STAT2 (signal transducer and activator of transcription 2) - Rat Genome Database

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Gene: STAT2 (signal transducer and activator of transcription 2) Homo sapiens
Analyze
Symbol: STAT2
Name: signal transducer and activator of transcription 2
RGD ID: 1323217
HGNC Page HGNC
Description: Exhibits identical protein binding activity and ubiquitin-like protein ligase binding activity. Involved in defense response to other organism; regulation of mitochondrial fission; and regulation of protein phosphorylation. Localizes to cytosol and plasma membrane. Implicated in immunodeficiency 44.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: IMD44; interferon alpha induced transcriptional activator; ISGF-3; MGC59816; P113; PTORCH3; signal transducer and activator of transcription 2, 113kD; signal transducer and activator of transcription 2, 113kDa; STAT113
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: This gene has been reviewed for its involvement in coronavirus biology, and is involved in immune response or antiviral activity.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1256,341,597 - 56,360,167 (-)EnsemblGRCh38hg38GRCh38
GRCh381256,341,597 - 56,360,161 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371256,735,381 - 56,753,891 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361255,021,648 - 55,040,176 (-)NCBINCBI36hg18NCBI36
Build 341255,021,650 - 55,040,176NCBI
Celera1256,388,733 - 56,407,397 (-)NCBI
Cytogenetic Map12q13.3NCBI
HuRef1253,774,045 - 53,793,077 (-)NCBIHuRef
CHM1_11256,702,765 - 56,721,407 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (EXP)
(S)-nicotine  (EXP)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-hydroxypropanoic acid  (EXP)
2-naphthylamine  (EXP)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-methylcholanthrene  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4-(ethoxymethylene)-2-phenyloxazol-5-one  (ISO)
aconitine  (ISO)
acrylamide  (ISO)
all-trans-retinoic acid  (EXP)
aristolochic acid  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-chloroethyl) sulfide  (EXP)
bisphenol A  (EXP,ISO)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
cisplatin  (EXP)
clopidogrel  (ISO)
copper atom  (EXP)
copper(0)  (EXP)
cyclosporin A  (EXP)
deoxynivalenol  (ISO)
dibutyl phthalate  (ISO)
diethylstilbestrol  (ISO)
doxorubicin  (EXP)
ethyl methanesulfonate  (EXP)
folic acid  (ISO)
formaldehyde  (EXP)
furan  (ISO)
gentamycin  (ISO)
geraniol  (EXP)
GW 4064  (ISO)
hydroxytyrosol  (EXP)
kaempferol  (EXP)
lipopolysaccharide  (EXP,ISO)
methyl methanesulfonate  (EXP)
monosodium L-glutamate  (ISO)
N-nitrosodiethylamine  (ISO)
nefazodone  (ISO)
nickel atom  (EXP)
nicotine  (EXP)
oxaliplatin  (ISO)
paracetamol  (EXP)
pentachlorophenol  (ISO)
pirinixic acid  (ISO)
poly(I:C)  (EXP)
poly(vinylpyrrolidone)  (ISO)
potassium chromate  (EXP)
potassium dichromate  (EXP)
quercetin  (EXP)
rac-lactic acid  (EXP)
silicon dioxide  (ISO)
silver atom  (ISO)
silver(0)  (ISO)
sodium fluoride  (ISO)
succimer  (EXP)
sunitinib  (EXP)
T-2 toxin  (ISO)
tamoxifen  (ISO)
testosterone  (ISO)
tetrachloromethane  (ISO)
tetraphene  (ISO)
titanium dioxide  (ISO)
tofacitinib  (EXP)
topotecan  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (ISO)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vitamin E  (EXP)
zidovudine  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
1. Ashour J, etal., Cell Host Microbe. 2010 Nov 18;8(5):410-21. doi: 10.1016/j.chom.2010.10.007.
2. Elsaesser HJ, etal., Proc Natl Acad Sci U S A. 2020 Mar 10;117(10):5420-5429. doi: 10.1073/pnas.1913776117. Epub 2020 Feb 24.
3. GOA_HUMAN data from the GO Consortium
4. Gopal R, etal., Front Immunol. 2018 Sep 25;9:2151. doi: 10.3389/fimmu.2018.02151. eCollection 2018.
5. Gorman MJ, etal., Cell Host Microbe. 2018 May 9;23(5):672-685.e6. doi: 10.1016/j.chom.2018.04.003.
6. Hahm B, etal., Immunity. 2005 Feb;22(2):247-57. doi: 10.1016/j.immuni.2005.01.005.
7. Kisseleva T, etal., Gene 2002 Feb 20;285(1-2):1-24.
8. Le-Trilling VTK, etal., J Virol. 2018 Jun 29;92(14). pii: JVI.00296-18. doi: 10.1128/JVI.00296-18. Print 2018 Jul 15.
9. Li W, etal., J Virol. 2014 Jul;88(13):7578-88. doi: 10.1128/JVI.03117-13. Epub 2014 Apr 23.
10. Miorin L, etal., J Virol. 2019 Jun 28;93(14). pii: JVI.00151-19. doi: 10.1128/JVI.00151-19. Print 2019 Jul 15.
11. Murray PJ J Immunol. 2007 Mar 1;178(5):2623-9.
12. OMIM Disease Annotation Pipeline
13. Perry ST, etal., PLoS Pathog. 2011 Feb;7(2):e1001297. doi: 10.1371/journal.ppat.1001297. Epub 2011 Feb 17.
14. Pipeline to import KEGG annotations from KEGG into RGD
15. Pipeline to import Pathway Interaction Database annotations from NCI into RGD
16. RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
17. RGD automated import pipeline for gene-chemical interactions
18. Song H, etal., J Immunol. 2019 Apr 15;202(8):2266-2275. doi: 10.4049/jimmunol.1800848. Epub 2019 Mar 6.
19. Sun SL, etal., Clin Exp Pharmacol Physiol. 2007 Nov;34(11):1097-101.
20. Sung PS, etal., Proc Natl Acad Sci U S A. 2015 Aug 18;112(33):10443-8. doi: 10.1073/pnas.1513341112. Epub 2015 Jul 27.
