CD37 (CD37 molecule) - Rat Genome Database

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Gene: CD37 (CD37 molecule) Homo sapiens
Analyze
Symbol: CD37
Name: CD37 molecule
RGD ID: 1346523
HGNC Page HGNC:1666
Description: Predicted to act upstream of or within several processes, including defense response to protozoan; negative regulation of leukocyte activation; and positive regulation of immunoglobulin production. Located in immunological synapse.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CD37 antigen; cell differentiation antigen 37; GP52-40; leukocyte antigen CD37; leukocyte surface antigen CD37; MGC120234; tetraspanin-26; tspan-26; TSPAN26
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
GRCh381949,335,406 - 49,340,606 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1949,335,171 - 49,343,335 (+)EnsemblGRCh38hg38GRCh38
GRCh371949,838,663 - 49,843,863 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361954,530,489 - 54,535,675 (+)NCBINCBI36Build 36hg18NCBI36
Build 341954,530,546 - 54,535,613NCBI
Celera1946,705,529 - 46,710,715 (+)NCBICelera
Cytogenetic Map19q13.33NCBI
HuRef1946,215,487 - 46,220,673 (+)NCBIHuRef
CHM1_11949,840,523 - 49,845,709 (+)NCBICHM1_1
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,6-di-tert-butyl-4-methylphenol  (ISO)
2-butoxyethanol  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4-hydroxyphenyl retinamide  (ISO)
9-cis-retinoic acid  (ISO)
acetamide  (ISO)
all-trans-retinoic acid  (EXP,ISO)
alpha-Zearalanol  (ISO)
ammonium chloride  (ISO)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
atrazine  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
beta-lapachone  (EXP)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (ISO)
buta-1,3-diene  (ISO)
carbon nanotube  (ISO)
chloroprene  (ISO)
choline  (ISO)
chrysene  (ISO)
cisplatin  (EXP)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
dichloromethane  (ISO)
dimethylarsinic acid  (ISO)
diuron  (EXP)
ethylbenzene  (ISO)
flavonoids  (ISO)
folic acid  (ISO)
gentamycin  (ISO)
glycidol  (ISO)
hexachlorobenzene  (ISO)
isotretinoin  (EXP)
L-methionine  (ISO)
lead(0)  (EXP)
methotrexate  (ISO)
methylarsonic acid  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
nitrates  (ISO)
ozone  (ISO)
paracetamol  (EXP,ISO)
piperonyl butoxide  (ISO)
prothioconazole  (EXP)
silicon dioxide  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (ISO)
tamoxifen  (ISO)
Tesaglitazar  (ISO)
testosterone  (EXP)
tetraphene  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
triphenyl phosphate  (EXP)
triptonide  (ISO)
troglitazone  (ISO)
valproic acid  (EXP)
vinclozolin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. The genes for CD37, CD53, and R2, all members of a novel gene family, are located on different chromosomes. Virtaneva KI, etal., Immunogenetics 1993;37(6):461-5.
Additional References at PubMed
PMID:1879540   PMID:2388030   PMID:2466944   PMID:3257508   PMID:8119731   PMID:8452817   PMID:10229664   PMID:10405235   PMID:10529602   PMID:11739647   PMID:12477932   PMID:14978098  
PMID:15342556   PMID:15489334   PMID:17182550   PMID:17440052   PMID:19913121   PMID:19946888   PMID:20458337   PMID:20628086   PMID:20709950   PMID:21873635   PMID:21930792   PMID:22624718  
PMID:23883821   PMID:24445867   PMID:25275127   PMID:25934707   PMID:26439863   PMID:26760575   PMID:27760757   PMID:28298427   PMID:30089630   PMID:30185523   PMID:30854931   PMID:31089249  
PMID:31366619   PMID:32296183   PMID:32400873   PMID:32513696   PMID:35171311   PMID:38846084  


Genomics

Comparative Map Data
CD37
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381949,335,406 - 49,340,606 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1949,335,171 - 49,343,335 (+)EnsemblGRCh38hg38GRCh38
GRCh371949,838,663 - 49,843,863 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361954,530,489 - 54,535,675 (+)NCBINCBI36Build 36hg18NCBI36
Build 341954,530,546 - 54,535,613NCBI
Celera1946,705,529 - 46,710,715 (+)NCBICelera
Cytogenetic Map19q13.33NCBI
HuRef1946,215,487 - 46,220,673 (+)NCBIHuRef
CHM1_11949,840,523 - 49,845,709 (+)NCBICHM1_1
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBIT2T-CHM13v2.0
Cd37
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39744,883,056 - 44,888,701 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl744,883,056 - 44,888,539 (-)EnsemblGRCm39 Ensembl
GRCm38745,233,632 - 45,239,340 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl745,233,632 - 45,239,115 (-)EnsemblGRCm38mm10GRCm38
MGSCv37752,489,002 - 52,494,209 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36745,101,674 - 45,106,882 (-)NCBIMGSCv36mm8
Celera740,689,498 - 40,694,754 (-)NCBICelera
Cytogenetic Map7B3NCBI
cM Map729.2NCBI
Cd37
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81104,855,622 - 104,861,111 (-)NCBIGRCr8
