RUNX1T1 (RUNX1 partner transcriptional co-repressor 1) - Rat Genome Database

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Gene: RUNX1T1 (RUNX1 partner transcriptional co-repressor 1) Homo sapiens
Analyze
Symbol: RUNX1T1
Name: RUNX1 partner transcriptional co-repressor 1
RGD ID: 1350261
HGNC Page HGNC
Description: Predicted to have identical protein binding activity and transcription corepressor activity. Involved in negative regulation of transcription, DNA-templated. Localizes to nuclear matrix and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: acute myelogenous leukemia 1 translocation 1, cyclin-D related; AML1-MTG8; AML1T1; CBFA2T1; CBFA2T1 isoform r1t1-11a61; CBFA2T1 isoform r1t1-11a62; CBFA2T1 isoform r1t1-11a63; CBFA2T1 isoform r1t1-11a64; CBFA2T1 isoform r1t1-11a65; CBFA2T1 isoform r1t1-7a47; CBFA2T1 isoform r1t1-7a48; CBFA2T1 isoform r1t1-7a49; CBFA2T1 isoform r1t1-7a50; CBFA2T1 isoform r1t1-7a51; CBFA2T1 isoform r1t1-7a52; CBFA2T1 isoform r1t1-7d53; CBFA2T1 isoform r1t1-7d54; CBFA2T1 isoform r1t1-7d55; CBFA2T1 isoform r1t1-7d56; CBFA2T1 isoform r1t1-8a57; CBFA2T1 isoform r1t1-8a58; CBFA2T1 isoform r1t1-8a59; CBFA2T1 isoform r1t1-8a60; CDR; core-binding factor, runt domain, alpha subunit 2; core-binding factor, runt domain, alpha subunit 2, translocated to, 1; cyclin D-related; cyclin-D-related protein; DKFZp564B213; eight twenty one protein; ETO; FLJ33145; MGC2796; MTG8; MTG8b; myeloid translocation gene on 8q22; runt related transcription factor 1; runt-related transcription factor 1; RUNX1 translocation partner 1; translocated to, 1; translocated to, 1 (cyclin D related); translocated to, 1 (cyclin D-related); zinc finger MYND domain-containing protein 2; ZMYND2
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
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl891,954,967 - 92,103,286 (-)EnsemblGRCh38hg38GRCh38
GRCh38891,954,967 - 92,103,451 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37892,967,195 - 93,115,613 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36893,040,328 - 93,176,619 (-)NCBINCBI36hg18NCBI36
Build 34893,040,327 - 93,144,367NCBI
Celera889,157,513 - 89,293,797 (-)NCBI
Cytogenetic Map8q21.3NCBI
HuRef888,174,218 - 88,322,535 (-)NCBIHuRef
CHM1_1893,007,519 - 93,155,728 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(S)-nicotine  (EXP)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-naphthylamine  (EXP)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
acrylamide  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (ISO)
Aroclor 1254  (EXP)
belinostat  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
buta-1,3-diene  (ISO)
cadmium dichloride  (ISO)
calciol  (ISO)
calcitriol  (ISO)
carbon nanotube  (ISO)
cefaloridine  (ISO)
chloroprene  (ISO)
choline  (ISO)
cocaine  (ISO)
crotonaldehyde  (EXP)
cyclosporin A  (EXP)
diethyl malate  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
elemental selenium  (EXP)
entinostat  (EXP)
fenvalerate  (ISO)
folic acid  (ISO)
furan  (ISO)
glyphosate  (ISO)
GW 4064  (ISO)
L-methionine  (ISO)
lead(0)  (EXP)
lead(2+)  (EXP)
melphalan  (EXP)
mercury dibromide  (EXP)
methylmercury chloride  (EXP)
N-methyl-4-phenylpyridinium  (EXP)
nickel atom  (EXP)
nicotine  (EXP)
panobinostat  (EXP)
PCB138  (ISO)
phenylephrine  (ISO)
phenylmercury acetate  (EXP)
pioglitazone  (ISO)
pirinixic acid  (ISO)
SB 431542  (EXP)
selenium atom  (EXP)
tamoxifen  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichostatin A  (EXP)
triptonide  (ISO)
tunicamycin  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vitamin E  (EXP)
vorinostat  (EXP)
XL147  (ISO)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
nuclear matrix  (IDA)
nucleoplasm  (IDA)
nucleus  (IBA,IEA)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Short stature  (IAGP)
References

Additional References at PubMed
PMID:1391946   PMID:1423235   PMID:7523801   PMID:7541640   PMID:7774816   PMID:7919324   PMID:8137293   PMID:8334990   PMID:8353289   PMID:8575770   PMID:8619474   PMID:8683993  
PMID:8781439   PMID:9110174   PMID:9618262   PMID:9632137   PMID:9661669   PMID:9790752   PMID:9819405   PMID:10076566   PMID:10675041   PMID:10688654   PMID:10861016   PMID:10882117  
PMID:10951564   PMID:10973986   PMID:11090081   PMID:11113190   PMID:11150306   PMID:11533236   PMID:11591653   PMID:11593431   PMID:11869944   PMID:11983111   PMID:11986950   PMID:12242670  
PMID:12393523   PMID:12427969   PMID:12460926   PMID:12477932   PMID:12557226   PMID:12773394   PMID:12874834   PMID:14551142   PMID:14702039   PMID:14703694   PMID:14751048   PMID:14982881  
PMID:15109542   PMID:15203865   PMID:15295650   PMID:15298716   PMID:15333839   PMID:15377655   PMID:15489334   PMID:15676213   PMID:15723339   PMID:15735013   PMID:15829516   PMID:16189514  
PMID:16227606   PMID:16344560   PMID:16502583   PMID:16616331   PMID:16652140   PMID:16713569   PMID:16741927   PMID:16892037   PMID:16966434   PMID:16990610   PMID:17058450   PMID:17244680  
PMID:17284535   PMID:17353931   PMID:17389244   PMID:17560011   PMID:17572682   PMID:17625612   PMID:17649722   PMID:17875504   PMID:17989718   PMID:17996649   PMID:18039847   PMID:18073335  
PMID:18156164   PMID:18183572   PMID:18205948   PMID:18258796   PMID:18332109   PMID:18519037   PMID:18548094   PMID:18586123   PMID:18687517   PMID:18952841   PMID:19001502   PMID:19043539  
PMID:19100510   PMID:19179469   PMID:19289505   PMID:19448675   PMID:19458628   PMID:19581587   PMID:20090777   PMID:20211142   PMID:20430957   PMID:20487545   PMID:20603019   PMID:20688956  
PMID:20708017   PMID:21200020   PMID:21245488   PMID:21499216   PMID:21516116   PMID:21540640   PMID:21764752   PMID:21873635   PMID:22025082   PMID:22101339   PMID:22201794   PMID:22343733  
PMID:22498736   PMID:22995345   PMID:23223432   PMID:23251453   PMID:23426948   PMID:24402164   PMID:24456692   PMID:24586690   PMID:24616160   PMID:24727677   PMID:24783204   PMID:24897507  
PMID:24973361   PMID:24976338   PMID:25082877   PMID:25101977   PMID:25184681   PMID:25241761   PMID:25416956   PMID:25609649   PMID:25928846   PMID:26320575   PMID:26546158   PMID:26706127  
PMID:27252013   PMID:27276256   PMID:27522676   PMID:27725192   PMID:27770540   PMID:27798886   PMID:28092997   PMID:28166825   PMID:28322996   PMID:28514442   PMID:28539478   PMID:28611288  
PMID:28640846   PMID:28650479   PMID:29413154   PMID:29472719   PMID:29568097   PMID:29892012   PMID:30050054   PMID:30093631   PMID:30499136   PMID:30569130   PMID:30637949   PMID:31119862  
PMID:31247675   PMID:31699991   PMID:31725954   PMID:31839036   PMID:31869378   PMID:32024815   PMID:32071087   PMID:32296183   PMID:32311890   PMID:33067946   PMID:33152396   PMID:33217477  
PMID:33382982   PMID:33483506  


Genomics

Comparative Map Data
RUNX1T1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl891,954,967 - 92,103,286 (-)EnsemblGRCh38hg38GRCh38
