided [RCV000683480] Chr12:173786..37869107 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33(chr12:1131052-1355047)x3 copy number gain not provided [RCV000683406] Chr12:1131052..1355047 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:310521-1550563)x1 copy number loss not provided [RCV000683461] Chr12:310521..1550563 [GRCh37]
Chr12:12p13.33
likely pathogenic
GRCh37/hg19 12p13.33-13.32(chr12:173786-4105910)x1 copy number loss not provided [RCV000683471] Chr12:173786..4105910 [GRCh37]
Chr12:12p13.33-13.32
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:173786-5952112)x1 copy number loss not provided [RCV000683474] Chr12:173786..5952112 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33(chr12:605963-1548851)x3 copy number gain not provided [RCV000683454] Chr12:605963..1548851 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33-13.31(chr12:173786-6201932)x1 copy number loss not provided [RCV000683476] Chr12:173786..6201932 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:191242-8122785)x3 copy number gain not provided [RCV000683477] Chr12:191242..8122785 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:173786-6039841)x1 copy number loss not provided [RCV000683475] Chr12:173786..6039841 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x2,3 copy number gain not provided [RCV000683478] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33(chr12:990136-1680695)x3 copy number gain not provided [RCV000683445] Chr12:990136..1680695 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3 copy number gain not provided [RCV000683479] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NC_000012.12:g.(1_3750000)_(5250000_9000000)del deletion Tumoral calcinosis, hyperphosphatemic, familial, 1 [RCV000758697] Chr12:3750000..5250000 [GRCh38]
Chr12:12p13.33-13.31
pathogenic|not provided
GRCh37/hg19 12p13.33(chr12:1253888-1350333)x1 copy number loss not provided [RCV000845621] Chr12:1253888..1350333 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33(chr12:1357860-1366511)x1 copy number loss not provided [RCV000737729] Chr12:1357860..1366511 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33(chr12:1365662-1366511)x1 copy number loss not provided [RCV000737730] Chr12:1365662..1366511 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33(chr12:1365662-1372010)x1 copy number loss not provided [RCV000737731] Chr12:1365662..1372010 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33-11.21(chr12:191619-31733044)x3 copy number gain not provided [RCV000750245] Chr12:191619..31733044 [GRCh37]
Chr12:12p13.33-11.21
pathogenic
GRCh37/hg19 12p13.33(chr12:1047531-1441137)x1 copy number loss not provided [RCV000750258] Chr12:1047531..1441137 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33(chr12:1098614-1366110)x3 copy number gain not provided [RCV000750259] Chr12:1098614..1366110 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33(chr12:1305357-1366314)x1 copy number loss not provided [RCV000750260] Chr12:1305357..1366314 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33(chr12:1344141-1366314)x1 copy number loss not provided [RCV000750261] Chr12:1344141..1366314 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33-13.31(chr12:189216-8185497) copy number gain not provided [RCV000767819] Chr12:189216..8185497 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-12.3(chr12:189216-15001420) copy number gain not provided [RCV000767817] Chr12:189216..15001420 [GRCh37]
Chr12:12p13.33-12.3
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:237588-8278292) copy number gain not provided [RCV000767818] Chr12:237588..8278292 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:173786-6346092)x1 copy number loss not provided [RCV000847821] Chr12:173786..6346092 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33(chr12:1436977-2156672)x3 copy number gain not provided [RCV000849160] Chr12:1436977..2156672 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.3037dup (p.Leu1013fs) duplication Macrocephaly, dysmorphic facies, and psychomotor retardation [RCV000991444] Chr12:1444570..1444571 [GRCh38]
Chr12:1553736..1553737 [GRCh37]
Chr12:12p13.33
likely pathogenic
GRCh37/hg19 12p13.33(chr12:1345909-1476210)x1 copy number loss Delayed speech and language development [RCV000787287] Chr12:1345909..1476210 [GRCh37]
Chr12:12p13.33
likely pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34496628)x3 copy number gain not provided [RCV000847209] Chr12:173786..34496628 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-13.31(chr12:173786-8393815)x3 copy number gain not provided [RCV000846343] Chr12:173786..8393815 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33(chr12:683945-1263167)x3 copy number gain not provided [RCV000847846] Chr12:683945..1263167 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:1168971-1268132)x1 copy number loss not provided [RCV000849144] Chr12:1168971..1268132 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:1019260-1562637)x3 copy number gain not provided [RCV000848785] Chr12:1019260..1562637 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:695863-1263167)x3 copy number gain not provided [RCV001006473] Chr12:695863..1263167 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33(chr12:937798-1289250)x3 copy number gain not provided [RCV001006474] Chr12:937798..1289250 [GRCh37]
Chr12:12p13.33
likely benign|uncertain significance
GRCh37/hg19 12p13.33(chr12:1550562-1861557)x1 copy number loss not provided [RCV000850007] Chr12:1550562..1861557 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:982093-1115007)x3 copy number gain not provided [RCV000845910] Chr12:982093..1115007 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1179T>A (p.Ser393=) single nucleotide variant ERC1-related disorder [RCV003915928]|not provided [RCV000957037] Chr12:1110209 [GRCh38]
Chr12:1219375 [GRCh37]
Chr12:12p13.33
benign
GRCh37/hg19 12p13.33(chr12:1037077-1487331)x3 copy number gain not provided [RCV002473500] Chr12:1037077..1487331 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:1018370-1680695)x3 copy number gain not provided [RCV001006475] Chr12:1018370..1680695 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33(chr12:1136914-1599259)x1 copy number loss not provided [RCV001092704] Chr12:1136914..1599259 [GRCh37]
Chr12:12p13.33
pathogenic
GRCh37/hg19 12p13.33(chr12:1024418-1401311)x3 copy number gain not provided [RCV001006476] Chr12:1024418..1401311 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33(chr12:1173101-1510756)x3 copy number gain not provided [RCV001006477] Chr12:1173101..1510756 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4 copy number gain not provided [RCV001006470] Chr12:274676..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33-13.32(chr12:191242-4683495)x1 copy number loss not provided [RCV001259134] Chr12:191242..4683495 [GRCh37]
Chr12:12p13.33-13.32
pathogenic
GRCh37/hg19 12p13.33(chr12:1111811-1622789)x3 copy number gain not provided [RCV001259129] Chr12:1111811..1622789 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33(chr12:1015338-1518434)x3 copy number gain not provided [RCV001259130] Chr12:1015338..1518434 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-13.31(chr12:189145-7730395)x3 copy number gain not provided [RCV001537906] Chr12:189145..7730395 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
NM_178040.4(ERC1):c.1957G>A (p.Asp653Asn) single nucleotide variant not specified [RCV004306251] Chr12:1182006 [GRCh38]
