RUNX1T1
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Homo sapiens |
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RUNX1T1 is differentially expressed in 310 experiments: 191 organism parts: cerebellum, brain, ... (189 more);, 255 disease states: normal, prostate carcinoma, ... (253 more);, 97 cell types 400 cell lines 36 compound treatments and 83 other conditions. |
| Synonyms |
CBFA2T1, ZMYND2, AML1T1, ETO, MTG8, CDR |
| Orthologs |
RUNX1T1
(Gallus gallus)
runx1t1
(Danio rerio)
Runx1t1
(Rattus norvegicus)
RUNX1T1
(Bos taurus)
Runx1t1
(Mus musculus)
nvy
(Drosophila melanogaster)
runx1t1
(Xenopus laevis)
RUNX1T1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0003677, GO:0008270, GO:0003700, GO:0051101, GO:0042803, GO:0042802, GO:0005515, GO:0005634, GO:0046872, GO:0006355, GO:0006351, GO:0006091, GO:0045444 |
| Gene Ontology Term |
DNA binding, protein binding, regulation of transcription, DNA-dependent, regulation of DNA binding, transcription, DNA-dependent, generation of precursor metabolites and energy, metal ion binding, identical protein binding, nucleus, protein homodimerization activity, zinc ion binding, fat cell differentiation, sequence-specific DNA binding transcription factor activity |
| InterPro ID |
IPR003894, IPR002893, IPR014896, IPR013290, IPR013289 |
| InterPro Term |
Znf_MYND, MTG8, ETO, TAFH_NHR1, NHR2 |
| Ensembl Family |
ENSFM00250000001209 |
| Ensembl Family Description |
CBF MTG8 |
| Description |
runt-related transcription factor 1; translocated to, 1 (cyclin D-related) [Source:HGNC Symbol;Acc:1535] |
| Ensembl Gene ID |
ENSG00000079102 |
| Ensembl Protein ID |
ENSP00000429940, ENSP00000429728, ENSP00000431094, ENSP00000429864, ENSP00000429857, ENSP00000429587, ENSP00000429506, ENSP00000429532, ENSP00000429653, ENSP00000429666, ENSP00000427763, ENSP00000265814, ENSP00000353504, ENSP00000429375, ENSP00000429137, ENSP00000429118, ENSP00000429085, ENSP00000429062, ENSP00000429034, ENSP00000428543, ENSP00000390137, ENSP00000428742, ENSP00000428100, ENSP00000428133, ENSP00000379520, ENSP00000428297, ENSP00000428408, ENSP00000428475, ENSP00000430334, ENSP00000430084, ENSP00000430070, ENSP00000430080, ENSP00000402257, ENSP00000430204, ENSP00000430728, ENSP00000430778, ENSP00000430863, ENSP00000430637 |
| EMBL-Bank ID |
BT009871, S78158, S78159, S50186, D13979, D43638, X79990, CR456792, BC067078, CH471060, D14823, D14822, D14821, AF198490, D14289, AB074982, AF018273, AF018272, AF018275, AF018274, AF018277, AF018276, AF018279, AF018278, AF018271, AF018270, AF018283, AF018282, AF018281, S74092, S74096, BC005850, AF181450, AC103680, AC104339 |
| RefSeq ID |
NM_175635, NM_175634, NM_175636, NM_004349, NP_783552, NP_783553, NP_783554, NP_004340, NP_001185558, NP_001185559, NP_001185556, NP_001185557, NP_001185554, NP_001185555, NP_001185561, NP_001185560, NP_001185563, NP_001185562, NP_001185608, NM_001198679, NM_001198629, NM_001198628, NM_001198627, NM_001198626, NM_001198625, NM_001198630, NM_001198632, NM_001198631, NM_001198634, NM_001198633 |
| UniGene ID |
Hs.368431, Hs.594620, Hs.624033, Hs.626145 |
| HGNC Symbol |
RUNX1T1 |
| UniProt Accession |
Q9HBV9, Q8TDW8, Q06455, Q7Z4J5, E7EQ59, E5RFQ3, E5RG85, E7EPN4, E7EQW7, E7EQW3, E7EQJ1, E7EQI9, E7ESA9, E7ERJ9, E5RJB3, E5RJE7, E7ETA8, E5RJ32, E7ESL1, E5RK76, E5RH72, E5RH30, E7EV92, E7EWJ9, E5RI38, E5RHJ8, E7EX23 |
| Entrez Gene ID |
862 |
| Ensembl Transcript ID |
ENST00000518449, ENST00000518361, ENST00000518317, ENST00000518256, ENST00000436581, ENST00000360348, ENST00000396218, ENST00000518954, ENST00000518992, ENST00000524215, ENST00000518823, ENST00000518844, ENST00000518832, ENST00000521078, ENST00000521054, ENST00000523290, ENST00000422361, ENST00000523629, ENST00000519061, ENST00000521902, ENST00000521897, ENST00000521733, ENST00000521751, ENST00000265814, ENST00000521553, ENST00000521375, ENST00000521319, ENST00000520047, ENST00000520172, ENST00000520556, ENST00000520583, ENST00000520428, ENST00000517919, ENST00000519422, ENST00000517792, ENST00000519577, ENST00000523168, ENST00000517493, ENST00000519847, ENST00000522316, ENST00000522467, ENST00000522163, ENST00000522065, ENST00000520978, ENST00000520974, ENST00000520724, ENST00000522860 |
| Gene-Disease Assocation |
COLORECTAL CANCER; CRC |
| Design Element |
ENST00000518844, ENST00000520047, ENST00000521733, 1564642_at, ENST00000522316, ENST00000518992, ENST00000518256, ENST00000518449, D14823_at, ENST00000422361, ENST00000523290, ENST00000519061, ENST00000521375, 35641_g_at, ENST00000517493, ENST00000522163, ENST00000522860, ENST00000518361, ENST00000360348, 35639_at, ENST00000517919, ENST00000521078, ENST00000265814, ENST00000524215, 228827_at, ENST00000520172, ENST00000523168, 242845_at, ENST00000520428, ENST00000518317, 91343_at, Hs.31551.0.S1_3p_s_at, Hs.144995.0.A1_3p_at, ENST00000518954, ENST00000520978, ENST00000523629, ENST00000518823, 71792_at, ENST00000520974, ENST00000396218, ENST00000521751, D43638_at, ENST00000521553, ENST00000521319, D14822_at, g4757915_3p_a_at, 35640_at, 65667_r_at, ENST00000519847, ENST00000520583, ENST00000522467, ENST00000518832, ENST00000519577, ENST00000521054, ENST00000521902, ENST00000520556, ENST00000436581, ENST00000519422, ENST00000520724, ENST00000522065, 216831_s_at, ENST00000521897, 205528_s_at, Hs.90858.0.S1_3p_at, 35638_at, 65252_at, 47161_at, Hs.307345.0.S1_3p_s_at, Hs2.434273.1.S1_3p_at, 205529_s_at, ENST00000517792, 216832_at |
| Search EB-eye |
ENSG00000079102
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