GRCh38891,954,967 - 92,103,451 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37892,967,195 - 93,115,613 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36893,040,328 - 93,176,619 (-)NCBINCBI36hg18NCBI36
Build 34893,040,327 - 93,144,367NCBI
Celera889,157,513 - 89,293,797 (-)NCBI
Cytogenetic Map8q21.3NCBI
HuRef888,174,218 - 88,322,535 (-)NCBIHuRef
CHM1_1893,007,519 - 93,155,728 (-)NCBICHM1_1
Runx1t1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39413,742,628 - 13,895,056 (+)NCBIGRCm39mm39
GRCm39 Ensembl413,743,436 - 13,893,649 (+)Ensembl
GRCm38413,742,628 - 13,895,056 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl413,743,436 - 13,893,649 (+)EnsemblGRCm38mm10GRCm38
MGSCv37413,670,449 - 13,820,796 (+)NCBIGRCm37mm9NCBIm37
MGSCv36413,711,929 - 13,818,264 (+)NCBImm8
Celera413,520,441 - 13,687,612 (+)NCBICelera
Cytogenetic Map4A1NCBI
cM Map45.88NCBI
Runx1t1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2527,187,674 - 27,338,070 (+)NCBI
Rnor_6.0 Ensembl527,312,928 - 27,442,841 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0527,284,921 - 27,440,802 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0531,976,957 - 32,132,101 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4528,230,322 - 28,338,441 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1528,188,640 - 28,338,441 (+)NCBI
Celera526,502,150 - 26,607,942 (+)NCBICelera
Cytogenetic Map5q13NCBI
Runx1t1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554178,580,363 - 8,721,416 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554178,580,355 - 8,714,267 (-)NCBIChiLan1.0ChiLan1.0
RUNX1T1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1890,538,965 - 90,686,689 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl890,538,965 - 90,686,689 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0888,588,560 - 88,736,614 (-)NCBIMhudiblu_PPA_v0panPan3
RUNX1T1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12937,156,861 - 37,289,934 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2937,158,659 - 37,297,879 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2937,305,761 - 37,440,000 (-)NCBI
ROS_Cfam_1.02937,355,710 - 37,490,023 (-)NCBI
UMICH_Zoey_3.12937,374,916 - 37,509,114 (-)NCBI
UNSW_CanFamBas_1.02937,356,296 - 37,490,752 (-)NCBI
UU_Cfam_GSD_1.02937,796,907 - 37,931,529 (-)NCBI
Runx1t1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440530342,278,379 - 42,410,876 (+)NCBI
SpeTri2.0NW_0049365445,381,829 - 5,514,364 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RUNX1T1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl444,599,760 - 44,743,448 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1444,600,292 - 44,745,954 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2448,029,947 - 48,172,694 (+)NCBISscrofa10.2Sscrofa10.2susScr3
RUNX1T1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1886,984,638 - 87,127,648 (-)NCBI
ChlSab1.1 Ensembl886,988,366 - 87,090,875 (-)Ensembl
Vero_WHO_p1.0NW_02366603953,720,972 - 53,868,048 (+)NCBI
Runx1t1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624744783 - 63,720 (+)NCBI

Position Markers
D8S270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,020,489 - 93,020,675UniSTSGRCh37
GRCh37893,020,370 - 93,020,487UniSTSGRCh37
Build 36893,089,665 - 93,089,851RGDNCBI36
Celera889,206,857 - 89,207,043RGD
Celera889,206,738 - 89,206,855UniSTS
Cytogenetic Map8q22UniSTS
HuRef888,227,384 - 88,227,501UniSTS
Marshfield Genetic Map8103.69RGD
Genethon Genetic Map8102.1UniSTS
deCODE Assembly Map897.29UniSTS
GeneMap99-GB4 RH Map8428.7UniSTS
Whitehead-YAC Contig Map8 UniSTS
NCBI RH Map8899.7UniSTS
GeneMap99-G3 RH Map83520.0UniSTS
SHGC-36696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,058,540 - 93,058,640UniSTSGRCh37
Build 36893,127,716 - 93,127,816RGDNCBI36
Celera889,244,904 - 89,245,004RGD
Cytogenetic Map8q22UniSTS
HuRef888,265,583 - 88,265,683UniSTS
GeneMap99-G3 RH Map83533.0UniSTS
WI-13899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,967,216 - 92,967,341UniSTSGRCh37
Build 36893,036,392 - 93,036,517RGDNCBI36
Celera889,153,578 - 89,153,703RGD
Cytogenetic Map8q22UniSTS
HuRef888,174,239 - 88,174,364UniSTS
GeneMap99-GB4 RH Map8430.62UniSTS
Whitehead-RH Map8537.3UniSTS
NCBI RH Map8899.7UniSTS
G15975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,972,289 - 92,972,417UniSTSGRCh37
Build 36893,041,465 - 93,041,593RGDNCBI36
Celera889,158,639 - 89,158,767RGD
Cytogenetic Map8q22UniSTS
HuRef888,179,289 - 88,179,417UniSTS
D8S1603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,023,017 - 93,023,198UniSTSGRCh37
Build 36893,092,193 - 93,092,374RGDNCBI36
Celera889,209,386 - 89,209,567RGD
Cytogenetic Map8q22UniSTS
HuRef888,230,150 - 88,230,331UniSTS
Stanford-G3 RH Map83443.0UniSTS
GeneMap99-GB4 RH Map8428.7UniSTS
Whitehead-RH Map8535.8UniSTS
Whitehead-YAC Contig Map8 UniSTS
NCBI RH Map8899.7UniSTS
GeneMap99-G3 RH Map83533.0UniSTS
RH12051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,967,219 - 92,967,339UniSTSGRCh37
Build 36893,036,395 - 93,036,515RGDNCBI36
Celera889,153,581 - 89,153,701RGD
Cytogenetic Map8q22UniSTS
HuRef888,174,242 - 88,174,362UniSTS
GeneMap99-GB4 RH Map8428.7UniSTS
NCBI RH Map8899.7UniSTS
D8S1648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,075,268 - 93,075,443UniSTSGRCh37
Build 36893,144,444 - 93,144,619RGDNCBI36
Celera889,261,622 - 89,261,797RGD
Cytogenetic Map8q22UniSTS
HuRef888,282,351 - 88,282,526UniSTS
Whitehead-YAC Contig Map8 UniSTS
RH80460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,968,788 - 92,969,015UniSTSGRCh37
Build 36893,037,964 - 93,038,191RGDNCBI36
Celera889,155,150 - 89,155,377RGD
Cytogenetic Map8q22UniSTS
HuRef888,175,811 - 88,176,038UniSTS
GeneMap99-GB4 RH Map8430.72UniSTS
SHGC-86338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,081,312 - 93,081,636UniSTSGRCh37
Build 36893,150,488 - 93,150,812RGDNCBI36
Celera889,267,666 - 89,267,990RGD
Cytogenetic Map8q22UniSTS
HuRef888,288,395 - 88,288,715UniSTS
TNG Radiation Hybrid Map834186.0UniSTS
RH121766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,097,266 - 93,097,551UniSTSGRCh37
Build 36893,166,442 - 93,166,727RGDNCBI36
Celera889,283,620 - 89,283,905RGD
Cytogenetic Map8q22UniSTS
HuRef888,304,345 - 88,304,630UniSTS
TNG Radiation Hybrid Map834194.0UniSTS
RH122838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,986,314 - 92,986,598UniSTSGRCh37
Build 36893,055,490 - 93,055,774RGDNCBI36
Celera889,172,682 - 89,172,966RGD
Cytogenetic Map8q22UniSTS
HuRef888,193,314 - 88,193,598UniSTS
TNG Radiation Hybrid Map834152.0UniSTS
GDB:196494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,029,490 - 93,029,577UniSTSGRCh37
Build 36893,098,666 - 93,098,753RGDNCBI36
Celera889,215,860 - 89,215,947RGD
Cytogenetic Map8q22UniSTS
HuRef888,236,619 - 88,236,706UniSTS
UniSTS:225014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,972,272 - 92,972,420UniSTSGRCh37
Build 36893,041,448 - 93,041,596RGDNCBI36
Celera889,158,622 - 89,158,770RGD
HuRef888,179,272 - 88,179,420UniSTS
STS-AA025270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,068,854 - 93,068,944UniSTSGRCh37