Chr12:1291172 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-13.31(chr12:146240-8330229)x3 copy number gain Obesity [RCV001801197] Chr12:146240..8330229 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
NM_178040.4(ERC1):c.297T>G (p.Pro99=) single nucleotide variant ERC1-related disorder [RCV003968566]|not provided [RCV001815735] Chr12:1028200 [GRCh38]
Chr12:1137366 [GRCh37]
Chr12:12p13.33
likely benign
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837) copy number gain not specified [RCV002052957] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q11(chr12:173786-37869301) copy number gain not specified [RCV002052958] Chr12:173786..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33-12.1(chr12:173786-25286865) copy number gain not specified [RCV002052955] Chr12:173786..25286865 [GRCh37]
Chr12:12p13.33-12.1
pathogenic
NC_000012.11:g.(?_862732)_(2800365_?)dup duplication not provided [RCV003113825] Chr12:862732..2800365 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-13.31(chr12:173787-8320544)x3 copy number gain not provided [RCV002472514] Chr12:173787..8320544 [GRCh37]
Chr12:12p13.33-13.31
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:176047-34179852)x4 copy number gain Pallister-Killian syndrome [RCV003154827] Chr12:176047..34179852 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33(chr12:817514-2205439)x1 copy number loss not provided [RCV002475589] Chr12:817514..2205439 [GRCh37]
Chr12:12p13.33
pathogenic
NM_178040.4(ERC1):c.2042A>G (p.His681Arg) single nucleotide variant not specified [RCV004144736] Chr12:1183306 [GRCh38]
Chr12:1292472 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.125C>T (p.Ser42Leu) single nucleotide variant not specified [RCV004118668] Chr12:1028028 [GRCh38]
Chr12:1137194 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1175C>G (p.Ser392Cys) single nucleotide variant not specified [RCV004112757] Chr12:1110205 [GRCh38]
Chr12:1219371 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2278C>G (p.Arg760Gly) single nucleotide variant not specified [RCV004081127] Chr12:1189979 [GRCh38]
Chr12:1299145 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1959T>A (p.Asp653Glu) single nucleotide variant not specified [RCV004127190] Chr12:1182008 [GRCh38]
Chr12:1291174 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1295A>G (p.His432Arg) single nucleotide variant not specified [RCV004105020] Chr12:1110325 [GRCh38]
Chr12:1219491 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.364A>G (p.Thr122Ala) single nucleotide variant not specified [RCV004200881] Chr12:1028267 [GRCh38]
Chr12:1137433 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.3218A>C (p.Gln1073Pro) single nucleotide variant not specified [RCV004132433] Chr12:1490097 [GRCh38]
Chr12:1599263 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1784G>A (p.Ser595Asn) single nucleotide variant not specified [RCV004136543] Chr12:1180586 [GRCh38]
Chr12:1289752 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2122G>C (p.Glu708Gln) single nucleotide variant ERC1-related disorder [RCV003953999]|not specified [RCV004160332] Chr12:1183386 [GRCh38]
Chr12:1292552 [GRCh37]
Chr12:12p13.33
likely benign|uncertain significance
NM_178040.4(ERC1):c.323G>A (p.Gly108Asp) single nucleotide variant not specified [RCV004123548] Chr12:1028226 [GRCh38]
Chr12:1137392 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2822A>G (p.Asn941Ser) single nucleotide variant not specified [RCV004166345] Chr12:1371874 [GRCh38]
Chr12:1481040 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.3080T>G (p.Ile1027Ser) single nucleotide variant not specified [RCV004145191] Chr12:1444617 [GRCh38]
Chr12:1553783 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.547A>G (p.Met183Val) single nucleotide variant not specified [RCV004190261] Chr12:1028450 [GRCh38]
Chr12:1137616 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2803A>G (p.Ile935Val) single nucleotide variant not specified [RCV004186649] Chr12:1371855 [GRCh38]
Chr12:1481021 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1244G>A (p.Ser415Asn) single nucleotide variant not specified [RCV004081176] Chr12:1110274 [GRCh38]
Chr12:1219440 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1880G>A (p.Arg627Gln) single nucleotide variant not specified [RCV004078076] Chr12:1181929 [GRCh38]
Chr12:1291095 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2864A>T (p.Gln955Leu) single nucleotide variant not specified [RCV004279970] Chr12:1371916 [GRCh38]
Chr12:1481082 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2365C>G (p.Gln789Glu) single nucleotide variant not specified [RCV004264802] Chr12:1236782 [GRCh38]
Chr12:1345948 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1102T>G (p.Phe368Val) single nucleotide variant not specified [RCV004257946] Chr12:1104765 [GRCh38]
Chr12:1213931 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2417A>G (p.Lys806Arg) single nucleotide variant not specified [RCV004266519] Chr12:1236834 [GRCh38]
Chr12:1346000 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1542G>T (p.Glu514Asp) single nucleotide variant not specified [RCV004331336] Chr12:1116006 [GRCh38]
Chr12:1225172 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1027G>A (p.Val343Ile) single nucleotide variant not specified [RCV004325689] Chr12:1083521 [GRCh38]
Chr12:1192687 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.520G>A (p.Val174Ile) single nucleotide variant not specified [RCV004269562] Chr12:1028423 [GRCh38]
Chr12:1137589 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1767C>A (p.Asp589Glu) single nucleotide variant not specified [RCV004271545] Chr12:1180569 [GRCh38]
Chr12:1289735 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1997G>A (p.Gly666Asp) single nucleotide variant not specified [RCV004360046] Chr12:1182046 [GRCh38]
Chr12:1291212 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-13.32(chr12:191243-5332596)x1 copy number loss not provided [RCV003483146] Chr12:191243..5332596 [GRCh37]
Chr12:12p13.33-13.32
pathogenic
Single allele duplication not provided [RCV003448692] Chr12:188053..34856694 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NM_178040.4(ERC1):c.3214-1G>A single nucleotide variant not provided [RCV003396107] Chr12:1490092 [GRCh38]
Chr12:1599258 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:332362-1590974)x3 copy number gain not provided [RCV003484859] Chr12:332362..1590974 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:173787-2431561)x1 copy number loss not provided [RCV003483145] Chr12:173787..2431561 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3 copy number gain not specified [RCV003986979] Chr12:173786..34835641 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33(chr12:1086096-1588778)x1 copy number loss not specified [RCV003986963] Chr12:1086096..1588778 [GRCh37]
Chr12:12p13.33
uncertain significance
GRCh37/hg19 12p13.33(chr12:922808-2129821)x1 copy number loss not provided [RCV003885454] Chr12:922808..2129821 [GRCh37]
Chr12:12p13.33
likely pathogenic
NM_178040.4(ERC1):c.3214-9246C>T single nucleotide variant ERC1-related disorder [RCV003982067] Chr12:1480847 [GRCh38]
Chr12:1590013 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.308G>C (p.Arg103Pro) single nucleotide variant ERC1-related disorder [RCV003966976] Chr12:1028211 [GRCh38]
Chr12:1137377 [GRCh37]
Chr12:12p13.33
likely benign
