SIX1
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Homo sapiens |
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SIX1 is differentially expressed in 246 experiments: 158 organism parts: pituitary gland, prostate, ... (156 more);, 175 disease states: normal, colon carcinoma, ... (173 more);, 70 cell types 375 cell lines 30 compound treatments and 61 other conditions. |
| Synonyms |
DFNA23 |
| Orthologs |
six1a
(Danio rerio)
Six1
(Mus musculus)
Six1
(Rattus norvegicus)
six1b
(Danio rerio)
so
(Drosophila melanogaster)
six1
(Xenopus laevis)
SIX1
(Canis familiaris)
(Compare orthologs)
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| Ensembl Family Description |
HOMEOBOX SINE OCULIS HOMEOBOX HOMOLOG |
| Gene Ontology Term |
pattern specification process, DNA binding, protein binding, regulation of transcription, DNA-dependent, transcription, DNA-dependent, sequence-specific DNA binding, positive regulation of transcription from RNA polymerase II promoter, regulation of neuron differentiation, nucleus, transcription factor complex, chromatin binding, skeletal muscle tissue development, positive regulation of transcription, DNA-dependent, nucleolus, negative regulation of neuron apoptosis, outflow tract morphogenesis, pharyngeal system development, kidney development, branching involved in ureteric bud morphogenesis, inner ear development, ureter smooth muscle cell differentiation, embryonic skeletal system morphogenesis, anatomical structure development, positive regulation of branching involved in ureteric bud morphogenesis, inner ear morphogenesis, regulation of branch elongation involved in ureteric bud branching, embryonic cranial skeleton morphogenesis, thymus development, generation of neurons, thyroid gland development, myoblast migration, ureteric bud development, epithelial cell differentiation, otic vesicle development, sequence-specific DNA binding transcription factor activity, protein localization to nucleus, positive regulation of mesenchymal cell proliferation involved in ureter development, positive regulation of ureteric bud formation, mesonephric tubule formation, metanephric mesenchyme development, transcription regulatory region DNA binding, organ induction, aorta morphogenesis, positive regulation of secondary heart field cardioblast proliferation |
| Gene Ontology ID |
GO:0003682, GO:0003677, GO:0003700, GO:0007389, GO:0007519, GO:0005515, GO:0005730, GO:0005634, GO:0005667, GO:0006355, GO:0006351, GO:0045664, GO:0045944, GO:0043524, GO:0043565, GO:0045893, GO:0060037, GO:0072095, GO:0072193, GO:0048856, GO:0048839, GO:0051451, GO:0048701, GO:0048704, GO:0048699, GO:0042472, GO:0048538, GO:0003151, GO:0030878, GO:0030855, GO:0090190, GO:0001759, GO:0001822, GO:0044212, GO:0001658, GO:0001657, GO:0034504, GO:0071599, GO:0072075, GO:2000729, GO:0072107, GO:0072172, GO:0035909, GO:0072513 |
| InterPro ID |
IPR001356 |
| InterPro Term |
Homeobox |
| Ensembl Family |
ENSFM00250000000696 |
| UniProt Accession |
Q15475 |
| UniGene ID |
Hs.633506, Hs.727889, Hs.630878 |
| RefSeq ID |
NM_005982, NP_005973 |
| Entrez Gene ID |
6495 |
| Ensembl Gene ID |
ENSG00000126778 |
| HGNC Symbol |
SIX1 |
| Ensembl Protein ID |
ENSP00000247182, ENSP00000450952, ENSP00000450739, ENSP00000452700 |
| EMBL-Bank ID |
BC008874, AF323497, X91868 |
| Description |
SIX homeobox 1 [Source:HGNC Symbol;Acc:10887] |
| Gene-Disease Assocation |
DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23, BRANCHIOOTIC SYNDROME 3; BOS3 |
| Ensembl Transcript ID |
ENST00000553535, ENST00000247182, ENST00000555627, ENST00000555955, ENST00000554986 |
| Design Element |
ENST00000247182, ENST00000553535, ENST00000555627, 228347_at, 205817_at, Hs.41295.0.S1_3p_at, g5174680_3p_at, ENST00000554986, 40004_at, 62110_at, 72890_at, ENST00000555955, X91868_at |
| Search EB-eye |
ENSG00000126778
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