Build 36893,138,030 - 93,138,120RGDNCBI36
Celera889,255,218 - 89,255,308RGD
Cytogenetic Map8q22UniSTS
HuRef888,275,899 - 88,275,989UniSTS
GeneMap99-GB4 RH Map8434.25UniSTS
D8S1952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,017,077 - 93,017,197UniSTSGRCh37
Build 36893,086,253 - 93,086,373RGDNCBI36
Celera889,203,445 - 89,203,565RGD
Cytogenetic Map8q22UniSTS
HuRef888,224,077 - 88,224,197UniSTS
GeneMap99-GB4 RH Map8428.7UniSTS
Whitehead-RH Map8535.8UniSTS
Whitehead-YAC Contig Map8 UniSTS
NCBI RH Map8899.7UniSTS
RH45255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37893,028,890 - 93,029,109UniSTSGRCh37
Build 36893,098,066 - 93,098,285RGDNCBI36
Celera889,215,260 - 89,215,479RGD
Cytogenetic Map8q22UniSTS
HuRef888,236,019 - 88,236,238UniSTS
GeneMap99-GB4 RH Map8430.41UniSTS
NCBI RH Map8899.7UniSTS
RH78563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,971,427 - 92,971,601UniSTSGRCh37
Build 36893,040,603 - 93,040,777RGDNCBI36
Celera889,157,788 - 89,157,962RGD
Cytogenetic Map8q22UniSTS
HuRef888,178,449 - 88,178,623UniSTS
GeneMap99-GB4 RH Map6183.02UniSTS
NCBI RH Map6693.7UniSTS
WI-17867  
Human AssemblyChrPosition (strand)SourceJBrowse
Celera889,209,042 - 89,209,191RGD
Cytogenetic Map8q22UniSTS
GeneMap99-GB4 RH Map8431.11UniSTS
Whitehead-RH Map8537.3UniSTS
NCBI RH Map8899.7UniSTS
G32207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,973,417 - 92,973,580UniSTSGRCh37
Build 36893,042,593 - 93,042,756RGDNCBI36
Celera889,159,767 - 89,159,930RGD
Cytogenetic Map8q22UniSTS
HuRef888,180,417 - 88,180,580UniSTS
D8S1950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,972,082 - 92,972,187UniSTSGRCh37
Build 36893,041,258 - 93,041,363RGDNCBI36
Celera889,158,432 - 89,158,537RGD
Cytogenetic Map8q22UniSTS
HuRef888,179,082 - 88,179,187UniSTS
Whitehead-YAC Contig Map8 UniSTS
Runx1t1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37892,972,282 - 92,972,701UniSTSGRCh37
Celera889,158,632 - 89,159,051UniSTS
HuRef888,179,282 - 88,179,701UniSTS
D8S270  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8q22UniSTS
Marshfield Genetic Map8103.69UniSTS
Genethon Genetic Map8102.1UniSTS
deCODE Assembly Map897.29UniSTS
Whitehead-YAC Contig Map8 UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:11109
Count of miRNA genes:1476
Interacting mature miRNAs:2002
Transcripts:ENST00000265814, ENST00000360348, ENST00000396218, ENST00000422361, ENST00000436581, ENST00000517493, ENST00000517792, ENST00000517919, ENST00000518256, ENST00000518317, ENST00000518361, ENST00000518449, ENST00000518823, ENST00000518832, ENST00000518844, ENST00000518954, ENST00000518992, ENST00000519061, ENST00000519422, ENST00000519577, ENST00000519847, ENST00000520047, ENST00000520172, ENST00000520428, ENST00000520556, ENST00000520583, ENST00000520724, ENST00000520974, ENST00000520978, ENST00000521054, ENST00000521078, ENST00000521319, ENST00000521375, ENST00000521553, ENST00000521733, ENST00000521751, ENST00000521897, ENST00000521902, ENST00000522065, ENST00000522163, ENST00000522316, ENST00000522467, ENST00000522860, ENST00000523168, ENST00000523290, ENST00000523629, ENST00000524215
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


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
High
Medium 253 57 15 1 17 1 782 71 1004 5 135 77 264 547
Low 2004 2151 1316 263 527 104 3458 2050 2667 240 1152 1345 162 1 940 2217 2
Below cutoff 68 658 356 329 731 327 61 53 47 129 100 73 4 24 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_023272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_175634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_175635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_175636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716676 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011517351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011517352 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011517353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017013941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_928359 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA506749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB074982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF018283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF131817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF181450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF198490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH006329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC067078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC139783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT009871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR456792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D14289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D14821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D43638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA499596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA500281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA503204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA504975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA770917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA774453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA776825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA776968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA777240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA779230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA787376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA795825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA796892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ177297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458797 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF946523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG551955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S45790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S50186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S74094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S74096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S82690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X79990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z35296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000265814   ⟹   ENSP00000265814
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,099,688 (-)Ensembl
RefSeq Acc Id: ENST00000360348   ⟹   ENSP00000353504
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,959,787 - 92,095,215 (-)Ensembl
RefSeq Acc Id: ENST00000396218   ⟹   ENSP00000379520
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,958,924 - 92,062,963 (-)Ensembl
RefSeq Acc Id: ENST00000422361   ⟹   ENSP00000390137
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,959,793 - 92,017,637 (-)Ensembl
RefSeq Acc Id: ENST00000436581   ⟹   ENSP00000402257