NM_178040.4(ERC1):c.1885A>G (p.Ile629Val) single nucleotide variant ERC1-related disorder [RCV003962111] Chr12:1181934 [GRCh38]
Chr12:1291100 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.48G>C (p.Gln16His) single nucleotide variant ERC1-related disorder [RCV003911371] Chr12:1027951 [GRCh38]
Chr12:1137117 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.1738-6A>C single nucleotide variant ERC1-related disorder [RCV003966767] Chr12:1180534 [GRCh38]
Chr12:1289700 [GRCh37]
Chr12:12p13.33
likely benign
NM_178040.4(ERC1):c.300C>T (p.Tyr100=) single nucleotide variant ERC1-related disorder [RCV003922134] Chr12:1028203 [GRCh38]
Chr12:1137369 [GRCh37]
Chr12:12p13.33
likely benign
NM_178040.4(ERC1):c.2820C>T (p.Ala940=) single nucleotide variant ERC1-related disorder [RCV003974119] Chr12:1371872 [GRCh38]
Chr12:1481038 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.1527C>T (p.Ser509=) single nucleotide variant ERC1-related disorder [RCV003947262] Chr12:1115991 [GRCh38]
Chr12:1225157 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.1372A>G (p.Lys458Glu) single nucleotide variant ERC1-related disorder [RCV003934253] Chr12:1112269 [GRCh38]
Chr12:1221435 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.3094A>G (p.Thr1032Ala) single nucleotide variant ERC1-related disorder [RCV003976331] Chr12:1444631 [GRCh38]
Chr12:1553797 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.2158-4G>A single nucleotide variant ERC1-related disorder [RCV003919389] Chr12:1189855 [GRCh38]
Chr12:1299021 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.2207G>A (p.Arg736Gln) single nucleotide variant ERC1-related disorder [RCV003949353] Chr12:1189908 [GRCh38]
Chr12:1299074 [GRCh37]
Chr12:12p13.33
likely benign
NM_178040.4(ERC1):c.148A>G (p.Ser50Gly) single nucleotide variant ERC1-related disorder [RCV003916797] Chr12:1028051 [GRCh38]
Chr12:1137217 [GRCh37]
Chr12:12p13.33
benign
NM_178040.4(ERC1):c.3214-9201G>T single nucleotide variant ERC1-related disorder [RCV003916857] Chr12:1480892 [GRCh38]
Chr12:1590058 [GRCh37]
Chr12:12p13.33
likely benign
NM_178040.4(ERC1):c.1026C>T (p.His342=) single nucleotide variant ERC1-related disorder [RCV003947239] Chr12:1083520 [GRCh38]
Chr12:1192686 [GRCh37]
Chr12:12p13.33
likely benign
NM_178040.4(ERC1):c.2158G>A (p.Ala720Thr) single nucleotide variant not specified [RCV004380502] Chr12:1189859 [GRCh38]
Chr12:1299025 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.85C>T (p.Arg29Cys) single nucleotide variant not specified [RCV004380511] Chr12:1027988 [GRCh38]
Chr12:1137154 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1097G>A (p.Arg366Gln) single nucleotide variant not specified [RCV004380500] Chr12:1104760 [GRCh38]
Chr12:1213926 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2447G>A (p.Arg816Gln) single nucleotide variant not specified [RCV004380505] Chr12:1236864 [GRCh38]
Chr12:1346030 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2302G>A (p.Val768Met) single nucleotide variant not specified [RCV004380503] Chr12:1190003 [GRCh38]
Chr12:1299169 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2675A>C (p.Lys892Thr) single nucleotide variant not specified [RCV004380508] Chr12:1289907 [GRCh38]
Chr12:1399073 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2485C>A (p.Gln829Lys) single nucleotide variant not specified [RCV004380506] Chr12:1236902 [GRCh38]
Chr12:1346068 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.64C>T (p.Pro22Ser) single nucleotide variant not specified [RCV004380510] Chr12:1027967 [GRCh38]
Chr12:1137133 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2441C>T (p.Ala814Val) single nucleotide variant not specified [RCV004380504] Chr12:1236858 [GRCh38]
Chr12:1346024 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1712G>A (p.Arg571Gln) single nucleotide variant not specified [RCV004380501] Chr12:1141762 [GRCh38]
Chr12:1250928 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.260G>T (p.Ser87Ile) single nucleotide variant not specified [RCV004380507] Chr12:1028163 [GRCh38]
Chr12:1137329 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2914C>T (p.Leu972Phe) single nucleotide variant not specified [RCV004380509] Chr12:1371966 [GRCh38]
Chr12:1481132 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2603C>T (p.Thr868Ile) single nucleotide variant not specified [RCV004617832] Chr12:1263149 [GRCh38]
Chr12:1372315 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2044G>T (p.Ala682Ser) single nucleotide variant not specified [RCV004617833] Chr12:1183308 [GRCh38]
Chr12:1292474 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.308G>A (p.Arg103Gln) single nucleotide variant not specified [RCV004617835] Chr12:1028211 [GRCh38]
Chr12:1137377 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.3127C>T (p.Arg1043Cys) single nucleotide variant not specified [RCV004617831] Chr12:1444664 [GRCh38]
Chr12:1553830 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.1861G>A (p.Ala621Thr) single nucleotide variant not specified [RCV004617840] Chr12:1180663 [GRCh38]
Chr12:1289829 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2459A>G (p.Asn820Ser) single nucleotide variant not specified [RCV004617829] Chr12:1236876 [GRCh38]
Chr12:1346042 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.3035C>G (p.Pro1012Arg) single nucleotide variant not specified [RCV004617834] Chr12:1444572 [GRCh38]
Chr12:1553738 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2140G>A (p.Glu714Lys) single nucleotide variant not specified [RCV004617841] Chr12:1183404 [GRCh38]
Chr12:1292570 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.953G>A (p.Ser318Asn) single nucleotide variant not specified [RCV004617830] Chr12:1083447 [GRCh38]
Chr12:1192613 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.595G>A (p.Ala199Thr) single nucleotide variant not specified [RCV004617836] Chr12:1028498 [GRCh38]
Chr12:1137664 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.3206G>C (p.Arg1069Pro) single nucleotide variant not specified [RCV004617837] Chr12:1444743 [GRCh38]
Chr12:1553909 [GRCh37]
Chr12:12p13.33
uncertain significance
NM_178040.4(ERC1):c.2731A>C (p.Asn911His) single nucleotide variant not specified [RCV004617838] Chr12:1289963 [GRCh38]
Chr12:1399129 [GRCh37]
Chr12:12p13.33
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:16884
Count of miRNA genes:1402
Interacting mature miRNAs:1876
Transcripts:ENST00000347735, ENST00000355446, ENST00000360905, ENST00000397203, ENST00000440394, ENST00000515210, ENST00000536573, ENST00000538971, ENST00000539007, ENST00000539802, ENST00000541503, ENST00000542302, ENST00000543086, ENST00000543151, ENST00000543263, ENST00000544277, ENST00000545318, ENST00000545948, ENST00000546231, ENST00000587595, ENST00000588412, ENST00000589028, ENST00000589132, ENST00000592048
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
597214489GWAS1310563_Hbody height QTL GWAS1310563 (human)1e-12body height (VT:0001253)body height (CMO:0000106)1214344241434425Human
597321624GWAS1417698_HX-11441 measurement QTL GWAS1417698 (human)0.000004X-11441 measurement1213942111394212Human
597291858GWAS1387932_Hpeptic ulcer disease, vital capacity QTL GWAS1387932 (human)2e-08peptic ulcer disease, vital capacity1212636751263676Human
597405579GWAS1501653_Hbody height QTL GWAS1501653 (human)9e-17body height (VT:0001253)body height (CMO:0000106)1213914371391438Human
597335435GWAS1431509_HS-warfarin measurement QTL GWAS1431509 (human)0.000008S-warfarin measurement1212892671289268Human
