STIL
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Homo sapiens |
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STIL is differentially expressed in 251 experiments: 100 organism parts: bone marrow, lung, ... (98 more);, 210 disease states: normal, colon carcinoma, ... (208 more);, 88 cell types 317 cell lines 24 compound treatments and 72 other conditions. |
| Synonyms |
MCPH7, SIL |
| Orthologs |
STIL
(Bos taurus)
Stil
(Mus musculus)
stil
(Danio rerio)
STIL
(Gallus gallus)
ENSCING00000013128
(Ciona intestinalis)
Stil
(Rattus norvegicus)
stil
(Xenopus laevis)
STIL
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
cytosol, cytoplasm, cell proliferation, negative regulation of apoptosis, smoothened signaling pathway, multicellular organism growth, centrosome, multicellular organismal development, embryonic axis specification, determination of left/right symmetry, neural tube closure, in utero embryonic development, forebrain development, notochord development, floor plate development, neural tube development, heart looping |
| Gene Ontology ID |
GO:0008283, GO:0007275, GO:0007224, GO:0007368, GO:0005737, GO:0005829, GO:0005813, GO:0000578, GO:0043066, GO:0035264, GO:0030900, GO:0030903, GO:0001947, GO:0001701, GO:0001843, GO:0021915, GO:0033504 |
| Ensembl Family |
ENSFM00250000004922 |
| Ensembl Family Description |
SCL INTERRUPTING LOCUS |
| Description |
SCL/TAL1 interrupting locus [Source:HGNC Symbol;Acc:10879] |
| UniProt Accession |
Q15468, Q5T0C7, Q5T0C6, Q5T0C9, Q5T0C8, Q5T0D4, Q5T0D0, E9PSF2 |
| Ensembl Protein ID |
ENSP00000412019, ENSP00000409087, ENSP00000353544, ENSP00000337367, ENSP00000411664, ENSP00000379523, ENSP00000360944, ENSP00000360941, ENSP00000243182 |
| RefSeq ID |
NM_003035, NM_001048166, NP_003026, NP_001041631 |
| EMBL-Bank ID |
CR749851, M74558, AL135960, AF349642, AF349643, AF349644, AF349645, AF349646, AF349647, AF349648, AF349649, AF349653, AF349654, AF349651, AF349652, AF349657, AF349655, AF349656, AF349650, BC126223, AL513322 |
| UniGene ID |
Hs.525198, Hs.673209 |
| Entrez Gene ID |
6491 |
| HGNC Symbol |
STIL |
| Ensembl Gene ID |
ENSG00000123473 |
| Ensembl Transcript ID |
ENST00000436811, ENST00000360380, ENST00000433827, ENST00000447475, ENST00000418131, ENST00000337817, ENST00000243182, ENST00000396221, ENST00000371874, ENST00000371877, ENST00000413565 |
| Gene-Disease Assocation |
MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE; MCPH7 |
| Design Element |
ENST00000413565, ENST00000396221, ENST00000337817, g4506958_3p_at, ENST00000371874, ENST00000360380, ENST00000243182, ENST00000418131, M74558_at, 205339_at, ENST00000447475, ENST00000433827, 32767_at, ENST00000371877, ENST00000436811 |
| Search EB-eye |
ENSG00000123473
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