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,095,654 (-)Ensembl
RefSeq Acc Id: ENST00000517493
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,263 - 92,095,472 (-)Ensembl
RefSeq Acc Id: ENST00000517792   ⟹   ENSP00000429940
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,011,088 - 92,071,387 (-)Ensembl
RefSeq Acc Id: ENST00000517919   ⟹   ENSP00000429506
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,641 - 92,095,637 (-)Ensembl
RefSeq Acc Id: ENST00000518256
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,304 - 92,095,229 (-)Ensembl
RefSeq Acc Id: ENST00000518317   ⟹   ENSP00000429062
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,757 - 92,095,235 (-)Ensembl
RefSeq Acc Id: ENST00000518361   ⟹   ENSP00000430863
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,986,917 - 92,005,160 (-)Ensembl
RefSeq Acc Id: ENST00000518449   ⟹   ENSP00000428133
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,062,624 - 92,095,261 (-)Ensembl
RefSeq Acc Id: ENST00000518823   ⟹   ENSP00000428475
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,728 - 92,095,416 (-)Ensembl
RefSeq Acc Id: ENST00000518832   ⟹   ENSP00000429864
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,798 - 92,103,286 (-)Ensembl
RefSeq Acc Id: ENST00000518844   ⟹   ENSP00000430728
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,960,242 - 92,095,613 (-)Ensembl
RefSeq Acc Id: ENST00000518954   ⟹   ENSP00000430080
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,290 - 92,095,443 (-)Ensembl
RefSeq Acc Id: ENST00000518992   ⟹   ENSP00000431094
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,005,168 - 92,095,230 (-)Ensembl
RefSeq Acc Id: ENST00000519061   ⟹   ENSP00000430334
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,293 - 92,095,482 (-)Ensembl
RefSeq Acc Id: ENST00000519422   ⟹   ENSP00000429587
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,766 - 92,095,482 (-)Ensembl
RefSeq Acc Id: ENST00000519577   ⟹   ENSP00000430084
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,725 - 92,102,907 (-)Ensembl
RefSeq Acc Id: ENST00000519847   ⟹   ENSP00000430204
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,011,053 - 92,095,654 (-)Ensembl
RefSeq Acc Id: ENST00000520047
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,991,671 - 92,006,768 (-)Ensembl
RefSeq Acc Id: ENST00000520172
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,248 - 92,095,230 (-)Ensembl
RefSeq Acc Id: ENST00000520428   ⟹   ENSP00000429857
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,307 - 92,095,228 (-)Ensembl
RefSeq Acc Id: ENST00000520556   ⟹   ENSP00000428100
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,661 - 92,095,235 (-)Ensembl
RefSeq Acc Id: ENST00000520583   ⟹   ENSP00000430070
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,686 - 92,095,478 (-)Ensembl
RefSeq Acc Id: ENST00000520724   ⟹   ENSP00000428742
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,960,131 - 92,095,611 (-)Ensembl
RefSeq Acc Id: ENST00000520974   ⟹   ENSP00000429375
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,792 - 92,095,510 (-)Ensembl
RefSeq Acc Id: ENST00000520978   ⟹   ENSP00000429085
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,970,771 - 92,005,174 (-)Ensembl
RefSeq Acc Id: ENST00000521054   ⟹   ENSP00000427763
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,005,231 - 92,019,175 (-)Ensembl
RefSeq Acc Id: ENST00000521078
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,960,240 - 91,971,160 (-)Ensembl
RefSeq Acc Id: ENST00000521319   ⟹   ENSP00000429137
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,670 - 92,095,236 (-)Ensembl
RefSeq Acc Id: ENST00000521375   ⟹   ENSP00000429666
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,766 - 92,095,257 (-)Ensembl
RefSeq Acc Id: ENST00000521553   ⟹   ENSP00000429728
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,004,422 - 92,017,363 (-)Ensembl
RefSeq Acc Id: ENST00000521733   ⟹   ENSP00000430637
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,661 - 92,063,623 (-)Ensembl
RefSeq Acc Id: ENST00000521751   ⟹   ENSP00000430778
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,960,441 - 91,991,728 (-)Ensembl
RefSeq Acc Id: ENST00000521897   ⟹   ENSP00000429653
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,747 - 92,095,450 (-)Ensembl
RefSeq Acc Id: ENST00000521902
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,346 - 92,095,478 (-)Ensembl
RefSeq Acc Id: ENST00000522065
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,266 - 92,095,230 (-)Ensembl
RefSeq Acc Id: ENST00000522163
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,346 - 92,095,235 (-)Ensembl
RefSeq Acc Id: ENST00000522316
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,005,166 - 92,103,228 (-)Ensembl
RefSeq Acc Id: ENST00000522467   ⟹   ENSP00000429532
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,579 - 92,099,656 (-)Ensembl
RefSeq Acc Id: ENST00000522860
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,017,400 - 92,095,484 (-)Ensembl
RefSeq Acc Id: ENST00000523168   ⟹   ENSP00000429118
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,688 - 92,099,688 (-)Ensembl
RefSeq Acc Id: ENST00000523290
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,009,646 - 92,095,262 (-)Ensembl
RefSeq Acc Id: ENST00000523629   ⟹   ENSP00000428543
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,975 - 92,103,226 (-)Ensembl
RefSeq Acc Id: ENST00000524215   ⟹   ENSP00000429034
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl892,014,788 - 92,102,913 (-)Ensembl
RefSeq Acc Id: ENST00000613302   ⟹   ENSP00000481799
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,095,654 (-)Ensembl
RefSeq Acc Id: ENST00000613886   ⟹   ENSP00000478331
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,095,262 (-)Ensembl
RefSeq Acc Id: ENST00000614812   ⟹   ENSP00000481315
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,095,654 (-)Ensembl
RefSeq Acc Id: ENST00000615601   ⟹   ENSP00000480500
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,103,226 (-)Ensembl
RefSeq Acc Id: ENST00000617740   ⟹   ENSP00000481112
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl891,954,967 - 92,095,654 (-)Ensembl
RefSeq Acc Id: NM_001198625   ⟹   NP_001185554
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,478 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,148,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198626   ⟹   NP_001185555
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,478 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,148,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198627   ⟹   NP_001185556
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,478 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,148,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198628   ⟹   NP_001185557
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,099,688 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,152,190 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198629   ⟹   NP_001185558