mRatBN7.2195,719,171 - 95,724,662 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl195,719,190 - 95,724,648 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1101,104,579 - 101,109,734 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01109,577,250 - 109,582,405 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01102,867,647 - 102,872,802 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01101,230,470 - 101,236,061 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1101,230,533 - 101,236,065 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01102,295,444 - 102,300,935 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4195,709,961 - 95,715,116 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1195,788,071 - 95,793,227 (-)NCBI
Celera189,977,460 - 89,982,615 (-)NCBICelera
Cytogenetic Map1q22NCBI
Cd37
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555591,465,937 - 1,471,249 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555591,465,937 - 1,471,249 (-)NCBIChiLan1.0ChiLan1.0
CD37
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22055,453,311 - 55,458,523 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11957,373,489 - 57,378,483 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01946,349,845 - 46,355,294 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11955,273,914 - 55,279,562 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1955,273,914 - 55,279,562 (+)Ensemblpanpan1.1panPan2
CD37
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11107,130,553 - 107,136,602 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1107,128,996 - 107,136,081 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1106,713,852 - 106,719,859 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01107,650,867 - 107,656,876 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.11107,323,776 - 107,329,780 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01106,965,941 - 106,971,950 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01107,807,087 - 107,813,087 (-)NCBIUU_Cfam_GSD_1.0
Cd37
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934921,619,176 - 21,624,634 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366643,237,597 - 3,242,806 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366643,237,747 - 3,242,824 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CD37
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl654,440,727 - 54,448,188 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1654,431,413 - 54,448,195 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CD37
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1642,516,901 - 42,522,695 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl642,517,571 - 42,525,598 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607322,439,360 - 22,444,685 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Cd37
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248324,837,247 - 4,841,756 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248324,837,247 - 4,842,126 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CD37
13 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.33(chr19:49839408-49844174)x3 copy number gain See cases [RCV000445983] Chr19:49839408..49844174 [GRCh37]
Chr19:19q13.33		 likely benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19q13.33(chr19:49645600-49891280)x3 copy number gain not provided [RCV000684076] Chr19:49645600..49891280 [GRCh37]
Chr19:19q13.33		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42		 pathogenic
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42		 not provided
GRCh37/hg19 19q13.33(chr19:49600909-51366070)x3 copy number gain not provided [RCV000847250] Chr19:49600909..51366070 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.685-7C>T single nucleotide variant not provided [RCV000887279] Chr19:49339323 [GRCh38]
Chr19:49842580 [GRCh37]
Chr19:19q13.33		 benign
NM_001774.3(CD37):c.132G>C (p.Val44=) single nucleotide variant not provided [RCV000972095] Chr19:49335776 [GRCh38]
Chr19:49839033 [GRCh37]
Chr19:19q13.33		 benign
NM_001774.3(CD37):c.364G>A (p.Val122Ile) single nucleotide variant not provided [RCV000912066] Chr19:49337946 [GRCh38]
Chr19:49841203 [GRCh37]
Chr19:19q13.33		 benign
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
NM_001774.3(CD37):c.698G>A (p.Gly233Asp) single nucleotide variant not specified [RCV004609943] Chr19:49339343 [GRCh38]
Chr19:49842600 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_48618906)_(50921204_?)dup duplication Developmental and epileptic encephalopathy, 12 [RCV001939968]|not provided [RCV001916178] Chr19:48618906..50921204 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_49519325)_(50366015_?)dup duplication Developmental and epileptic encephalopathy, 12 [RCV002030046] Chr19:49519325..50366015 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.740G>T (p.Gly247Val) single nucleotide variant not specified [RCV004240170] Chr19:49339385 [GRCh38]