21. Tripathi S, etal., PLoS Pathog. 2017 Mar 9;13(3):e1006258. doi: 10.1371/journal.ppat.1006258. eCollection 2017 Mar.
22. Wada M, etal., J Viral Hepat. 2009 Jun;16(6):388-96. doi: 10.1111/j.1365-2893.2009.01095.x. Epub 2009 Feb 5.
23. Wang Y, etal., Cell Res. 2021 Feb;31(2):206-218. doi: 10.1038/s41422-020-0386-6. Epub 2020 Aug 5.
24. Yoshikawa R, etal., J Virol. 2019 May 1;93(10). pii: JVI.02226-18. doi: 10.1128/JVI.02226-18. Print 2019 May 15.
Additional References at PubMed
PMID:1502204   PMID:7559568   PMID:7746328   PMID:7885841   PMID:8601453   PMID:8605876   PMID:8605877   PMID:8621447   PMID:8848048   PMID:8943351   PMID:9020188   PMID:9121453  
PMID:9242679   PMID:9677371   PMID:9724754   PMID:9804758   PMID:10446176   PMID:10464260   PMID:10490982   PMID:10506573   PMID:10702714   PMID:11150296   PMID:11564163   PMID:11694501  
PMID:11786546   PMID:11804954   PMID:11932384   PMID:12048190   PMID:12050355   PMID:12167251   PMID:12220192   PMID:12244326   PMID:12388709   PMID:12477932   PMID:12509459   PMID:12610111  
PMID:12777975   PMID:12804771   PMID:14557668   PMID:14645718   PMID:14702039   PMID:14722125   PMID:15154850   PMID:15165826   PMID:15175343   PMID:15221897   PMID:15356134   PMID:15467722  
PMID:15489334   PMID:15650219   PMID:15668228   PMID:15717316   PMID:15825084   PMID:16227264   PMID:16501077   PMID:16689942   PMID:16918696   PMID:16978698   PMID:17351669   PMID:17442890  
PMID:17538964   PMID:17596301   PMID:17923090   PMID:18029348   PMID:18338947   PMID:18370868   PMID:18456457   PMID:18579593   PMID:18678383   PMID:18701593   PMID:18771758   PMID:18796709  
PMID:19007958   PMID:19159017   PMID:19169254   PMID:19274049   PMID:19279106   PMID:19322201   PMID:19351818   PMID:19423540   PMID:19434718   PMID:19561067   PMID:19730683   PMID:19754307  
PMID:19913121   PMID:20068068   PMID:20331378   PMID:20403236   PMID:20404187   PMID:20406964   PMID:20428775   PMID:20438785   PMID:20533260   PMID:20588308   PMID:20628086   PMID:20881960  
PMID:20937132   PMID:20953190   PMID:21268015   PMID:21354905   PMID:21399658   PMID:21498520   PMID:21795355   PMID:21873635   PMID:21886773   PMID:21903422   PMID:21988832   PMID:22020285  
PMID:22022391   PMID:22238643   PMID:22426484   PMID:22523757   PMID:22634037   PMID:22859983   PMID:22883142   PMID:22939624   PMID:23139419   PMID:23391734   PMID:23456168   PMID:23487038  
PMID:23555265   PMID:23878400   PMID:24065129   PMID:24144296   PMID:24480984   PMID:24658140   PMID:24814927   PMID:25008924   PMID:25293394   PMID:25402006   PMID:25429064   PMID:25468996  
PMID:25529283   PMID:25773664   PMID:25812002   PMID:25814554   PMID:25921106   PMID:25965795   PMID:26122121   PMID:26186194   PMID:26335850   PMID:26397446   PMID:26496610   PMID:26559840  
PMID:26673895   PMID:26897526   PMID:26945968   PMID:26966684   PMID:27053489   PMID:27304884   PMID:27782195   PMID:27802159   PMID:27852626   PMID:27855377   PMID:27929099   PMID:28165510  
PMID:28218735   PMID:28242623   PMID:28250121   PMID:28365387   PMID:28440504   PMID:28441586   PMID:28442624   PMID:28472186   PMID:28514442   PMID:28707474   PMID:28978648   PMID:29031523  
PMID:29089085   PMID:29317535   PMID:29509190   PMID:29581268   PMID:29886262   PMID:30412483   PMID:30623419   PMID:31091453   PMID:31102697   PMID:31697988   PMID:31836668   PMID:31843895  
PMID:31974171   PMID:32092142   PMID:32376554   PMID:32581091   PMID:32635475   PMID:32953130  


Genomics

Comparative Map Data
STAT2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1256,341,597 - 56,360,167 (-)EnsemblGRCh38hg38GRCh38
GRCh381256,341,597 - 56,360,161 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371256,735,381 - 56,753,891 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361255,021,648 - 55,040,176 (-)NCBINCBI36hg18NCBI36
Build 341255,021,650 - 55,040,176NCBI
Celera1256,388,733 - 56,407,397 (-)NCBI
Cytogenetic Map12q13.3NCBI
HuRef1253,774,045 - 53,793,077 (-)NCBIHuRef
CHM1_11256,702,765 - 56,721,407 (-)NCBICHM1_1
Stat2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3910128,106,367 - 128,128,722 (+)NCBIGRCm39mm39
GRCm39 Ensembl10128,106,428 - 128,128,718 (+)Ensembl
GRCm3810128,270,498 - 128,292,853 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl10128,270,559 - 128,292,849 (+)EnsemblGRCm38mm10GRCm38
MGSCv3710127,707,632 - 127,729,905 (+)NCBIGRCm37mm9NCBIm37
MGSCv3610127,673,525 - 127,695,798 (+)NCBImm8
Celera10130,656,386 - 130,681,169 (+)NCBICelera
Cytogenetic Map10D3NCBI
cM Map1076.5NCBI
Stat2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.27702,565 - 718,349 (+)NCBI
Rnor_6.0 Ensembl72,691,369 - 2,707,741 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.072,691,064 - 2,707,530 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.072,669,952 - 2,685,673 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.471,564,385 - 1,580,652 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.171,564,384 - 1,580,651 (+)NCBI
Celera7578,845 - 593,799 (+)NCBICelera
Cytogenetic Map7q11NCBI
Stat2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554583,952,738 - 3,970,668 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554583,953,019 - 3,973,151 (-)NCBIChiLan1.0ChiLan1.0
STAT2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11232,808,586 - 32,827,732 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1232,808,586 - 32,827,732 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01232,555,523 - 32,574,137 (+)NCBIMhudiblu_PPA_v0panPan3
STAT2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.110641,543 - 660,882 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl10642,718 - 658,546 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha10704,962 - 724,101 (-)NCBI
ROS_Cfam_1.010650,365 - 669,707 (-)NCBI
UMICH_Zoey_3.110627,617 - 646,943 (-)NCBI
UNSW_CanFamBas_1.010870,771 - 890,099 (-)NCBI
UU_Cfam_GSD_1.010994,493 - 1,013,823 (-)NCBI
Stat2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494558,106,734 - 58,122,062 (+)NCBI
SpeTri2.0NW_004936646747,178 - 763,449 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
STAT2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl521,733,035 - 21,751,354 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1521,733,030 - 21,748,960 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2523,280,591 - 23,294,360 (-)NCBISscrofa10.2Sscrofa10.2susScr3
STAT2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11152,297,890 - 52,316,089 (-)NCBI
ChlSab1.1 Ensembl1152,297,543 - 52,316,105 (-)Ensembl
Vero_WHO_p1.0NW_023666037193,669,493 - 193,688,727 (+)NCBI
Stat2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462480211,645,851 - 11,662,812 (+)NCBI

Position Markers
STS-L27050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,755,142 - 56,755,280UniSTSGRCh37
Build 361255,041,409 - 55,041,547RGDNCBI36
Celera1256,408,502 - 56,408,640RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,794,182 - 53,794,320UniSTS
GeneMap99-GB4 RH Map12249.32UniSTS
RH40514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,735,387 - 56,735,606UniSTSGRCh37
GRCh37817,142,329 - 17,142,553UniSTSGRCh37
Build 36817,186,700 - 17,186,924RGDNCBI36
Celera1256,388,739 - 56,388,958UniSTS
Celera816,108,372 - 16,108,596RGD
Cytogenetic Map8p22UniSTS
Cytogenetic Map12q13.3UniSTS
HuRef1253,774,051 - 53,774,270UniSTS
HuRef815,687,197 - 15,687,421UniSTS
RH99119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,735,416 - 56,735,570UniSTSGRCh37
GRCh37817,142,365 - 17,142,524UniSTSGRCh37
Build 36817,186,736 - 17,186,895RGDNCBI36
Celera816,108,408 - 16,108,567RGD
Celera1256,388,768 - 56,388,922UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map8p22UniSTS
HuRef1253,774,080 - 53,774,234UniSTS
HuRef815,687,233 - 15,687,392UniSTS
GeneMap99-GB4 RH Map12248.88UniSTS
G67915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,753,702 - 56,753,952UniSTSGRCh37
Build 361255,039,969 - 55,040,219RGDNCBI36
Celera1256,407,062 - 56,407,312RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,792,742 - 53,792,992UniSTS
G67921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,743,265 - 56,743,543UniSTSGRCh37
Build 361255,029,532 - 55,029,810RGDNCBI36
Celera1256,396,617 - 56,396,895RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,781,962 - 53,782,240UniSTS