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,230 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,147,764 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198630   ⟹   NP_001185559
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,230 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,147,764 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198631   ⟹   NP_001185560
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,478 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,148,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198632   ⟹   NP_001185561
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,230 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,147,764 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198633   ⟹   NP_001185562
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,103,385 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,155,728 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198634   ⟹   NP_001185563
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,478 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,148,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198679   ⟹   NP_001185608
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,478 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,148,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_004349   ⟹   NP_004340
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,062,634 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
Build 36893,040,328 - 93,144,367 (-)NCBI Archive
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,115,468 (-)NCBI
Sequence:
RefSeq Acc Id: NM_175634   ⟹   NP_783552
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,103,385 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
Build 36893,040,328 - 93,157,540 (-)NCBI Archive
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,155,728 (-)NCBI
Sequence:
RefSeq Acc Id: NM_175635   ⟹   NP_783553
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,972 - 92,095,230 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
Build 36893,040,328 - 93,176,619 (-)NCBI Archive
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,147,764 (-)NCBI
Sequence:
RefSeq Acc Id: NM_175636   ⟹   NP_783554
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,967 - 92,017,680 (-)NCBI
GRCh37892,967,195 - 93,115,454 (-)ENTREZGENE
Build 36893,040,328 - 93,099,084 (-)NCBI Archive
HuRef888,174,218 - 88,322,535 (-)ENTREZGENE
CHM1_1893,007,519 - 93,070,187 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716676   ⟹   XP_006716739
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,102,907 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011517351   ⟹   XP_011515653
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,510 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011517352   ⟹   XP_011515654
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,103,114 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011517353   ⟹   XP_011515655
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,450 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013930   ⟹   XP_016869419
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,103,451 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013932   ⟹   XP_016869421
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,230 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013933   ⟹   XP_016869422
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,261 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013934   ⟹   XP_016869423
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013935   ⟹   XP_016869424
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,478 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013936   ⟹   XP_016869425
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,103,226 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013937   ⟹   XP_016869426
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,482 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013938   ⟹   XP_016869427
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,975,905 - 92,095,503 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013939   ⟹   XP_016869428
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 91,993,735 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013940   ⟹   XP_016869429
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 91,996,226 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017013941   ⟹   XP_016869430
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 91,996,225 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024447317   ⟹   XP_024303085
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,095,482 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024447318   ⟹   XP_024303086
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,954,975 - 92,102,933 (-)NCBI
Sequence:
RefSeq Acc Id: XR_928359
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38891,960,441 - 92,095,503 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001185554 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185555 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185556 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185557 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185558 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185559 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185560 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185561 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185562 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185563 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185608 (Get FASTA)   NCBI Sequence Viewer  
  NP_004340 (Get FASTA)   NCBI Sequence Viewer  
  NP_783552 (Get FASTA)   NCBI Sequence Viewer  
  NP_783553 (Get FASTA)   NCBI Sequence Viewer  
  NP_783554 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716739 (Get FASTA)   NCBI Sequence Viewer  
  XP_011515653 (Get FASTA)   NCBI Sequence Viewer  
  XP_011515654 (Get FASTA)   NCBI Sequence Viewer  
  XP_011515655 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869419 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869421 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869422 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869423 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869424 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869425 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869426 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869427 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869428 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869429 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869430 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303085 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303086 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB32126 (Get FASTA)   NCBI Sequence Viewer  