Chr19:49842642 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.825C>A (p.Asn275Lys) single nucleotide variant not specified [RCV004225049] Chr19:49340307 [GRCh38]
Chr19:49843564 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.508A>G (p.Asn170Asp) single nucleotide variant not specified [RCV004124471] Chr19:49338760 [GRCh38]
Chr19:49842017 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.173C>A (p.Ser58Tyr) single nucleotide variant not specified [RCV004265916] Chr19:49336939 [GRCh38]
Chr19:49840196 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.638G>A (p.Ser213Asn) single nucleotide variant not specified [RCV004271202] Chr19:49338890 [GRCh38]
Chr19:49842147 [GRCh37]
Chr19:19q13.33		 likely benign
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43		 likely pathogenic
GRCh37/hg19 19q13.33-13.41(chr19:48905537-51614930)x3 copy number gain not specified [RCV003986127] Chr19:48905537..51614930 [GRCh37]
Chr19:19q13.33-13.41		 likely pathogenic
NM_001774.3(CD37):c.841C>T (p.Arg281Cys) single nucleotide variant not specified [RCV004435448] Chr19:49340323 [GRCh38]
Chr19:49843580 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.367G>T (p.Val123Leu) single nucleotide variant not specified [RCV004435447] Chr19:49337949 [GRCh38]
Chr19:49841206 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_49713446)_(50413064_?)dup duplication Developmental and epileptic encephalopathy, 12 [RCV004581120] Chr19:49713446..50413064 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.299C>T (p.Thr100Ile) single nucleotide variant not specified [RCV004606552] Chr19:49337178 [GRCh38]
Chr19:49840435 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001774.3(CD37):c.130G>A (p.Val44Met) single nucleotide variant not specified [RCV004606551] Chr19:49335774 [GRCh38]
Chr19:49839031 [GRCh37]
Chr19:19q13.33		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4974
Count of miRNA genes:983
Interacting mature miRNAs:1230
Transcripts:ENST00000323906, ENST00000391859, ENST00000426897, ENST00000535669, ENST00000593512, ENST00000594743, ENST00000595660, ENST00000595725, ENST00000596426, ENST00000597033, ENST00000597602, ENST00000597852, ENST00000598095, ENST00000598134, ENST00000600121
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1559110SCL22_HSerum cholesterol level QTL 22 (human)3.590.000241Lipid levelLDL cholesterol193190759457907594Human
1331657COPD9_HChronic obstructive pulmonary disease QTL 9 (human)1.94Chronic airflow obstructionpost-bronchodilator FEV1193102176057021760Human

Markers in Region
WI-15345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371949,843,730 - 49,843,830UniSTSGRCh37
Build 361954,535,542 - 54,535,642RGDNCBI36
Celera1946,710,582 - 46,710,682RGD
Cytogenetic Map19q13.3UniSTS
HuRef1946,220,540 - 46,220,640UniSTS
GeneMap99-GB4 RH Map19268.85UniSTS
Whitehead-RH Map19347.2UniSTS
NCBI RH Map19533.4UniSTS
RH93092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371949,843,898 - 49,844,017UniSTSGRCh37
Build 361954,535,710 - 54,535,829RGDNCBI36
Celera1946,710,750 - 46,710,869RGD
Cytogenetic Map19q13.3UniSTS
HuRef1946,220,708 - 46,220,827UniSTS
GeneMap99-GB4 RH Map19270.08UniSTS
STS-AA024912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371949,843,554 - 49,843,794UniSTSGRCh37
Build 361954,535,366 - 54,535,606RGDNCBI36
Celera1946,710,406 - 46,710,646RGD
Cytogenetic Map19q13.3UniSTS
HuRef1946,220,364 - 46,220,604UniSTS
GeneMap99-GB4 RH Map19270.18UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
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Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2428 2788 2253 4971 1725 2337 6 624 1951 465 2267 7293 6468 48 3734 1 847 1741 1604 174 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_033941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001040031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005259435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005259436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011527542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011527543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011527544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA767248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK058093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC106752 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP309557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT019851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR541877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HI179050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HI179052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X14046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000323906   ⟹   ENSP00000325708