597342920GWAS1438994_Hfemoral neck size QTL GWAS1438994 (human)1e-08femoral neck sizefemoral neck morphological measurement (CMO:0001672)1213099611309962Human
597333001GWAS1429075_HR-warfarin measurement QTL GWAS1429075 (human)0.000004R-warfarin measurement1212628501262851Human
597585798GWAS1642658_Hbody height QTL GWAS1642658 (human)1e-15body height (VT:0001253)body height (CMO:0000106)1213940451394046Human
597061261GWAS1157335_HFEV/FVC ratio QTL GWAS1157335 (human)1e-18FEV/FVC ratioforced expiratory volume to forced vital capacity ratio (CMO:0000241)1214043601404361Human
597582978GWAS1639838_Hbody height QTL GWAS1639838 (human)6e-16body height (VT:0001253)body height (CMO:0000106)1213940451394046Human
597052616GWAS1148690_Hbody height QTL GWAS1148690 (human)0.0000002body height (VT:0001253)body height (CMO:0000106)1214043601404361Human
597081289GWAS1177363_Hattention deficit hyperactivity disorder QTL GWAS1177363 (human)0.000003attention deficit hyperactivity disorder1213400331340034Human
597357179GWAS1453253_Hbody height QTL GWAS1453253 (human)1e-10body height (VT:0001253)body height (CMO:0000106)12992098992099Human
597253816GWAS1349890_Hurate measurement, bone density QTL GWAS1349890 (human)4e-11bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)1210961431096144Human
597290682GWAS1386756_Hsize QTL GWAS1386756 (human)4e-11size1213880121388013Human
597357180GWAS1453254_Hbody height QTL GWAS1453254 (human)8e-49body height (VT:0001253)body height (CMO:0000106)1210250981025099Human
597357181GWAS1453255_Hbody height QTL GWAS1453255 (human)8e-86body height (VT:0001253)body height (CMO:0000106)1213875381387539Human
597254193GWAS1350267_Hurate measurement, bone density QTL GWAS1350267 (human)2e-09bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)1210961431096144Human
597325107GWAS1421181_Hvital capacity QTL GWAS1421181 (human)4e-14vital capacity1211284951128496Human
597343472GWAS1439546_Hdiverticular disease QTL GWAS1439546 (human)2e-11diverticular disease1210539491053950Human
597536695GWAS1632769_Hbody height QTL GWAS1632769 (human)3e-20body height (VT:0001253)body height (CMO:0000106)1214442841444285Human
597536694GWAS1632768_Hbody height QTL GWAS1632768 (human)3e-32body height (VT:0001253)body height (CMO:0000106)1211157511115752Human
597025022GWAS1121096_Hacute myeloid leukemia QTL GWAS1121096 (human)0.0000001leukocyte integrity trait (VT:0010898)1213892671389268Human
597045560GWAS1141634_Hbody height QTL GWAS1141634 (human)2e-14body height (VT:0001253)body height (CMO:0000106)1213852661385267Human
597582128GWAS1638988_Hbody height QTL GWAS1638988 (human)2e-16body height (VT:0001253)body height (CMO:0000106)1213940451394046Human
596953702GWAS1073221_Hsize QTL GWAS1073221 (human)4e-11size1213880121388013Human
597357422GWAS1453496_Hbody height QTL GWAS1453496 (human)1e-13body height (VT:0001253)body height (CMO:0000106)1214651111465112Human
597357423GWAS1453497_Hbody height QTL GWAS1453497 (human)2e-09body height (VT:0001253)body height (CMO:0000106)1214809031480904Human
597059310GWAS1155384_Hvital capacity QTL GWAS1155384 (human)3e-17vital capacity1213497191349720Human
596976495GWAS1096014_Hbody height QTL GWAS1096014 (human)9e-17body height (VT:0001253)body height (CMO:0000106)1213914371391438Human
596962536GWAS1082055_Hpeptic ulcer disease, vital capacity QTL GWAS1082055 (human)2e-08peptic ulcer disease, vital capacity1212636751263676Human
597101288GWAS1197362_Htemporal lobe volume measurement, volumetric brain MRI QTL GWAS1197362 (human)3e-09temporal lobe volume measurement, volumetric brain MRI1211776751177676Human

Markers in Region
D12S1587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,334,584 - 1,334,824UniSTSGRCh37
Build 36121,204,845 - 1,205,085RGDNCBI36
Celera122,941,166 - 2,941,406RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,187,201 - 1,187,439UniSTS
Marshfield Genetic Map121.71RGD
Marshfield Genetic Map121.71UniSTS
Genethon Genetic Map121.6UniSTS
deCODE Assembly Map121.69UniSTS
Stanford-G3 RH Map1268.0UniSTS
NCBI RH Map1228.3UniSTS
GeneMap99-G3 RH Map1268.0UniSTS
D12S389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,113,938 - 1,114,100UniSTSGRCh37
Build 3612984,199 - 984,361RGDNCBI36
Celera122,720,610 - 2,720,760RGD
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map12p13.33UniSTS
HuRef12965,493 - 965,638UniSTS
Marshfield Genetic Map121.71RGD
Marshfield Genetic Map121.71UniSTS
deCODE Assembly Map121.69UniSTS
STS-W47124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,602,270 - 1,602,404UniSTSGRCh37
Build 36121,472,531 - 1,472,665RGDNCBI36
Celera123,208,827 - 3,208,961RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,455,143 - 1,455,277UniSTS
GeneMap99-GB4 RH Map1218.9UniSTS
NCBI RH Map1236.4UniSTS
WI-13645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,417,329 - 1,417,478UniSTSGRCh37
Build 36121,287,590 - 1,287,739RGDNCBI36
Celera123,023,911 - 3,024,060RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,269,937 - 1,270,086UniSTS
GeneMap99-GB4 RH Map1216.74UniSTS
Whitehead-RH Map1233.3UniSTS
NCBI RH Map1220.4UniSTS
G24041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,394,443 - 1,394,571UniSTSGRCh37
Build 36121,264,704 - 1,264,832RGDNCBI36
Celera123,001,025 - 3,001,153RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,247,061 - 1,247,189UniSTS
RH91161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,604,826 - 1,604,950UniSTSGRCh37
Build 36121,475,087 - 1,475,211RGDNCBI36
Celera123,211,383 - 3,211,507RGD
Cytogenetic Map12p13UniSTS
Cytogenetic Map12p13.3UniSTS
HuRef121,457,707 - 1,457,831UniSTS
GeneMap99-GB4 RH Map1217.99UniSTS
RH48779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,238,822 - 1,238,955UniSTSGRCh37
Build 36121,109,083 - 1,109,216RGDNCBI36
Celera122,845,364 - 2,845,497RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,091,437 - 1,091,570UniSTS
G42667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,273,230 - 1,273,314UniSTSGRCh37
Build 36121,143,491 - 1,143,575RGDNCBI36
Celera122,879,815 - 2,879,899RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,125,851 - 1,125,935UniSTS
RH120809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,106,649 - 1,106,968UniSTSGRCh37
Build 3612976,910 - 977,229RGDNCBI36
Celera122,713,321 - 2,713,640RGD
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map12p13.3UniSTS
HuRef12958,296 - 958,615UniSTS
TNG Radiation Hybrid Map12458.0UniSTS
RH118903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,414,416 - 1,414,703UniSTSGRCh37
Build 36121,284,677 - 1,284,964RGDNCBI36
Celera123,020,998 - 3,021,285RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,267,024 - 1,267,311UniSTS
D12S388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,228,616 - 1,228,750UniSTSGRCh37
Build 36121,098,877 - 1,099,011RGDNCBI36
Celera122,835,143 - 2,835,265RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,080,851 - 1,080,973UniSTS
Marshfield Genetic Map121.71UniSTS
D12S972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,527,021 - 1,527,239UniSTSGRCh37
Build 36121,397,282 - 1,397,500RGDNCBI36
Celera123,133,599 - 3,133,817RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,379,575 - 1,379,793UniSTS
D12S1227E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,603,512 - 1,603,593UniSTSGRCh37
GRCh37121,603,512 - 1,603,660UniSTSGRCh37
Build 36121,473,773 - 1,473,854RGDNCBI36
Celera123,210,069 - 3,210,150RGD