  AAB46751 (Get FASTA)   NCBI Sequence Viewer  
  AAC26143 (Get FASTA)   NCBI Sequence Viewer  
  AAC28932 (Get FASTA)   NCBI Sequence Viewer  
  AAC28933 (Get FASTA)   NCBI Sequence Viewer  
  AAC28934 (Get FASTA)   NCBI Sequence Viewer  
  AAD14974 (Get FASTA)   NCBI Sequence Viewer  
  AAG33024 (Get FASTA)   NCBI Sequence Viewer  
  AAH05850 (Get FASTA)   NCBI Sequence Viewer  
  AAH67078 (Get FASTA)   NCBI Sequence Viewer  
  AAP88873 (Get FASTA)   NCBI Sequence Viewer  
  AHK05721 (Get FASTA)   NCBI Sequence Viewer  
  AHK05722 (Get FASTA)   NCBI Sequence Viewer  
  AHK05723 (Get FASTA)   NCBI Sequence Viewer  
  AHK05724 (Get FASTA)   NCBI Sequence Viewer  
  AHK05725 (Get FASTA)   NCBI Sequence Viewer  
  AHK05726 (Get FASTA)   NCBI Sequence Viewer  
  AHK05727 (Get FASTA)   NCBI Sequence Viewer  
  AHK05728 (Get FASTA)   NCBI Sequence Viewer  
  AHK05729 (Get FASTA)   NCBI Sequence Viewer  
  AHK05730 (Get FASTA)   NCBI Sequence Viewer  
  AHK05731 (Get FASTA)   NCBI Sequence Viewer  
  AHK05732 (Get FASTA)   NCBI Sequence Viewer  
  AHK05733 (Get FASTA)   NCBI Sequence Viewer  
  AHK05734 (Get FASTA)   NCBI Sequence Viewer  
  AHK05735 (Get FASTA)   NCBI Sequence Viewer  
  AHK05736 (Get FASTA)   NCBI Sequence Viewer  
  AHK05737 (Get FASTA)   NCBI Sequence Viewer  
  AHK05738 (Get FASTA)   NCBI Sequence Viewer  
  AHK05739 (Get FASTA)   NCBI Sequence Viewer  
  BAA03247 (Get FASTA)   NCBI Sequence Viewer  
  BAA03558 (Get FASTA)   NCBI Sequence Viewer  
  BAA07755 (Get FASTA)   NCBI Sequence Viewer  
  BAB88555 (Get FASTA)   NCBI Sequence Viewer  
  BAG35486 (Get FASTA)   NCBI Sequence Viewer  
  BAH12630 (Get FASTA)   NCBI Sequence Viewer  
  CAA56311 (Get FASTA)   NCBI Sequence Viewer  
  CAG33073 (Get FASTA)   NCBI Sequence Viewer  
  EAW91681 (Get FASTA)   NCBI Sequence Viewer  
  EAW91682 (Get FASTA)   NCBI Sequence Viewer  
  EAW91683 (Get FASTA)   NCBI Sequence Viewer  
  EAW91684 (Get FASTA)   NCBI Sequence Viewer  
  EAW91685 (Get FASTA)   NCBI Sequence Viewer  
  EAW91686 (Get FASTA)   NCBI Sequence Viewer  
  Q06455 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001185562   ⟸   NM_001198633
- Peptide Label: isoform D
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   A0A087WWT6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_783552   ⟸   NM_175634
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185557   ⟸   NM_001198628
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185563   ⟸   NM_001198634
- Peptide Label: isoform E
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185560   ⟸   NM_001198631
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185608   ⟸   NM_001198679
- Peptide Label: isoform F
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   A0A0A0MSU1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185555   ⟸   NM_001198626
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185556   ⟸   NM_001198627
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185554   ⟸   NM_001198625
- Peptide Label: isoform A
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   B2R6I9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_783553   ⟸   NM_175635
- Peptide Label: isoform C
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185561   ⟸   NM_001198632
- Peptide Label: isoform A
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185558   ⟸   NM_001198629
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001185559   ⟸   NM_001198630
- Peptide Label: isoform B
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_004340   ⟸   NM_004349
- Peptide Label: isoform A
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_783554   ⟸   NM_175636
- Peptide Label: isoform C
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006716739   ⟸   XM_006716676
- Peptide Label: isoform X4
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011515654   ⟸   XM_011517352
- Peptide Label: isoform X3
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011515653   ⟸   XM_011517351
- Peptide Label: isoform X2
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011515655   ⟸   XM_011517353
- Peptide Label: isoform X4
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016869419   ⟸   XM_017013930
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016869425   ⟸   XM_017013936
- Peptide Label: isoform X4
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016869423   ⟸   XM_017013934
- Peptide Label: isoform X4
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016869426   ⟸   XM_017013937
- Peptide Label: isoform X4
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016869424   ⟸   XM_017013935
- Peptide Label: isoform X4
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot),   W8FW32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016869422   ⟸   XM_017013933
- Peptide Label: isoform X3
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016869421   ⟸   XM_017013932
- Peptide Label: isoform X3
- UniProtKB: Q06455 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016869429   ⟸   XM_017013940
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016869430   ⟸   XM_017013941
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016869428   ⟸   XM_017013939
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016869427   ⟸   XM_017013938
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_024303086   ⟸   XM_024447318
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_024303085   ⟸   XM_024447317
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000429940   ⟸   ENST00000517792
RefSeq Acc Id: ENSP00000429506   ⟸   ENST00000517919
RefSeq Acc Id: ENSP00000431094   ⟸   ENST00000518992
RefSeq Acc Id: ENSP00000430080   ⟸   ENST00000518954
RefSeq Acc Id: ENSP00000428475   ⟸   ENST00000518823
RefSeq Acc Id: ENSP00000429864   ⟸   ENST00000518832
RefSeq Acc Id: ENSP00000430728   ⟸   ENST00000518844
RefSeq Acc Id: ENSP00000428133   ⟸   ENST00000518449
RefSeq Acc Id: ENSP00000430863   ⟸   ENST00000518361
RefSeq Acc Id: ENSP00000429062   ⟸   ENST00000518317
RefSeq Acc Id: ENSP00000430334   ⟸   ENST00000519061
RefSeq Acc Id: ENSP00000429587   ⟸   ENST00000519422
RefSeq Acc Id: ENSP00000430204   ⟸   ENST00000519847
RefSeq Acc Id: ENSP00000430084   ⟸   ENST00000519577
RefSeq Acc Id: ENSP00000353504   ⟸   ENST00000360348
RefSeq Acc Id: ENSP00000481799   ⟸   ENST00000613302
RefSeq Acc Id: ENSP00000478331   ⟸   ENST00000613886
RefSeq Acc Id: ENSP00000429857   ⟸   ENST00000520428
RefSeq Acc Id: ENSP00000429375   ⟸   ENST00000520974
RefSeq Acc Id: ENSP00000429085   ⟸   ENST00000520978
RefSeq Acc Id: ENSP00000428742   ⟸   ENST00000520724
RefSeq Acc Id: ENSP00000428100   ⟸   ENST00000520556
RefSeq Acc Id: ENSP00000430070   ⟸   ENST00000520583
RefSeq Acc Id: ENSP00000429666   ⟸   ENST00000521375
RefSeq Acc Id: ENSP00000429137   ⟸   ENST00000521319
RefSeq Acc Id: ENSP00000427763   ⟸   ENST00000521054
RefSeq Acc Id: ENSP00000481315   ⟸   ENST00000614812