G67923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,743,127 - 56,743,425UniSTSGRCh37
Build 361255,029,394 - 55,029,692RGDNCBI36
Celera1256,396,479 - 56,396,777RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,781,824 - 53,782,122UniSTS
G67924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,742,822 - 56,743,195UniSTSGRCh37
Build 361255,029,089 - 55,029,462RGDNCBI36
Celera1256,396,174 - 56,396,547RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,781,519 - 53,781,892UniSTS
G67925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,742,665 - 56,742,991UniSTSGRCh37
Build 361255,028,932 - 55,029,258RGDNCBI36
Celera1256,396,017 - 56,396,343RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,781,362 - 53,781,688UniSTS
G67927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,742,213 - 56,742,507UniSTSGRCh37
Build 361255,028,480 - 55,028,774RGDNCBI36
Celera1256,395,565 - 56,395,859RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,780,910 - 53,781,204UniSTS
G67917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,750,071 - 56,750,418UniSTSGRCh37
Build 361255,036,338 - 55,036,685RGDNCBI36
Celera1256,403,431 - 56,403,778RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,788,802 - 53,789,149UniSTS
G67916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,740,503 - 56,740,823UniSTSGRCh37
Build 361255,026,770 - 55,027,090RGDNCBI36
Celera1256,393,855 - 56,394,175RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,779,200 - 53,779,520UniSTS
G67920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,737,560 - 56,738,063UniSTSGRCh37
Build 361255,023,827 - 55,024,330RGDNCBI36
Celera1256,390,912 - 56,391,415RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,776,224 - 53,776,727UniSTS
G67922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,736,341 - 56,737,454UniSTSGRCh37
GRCh37753,126,119 - 53,126,955UniSTSGRCh37
Build 361255,022,608 - 55,023,721RGDNCBI36
Celera1256,389,693 - 56,390,806RGD
Celera753,186,858 - 53,187,694UniSTS
Cytogenetic Map12q13.3UniSTS
HuRef752,975,548 - 52,976,384UniSTS
HuRef1253,775,005 - 53,776,118UniSTS
CRA_TCAGchr7v2753,131,640 - 53,132,476UniSTS
G67918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,749,784 - 56,750,204UniSTSGRCh37
Build 361255,036,051 - 55,036,471RGDNCBI36
Celera1256,403,144 - 56,403,564RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,788,515 - 53,788,935UniSTS
G67919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,749,427 - 56,749,709UniSTSGRCh37
Build 361255,035,694 - 55,035,976RGDNCBI36
Celera1256,402,787 - 56,403,069RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,788,158 - 53,788,440UniSTS
G67926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,748,185 - 56,748,547UniSTSGRCh37
Build 361255,034,452 - 55,034,814RGDNCBI36
Celera1256,401,545 - 56,401,907RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,786,916 - 53,787,278UniSTS
STAT2_258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,736,477 - 56,737,311UniSTSGRCh37
Build 361255,022,744 - 55,023,578RGDNCBI36
Celera1256,389,829 - 56,390,663RGD
HuRef1253,775,141 - 53,775,975UniSTS
D12S1878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,746,360 - 56,746,471UniSTSGRCh37
Build 361255,032,627 - 55,032,738RGDNCBI36
Celera1256,399,712 - 56,399,823RGD
Cytogenetic Map12q13.3UniSTS
HuRef1253,785,057 - 53,785,168UniSTS
GDB:335751  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map3q22.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map9q22.32UniSTS
D10S275  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map6q24UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map20pter-q11.23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11p14.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map6q12-q13UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
RH36905  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map3q27-q28UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map3q12.2-q12.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q12-q13.1UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map9q31.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map10q21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map10q25-q26UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map16q22.1UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS
RH80815  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map12q13.3UniSTS
GeneMap99-GB4 RH Map12247.26UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3024
Count of miRNA genes:980
Interacting mature miRNAs:1197
Transcripts:ENST00000314128, ENST00000418572, ENST00000555488, ENST00000555519, ENST00000555646, ENST00000556140, ENST00000556539, ENST00000557156, ENST00000557199, ENST00000557235, ENST00000557252, ENST00000557417
Prediction methods:Microtar, Miranda, Rnahybrid
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.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2432 2792 1721 622 1870 463 4180 1909 3463 392 1458 1610 175 1 1204 2612 6 2
Low 7 199 5 2 81 2 177 288 271 27 2 3 176
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_046314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_198332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748858 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_245953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC025574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY525126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD684210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS542453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB482283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX178291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M97934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S81491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U18671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000314128   ⟹   ENSP00000315768
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,597 - 56,360,107 (-)Ensembl
RefSeq Acc Id: ENST00000418572   ⟹   ENSP00000387354
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,348,752 - 56,360,126 (-)Ensembl
RefSeq Acc Id: ENST00000555488
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,344,085 - 56,346,868 (-)Ensembl
RefSeq Acc Id: ENST00000555519
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,349,501 - 56,354,507 (-)Ensembl
RefSeq Acc Id: ENST00000555646   ⟹   ENSP00000450985
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,355,273 - 56,360,107 (-)Ensembl
RefSeq Acc Id: ENST00000556140
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,342,298 - 56,360,165 (-)Ensembl
RefSeq Acc Id: ENST00000556539
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,597 - 56,349,775 (-)Ensembl
RefSeq Acc Id: ENST00000557156
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,351,203 - 56,354,872 (-)Ensembl
RefSeq Acc Id: ENST00000557199
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,346,678 - 56,348,912 (-)Ensembl
RefSeq Acc Id: ENST00000557235   ⟹   ENSP00000450751
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,342,936 - 56,360,126 (-)Ensembl
RefSeq Acc Id: ENST00000557252
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,349,860 - 56,351,181 (-)Ensembl
RefSeq Acc Id: ENST00000557417
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,354,555 - 56,360,155 (-)Ensembl
RefSeq Acc Id: ENST00000650805   ⟹   ENSP00000498710
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,618 - 56,360,142 (-)Ensembl
RefSeq Acc Id: ENST00000651078
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,613 - 56,360,100 (-)Ensembl
RefSeq Acc Id: ENST00000651301   ⟹   ENSP00000498470
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,605 - 56,360,106 (-)Ensembl
RefSeq Acc Id: ENST00000651339
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,342,630 - 56,349,473 (-)Ensembl
RefSeq Acc Id: ENST00000651805
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,613 - 56,360,134 (-)Ensembl
RefSeq Acc Id: ENST00000651915   ⟹   ENSP00000498876
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,608 - 56,360,131 (-)Ensembl
RefSeq Acc Id: ENST00000651934
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,613 - 56,360,167 (-)Ensembl
RefSeq Acc Id: ENST00000651967
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,342,618 - 56,356,219 (-)Ensembl