Celera123,210,069 - 3,210,217UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map12p13.3UniSTS
HuRef121,456,393 - 1,456,474UniSTS
HuRef121,456,393 - 1,456,541UniSTS
SHGC-152870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,334,575 - 1,334,845UniSTSGRCh37
Build 36121,204,836 - 1,205,106RGDNCBI36
Celera122,941,157 - 2,941,427RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,187,192 - 1,187,460UniSTS
TNG Radiation Hybrid Map364999.0UniSTS
G41234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,399,943 - 1,400,114UniSTSGRCh37
Build 36121,270,204 - 1,270,375RGDNCBI36
Celera123,006,525 - 3,006,696RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,252,562 - 1,252,733UniSTS
SHGC-144473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,517,374 - 1,517,664UniSTSGRCh37
Build 36121,387,635 - 1,387,925RGDNCBI36
Celera123,123,952 - 3,124,242RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,369,928 - 1,370,218UniSTS
TNG Radiation Hybrid Map1225643.0UniSTS
G41233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,334,585 - 1,334,818UniSTSGRCh37
Build 36121,204,846 - 1,205,079RGDNCBI36
Celera122,941,167 - 2,941,400RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,187,202 - 1,187,433UniSTS
G41235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,408,757 - 1,408,871UniSTSGRCh37
Build 36121,279,018 - 1,279,132RGDNCBI36
Celera123,015,339 - 3,015,453RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,261,365 - 1,261,479UniSTS
G41232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,300,215 - 1,300,348UniSTSGRCh37
Build 36121,170,476 - 1,170,609RGDNCBI36
Celera122,906,801 - 2,906,934RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,152,838 - 1,152,971UniSTS
D12S2047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,552,901 - 1,553,089UniSTSGRCh37
Build 36121,423,162 - 1,423,350RGDNCBI36
Celera123,159,460 - 3,159,648RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,405,424 - 1,405,612UniSTS
G41791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,520,481 - 1,520,706UniSTSGRCh37
Build 36121,390,742 - 1,390,967RGDNCBI36
Celera123,127,059 - 3,127,284RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,373,035 - 1,373,260UniSTS
G41231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,176,302 - 1,176,441UniSTSGRCh37
Build 36121,046,563 - 1,046,702RGDNCBI36
Celera122,783,280 - 2,783,419RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,027,704 - 1,027,843UniSTS
RH45217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,208,485 - 1,208,684UniSTSGRCh37
Build 36121,078,746 - 1,078,945RGDNCBI36
Celera122,815,014 - 2,815,213RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,060,728 - 1,060,927UniSTS
GeneMap99-GB4 RH Map1216.12UniSTS
NCBI RH Map1219.3UniSTS
A004N30  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,404,975 - 1,405,120UniSTSGRCh37
Build 36121,275,236 - 1,275,381RGDNCBI36
Celera123,011,557 - 3,011,702RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,257,594 - 1,257,739UniSTS
GeneMap99-GB4 RH Map1219.0UniSTS
NCBI RH Map1210.0UniSTS
D12S1406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,604,826 - 1,604,985UniSTSGRCh37
Build 36121,475,087 - 1,475,246RGDNCBI36
Celera123,211,383 - 3,211,542RGD
Cytogenetic Map12p13UniSTS
Cytogenetic Map12p13.3UniSTS
HuRef121,457,707 - 1,457,866UniSTS
Whitehead-YAC Contig Map12 UniSTS
D12S1285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37121,533,801 - 1,534,112UniSTSGRCh37
Build 36121,404,062 - 1,404,373RGDNCBI36
Celera123,140,370 - 3,140,674RGD
Cytogenetic Map12p13.3UniSTS
HuRef121,386,346 - 1,386,641UniSTS
Marshfield Genetic Map121.71UniSTS
Whitehead-YAC Contig Map12 UniSTS
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
D12S40  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map12p13.3UniSTS
HuRef121,051,758 - 1,052,770UniSTS


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
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2438 2788 2251 4973 1726 2351 5 624 1951 465 2269 7302 6469 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001301248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_178039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_178040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_027946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_027948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_027949 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019074 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428571 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047428584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371535 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054371536 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB015617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB029004 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB053468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB053469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB053470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB053471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC234852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC037377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC068006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC132782 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC132784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM984956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR000847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X58046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000347735   ⟹   ENSP00000340054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,238 - 1,491,567 (+)Ensembl
Ensembl Acc Id: ENST00000355446   ⟹   ENSP00000347621
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,027,772 - 1,492,487 (+)Ensembl
Ensembl Acc Id: ENST00000360905   ⟹   ENSP00000354158
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,223 - 1,495,931 (+)Ensembl
Ensembl Acc Id: ENST00000397203   ⟹   ENSP00000380386
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,248 - 1,493,516 (+)Ensembl
Ensembl Acc Id: ENST00000440394   ⟹   ENSP00000410064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,267 - 1,493,549 (+)Ensembl
Ensembl Acc Id: ENST00000515210
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,430,277 - 1,444,630 (+)Ensembl
Ensembl Acc Id: ENST00000536573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,253 - 1,245,024 (+)Ensembl
Ensembl Acc Id: ENST00000538971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,083,141 - 1,444,589 (+)Ensembl
Ensembl Acc Id: ENST00000539007
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,083,484 - 1,116,201 (+)Ensembl
Ensembl Acc Id: ENST00000539802   ⟹   ENSP00000467196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,408,192 - 1,445,055 (+)Ensembl
Ensembl Acc Id: ENST00000541503
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,115,624 - 1,141,740 (+)Ensembl
Ensembl Acc Id: ENST00000542302   ⟹   ENSP00000445336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,233 - 1,490,729 (+)Ensembl
Ensembl Acc Id: ENST00000543086   ⟹   ENSP00000438546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,208 - 1,495,933 (+)Ensembl
Ensembl Acc Id: ENST00000543151
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,443,291 - 1,491,079 (+)Ensembl
Ensembl Acc Id: ENST00000543263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,257,138 - 1,371,952 (+)Ensembl