RefSeq Acc Id: ENSP00000430778   ⟸   ENST00000521751
RefSeq Acc Id: ENSP00000430637   ⟸   ENST00000521733
RefSeq Acc Id: ENSP00000429728   ⟸   ENST00000521553
RefSeq Acc Id: ENSP00000429653   ⟸   ENST00000521897
RefSeq Acc Id: ENSP00000429532   ⟸   ENST00000522467
RefSeq Acc Id: ENSP00000480500   ⟸   ENST00000615601
RefSeq Acc Id: ENSP00000428543   ⟸   ENST00000523629
RefSeq Acc Id: ENSP00000429118   ⟸   ENST00000523168
RefSeq Acc Id: ENSP00000429034   ⟸   ENST00000524215
RefSeq Acc Id: ENSP00000481112   ⟸   ENST00000617740
RefSeq Acc Id: ENSP00000379520   ⟸   ENST00000396218
RefSeq Acc Id: ENSP00000265814   ⟸   ENST00000265814
RefSeq Acc Id: ENSP00000402257   ⟸   ENST00000436581
RefSeq Acc Id: ENSP00000390137   ⟸   ENST00000422361
Protein Domains
MYND-type   NHR2   TAFH

Promoters
RGD ID:7213745
Promoter ID:EPDNEW_H12618
Type:initiation region
Name:RUNX1T1_3
Description:RUNX1 translocation partner 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12619  EPDNEW_H12620  EPDNEW_H12621  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38892,017,299 - 92,017,359EPDNEW
RGD ID:7213747
Promoter ID:EPDNEW_H12619
Type:multiple initiation site
Name:RUNX1T1_2
Description:RUNX1 translocation partner 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12618  EPDNEW_H12620  EPDNEW_H12621  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38892,017,657 - 92,017,717EPDNEW
RGD ID:7213749
Promoter ID:EPDNEW_H12620
Type:initiation region
Name:RUNX1T1_1
Description:RUNX1 translocation partner 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12618  EPDNEW_H12619  EPDNEW_H12621  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38892,095,230 - 92,095,290EPDNEW
RGD ID:7213751
Promoter ID:EPDNEW_H12621
Type:initiation region
Name:RUNX1T1_4
Description:RUNX1 translocation partner 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12618  EPDNEW_H12619  EPDNEW_H12620  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38892,095,478 - 92,095,538EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-22.1(chr8:85835757-93610142)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053676]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053676]|See cases [RCV000053676] Chr8:85835757..93610142 [GRCh38]
Chr8:86847986..94622370 [GRCh37]
Chr8:86917086..94691546 [NCBI36]
Chr8:8q21.2-22.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-22.1(chr8:78672463-95366868)x1 copy number loss See cases [RCV000054262] Chr8:78672463..95366868 [GRCh38]
Chr8:79584698..96379096 [GRCh37]
Chr8:79747253..96448272 [NCBI36]
Chr8:8q21.13-22.1
pathogenic
GRCh38/hg38 8q21.3-22.1(chr8:90940996-94538343)x1 copy number loss See cases [RCV000054263] Chr8:90940996..94538343 [GRCh38]
Chr8:91953224..95550571 [GRCh37]
Chr8:92022400..95619747 [NCBI36]
Chr8:8q21.3-22.1
pathogenic
NM_175635.2(RUNX1T1):c.1169-25C>T single nucleotide variant Lung cancer [RCV000107883] Chr8:91975998 [GRCh38]
Chr8:92988226 [GRCh37]
Chr8:8q21.3
uncertain significance
NM_175635.2(RUNX1T1):c.630-725T>G single nucleotide variant Lung cancer [RCV000107884] Chr8:91992614 [GRCh38]
Chr8:93004842 [GRCh37]
Chr8:8q21.3
uncertain significance
NM_175635.2(RUNX1T1):c.-24+20949C>A single nucleotide variant Lung cancer [RCV000107885] Chr8:92074079 [GRCh38]
Chr8:93086307 [GRCh37]
Chr8:8q21.3
uncertain significance
GRCh38/hg38 8q21.3-24.23(chr8:86300584-137022587)x3 copy number gain See cases [RCV000135621] Chr8:86300584..137022587 [GRCh38]
Chr8:87312813..138034830 [GRCh37]
Chr8:87381929..138104012 [NCBI36]
Chr8:8q21.3-24.23
pathogenic|likely pathogenic
GRCh38/hg38 8q13.1-22.1(chr8:66171669-93505509)x3 copy number gain See cases [RCV000137050] Chr8:66171669..93505509 [GRCh38]
Chr8:67083904..94517737 [GRCh37]
Chr8:67246458..94586913 [NCBI36]
Chr8:8q13.1-22.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.3-24.3(chr8:93047482-141355635)x3 copy number gain See cases [RCV000511761] Chr8:93047482..141355635 [GRCh37]
Chr8:8q21.3-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3 copy number gain See cases [RCV000511002] Chr8:86841154..146295771 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3 copy number gain See cases [RCV000510854] Chr8:86841228..142689874 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3
pathogenic
GRCh37/hg19 8q21.3(chr8:92378841-93053423)x1 copy number loss not provided [RCV000682995] Chr8:92378841..93053423 [GRCh37]
Chr8:8q21.3
uncertain significance
GRCh37/hg19 8q21.3-22.1(chr8:91914994-93365750)x1 copy number loss not provided [RCV000683011] Chr8:91914994..93365750 [GRCh37]
Chr8:8q21.3-22.1
uncertain significance
GRCh37/hg19 8q21.2-23.3(chr8:86841154-116518125)x3 copy number gain not provided [RCV000683045] Chr8:86841154..116518125 [GRCh37]
Chr8:8q21.2-23.3
pathogenic
NM_175635.3(RUNX1T1):c.66_67insT (p.Pro23fs) insertion Short stature [RCV000736228] Chr8:92017274..92017275 [GRCh38]
Chr8:93029502..93029503 [GRCh37]
Chr8:8q21.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
NM_175635.3(RUNX1T1):c.1290C>T (p.Ala430=) single nucleotide variant not provided [RCV000919573] Chr8:91970796 [GRCh38]
Chr8:92983024 [GRCh37]
Chr8:8q21.3
likely benign
NM_175635.3(RUNX1T1):c.717C>T (p.Tyr239=) single nucleotide variant not provided [RCV000881739] Chr8:91991802 [GRCh38]
Chr8:93004030 [GRCh37]
Chr8:8q21.3
benign
NM_175635.3(RUNX1T1):c.966+7C>T single nucleotide variant not provided [RCV000965779] Chr8:91986880 [GRCh38]
Chr8:92999108 [GRCh37]
Chr8:8q21.3
benign
NM_175635.3(RUNX1T1):c.1054T>C (p.Leu352=) single nucleotide variant not provided [RCV000967095] Chr8:91986238 [GRCh38]
Chr8:92998466 [GRCh37]
Chr8:8q21.3
benign
NM_175635.3(RUNX1T1):c.127A>C (p.Thr43Pro) single nucleotide variant NK-cell enteropathy [RCV000791310] Chr8:92014809 [GRCh38]
Chr8:93027037 [GRCh37]
Chr8:8q21.3
likely pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3
pathogenic
NM_175635.3(RUNX1T1):c.354A>G (p.Leu118=) single nucleotide variant not provided [RCV000892795] Chr8:92014582 [GRCh38]
Chr8:93026810 [GRCh37]
Chr8:8q21.3
benign
NM_175635.3(RUNX1T1):c.1455G>A (p.Ala485=) single nucleotide variant not provided [RCV000899686] Chr8:91960491 [GRCh38]
Chr8:92972719 [GRCh37]
Chr8:8q21.3
benign
NM_175635.3(RUNX1T1):c.1245C>T (p.Ala415=) single nucleotide variant not provided [RCV000956649] Chr8:91970841 [GRCh38]
Chr8:92983069 [GRCh37]
Chr8:8q21.3
benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1535 AgrOrtholog
COSMIC RUNX1T1 COSMIC
Ensembl Genes ENSG00000079102 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000265814 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000353504 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000379520 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000390137 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000402257 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000427763 UniProtKB/TrEMBL
  ENSP00000428100 UniProtKB/TrEMBL
  ENSP00000428133 UniProtKB/TrEMBL
  ENSP00000428475 UniProtKB/TrEMBL