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,406 - 49,340,606 (+)Ensembl
Ensembl Acc Id: ENST00000391859   ⟹   ENSP00000375732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,171 - 49,340,602 (+)Ensembl
Ensembl Acc Id: ENST00000426897   ⟹   ENSP00000413151
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,396 - 49,340,575 (+)Ensembl
Ensembl Acc Id: ENST00000535669   ⟹   ENSP00000441037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,427 - 49,340,205 (+)Ensembl
Ensembl Acc Id: ENST00000593512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,406 - 49,337,961 (+)Ensembl
Ensembl Acc Id: ENST00000594743   ⟹   ENSP00000470683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,337,215 - 49,340,027 (+)Ensembl
Ensembl Acc Id: ENST00000595660   ⟹   ENSP00000470260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,464 - 49,337,217 (+)Ensembl
Ensembl Acc Id: ENST00000595725   ⟹   ENSP00000471902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,400 - 49,340,466 (+)Ensembl
Ensembl Acc Id: ENST00000596426
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,434 - 49,338,201 (+)Ensembl
Ensembl Acc Id: ENST00000597033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,205 - 49,337,682 (+)Ensembl
Ensembl Acc Id: ENST00000597602   ⟹   ENSP00000471078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,457 - 49,337,163 (+)Ensembl
Ensembl Acc Id: ENST00000597852
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,418 - 49,340,606 (+)Ensembl
Ensembl Acc Id: ENST00000598095   ⟹   ENSP00000470394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,396 - 49,340,132 (+)Ensembl
Ensembl Acc Id: ENST00000598134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,335,446 - 49,337,246 (+)Ensembl
Ensembl Acc Id: ENST00000600121
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1949,340,595 - 49,343,335 (+)Ensembl
RefSeq Acc Id: NM_001040031   ⟹   NP_001035120
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381949,335,406 - 49,340,606 (+)NCBI
GRCh371949,838,632 - 49,843,863 (+)NCBI
Build 361954,530,489 - 54,535,675 (+)NCBI Archive
HuRef1946,215,487 - 46,220,673 (+)ENTREZGENE
CHM1_11949,840,523 - 49,845,709 (+)NCBI
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001774   ⟹   NP_001765
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381949,335,406 - 49,340,606 (+)NCBI
GRCh371949,838,632 - 49,843,863 (+)NCBI
Build 361954,530,489 - 54,535,675 (+)NCBI Archive
HuRef1946,215,487 - 46,220,673 (+)ENTREZGENE
CHM1_11949,840,523 - 49,845,709 (+)NCBI
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005259435   ⟹   XP_005259492
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381949,335,406 - 49,340,606 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011527542   ⟹   XP_011525844
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381949,335,406 - 49,340,606 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011527543   ⟹   XP_011525845
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381949,335,406 - 49,340,606 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054322710   ⟹   XP_054178685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
RefSeq Acc Id: XM_054322711   ⟹   XP_054178686
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
RefSeq Acc Id: XM_054322712   ⟹   XP_054178687
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
RefSeq Acc Id: XM_054322713   ⟹   XP_054178688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
RefSeq Acc Id: XM_054322714   ⟹   XP_054178689
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01952,332,834 - 52,338,034 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001035120 (Get FASTA)   NCBI Sequence Viewer  
  NP_001765 (Get FASTA)   NCBI Sequence Viewer  
  XP_005259492 (Get FASTA)   NCBI Sequence Viewer  
  XP_011525844 (Get FASTA)   NCBI Sequence Viewer  
  XP_011525845 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178685 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178686 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178687 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178688 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178689 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI06753 (Get FASTA)   NCBI Sequence Viewer  
  AAI10380 (Get FASTA)   NCBI Sequence Viewer  
  AAV38654 (Get FASTA)   NCBI Sequence Viewer  
  BAB71662 (Get FASTA)   NCBI Sequence Viewer  
  BAG62633 (Get FASTA)   NCBI Sequence Viewer  
  BAG62877 (Get FASTA)   NCBI Sequence Viewer  
  BAH14719 (Get FASTA)   NCBI Sequence Viewer  
  CAA32204 (Get FASTA)   NCBI Sequence Viewer  
  CAG46675 (Get FASTA)   NCBI Sequence Viewer  
  CBX53834 (Get FASTA)   NCBI Sequence Viewer  
  CBX53835 (Get FASTA)   NCBI Sequence Viewer  
  EAW52466 (Get FASTA)   NCBI Sequence Viewer  
