ERCC8
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Homo sapiens |
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ERCC8 is differentially expressed in 266 experiments: 119 organism parts: lung, bone marrow, ... (117 more);, 179 disease states: normal, breast carcinoma, ... (177 more);, 87 cell types 345 cell lines 33 compound treatments and 78 other conditions. |
| Synonyms |
CSA, CKN1 |
| Orthologs |
ERCC8
(Gallus gallus)
Ercc8
(Mus musculus)
Q4H3S8_CIOIN
(Ciona intestinalis)
ercc8
(Danio rerio)
RAD28
(Saccharomyces cerevisiae)
ERCC8_BOVIN
(Bos taurus)
Ercc8
(Rattus norvegicus)
ercc8
(Xenopus laevis)
ENSXETG00000031181
(Xenopus laevis)
ERCC8
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
response to UV, response to oxidative stress, nucleotide-excision repair, proteasomal ubiquitin-dependent protein catabolic process, protein binding, protein autoubiquitination, DNA repair, protein complex, nuclear matrix, soluble fraction, nucleus, protein polyubiquitination, ubiquitin-protein ligase activity, nucleoplasm, response to DNA damage stimulus, response to X-ray, transcription-coupled nucleotide-excision repair, nucleotide-excision repair complex, positive regulation of DNA repair, Cul4A-RING ubiquitin ligase complex, protein complex binding |
| InterPro Term |
WD40_repeat_dom, WD40_repeat, WD40_repeat_2, G-protein_beta_WD-40_rep, WD40_repeat_subgr |
| InterPro ID |
IPR001680, IPR017986, IPR019781, IPR019782, IPR020472 |
| Gene Ontology ID |
GO:0009411, GO:0010165, GO:0016363, GO:0005625, GO:0005515, GO:0004842, GO:0005634, GO:0005654, GO:0006979, GO:0006974, GO:0043161, GO:0051865, GO:0043234, GO:0000209, GO:0006289, GO:0006281, GO:0032403, GO:0045739, GO:0000109, GO:0006283, GO:0031464 |
| Ensembl Family |
ENSFM00250000006144 |
| Ensembl Family Description |
DNA EXCISION REPAIR ERCC 8 COCKAYNE SYNDROME WD REPEAT CSA |
| HGNC Symbol |
ERCC8 |
| Ensembl Protein ID |
ENSP00000265038, ENSP00000408344, ENSP00000370510, ENSP00000400110, ENSP00000441732, ENSP00000442219 |
| UniProt Accession |
Q13216, C9JNT2, B4E383, B4DGZ9, B3KPW7 |
| EMBL-Bank ID |
CR536563, AC022445, AY213194, BC009793, BT020021, U28413, AK314511, CH471123, AK294856, AK304610, AC104113, AK056931 |
| Ensembl Gene ID |
ENSG00000049167 |
| Entrez Gene ID |
1161 |
| Description |
excision repair cross-complementing rodent repair deficiency, complementation group 8 [Source:HGNC Symbol;Acc:3439] |
| RefSeq ID |
NP_000073, NM_000082 |
| Ensembl Transcript ID |
ENST00000495985, ENST00000543101, ENST00000426742, ENST00000536596, ENST00000265038, ENST00000497892, ENST00000381118, ENST00000462279, ENST00000477893, ENST00000484330, ENST00000439176 |
| Gene-Disease Assocation |
COCKAYNE SYNDROME, TYPE A; CSA |
| Design Element |
ENST00000543101, 205162_at, ENST00000381118, 39664_at, 1554883_a_at, 220716_3p_at, ENST00000497892, ENST00000495985, 1554882_at, 220716_at, ENST00000536596, ENST00000484330, ENST00000477893, ENST00000462279, g4557466_3p_at, ENST00000426742, ENST00000265038, Hs2.32967.2.S1_3p_at, U28413_at, ENST00000439176 |
| Search EB-eye |
ENSG00000049167
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