Ensembl Acc Id: ENST00000544277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,203,966 - 1,263,073 (+)Ensembl
Ensembl Acc Id: ENST00000545318   ⟹   ENSP00000465628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,233 - 1,189,969 (+)Ensembl
Ensembl Acc Id: ENST00000545948   ⟹   ENSP00000442976
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,273 - 1,490,377 (+)Ensembl
Ensembl Acc Id: ENST00000546231   ⟹   ENSP00000442739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,233 - 1,490,729 (+)Ensembl
Ensembl Acc Id: ENST00000587595
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12998,322 - 1,027,842 (+)Ensembl
Ensembl Acc Id: ENST00000588412   ⟹   ENSP00000467339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,189,896 - 1,491,079 (+)Ensembl
Ensembl Acc Id: ENST00000589028   ⟹   ENSP00000468263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,597 - 1,493,516 (+)Ensembl
Ensembl Acc Id: ENST00000589132   ⟹   ENSP00000464959
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,622 - 1,028,339 (+)Ensembl
Ensembl Acc Id: ENST00000592048   ⟹   ENSP00000467476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,263 - 1,116,033 (+)Ensembl
Ensembl Acc Id: ENST00000611180   ⟹   ENSP00000479523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12990,509 - 1,236,834 (+)Ensembl
Ensembl Acc Id: ENST00000686476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,253 - 1,184,122 (+)Ensembl
Ensembl Acc Id: ENST00000688324   ⟹   ENSP00000510615
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,112,233 - 1,190,052 (+)Ensembl
Ensembl Acc Id: ENST00000689995   ⟹   ENSP00000509777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,083,173 - 1,182,005 (+)Ensembl
Ensembl Acc Id: ENST00000690222
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,253 - 1,188,497 (+)Ensembl
Ensembl Acc Id: ENST00000690948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,229 - 1,399,822 (+)Ensembl
Ensembl Acc Id: ENST00000691018
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,225 - 1,190,375 (+)Ensembl
Ensembl Acc Id: ENST00000691140
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,417,974 - 1,493,514 (+)Ensembl
Ensembl Acc Id: ENST00000691177   ⟹   ENSP00000510024
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl121,115,912 - 1,182,005 (+)Ensembl
Ensembl Acc Id: ENST00000692909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12991,253 - 1,142,195 (+)Ensembl
RefSeq Acc Id: NM_001301248   ⟹   NP_001288177
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38121,027,748 - 1,495,933 (+)NCBI
CHM1_1121,135,894 - 1,604,090 (+)NCBI
T2T-CHM13v2.0121,023,615 - 1,490,194 (+)NCBI
Sequence:
RefSeq Acc Id: NM_178039   ⟹   NP_829883
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
GRCh37121,100,404 - 1,605,099 (+)ENTREZGENE
Build 3612970,665 - 1,472,958 (+)NCBI Archive
HuRef12952,225 - 1,457,980 (+)ENTREZGENE
CHM1_1121,099,378 - 1,604,090 (+)NCBI
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
Sequence:
RefSeq Acc Id: NM_178040   ⟹   NP_829884
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
GRCh37121,100,404 - 1,605,099 (+)ENTREZGENE
Build 3612970,665 - 1,472,958 (+)NCBI Archive
HuRef12952,225 - 1,457,980 (+)ENTREZGENE
CHM1_1121,099,378 - 1,604,090 (+)NCBI
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
Sequence:
RefSeq Acc Id: NR_027946
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
GRCh37121,100,404 - 1,605,099 (+)ENTREZGENE
HuRef12952,225 - 1,457,980 (+)ENTREZGENE
CHM1_1121,099,378 - 1,604,090 (+)NCBI
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
Sequence:
RefSeq Acc Id: NR_027948
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
GRCh37121,100,404 - 1,605,099 (+)ENTREZGENE
HuRef12952,225 - 1,457,980 (+)ENTREZGENE
CHM1_1121,099,378 - 1,604,090 (+)NCBI
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
Sequence:
RefSeq Acc Id: NR_027949
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
GRCh37121,100,404 - 1,605,099 (+)ENTREZGENE
HuRef12952,225 - 1,457,980 (+)ENTREZGENE
CHM1_1121,099,378 - 1,604,090 (+)NCBI
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019052   ⟹   XP_016874541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019054   ⟹   XP_016874543
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019055   ⟹   XP_016874544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,017 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019056   ⟹   XP_016874545
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019057   ⟹   XP_016874546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019059   ⟹   XP_016874548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019060   ⟹   XP_016874549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019061   ⟹   XP_016874550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019062   ⟹   XP_016874551
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019063   ⟹   XP_016874552
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019064   ⟹   XP_016874553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019065   ⟹   XP_016874554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019066   ⟹   XP_016874555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019067   ⟹   XP_016874556
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019069   ⟹   XP_016874558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019070   ⟹   XP_016874559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019072   ⟹   XP_016874561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,642 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019074   ⟹   XP_016874563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38121,167,940 - 1,495,931 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047428556   ⟹   XP_047284512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428557   ⟹   XP_047284513
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428558   ⟹   XP_047284514
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,017 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428559   ⟹   XP_047284515
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428560   ⟹   XP_047284516
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428561   ⟹   XP_047284517
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428562   ⟹   XP_047284518
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812989,998 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428563   ⟹   XP_047284519
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,017 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428564   ⟹   XP_047284520
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428565   ⟹   XP_047284521
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428566   ⟹   XP_047284522
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812989,959 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428567   ⟹   XP_047284523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428568   ⟹   XP_047284524
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428569   ⟹   XP_047284525
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428570   ⟹   XP_047284526
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,017 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428571   ⟹   XP_047284527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428572   ⟹   XP_047284528
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428573   ⟹   XP_047284529
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428574   ⟹   XP_047284530
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428575   ⟹   XP_047284531