  EAW52467 (Get FASTA)   NCBI Sequence Viewer  
  EAW52468 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000325708
  ENSP00000325708.3
  ENSP00000375732.2
  ENSP00000413151
  ENSP00000413151.1
  ENSP00000441037.1
  ENSP00000470260.1
  ENSP00000470394.1
  ENSP00000470683
  ENSP00000470683.1
  ENSP00000471078.1
  ENSP00000471902.1
GenBank Protein P11049 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001765   ⟸   NM_001774
- Peptide Label: isoform A
- UniProtKB: P11049 (UniProtKB/Swiss-Prot),   B4DVC1 (UniProtKB/Swiss-Prot),   Q3KPF9 (UniProtKB/Swiss-Prot),   B7ZAN3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001035120   ⟸   NM_001040031
- Peptide Label: isoform B
- UniProtKB: P11049 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005259492   ⟸   XM_005259435
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011525845   ⟸   XM_011527543
- Peptide Label: isoform X2
- UniProtKB: M0QZP6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011525844   ⟸   XM_011527542
- Peptide Label: isoform X2
- UniProtKB: M0QZP6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000470683   ⟸   ENST00000594743
Ensembl Acc Id: ENSP00000470260   ⟸   ENST00000595660
Ensembl Acc Id: ENSP00000471902   ⟸   ENST00000595725
Ensembl Acc Id: ENSP00000471078   ⟸   ENST00000597602
Ensembl Acc Id: ENSP00000413151   ⟸   ENST00000426897
Ensembl Acc Id: ENSP00000470394   ⟸   ENST00000598095
Ensembl Acc Id: ENSP00000325708   ⟸   ENST00000323906
Ensembl Acc Id: ENSP00000441037   ⟸   ENST00000535669
Ensembl Acc Id: ENSP00000375732   ⟸   ENST00000391859
RefSeq Acc Id: XP_054178685   ⟸   XM_054322710
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054178686   ⟸   XM_054322711
- Peptide Label: isoform X2
- UniProtKB: M0QZP6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054178689   ⟸   XM_054322714
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054178687   ⟸   XM_054322712
- Peptide Label: isoform X2
- UniProtKB: M0QZP6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054178688   ⟸   XM_054322713
- Peptide Label: isoform X2
- UniProtKB: M0QZP6 (UniProtKB/TrEMBL)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P11049-F1-model_v2 AlphaFold P11049 1-281 view protein structure

Promoters
RGD ID:13205101
Promoter ID:EPDNEW_H26131
Type:initiation region
Name:CD37_1
Description:CD37 molecule
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381949,335,427 - 49,335,487EPDNEW
RGD ID:6795268
Promoter ID:HG_KWN:30527
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000391859,   NM_001040031,   NM_001774,   UC002PNC.1,   UC002PNF.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361954,530,244 - 54,530,744 (+)MPROMDB
RGD ID:6852354
Promoter ID:EP73984
Type:initiation region
Name:HS_CD37
Description:CD37 antigen.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 361954,530,537 - 54,530,597EPD

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1666 AgrOrtholog
COSMIC CD37 COSMIC
Ensembl Genes ENSG00000104894 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000323906 ENTREZGENE
  ENST00000323906.9 UniProtKB/Swiss-Prot
  ENST00000391859.6 UniProtKB/TrEMBL
  ENST00000426897 ENTREZGENE
  ENST00000426897.6 UniProtKB/Swiss-Prot
  ENST00000535669.6 UniProtKB/TrEMBL
  ENST00000594743 ENTREZGENE
  ENST00000594743.1 UniProtKB/TrEMBL
  ENST00000595660.1 UniProtKB/TrEMBL
  ENST00000595725.5 UniProtKB/TrEMBL
  ENST00000597602.1 UniProtKB/TrEMBL
  ENST00000598095.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.1450.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000104894 GTEx
HGNC ID HGNC:1666 ENTREZGENE
Human Proteome Map CD37 Human Proteome Map
InterPro Tetraspanin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tetraspanin/Peripherin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tetraspanin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tetraspanin_EC2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:951 UniProtKB/Swiss-Prot
NCBI Gene 951 ENTREZGENE
OMIM 151523 OMIM
PANTHER LEUKOCYTE ANTIGEN CD37 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR19282 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Tetraspanin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26213 PharmGKB
PIRSF Tetraspanin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS TMFOUR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE TM4_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48652 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B4DVC1 ENTREZGENE
  B7ZAN3 ENTREZGENE, UniProtKB/TrEMBL
  CD37_HUMAN UniProtKB/Swiss-Prot
  M0QZ33_HUMAN UniProtKB/TrEMBL
  M0QZP6 ENTREZGENE, UniProtKB/TrEMBL
  M0R083_HUMAN UniProtKB/TrEMBL
  M0R1J1_HUMAN UniProtKB/TrEMBL
  P11049 ENTREZGENE
  Q3KPF9 ENTREZGENE
  Q96LM7_HUMAN UniProtKB/TrEMBL
UniProt Secondary B4DVC1 UniProtKB/Swiss-Prot
  Q3KPF9 UniProtKB/Swiss-Prot