RefSeq Acc Id: ENST00000652091
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,613 - 56,360,161 (-)Ensembl
RefSeq Acc Id: ENST00000652398   ⟹   ENSP00000499022
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,342,618 - 56,360,110 (-)Ensembl
RefSeq Acc Id: ENST00000652624   ⟹   ENSP00000499108
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,800 - 56,360,117 (-)Ensembl
RefSeq Acc Id: ENST00000652741   ⟹   ENSP00000498704
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,341,618 - 56,360,096 (-)Ensembl
RefSeq Acc Id: NM_001385110   ⟹   NP_001372039
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
RefSeq Acc Id: NM_001385111   ⟹   NP_001372040
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
RefSeq Acc Id: NM_001385113   ⟹   NP_001372042
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
RefSeq Acc Id: NM_001385114   ⟹   NP_001372043
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
RefSeq Acc Id: NM_001385115   ⟹   NP_001372044
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
RefSeq Acc Id: NM_005419   ⟹   NP_005410
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
GRCh371256,735,381 - 56,754,058 (-)NCBI
Build 361255,021,648 - 55,040,176 (-)NCBI Archive
HuRef1253,774,045 - 53,793,077 (-)ENTREZGENE
CHM1_11256,702,765 - 56,721,407 (-)NCBI
Sequence:
RefSeq Acc Id: NM_198332   ⟹   NP_938146
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,107 (-)NCBI
GRCh371256,735,381 - 56,754,058 (-)NCBI
HuRef1253,774,045 - 53,793,077 (-)ENTREZGENE
CHM1_11256,702,765 - 56,721,407 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538697   ⟹   XP_011536999
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,161 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538698   ⟹   XP_011537000
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,131 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538699   ⟹   XP_011537001
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,346,981 - 56,360,161 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011538700   ⟹   XP_011537002
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,354,872 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017019904   ⟹   XP_016875393
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,126 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001748856
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,161 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001748857
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,161 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001748858
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,131 (-)NCBI
Sequence:
RefSeq Acc Id: XR_002957375
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,161 (-)NCBI
Sequence:
RefSeq Acc Id: XR_002957376
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,341,597 - 56,360,131 (-)NCBI
Sequence:
RefSeq Acc Id: XR_245953
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,348,529 - 56,360,161 (-)NCBI
GRCh371256,735,381 - 56,754,058 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001372039 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372040 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372042 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372043 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372044 (Get FASTA)   NCBI Sequence Viewer  
  NP_005410 (Get FASTA)   NCBI Sequence Viewer  
  NP_938146 (Get FASTA)   NCBI Sequence Viewer  
  XP_011536999 (Get FASTA)   NCBI Sequence Viewer  
  XP_011537000 (Get FASTA)   NCBI Sequence Viewer  
  XP_011537001 (Get FASTA)   NCBI Sequence Viewer  
  XP_011537002 (Get FASTA)   NCBI Sequence Viewer  
  XP_016875393 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA98760 (Get FASTA)   NCBI Sequence Viewer  
  AAB36225 (Get FASTA)   NCBI Sequence Viewer  
  AAB36226 (Get FASTA)   NCBI Sequence Viewer  
  AAB36227 (Get FASTA)   NCBI Sequence Viewer  
  AAH06092 (Get FASTA)   NCBI Sequence Viewer  
  AAH51284 (Get FASTA)   NCBI Sequence Viewer  
  AAS00091 (Get FASTA)   NCBI Sequence Viewer  
  AFM91190 (Get FASTA)   NCBI Sequence Viewer  
  AFM91191 (Get FASTA)   NCBI Sequence Viewer  
  AFM91192 (Get FASTA)   NCBI Sequence Viewer  
  AFM91193 (Get FASTA)   NCBI Sequence Viewer  
  AFM91194 (Get FASTA)   NCBI Sequence Viewer  
  AFM91195 (Get FASTA)   NCBI Sequence Viewer  
  AFM91196 (Get FASTA)   NCBI Sequence Viewer  
  AFM91197 (Get FASTA)   NCBI Sequence Viewer  
  AFM91198 (Get FASTA)   NCBI Sequence Viewer  
  AFM91199 (Get FASTA)   NCBI Sequence Viewer  
  AFM91200 (Get FASTA)   NCBI Sequence Viewer  
  AFM91201 (Get FASTA)   NCBI Sequence Viewer  
  AFM91202 (Get FASTA)   NCBI Sequence Viewer  
  AFM91203 (Get FASTA)   NCBI Sequence Viewer  
  AFM91204 (Get FASTA)   NCBI Sequence Viewer  
  AFM91205 (Get FASTA)   NCBI Sequence Viewer  
  AFM91206 (Get FASTA)   NCBI Sequence Viewer  
  AFM91207 (Get FASTA)   NCBI Sequence Viewer  
  AFM91208 (Get FASTA)   NCBI Sequence Viewer  
  AFM91209 (Get FASTA)   NCBI Sequence Viewer  
  AFM91210 (Get FASTA)   NCBI Sequence Viewer  
  AFM91211 (Get FASTA)   NCBI Sequence Viewer  
  AFM91212 (Get FASTA)   NCBI Sequence Viewer  
  AFM91213 (Get FASTA)   NCBI Sequence Viewer  
  AFM91214 (Get FASTA)   NCBI Sequence Viewer  
  AFM91215 (Get FASTA)   NCBI Sequence Viewer  
  AFM91216 (Get FASTA)   NCBI Sequence Viewer  
  AFM91217 (Get FASTA)   NCBI Sequence Viewer  
  AFM91218 (Get FASTA)   NCBI Sequence Viewer  
  AFM91219 (Get FASTA)   NCBI Sequence Viewer  
  AFM91220 (Get FASTA)   NCBI Sequence Viewer  
  AFM91221 (Get FASTA)   NCBI Sequence Viewer  
  AFM91222 (Get FASTA)   NCBI Sequence Viewer  
  AFM91223 (Get FASTA)   NCBI Sequence Viewer  
  AFM91224 (Get FASTA)   NCBI Sequence Viewer  
  AFM91225 (Get FASTA)   NCBI Sequence Viewer  
  AFM91226 (Get FASTA)   NCBI Sequence Viewer  
  AFM91227 (Get FASTA)   NCBI Sequence Viewer  
  AFM91228 (Get FASTA)   NCBI Sequence Viewer  
  AFM91229 (Get FASTA)   NCBI Sequence Viewer  
  AFM91230 (Get FASTA)   NCBI Sequence Viewer  
  AFM91231 (Get FASTA)   NCBI Sequence Viewer  
  AFM91232 (Get FASTA)   NCBI Sequence Viewer  
  AFM91233 (Get FASTA)   NCBI Sequence Viewer  
  AFM91234 (Get FASTA)   NCBI Sequence Viewer  
  AFM91235 (Get FASTA)   NCBI Sequence Viewer  
  AFM91236 (Get FASTA)   NCBI Sequence Viewer  
  AFM91237 (Get FASTA)   NCBI Sequence Viewer  
  AFM91238 (Get FASTA)   NCBI Sequence Viewer  
  AFM91239 (Get FASTA)   NCBI Sequence Viewer  
  AFM91240 (Get FASTA)   NCBI Sequence Viewer  
  AFM91241 (Get FASTA)   NCBI Sequence Viewer  
  AFM91242 (Get FASTA)   NCBI Sequence Viewer  
  AFM91243 (Get FASTA)   NCBI Sequence Viewer  
  AFM91244 (Get FASTA)   NCBI Sequence Viewer  
  AFM91245 (Get FASTA)   NCBI Sequence Viewer  
  AFM91246 (Get FASTA)   NCBI Sequence Viewer  
  AFM91247 (Get FASTA)   NCBI Sequence Viewer  
  AFM91248 (Get FASTA)   NCBI Sequence Viewer  
  AFM91249 (Get FASTA)   NCBI Sequence Viewer  
  AFM91250 (Get FASTA)   NCBI Sequence Viewer  
  AFM91251 (Get FASTA)   NCBI Sequence Viewer  
  AFM91252 (Get FASTA)   NCBI Sequence Viewer  
  AFM91253 (Get FASTA)   NCBI Sequence Viewer  
  AFM91254 (Get FASTA)   NCBI Sequence Viewer  
  AFM91255 (Get FASTA)   NCBI Sequence Viewer  
  AFM91256 (Get FASTA)   NCBI Sequence Viewer  
  AFM91257 (Get FASTA)   NCBI Sequence Viewer  
  AFM91258 (Get FASTA)   NCBI Sequence Viewer  
  AFM91259 (Get FASTA)   NCBI Sequence Viewer  
  AFM91260 (Get FASTA)   NCBI Sequence Viewer  
  AFM91261 (Get FASTA)   NCBI Sequence Viewer  
  AFM91262 (Get FASTA)   NCBI Sequence Viewer  
  AFM91263 (Get FASTA)   NCBI Sequence Viewer  
  AFM91264 (Get FASTA)   NCBI Sequence Viewer  
  AFM91265 (Get FASTA)   NCBI Sequence Viewer  
  AFM91266 (Get FASTA)   NCBI Sequence Viewer  
  AFM91267 (Get FASTA)   NCBI Sequence Viewer  
  AFM91268 (Get FASTA)   NCBI Sequence Viewer  
  AFM91269 (Get FASTA)   NCBI Sequence Viewer  
  AFM91270 (Get FASTA)   NCBI Sequence Viewer  
  AFM91271 (Get FASTA)   NCBI Sequence Viewer  
  AFM91272 (Get FASTA)   NCBI Sequence Viewer  
  AFM91273 (Get FASTA)   NCBI Sequence Viewer  
  AFM91274 (Get FASTA)   NCBI Sequence Viewer  
  AFM91275 (Get FASTA)   NCBI Sequence Viewer  
  AFM91276 (Get FASTA)   NCBI Sequence Viewer  
  AFM91277 (Get FASTA)   NCBI Sequence Viewer  
