TCF12
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Homo sapiens |
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TCF12 is differentially expressed in 322 experiments: 112 organism parts: bone marrow, thymus, ... (110 more);, 165 disease states: normal, control, ... (163 more);, 94 cell types 433 cell lines 49 compound treatments and 75 other conditions. |
| Synonyms |
HsT17266, HTF4, HEB, bHLHb20 |
| Orthologs |
tcf12
(Danio rerio)
Tcf12
(Rattus norvegicus)
Tcf12
(Mus musculus)
TCF12
(Gallus gallus)
TCF12
(Bos taurus)
tcf12
(Xenopus laevis)
TCF12
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0003677, GO:0010628, GO:0003700, GO:0007275, GO:0007399, GO:0007517, GO:0005515, GO:0006955, GO:0005634, GO:0005667, GO:0006355, GO:0006357, GO:0006351, GO:0046982, GO:0045893, GO:0030154, GO:0045666, GO:0044212, GO:0070888 |
| Gene Ontology Term |
DNA binding, protein binding, regulation of transcription, DNA-dependent, transcription, DNA-dependent, positive regulation of gene expression, cell differentiation, multicellular organismal development, nucleus, muscle organ development, protein heterodimerization activity, transcription factor complex, immune response, nervous system development, regulation of transcription from RNA polymerase II promoter, positive regulation of transcription, DNA-dependent, positive regulation of neuron differentiation, E-box binding, sequence-specific DNA binding transcription factor activity, transcription regulatory region DNA binding |
| InterPro ID |
IPR011598 |
| Ensembl Family Description |
TRANSCRIPTION FACTOR TCF TRANSCRIPTION FACTOR |
| Ensembl Family |
ENSFM00250000000724 |
| InterPro Term |
HLH_DNA-bd |
| EMBL-Bank ID |
AL831981, BX537967, AK303028, M83233, M65209, BC050556, CH471082, M80627, AK294617, BK001049, AK304007, AF271611, AF271613, AF271612, AF271615, AF271614, AF271616, AF271617, AF271609, AC016525, AC090532, AC090511, AC010999 |
| UniProt Accession |
Q99081, Q9NQY4, Q9NQY5, Q9NQY6, Q9NQY7, Q9NQY9, Q9NQY1, Q9NQY2, Q9NQY3, B4DZP2, B4E1W1, B4DGI9, F5GY10, E9PGY0, F5H6Z6, F5H5E9 |
| Ensembl Protein ID |
ENSP00000342459, ENSP00000267811, ENSP00000331057, ENSP00000396881, ENSP00000388940, ENSP00000444696, ENSP00000440017, ENSP00000443452, ENSP00000442910, ENSP00000454109, ENSP00000454102, ENSP00000453653, ENSP00000453737, ENSP00000453876, ENSP00000453216, ENSP00000453264 |
| RefSeq ID |
NM_003205, NP_003196, NP_996923, NP_996920, NP_996921, NP_996919, NM_207040, NM_207036, NM_207037, NM_207038 |
| UniGene ID |
Hs.608843, Hs.659471, Hs.595728, Hs.511504, Hs.682266 |
| Entrez Gene ID |
6938 |
| Ensembl Gene ID |
ENSG00000140262 |
| HGNC Symbol |
TCF12 |
| Description |
transcription factor 12 [Source:HGNC Symbol;Acc:11623] |
| Ensembl Transcript ID |
ENST00000543417, ENST00000543579, ENST00000452095, ENST00000543236, ENST00000438423, ENST00000267811, ENST00000343827, ENST00000537840, ENST00000333725, ENST00000559922, ENST00000559609, ENST00000559710, ENST00000559703, ENST00000559216, ENST00000560836, ENST00000560887, ENST00000560948, ENST00000560191, ENST00000560190, ENST00000560764, ENST00000560506, ENST00000557947, ENST00000558210, ENST00000557843, ENST00000561346, ENST00000561152, ENST00000561235, ENST00000561454, ENST00000561449, ENST00000561420, ENST00000558908 |
| Design Element |
ENST00000559710, ENST00000560836, 238041_at, ENST00000452095, ENST00000560190, ENST00000561449, ENST00000560887, Hs.82572.0.A1_3p_at, ENST00000343827, ENST00000561152, 208986_at, ENST00000561346, ENST00000543579, ENST00000543417, ENST00000267811, ENST00000543236, ENST00000559216, ENST00000561420, ENST00000560764, ENST00000558210, ENST00000438423, ENST00000558908, 54311_at, ENST00000333725, ENST00000561454, ENST00000559609, gnf1h02919_s_at, ENST00000559703, ENST00000560948, ENST00000537840, Hs.21704.0.S2_3p_at, ENST00000560506, ENST00000557947, ENST00000557843, ENST00000560191, ENST00000561235, M83233_at, ENST00000559922, 33348_at |
| Search EB-eye |
ENSG00000140262
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