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428576   ⟹   XP_047284532
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,017 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428577   ⟹   XP_047284533
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,550 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428578   ⟹   XP_047284534
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428579   ⟹   XP_047284535
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812990,546 - 1,495,931 (+)NCBI
RefSeq Acc Id: XM_047428580   ⟹   XP_047284536
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,642 (+)NCBI
RefSeq Acc Id: XM_047428581   ⟹   XP_047284537
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,642 (+)NCBI
RefSeq Acc Id: XM_047428582   ⟹   XP_047284538
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,642 (+)NCBI
RefSeq Acc Id: XM_047428583   ⟹   XP_047284539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,642 (+)NCBI
RefSeq Acc Id: XM_047428584   ⟹   XP_047284540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,642 (+)NCBI
RefSeq Acc Id: XM_054371489   ⟹   XP_054227464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371490   ⟹   XP_054227465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371491   ⟹   XP_054227466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371492   ⟹   XP_054227467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,908 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371493   ⟹   XP_054227468
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371494   ⟹   XP_054227469
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371495   ⟹   XP_054227470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371496   ⟹   XP_054227471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,908 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371497   ⟹   XP_054227472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371498   ⟹   XP_054227473
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371499   ⟹   XP_054227474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371500   ⟹   XP_054227475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371501   ⟹   XP_054227476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,889 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371502   ⟹   XP_054227477
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371503   ⟹   XP_054227478
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371504   ⟹   XP_054227479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371505   ⟹   XP_054227480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371506   ⟹   XP_054227481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371507   ⟹   XP_054227482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,908 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371508   ⟹   XP_054227483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371509   ⟹   XP_054227484
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,850 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371510   ⟹   XP_054227485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371511   ⟹   XP_054227486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371512   ⟹   XP_054227487
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371513   ⟹   XP_054227488
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371514   ⟹   XP_054227489
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,908 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371515   ⟹   XP_054227490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371516   ⟹   XP_054227491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371517   ⟹   XP_054227492
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371518   ⟹   XP_054227493
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371519   ⟹   XP_054227494
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371520   ⟹   XP_054227495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012985,908 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371521   ⟹   XP_054227496
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371522   ⟹   XP_054227497
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371523   ⟹   XP_054227498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371524   ⟹   XP_054227499
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371525   ⟹   XP_054227500
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371526   ⟹   XP_054227501
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371527   ⟹   XP_054227502
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,490,192 (+)NCBI
RefSeq Acc Id: XM_054371528   ⟹   XP_054227503
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371529   ⟹   XP_054227504
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371530   ⟹   XP_054227505
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371531   ⟹   XP_054227506
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012987,116 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371532   ⟹   XP_054227507
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371533   ⟹   XP_054227508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371534   ⟹   XP_054227509
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371535   ⟹   XP_054227510
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012986,436 - 1,438,908 (+)NCBI
RefSeq Acc Id: XM_054371536   ⟹   XP_054227511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0121,162,256 - 1,490,192 (+)NCBI
RefSeq Acc Id: XR_001748631
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812991,223 - 1,444,620 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001288177 (Get FASTA)   NCBI Sequence Viewer  
  NP_829883 (Get FASTA)   NCBI Sequence Viewer  
  NP_829884 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874541 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874543 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874544 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874545 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874546 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874548 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874549 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874550 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874551 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874552 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874553 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874554 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874555 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874556 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874558 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874559 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874561 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874563 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284512 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284513 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284514 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284515 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284516 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284517 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284518 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284519 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284520 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284521 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284522 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284523 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284524 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284525 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284526 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284527 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284528 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284529 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284530 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284531 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284532 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284533 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284534 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284535 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284536 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284537 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284538 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284539 (Get FASTA)   NCBI Sequence Viewer  