  AFM91278 (Get FASTA)   NCBI Sequence Viewer  
  AFM91279 (Get FASTA)   NCBI Sequence Viewer  
  AFM91280 (Get FASTA)   NCBI Sequence Viewer  
  BAG58101 (Get FASTA)   NCBI Sequence Viewer  
  BAG58143 (Get FASTA)   NCBI Sequence Viewer  
  BAG59489 (Get FASTA)   NCBI Sequence Viewer  
  BAG59490 (Get FASTA)   NCBI Sequence Viewer  
  BAH14887 (Get FASTA)   NCBI Sequence Viewer  
  CAE45713 (Get FASTA)   NCBI Sequence Viewer  
  CAM91176 (Get FASTA)   NCBI Sequence Viewer  
  EAW96934 (Get FASTA)   NCBI Sequence Viewer  
  EAW96935 (Get FASTA)   NCBI Sequence Viewer  
  EAW96936 (Get FASTA)   NCBI Sequence Viewer  
  EAW96937 (Get FASTA)   NCBI Sequence Viewer  
  P52630 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_938146   ⟸   NM_198332
- Peptide Label: isoform 2
- UniProtKB: P52630 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_005410   ⟸   NM_005419
- Peptide Label: isoform 1
- UniProtKB: P52630 (UniProtKB/Swiss-Prot),   R9QE65 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011536999   ⟸   XM_011538697
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011537000   ⟸   XM_011538698
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011537002   ⟸   XM_011538700
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011537001   ⟸   XM_011538699
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016875393   ⟸   XM_017019904
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: ENSP00000450985   ⟸   ENST00000555646
RefSeq Acc Id: ENSP00000450751   ⟸   ENST00000557235
RefSeq Acc Id: ENSP00000498710   ⟸   ENST00000650805
RefSeq Acc Id: ENSP00000498876   ⟸   ENST00000651915
RefSeq Acc Id: ENSP00000498470   ⟸   ENST00000651301
RefSeq Acc Id: ENSP00000498704   ⟸   ENST00000652741
RefSeq Acc Id: ENSP00000499108   ⟸   ENST00000652624
RefSeq Acc Id: ENSP00000499022   ⟸   ENST00000652398
RefSeq Acc Id: ENSP00000387354   ⟸   ENST00000418572
RefSeq Acc Id: ENSP00000315768   ⟸   ENST00000314128
RefSeq Acc Id: NP_001372039   ⟸   NM_001385110
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372044   ⟸   NM_001385115
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001372043   ⟸   NM_001385114
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001372040   ⟸   NM_001385111
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372042   ⟸   NM_001385113
- Peptide Label: isoform 5
Protein Domains
SH2   STAT_int

Promoters
RGD ID:6790517
Promoter ID:HG_KWN:15905
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC001SLB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361255,029,181 - 55,029,681 (-)MPROMDB
RGD ID:6790519
Promoter ID:HG_KWN:15906
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC001SLD.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361255,036,281 - 55,036,781 (-)MPROMDB
RGD ID:6790518
Promoter ID:HG_KWN:15907
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000314128,   NM_198332,   UC001SLC.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361255,040,006 - 55,040,537 (-)MPROMDB
RGD ID:7224429
Promoter ID:EPDNEW_H17960
Type:initiation region
Name:STAT2_1
Description:signal transducer and activator of transcription 2
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
GRCh381256,360,107 - 56,360,167EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_005419.4(STAT2):c.165G>A (p.Lys55=) single nucleotide variant Immunodeficiency 44 [RCV000544491] Chr12:56356252 [GRCh38]
Chr12:56750036 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.116T>C (p.Ile39Thr) single nucleotide variant Immunodeficiency 44 [RCV000545981] Chr12:56356456 [GRCh38]
Chr12:56750240 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2478G>T (p.Gln826His) single nucleotide variant Immunodeficiency 44 [RCV000548114] Chr12:56343467 [GRCh38]
Chr12:56737251 [GRCh37]
Chr12:12q13.3
benign
NM_001638.2(APOF):c.486C>T (p.Val162=) single nucleotide variant Malignant melanoma [RCV000070111] Chr12:56361720 [GRCh38]
Chr12:56755504 [GRCh37]
Chr12:55041771 [NCBI36]
Chr12:12q13.3
not provided
NM_005419.4(STAT2):c.598C>T (p.Gln200Ter) single nucleotide variant not provided [RCV000122521] Chr12:56354813 [GRCh38]
Chr12:56748597 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.382-9dup duplication not provided [RCV000514180] Chr12:56355535..56355536 [GRCh38]
Chr12:56749319..56749320 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.989G>A (p.Arg330Gln) single nucleotide variant Immunodeficiency 44 [RCV000791837]|Inborn genetic diseases [RCV000190677] Chr12:56351143 [GRCh38]
Chr12:56744927 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.633+6A>C single nucleotide variant Immunodeficiency 44 [RCV001294273] Chr12:56354772 [GRCh38]
Chr12:56748556 [GRCh37]
Chr12:12q13.3
uncertain significance
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
NM_005419.4(STAT2):c.381+5G>C single nucleotide variant Immunodeficiency 44 [RCV000202375] Chr12:56355703 [GRCh38]
Chr12:56749487 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.1836C>A (p.Cys612Ter) single nucleotide variant Immunodeficiency 44 [RCV000202385] Chr12:56346844 [GRCh38]
Chr12:56740628 [GRCh37]
Chr12:12q13.3
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
NM_005419.4(STAT2):c.379T>C (p.Leu127=) single nucleotide variant Immunodeficiency 44 [RCV000527071] Chr12:56355710 [GRCh38]
Chr12:56749494 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.400C>T (p.Leu134Phe) single nucleotide variant Immunodeficiency 44 [RCV000537418] Chr12:56355514 [GRCh38]
Chr12:56749298 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2473G>T (p.Gly825Cys) single nucleotide variant not specified [RCV000454428] Chr12:56343472 [GRCh38]
Chr12:56737256 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.759C>T (p.His253=) single nucleotide variant Immunodeficiency 44 [RCV000652754]|not specified [RCV000454686] Chr12:56354489 [GRCh38]
Chr12:56748273 [GRCh37]
Chr12:12q13.3
benign|likely benign
NM_005419.4(STAT2):c.2472T>C (p.Ala824=) single nucleotide variant not specified [RCV000455107] Chr12:56343473 [GRCh38]
Chr12:56737257 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.1782G>C (p.Met594Ile) single nucleotide variant Immunodeficiency 44 [RCV000559305]|not specified [RCV000455792] Chr12:56346898 [GRCh38]
Chr12:56740682 [GRCh37]
Chr12:12q13.3
benign
NM_016584.3(IL23A):c.318G>A (p.Ser106=) single nucleotide variant not specified [RCV000455797] Chr12:56339747 [GRCh38]
Chr12:56733531 [GRCh37]
Chr12:12q13.3
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-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NM_005419.4(STAT2):c.1343C>T (p.Thr448Met) single nucleotide variant Immunodeficiency 44 [RCV000560792] Chr12:56349260 [GRCh38]
Chr12:56743044 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.2472_2473delinsCT (p.Gly825Cys) indel Immunodeficiency 44 [RCV000537740] Chr12:56343472..56343473 [GRCh38]
Chr12:56737256..56737257 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.1390A>G (p.Ile464Val) single nucleotide variant Immunodeficiency 44 [RCV000534703] Chr12:56349213 [GRCh38]
Chr12:56742997 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.2004C>G (p.Ile668Met) single nucleotide variant Immunodeficiency 44 [RCV000652750]|not provided [RCV000788168] Chr12:56346482 [GRCh38]
Chr12:56740266 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1301C>T (p.Thr434Met) single nucleotide variant Immunodeficiency 44 [RCV000652751] Chr12:56349466 [GRCh38]
Chr12:56743250 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1727G>T (p.Arg576Leu) single nucleotide variant Immunodeficiency 44 [RCV000652752] Chr12:56346953 [GRCh38]
Chr12:56740737 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.903C>T (p.Asn301=) single nucleotide variant Immunodeficiency 44 [RCV000652753] Chr12:56351330 [GRCh38]
Chr12:56745114 [GRCh37]
Chr12:12q13.3
likely benign|conflicting interpretations of pathogenicity
NM_005419.4(STAT2):c.2044+9C>T single nucleotide variant Immunodeficiency 44 [RCV000652755] Chr12:56346433 [GRCh38]
Chr12:56740217 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2044+10G>A single nucleotide variant Immunodeficiency 44 [RCV000652756] Chr12:56346432 [GRCh38]
Chr12:56740216 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1326G>A (p.Leu442=) single nucleotide variant Immunodeficiency 44 [RCV000652757] Chr12:56349441 [GRCh38]
Chr12:56743225 [GRCh37]