  ENSP00000428543 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000428742 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000429034 UniProtKB/TrEMBL
  ENSP00000429062 UniProtKB/TrEMBL
  ENSP00000429085 UniProtKB/TrEMBL
  ENSP00000429118 UniProtKB/TrEMBL
  ENSP00000429137 UniProtKB/TrEMBL
  ENSP00000429375 UniProtKB/TrEMBL
  ENSP00000429506 UniProtKB/TrEMBL
  ENSP00000429532 UniProtKB/TrEMBL
  ENSP00000429587 UniProtKB/TrEMBL
  ENSP00000429653 UniProtKB/TrEMBL
  ENSP00000429666 UniProtKB/TrEMBL
  ENSP00000429728 UniProtKB/TrEMBL
  ENSP00000429857 UniProtKB/TrEMBL
  ENSP00000429864 UniProtKB/TrEMBL
  ENSP00000429940 UniProtKB/TrEMBL
  ENSP00000430070 UniProtKB/TrEMBL
  ENSP00000430080 UniProtKB/TrEMBL
  ENSP00000430084 UniProtKB/TrEMBL
  ENSP00000430204 UniProtKB/TrEMBL
  ENSP00000430334 UniProtKB/TrEMBL
  ENSP00000430637 UniProtKB/TrEMBL
  ENSP00000430728 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000430778 UniProtKB/TrEMBL
  ENSP00000430863 UniProtKB/TrEMBL
  ENSP00000431094 UniProtKB/TrEMBL
  ENSP00000478331 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000480500 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000481112 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000481315 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000481799 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000265814 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000360348 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000396218 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000422361 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000436581 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000517792 UniProtKB/TrEMBL
  ENST00000517919 UniProtKB/TrEMBL
  ENST00000518317 UniProtKB/TrEMBL
  ENST00000518361 UniProtKB/TrEMBL
  ENST00000518449 UniProtKB/TrEMBL
  ENST00000518823 UniProtKB/TrEMBL
  ENST00000518832 UniProtKB/TrEMBL
  ENST00000518844 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000518954 UniProtKB/TrEMBL
  ENST00000518992 UniProtKB/TrEMBL
  ENST00000519061 UniProtKB/TrEMBL
  ENST00000519422 UniProtKB/TrEMBL
  ENST00000519577 UniProtKB/TrEMBL
  ENST00000519847 UniProtKB/TrEMBL
  ENST00000520428 UniProtKB/TrEMBL
  ENST00000520556 UniProtKB/TrEMBL
  ENST00000520583 UniProtKB/TrEMBL
  ENST00000520724 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000520974 UniProtKB/TrEMBL
  ENST00000520978 UniProtKB/TrEMBL
  ENST00000521054 UniProtKB/TrEMBL
  ENST00000521319 UniProtKB/TrEMBL
  ENST00000521375 UniProtKB/TrEMBL
  ENST00000521553 UniProtKB/TrEMBL
  ENST00000521733 UniProtKB/TrEMBL
  ENST00000521751 UniProtKB/TrEMBL
  ENST00000521897 UniProtKB/TrEMBL
  ENST00000522467 UniProtKB/TrEMBL
  ENST00000523168 UniProtKB/TrEMBL
  ENST00000523629 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000524215 UniProtKB/TrEMBL
  ENST00000613302 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000613886 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000614812 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000615601 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000617740 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.120.1110 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000079102 GTEx
HGNC ID HGNC:1535 ENTREZGENE
Human Proteome Map RUNX1T1 Human Proteome Map
InterPro CBFA2T1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CBFA2T1/2/3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NHR2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TAFH/NHR1_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TAFH_NHR1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_MYND UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:862 UniProtKB/Swiss-Prot
NCBI Gene 862 ENTREZGENE
OMIM 133435 OMIM
PANTHER PTHR10379 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10379:SF5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam NHR2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TAFH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-MYND UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26111 PharmGKB
PRINTS ETOFAMILY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MTG8PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE TAFH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_MYND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_MYND_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART TAFH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF158553 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WWT6 ENTREZGENE, UniProtKB/TrEMBL
  A0A0A0MSU1 ENTREZGENE, UniProtKB/TrEMBL
  A0A1B0GX92_HUMAN UniProtKB/TrEMBL
  B2R6I9 ENTREZGENE, UniProtKB/TrEMBL
  E5RFQ3_HUMAN UniProtKB/TrEMBL
  E5RG85_HUMAN UniProtKB/TrEMBL
  E5RH30_HUMAN UniProtKB/TrEMBL
  E5RH72_HUMAN UniProtKB/TrEMBL
  E5RHJ8_HUMAN UniProtKB/TrEMBL
  E5RI38_HUMAN UniProtKB/TrEMBL
  E5RJ32_HUMAN UniProtKB/TrEMBL
  E5RJB3_HUMAN UniProtKB/TrEMBL
  E5RJE7_HUMAN UniProtKB/TrEMBL
  E5RK76_HUMAN UniProtKB/TrEMBL
  E7EQ59_HUMAN UniProtKB/TrEMBL
  E7EQI9_HUMAN UniProtKB/TrEMBL
  E7EQJ1_HUMAN UniProtKB/TrEMBL
  E7EQW3_HUMAN UniProtKB/TrEMBL
  E7EQW7_HUMAN UniProtKB/TrEMBL
  E7ERJ9_HUMAN UniProtKB/TrEMBL
  E7ESA9_HUMAN UniProtKB/TrEMBL
  E7ESL1_HUMAN UniProtKB/TrEMBL
  E7ETA8_HUMAN UniProtKB/TrEMBL
  E7EV92_HUMAN UniProtKB/TrEMBL
  E7EWJ9_HUMAN UniProtKB/TrEMBL
  E7EX23_HUMAN UniProtKB/TrEMBL
  H0YBA6_HUMAN UniProtKB/TrEMBL
  H0YC25_HUMAN UniProtKB/TrEMBL
  H0YC43_HUMAN UniProtKB/TrEMBL
  MTG8_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  W8FK78_HUMAN UniProtKB/TrEMBL
  W8FK92_HUMAN UniProtKB/TrEMBL
  W8FKX0_HUMAN UniProtKB/TrEMBL
  W8FP49_HUMAN UniProtKB/TrEMBL
  W8FP57_HUMAN UniProtKB/TrEMBL
  W8FP62_HUMAN UniProtKB/TrEMBL
  W8FSP9_HUMAN UniProtKB/TrEMBL
  W8FSQ2_HUMAN UniProtKB/TrEMBL
  W8FSQ5_HUMAN UniProtKB/TrEMBL
  W8FSQ8_HUMAN UniProtKB/TrEMBL
  W8FW28_HUMAN UniProtKB/TrEMBL
  W8FW32 ENTREZGENE, UniProtKB/TrEMBL
  W8FW37_HUMAN UniProtKB/TrEMBL
UniProt Secondary A0A0A6YYQ5 UniProtKB/TrEMBL
  A0A0K0K188 UniProtKB/TrEMBL
  B7Z4P4 UniProtKB/Swiss-Prot
  E7EPN4 UniProtKB/Swiss-Prot
  E7EX26 UniProtKB/TrEMBL
  O14784 UniProtKB/Swiss-Prot
  Q06456 UniProtKB/Swiss-Prot
  Q14873 UniProtKB/Swiss-Prot
  Q16239 UniProtKB/Swiss-Prot
  Q16346 UniProtKB/Swiss-Prot
  Q16347 UniProtKB/Swiss-Prot
  Q6IBL1 UniProtKB/Swiss-Prot
  Q6NXH1 UniProtKB/Swiss-Prot
  Q7Z4J5 UniProtKB/Swiss-Prot
  Q92479 UniProtKB/Swiss-Prot
  Q9BRZ0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-05-21 RUNX1T1  RUNX1 partner transcriptional co-repressor 1  RUNX1T1  RUNX1 translocation partner 1  Symbol and/or name change 5135510 APPROVED
2016-03-28 RUNX1T1  RUNX1 translocation partner 1    runt related transcription factor 1; translocated to, 1 (cyclin D related)  Symbol and/or name change 5135510 APPROVED
2016-02-02 RUNX1T1  runt related transcription factor 1; translocated to, 1 (cyclin D related)    runt-related transcription factor 1; translocated to, 1 (cyclin D-related)  Symbol and/or name change 5135510 APPROVED