  XP_047284540 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227464 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227465 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227466 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227467 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227468 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227469 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227470 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227471 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227472 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227473 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227474 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227475 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227476 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227477 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227478 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227479 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227480 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227481 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227482 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227483 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227484 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227485 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227486 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227487 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227488 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227489 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227490 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227491 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227492 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227493 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227494 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227495 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227496 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227497 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227498 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227499 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227500 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227501 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227502 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227503 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227504 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227505 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227506 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227507 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227508 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227509 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227510 (Get FASTA)   NCBI Sequence Viewer  
  XP_054227511 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH68006 (Get FASTA)   NCBI Sequence Viewer  
  AAI32783 (Get FASTA)   NCBI Sequence Viewer  
  AAI32785 (Get FASTA)   NCBI Sequence Viewer  
  BAA83033 (Get FASTA)   NCBI Sequence Viewer  
  BAA88763 (Get FASTA)   NCBI Sequence Viewer  
  BAA90975 (Get FASTA)   NCBI Sequence Viewer  
  BAC03827 (Get FASTA)   NCBI Sequence Viewer  
  BAC54107 (Get FASTA)   NCBI Sequence Viewer  
  BAC54108 (Get FASTA)   NCBI Sequence Viewer  
  BAC54109 (Get FASTA)   NCBI Sequence Viewer  
  BAC54110 (Get FASTA)   NCBI Sequence Viewer  
  BAG57618 (Get FASTA)   NCBI Sequence Viewer  
  EAW88932 (Get FASTA)   NCBI Sequence Viewer  
  EAW88933 (Get FASTA)   NCBI Sequence Viewer  
  EAW88934 (Get FASTA)   NCBI Sequence Viewer  
  EAW88935 (Get FASTA)   NCBI Sequence Viewer  
  EAW88936 (Get FASTA)   NCBI Sequence Viewer  
  EAW88937 (Get FASTA)   NCBI Sequence Viewer  
  EAW88938 (Get FASTA)   NCBI Sequence Viewer  
  EAW88939 (Get FASTA)   NCBI Sequence Viewer  
  EAW88940 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000340054.6
  ENSP00000347621
  ENSP00000347621.5
  ENSP00000354158
  ENSP00000354158.3
  ENSP00000380386
  ENSP00000380386.4
  ENSP00000410064
  ENSP00000410064.2
  ENSP00000438546
  ENSP00000438546.1
  ENSP00000442739
  ENSP00000442739.2
  ENSP00000442976.1
  ENSP00000445336
  ENSP00000445336.2
  ENSP00000464959.1
  ENSP00000465628.2
  ENSP00000467196.1
  ENSP00000467339.1
  ENSP00000467476.1
  ENSP00000468263
  ENSP00000468263.1
  ENSP00000479523.2
  ENSP00000509777.1
  ENSP00000510024.1
  ENSP00000510615.1
GenBank Protein Q8IUD2 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_829884   ⟸   NM_178040
- Peptide Label: isoform epsilon
- UniProtKB: Q8IUD2 (UniProtKB/Swiss-Prot),   Q9UIK7 (UniProtKB/Swiss-Prot),   Q9NXN5 (UniProtKB/Swiss-Prot),   Q8NAS1 (UniProtKB/Swiss-Prot),   Q8IUD5 (UniProtKB/Swiss-Prot),   Q8IUD4 (UniProtKB/Swiss-Prot),   Q8IUD3 (UniProtKB/Swiss-Prot),   Q6NVK2 (UniProtKB/Swiss-Prot),   D3DUP8 (UniProtKB/Swiss-Prot),   D3DUP7 (UniProtKB/Swiss-Prot),   A7E295 (UniProtKB/Swiss-Prot),   A2RU77 (UniProtKB/Swiss-Prot),   Q9UPS1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_829883   ⟸   NM_178039
- Peptide Label: isoform delta
- UniProtKB: Q8IUD2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001288177   ⟸   NM_001301248
- Peptide Label: isoform zeta
- UniProtKB: G8JLD3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016874544   ⟸   XM_017019055
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016874543   ⟸   XM_017019054
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016874541   ⟸   XM_017019052
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016874553   ⟸   XM_017019064
- Peptide Label: isoform X8
- UniProtKB: Q8IUD2 (UniProtKB/Swiss-Prot),   Q9UIK7 (UniProtKB/Swiss-Prot),   Q9NXN5 (UniProtKB/Swiss-Prot),   Q8NAS1 (UniProtKB/Swiss-Prot),   Q8IUD5 (UniProtKB/Swiss-Prot),   Q8IUD4 (UniProtKB/Swiss-Prot),   Q8IUD3 (UniProtKB/Swiss-Prot),   Q6NVK2 (UniProtKB/Swiss-Prot),   D3DUP8 (UniProtKB/Swiss-Prot),   D3DUP7 (UniProtKB/Swiss-Prot),   A7E295 (UniProtKB/Swiss-Prot),   A2RU77 (UniProtKB/Swiss-Prot),   Q9UPS1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016874556   ⟸   XM_017019067
- Peptide Label: isoform X12
- UniProtKB: Q8IUD2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016874550   ⟸   XM_017019061
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016874552   ⟸   XM_017019063