Chr12:12q13.3
benign
NM_005419.4(STAT2):c.285+5T>C single nucleotide variant Immunodeficiency 44 [RCV000652758] Chr12:56356127 [GRCh38]
Chr12:56749911 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1629+7C>T single nucleotide variant Immunodeficiency 44 [RCV000652759] Chr12:56348745 [GRCh38]
Chr12:56742529 [GRCh37]
Chr12:12q13.3
likely benign
NC_000012.11:g.(?_56737153)_(56750375_?)dup duplication Immunodeficiency 44 [RCV000652760] Chr12:56343369..56356591 [GRCh38]
Chr12:56737153..56750375 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.331C>T (p.Leu111Phe) single nucleotide variant Immunodeficiency 44 [RCV000698784] Chr12:56355758 [GRCh38]
Chr12:56749542 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1999C>T (p.Arg667Ter) single nucleotide variant Immunodeficiency 44 [RCV000701416] Chr12:56346487 [GRCh38]
Chr12:56740271 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.109G>T (p.Val37Phe) single nucleotide variant Immunodeficiency 44 [RCV000690233] Chr12:56356463 [GRCh38]
Chr12:56750247 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1957GAG[1] (p.Glu654del) microsatellite Immunodeficiency 44 [RCV000700216] Chr12:56346524..56346526 [GRCh38]
Chr12:56740308..56740310 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1345G>A (p.Asp449Asn) single nucleotide variant Immunodeficiency 44 [RCV000703937] Chr12:56349258 [GRCh38]
Chr12:56743042 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1294A>G (p.Ser432Gly) single nucleotide variant Immunodeficiency 44 [RCV000695815] Chr12:56349473 [GRCh38]
Chr12:56743257 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1864A>C (p.Lys622Gln) single nucleotide variant Immunodeficiency 44 [RCV000691263] Chr12:56346622 [GRCh38]
Chr12:56740406 [GRCh37]
Chr12:12q13.3
uncertain significance
NC_000012.11:g.(?_56739910)_(56750375_?)dup duplication Immunodeficiency 44 [RCV000708000] Chr12:56346126..56356591 [GRCh38]
Chr12:56739910..56750375 [GRCh37]
Chr12:12q13.3
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
NM_005419.4(STAT2):c.2000G>A (p.Arg667Gln) single nucleotide variant Immunodeficiency 44 [RCV001066299] Chr12:56346486 [GRCh38]
Chr12:56740270 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.804GTT[1] (p.Leu269del) microsatellite not provided [RCV000788134] Chr12:56351424..56351426 [GRCh38]
Chr12:56745208..56745210 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1611C>G (p.Ser537=) single nucleotide variant not provided [RCV000944894] Chr12:56348770 [GRCh38]
Chr12:56742554 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1111C>G (p.Gln371Glu) single nucleotide variant Immunodeficiency 44 [RCV000907041] Chr12:56350416 [GRCh38]
Chr12:56744200 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1062T>C (p.Asn354=) single nucleotide variant Immunodeficiency 44 [RCV000936326] Chr12:56350861 [GRCh38]
Chr12:56744645 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.378A>G (p.Gln126=) single nucleotide variant Immunodeficiency 44 [RCV000944146] Chr12:56355711 [GRCh38]
Chr12:56749495 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.897A>T (p.Leu299=) single nucleotide variant Immunodeficiency 44 [RCV001439890]|not provided [RCV000966460] Chr12:56351336 [GRCh38]
Chr12:56745120 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2451G>A (p.Pro817=) single nucleotide variant not provided [RCV000921405] Chr12:56343494 [GRCh38]
Chr12:56737278 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2127G>A (p.Pro709=) single nucleotide variant Immunodeficiency 44 [RCV000948398] Chr12:56344111 [GRCh38]
Chr12:56737895 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.340G>A (p.Glu114Lys) single nucleotide variant Immunodeficiency 44 [RCV001049114] Chr12:56355749 [GRCh38]
Chr12:56749533 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1612T>C (p.Trp538Arg) single nucleotide variant Immunodeficiency 44 [RCV001059438] Chr12:56348769 [GRCh38]
Chr12:56742553 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1061A>G (p.Asn354Ser) single nucleotide variant Immunodeficiency 44 [RCV001059694] Chr12:56350862 [GRCh38]
Chr12:56744646 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1344G>A (p.Thr448=) single nucleotide variant Immunodeficiency 44 [RCV000807883] Chr12:56349259 [GRCh38]
Chr12:56743043 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.34A>G (p.Ser12Gly) single nucleotide variant Immunodeficiency 44 [RCV000768098] Chr12:56356538 [GRCh38]
Chr12:56750322 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1088T>C (p.Ile363Thr) single nucleotide variant Immunodeficiency 44 [RCV000808355] Chr12:56350835 [GRCh38]
Chr12:56744619 [GRCh37]
Chr12:12q13.3
uncertain significance
NC_000012.11:g.(?_56737153)_(56737939_?)dup duplication Immunodeficiency 44 [RCV000815900] Chr12:56343369..56344155 [GRCh38]
Chr12:56737153..56737939 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1693C>T (p.His565Tyr) single nucleotide variant Immunodeficiency 44 [RCV000806496] Chr12:56348560 [GRCh38]
Chr12:56742344 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1258-4C>T single nucleotide variant not provided [RCV000982082] Chr12:56349513 [GRCh38]
Chr12:56743297 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1239A>G (p.Ser413=) single nucleotide variant Immunodeficiency 44 [RCV001418458]|not provided [RCV000943468] Chr12:56349607 [GRCh38]
Chr12:56743391 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.531T>C (p.Tyr177=) single nucleotide variant not provided [RCV000942384] Chr12:56355292 [GRCh38]
Chr12:56749076 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1035-4C>T single nucleotide variant Immunodeficiency 44 [RCV001418418]|not provided [RCV000920392] Chr12:56350892 [GRCh38]
Chr12:56744676 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.548-10C>T single nucleotide variant not provided [RCV000936864] Chr12:56354873 [GRCh38]
Chr12:56748657 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2507G>A (p.Arg836His) single nucleotide variant Immunodeficiency 44 [RCV000810155] Chr12:56343438 [GRCh38]
Chr12:56737222 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.538C>G (p.Gln180Glu) single nucleotide variant Immunodeficiency 44 [RCV000807124] Chr12:56355285 [GRCh38]
Chr12:56749069 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1827_1829del (p.Ile610del) deletion Immunodeficiency 44 [RCV000816111] Chr12:56346851..56346853 [GRCh38]
Chr12:56740635..56740637 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2191C>T (p.Pro731Ser) single nucleotide variant Immunodeficiency 44 [RCV000805508] Chr12:56344047 [GRCh38]
Chr12:56737831 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1320G>A (p.Gln440=) single nucleotide variant Immunodeficiency 44 [RCV000809332] Chr12:56349447 [GRCh38]
Chr12:56743231 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.694C>A (p.Leu232Met) single nucleotide variant Immunodeficiency 44 [RCV000818829] Chr12:56354554 [GRCh38]
Chr12:56748338 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1873A>T (p.Ile625Phe) single nucleotide variant not provided [RCV000788167] Chr12:56346613 [GRCh38]
Chr12:56740397 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2506C>T (p.Arg836Cys) single nucleotide variant Immunodeficiency 44 [RCV000798430] Chr12:56343439 [GRCh38]
Chr12:56737223 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2525C>A (p.Thr842Asn) single nucleotide variant Immunodeficiency 44 [RCV000793646] Chr12:56343420 [GRCh38]
Chr12:56737204 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.250C>A (p.Gln84Lys) single nucleotide variant Immunodeficiency 44 [RCV000802910]|not provided [RCV000788163] Chr12:56356167 [GRCh38]
Chr12:56749951 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2491G>A (p.Glu831Lys) single nucleotide variant Immunodeficiency 44 [RCV000810908] Chr12:56343454 [GRCh38]
Chr12:56737238 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2030A>G (p.Tyr677Cys) single nucleotide variant Immunodeficiency 44 [RCV000813545] Chr12:56346456 [GRCh38]
Chr12:56740240 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1209+1del deletion Immunodeficiency 44 [RCV000821148] Chr12:56350096 [GRCh38]
Chr12:56743880 [GRCh37]
Chr12:12q13.3
pathogenic|likely pathogenic
NM_005419.4(STAT2):c.772C>T (p.Leu258=) single nucleotide variant Immunodeficiency 44 [RCV000938496] Chr12:56354476 [GRCh38]
Chr12:56748260 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1466C>T (p.Pro489Leu) single nucleotide variant Immunodeficiency 44 [RCV000802302]|not provided [RCV000788162] Chr12:56349034 [GRCh38]
Chr12:56742818 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.286-5T>C single nucleotide variant Immunodeficiency 44 [RCV000975308] Chr12:56355808 [GRCh38]
Chr12:56749592 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.904G>A (p.Ala302Thr) single nucleotide variant Immunodeficiency 44 [RCV001066159] Chr12:56351329 [GRCh38]
Chr12:56745113 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1791del (p.Leu599fs) deletion Immunodeficiency 44 [RCV001241439] Chr12:56346889 [GRCh38]
Chr12:56740673 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.442C>T (p.Arg148Trp) single nucleotide variant Pseudo-TORCH syndrome 3 [RCV001249565] Chr12:56355472 [GRCh38]
Chr12:56749256 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.1922T>C (p.Leu641Pro) single nucleotide variant Immunodeficiency 44 [RCV001209794] Chr12:56346564 [GRCh38]
Chr12:56740348 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.429T>A (p.His143Gln) single nucleotide variant Immunodeficiency 44 [RCV001223533] Chr12:56355485 [GRCh38]
Chr12:56749269 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.403G>A (p.Glu135Lys) single nucleotide variant Immunodeficiency 44 [RCV001230385] Chr12:56355511 [GRCh38]
Chr12:56749295 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.418A>G (p.Ser140Gly) single nucleotide variant Immunodeficiency 44 [RCV001210593] Chr12:56355496 [GRCh38]
Chr12:56749280 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2269T>C (p.Ser757Pro) single nucleotide variant Immunodeficiency 44 [RCV001212070] Chr12:56343969 [GRCh38]
Chr12:56737753 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1263A>C (p.Pro421=) single nucleotide variant Immunodeficiency 44 [RCV000974767] Chr12:56349504 [GRCh38]
Chr12:56743288 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1095-8C>G single nucleotide variant Immunodeficiency 44 [RCV001440453]|not provided [RCV000928771] Chr12:56350440 [GRCh38]
Chr12:56744224 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1462C>G (p.Pro488Ala) single nucleotide variant Immunodeficiency 44 [RCV000948896] Chr12:56349038 [GRCh38]
Chr12:56742822 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.948del (p.Phe316fs) deletion not provided [RCV001092489] Chr12:56351184 [GRCh38]
Chr12:56744968 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.2060G>A (p.Arg687Gln) single nucleotide variant Immunodeficiency 44 [RCV001043810] Chr12:56346188 [GRCh38]
Chr12:56739972 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1466C>A (p.Pro489His) single nucleotide variant Immunodeficiency 44 [RCV001048902] Chr12:56349034 [GRCh38]
Chr12:56742818 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1602ATT[1] (p.Leu536del) microsatellite Immunodeficiency 44 [RCV001070574] Chr12:56348774..56348776 [GRCh38]
Chr12:56742558..56742560 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.443G>A (p.Arg148Gln) single nucleotide variant Pseudo-TORCH syndrome 3 [RCV001156646] Chr12:56355471 [GRCh38]
Chr12:56749255 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.1045_1046insCA (p.Arg349fs) insertion not provided [RCV001092488] Chr12:56350877..56350878 [GRCh38]
Chr12:56744661..56744662 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.2450C>T (p.Pro817Leu) single nucleotide variant Immunodeficiency 44 [RCV001048561] Chr12:56343495 [GRCh38]
Chr12:56737279 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2474G>A (p.Gly825Asp) single nucleotide variant Immunodeficiency 44 [RCV001204786] Chr12:56343471 [GRCh38]
Chr12:56737255 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.135G>T (p.Gln45His) single nucleotide variant Immunodeficiency 44 [RCV001247040] Chr12:56356282 [GRCh38]
Chr12:56750066 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.124C>A (p.Gln42Lys) single nucleotide variant Immunodeficiency 44 [RCV001220034] Chr12:56356448 [GRCh38]
Chr12:56750232 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1823G>C (p.Gly608Ala) single nucleotide variant Immunodeficiency 44 [RCV001061575] Chr12:56346857 [GRCh38]
Chr12:56740641 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.724C>G (p.Gln242Glu) single nucleotide variant Immunodeficiency 44 [RCV001214005] Chr12:56354524 [GRCh38]
Chr12:56748308 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.106G>A (p.Ala36Thr) single nucleotide variant Immunodeficiency 44 [RCV001208734] Chr12:56356466 [GRCh38]
Chr12:56750250 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.737G>C (p.Cys246Ser) single nucleotide variant Immunodeficiency 44 [RCV001059695] Chr12:56354511 [GRCh38]
Chr12:56748295 [GRCh37]
Chr12:12q13.3
uncertain significance
GRCh37/hg19 12q13.2-14.1(chr12:55552371-62126304)x3 copy number gain not provided [RCV001006505] Chr12:55552371..62126304 [GRCh37]
Chr12:12q13.2-14.1
pathogenic
NM_005419.4(STAT2):c.1903G>A (p.Val635Met) single nucleotide variant Immunodeficiency 44 [RCV001040166] Chr12:56346583 [GRCh38]
Chr12:56740367 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.297G>C (p.Gln99His) single nucleotide variant Immunodeficiency 44 [RCV001233807] Chr12:56355792 [GRCh38]
Chr12:56749576 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.47A>G (p.Asp16Gly) single nucleotide variant Immunodeficiency 44 [RCV001070160] Chr12:56356525 [GRCh38]
Chr12:56750309 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1762C>T (p.Arg588Trp) single nucleotide variant Immunodeficiency 44 [RCV001203392] Chr12:56346918 [GRCh38]
Chr12:56740702 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.788C>T (p.Thr263Ile) single nucleotide variant Immunodeficiency 44 [RCV001304261] Chr12:56351445 [GRCh38]
Chr12:56745229 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.274C>T (p.Arg92Trp) single nucleotide variant Immunodeficiency 44 [RCV001257209] Chr12:56356143 [GRCh38]
Chr12:56749927 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2555A>G (p.Ter852Trp) single nucleotide variant Immunodeficiency 44 [RCV001294212] Chr12:56343390 [GRCh38]
Chr12:56737174 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.567C>A (p.Asp189Glu) single nucleotide variant Immunodeficiency 44 [RCV001352223] Chr12:56354844 [GRCh38]
Chr12:56748628 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2239C>A (p.Leu747Met) single nucleotide variant Immunodeficiency 44 [RCV001295286] Chr12:56343999 [GRCh38]
Chr12:56737783 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2236G>C (p.Asp746His) single nucleotide variant Immunodeficiency 44 [RCV001316756] Chr12:56344002 [GRCh38]
Chr12:56737786 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1766T>C (p.Leu589Pro) single nucleotide variant Immunodeficiency 44 [RCV001342111] Chr12:56346914 [GRCh38]
Chr12:56740698 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.970A>C (p.Met324Leu) single nucleotide variant Immunodeficiency 44 [RCV001337235] Chr12:56351162 [GRCh38]
Chr12:56744946 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2284G>A (p.Val762Met) single nucleotide variant Immunodeficiency 44 [RCV001296182] Chr12:56343954 [GRCh38]
Chr12:56737738 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2116C>T (p.Leu706=) single nucleotide variant Immunodeficiency 44 [RCV001415294] Chr12:56344122 [GRCh38]
Chr12:56737906 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1558C>G (p.Leu520Val) single nucleotide variant Immunodeficiency 44 [RCV001361967] Chr12:56348942 [GRCh38]
Chr12:56742726 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2130_2135del (p.Glu711_Leu712del) deletion Immunodeficiency 44 [RCV001345666] Chr12:56344103..56344108 [GRCh38]
Chr12:56737887..56737892 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1102C>G (p.Pro368Ala) single nucleotide variant Immunodeficiency 44 [RCV001368326] Chr12:56350425 [GRCh38]
Chr12:56744209 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.820C>T (p.Gln274Ter) single nucleotide variant Immunodeficiency 44 [RCV001330058] Chr12:56351413 [GRCh38]
Chr12:56745197 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.1618G>A (p.Asp540Asn) single nucleotide variant Immunodeficiency 44 [RCV001349708] Chr12:56348763 [GRCh38]
Chr12:56742547 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1745G>A (p.Ser582Asn) single nucleotide variant Immunodeficiency 44 [RCV001344062] Chr12:56346935 [GRCh38]
Chr12:56740719 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2008C>T (p.Arg670Trp) single nucleotide variant Immunodeficiency 44 [RCV001319190] Chr12:56346478 [GRCh38]
Chr12:56740262 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.874C>G (p.Pro292Ala) single nucleotide variant Immunodeficiency 44 [RCV001342850] Chr12:56351359 [GRCh38]
Chr12:56745143 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2045-9T>G single nucleotide variant Immunodeficiency 44 [RCV001335269] Chr12:56346212 [GRCh38]
Chr12:56739996 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2485G>A (p.Val829Met) single nucleotide variant Immunodeficiency 44 [RCV001343134] Chr12:56343460 [GRCh38]
Chr12:56737244 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.2059C>T (p.Arg687Trp) single nucleotide variant Immunodeficiency 44 [RCV001321281] Chr12:56346189 [GRCh38]
Chr12:56739973 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.381+3G>A single nucleotide variant Immunodeficiency 44 [RCV001318374] Chr12:56355705 [GRCh38]
Chr12:56749489 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1435del (p.Leu479fs) deletion Immunodeficiency 44 [RCV001335268] Chr12:56349168 [GRCh38]
Chr12:56742952 [GRCh37]
Chr12:12q13.3
pathogenic
NM_005419.4(STAT2):c.275G>A (p.Arg92Gln) single nucleotide variant Immunodeficiency 44 [RCV001366926] Chr12:56356142 [GRCh38]
Chr12:56749926 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.402C>T (p.Leu134=) single nucleotide variant Immunodeficiency 44 [RCV001421136] Chr12:56355512 [GRCh38]
Chr12:56749296 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1985G>A (p.Arg662His) single nucleotide variant Immunodeficiency 44 [RCV001297508] Chr12:56346501 [GRCh38]
Chr12:56740285 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.1466C>G (p.Pro489Arg) single nucleotide variant Immunodeficiency 44 [RCV001365482] Chr12:56349034 [GRCh38]
Chr12:56742818 [GRCh37]
Chr12:12q13.3
uncertain significance
NM_005419.4(STAT2):c.72C>T (p.His24=) single nucleotide variant Immunodeficiency 44 [RCV001405590] Chr12:56356500 [GRCh38]
Chr12:56750284 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2109G>A (p.Val703=) single nucleotide variant Immunodeficiency 44 [RCV001440601] Chr12:56344129 [GRCh38]
Chr12:56737913 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2103-17T>C single nucleotide variant Immunodeficiency 44 [RCV001412067] Chr12:56344152 [GRCh38]
Chr12:56737936 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.510G>A (p.Gln170=) single nucleotide variant Immunodeficiency 44 [RCV001444539] Chr12:56355313 [GRCh38]
Chr12:56749097 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1749G>C (p.Arg583=) single nucleotide variant Immunodeficiency 44 [RCV001423666] Chr12:56346931 [GRCh38]
Chr12:56740715 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2414-4C>T single nucleotide variant Immunodeficiency 44 [RCV001438203] Chr12:56343535 [GRCh38]
Chr12:56737319 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.291T>C (p.Phe97=) single nucleotide variant Immunodeficiency 44 [RCV001438275] Chr12:56355798 [GRCh38]
Chr12:56749582 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1350C>T (p.Thr450=) single nucleotide variant Immunodeficiency 44 [RCV001427620] Chr12:56349253 [GRCh38]
Chr12:56743037 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.2271C>T (p.Ser757=) single nucleotide variant Immunodeficiency 44 [RCV001441092] Chr12:56343967 [GRCh38]
Chr12:56737751 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1890G>A (p.Pro630=) single nucleotide variant Immunodeficiency 44 [RCV001435394] Chr12:56346596 [GRCh38]
Chr12:56740380 [GRCh37]
Chr12:12q13.3
likely benign
NM_005419.4(STAT2):c.1440+9G>A single nucleotide variant Immunodeficiency 44 [RCV001441744] Chr12:56349154 [GRCh38]
Chr12:56742938 [GRCh37]
Chr12:12q13.3
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11363 AgrOrtholog
COSMIC STAT2 COSMIC
Ensembl Genes ENSG00000170581 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000315768 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000387354 UniProtKB/TrEMBL
  ENSP00000450751 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000450985 UniProtKB/TrEMBL
  ENSP00000498470 UniProtKB/TrEMBL
  ENSP00000498704 UniProtKB/TrEMBL
  ENSP00000498710 UniProtKB/TrEMBL
  ENSP00000498876 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000499022 UniProtKB/TrEMBL
  ENSP00000499108 UniProtKB/TrEMBL
Ensembl Transcript ENST00000314128 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000418572 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000555646 UniProtKB/TrEMBL
  ENST00000557235 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000650805 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000651301 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000651805 ENTREZGENE
  ENST00000651915 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000652091 ENTREZGENE
  ENST00000652398 UniProtKB/TrEMBL
  ENST00000652624 UniProtKB/TrEMBL
  ENST00000652741 ENTREZGENE, UniProtKB/TrEMBL
Gene3D-CATH 1.10.532.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.40.630 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.505.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000170581 GTEx
HGNC ID HGNC:11363 ENTREZGENE
Human Proteome Map STAT2 Human Proteome Map
InterPro p53-like_TF_DNA-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH2_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT2_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT2_SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_N_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_TF_alpha UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_TF_coiled-coil UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_TF_DNA-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_TF_DNA-bd_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_TF_prot_interaction UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6773 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 6773 ENTREZGENE
OMIM 600556 OMIM
  616636 OMIM
  618886 OMIM
PANTHER PTHR11801 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT2_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_alpha UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_bind UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_int UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36184 PharmGKB
PROSITE SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAT_int UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47655 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48092 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49417 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF55550 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A494C0B5_HUMAN UniProtKB/TrEMBL
  A0A494C164_HUMAN UniProtKB/TrEMBL
  A0A494C1L3_HUMAN UniProtKB/TrEMBL
  A0JLQ9_HUMAN UniProtKB/TrEMBL
  B4DHE0_HUMAN UniProtKB/TrEMBL
  B4DLC8_HUMAN UniProtKB/TrEMBL
  G3V319_HUMAN UniProtKB/TrEMBL
  P52630 ENTREZGENE
  Q6LD48_HUMAN UniProtKB/TrEMBL
  R9QDW3_HUMAN UniProtKB/TrEMBL
  R9QDW5_HUMAN UniProtKB/TrEMBL
  R9QDY3_HUMAN UniProtKB/TrEMBL
  R9QDY7_HUMAN UniProtKB/TrEMBL
  R9QDZ0_HUMAN UniProtKB/TrEMBL
  R9QE44_HUMAN UniProtKB/TrEMBL
  R9QE53_HUMAN UniProtKB/TrEMBL
  R9QE63_HUMAN UniProtKB/TrEMBL
  R9QE65 ENTREZGENE, UniProtKB/TrEMBL
  R9QE71_HUMAN UniProtKB/TrEMBL
  R9QF58_HUMAN UniProtKB/TrEMBL
  R9QF97_HUMAN UniProtKB/TrEMBL
  R9QF99_HUMAN UniProtKB/TrEMBL
  R9QFA2_HUMAN UniProtKB/TrEMBL
  R9QFA6_HUMAN UniProtKB/TrEMBL
  R9QFC5_HUMAN UniProtKB/TrEMBL
  R9QG79_HUMAN UniProtKB/TrEMBL
  R9QG81_HUMAN UniProtKB/TrEMBL
  R9QG88_HUMAN UniProtKB/TrEMBL
  R9QG91_HUMAN UniProtKB/TrEMBL
  R9QGC0_HUMAN UniProtKB/TrEMBL
  STAT2_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B4DLC7 UniProtKB/Swiss-Prot
  G3V2M6 UniProtKB/Swiss-Prot
  Q16430 UniProtKB/Swiss-Prot
  Q16431 UniProtKB/Swiss-Prot
  Q9UDL4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-17 STAT2  signal transducer and activator of transcription 2    signal transducer and activator of transcription 2, 113kDa  Symbol and/or name change 5135510 APPROVED