ERCC6
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Homo sapiens |
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ERCC6 is differentially expressed in 216 experiments: 85 organism parts: blood, cervix, ... (83 more);, 114 disease states: normal, adenocarcinoma, ... (112 more);, 72 cell types 259 cell lines 31 compound treatments and 67 other conditions. |
| Synonyms |
CSB, RAD26, CKN2 |
| Orthologs |
RAD26
(Saccharomyces cerevisiae)
ercc6
(Danio rerio)
ERCC6
(Bos taurus)
Ercc6
(Mus musculus)
ERCC6
(Gallus gallus)
Ercc6
(Rattus norvegicus)
pgbd3
(Xenopus laevis)
ERCC6
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
response to UV, response to oxidative stress, DNA binding, nucleotide-excision repair, protein binding, DNA repair, DNA damage response, signal transduction resulting in induction of apoptosis, response to toxin, protein N-terminus binding, nucleic acid binding, activation of JNKK activity, transcription from RNA polymerase II promoter, photoreceptor cell maintenance, soluble fraction, ATP binding, activation of JUN kinase activity, DNA-dependent ATPase activity, nucleus, transcription elongation factor complex, nucleotide binding, chromatin binding, hydrolase activity, protein C-terminus binding, nucleoplasm, base-excision repair, response to DNA damage stimulus, response to gamma radiation, response to X-ray, nucleolus, helicase activity, pyrimidine dimer repair, transcription-coupled nucleotide-excision repair, response to superoxide, response to UV-B, protein complex binding, regulation of transcription elongation, DNA-dependent, positive regulation of transcription elongation, DNA-dependent |
| Gene Ontology ID |
GO:0003682, GO:0003676, GO:0003677, GO:0008094, GO:0008023, GO:0008022, GO:0010332, GO:0009411, GO:0008630, GO:0010165, GO:0009636, GO:0007256, GO:0007257, GO:0004386, GO:0016787, GO:0005625, GO:0005524, GO:0005515, GO:0047485, GO:0005730, GO:0005634, GO:0005654, GO:0006979, GO:0006974, GO:0000166, GO:0006366, GO:0006284, GO:0006289, GO:0006281, GO:0045494, GO:0010224, GO:0032403, GO:0032786, GO:0006290, GO:0006283, GO:0000303, GO:0032784 |
| InterPro ID |
IPR001650, IPR000330, IPR014001 |
| InterPro Term |
SNF2_N, Helicase_C, DEAD-like_helicase |
| Ensembl Family |
ENSFM00560000771020 |
| Ensembl Family Description |
DNA EXCISION REPAIR ERCC 6 EC_3.6.4.12 ATP DEPENDENT HELICASE ERCC6 |
| UniGene ID |
Hs.682679, Hs.654449 |
| Ensembl Protein ID |
ENSP00000363244, ENSP00000422827, ENSP00000348089, ENSP00000439608, ENSP00000445134 |
| HGNC Symbol |
ERCC6 |
| Entrez Gene ID |
2074 |
| UniProt Accession |
D6R9X7, Q03468, Q68DI2, F5H1J0, F5H493 |
| Ensembl Gene ID |
ENSG00000225830 |
| Description |
excision repair cross-complementing rodent repair deficiency, complementation group 6 [Source:HGNC Symbol;Acc:3438] |
| EMBL-Bank ID |
L04791, CH471187, AL138760, AY204752, AC073366, CR749388 |
| Gene-Disease Assocation |
LUNG CANCER, DE SANCTIS-CACCHIONE SYNDROME, COCKAYNE SYNDROME, TYPE B; CSB, CEREBROOCULOFACIOSKELETAL SYNDROME 1; COFS1, MACULAR DEGENERATION, AGE-RELATED, 5; ARMD5, UV-SENSITIVE SYNDROME; UVS |
| RefSeq ID |
NP_000115, NM_000124 |
| Ensembl Transcript ID |
ENST00000355832, ENST00000542458, ENST00000465653, ENST00000539110, ENST00000462247, ENST00000374129, ENST00000475116, ENST00000479652 |
| Design Element |
ENST00000539110, 82563_at, ENST00000465653, Hs.98361.0.A1_3p_at, 49088_at, ENST00000475116, ENST00000479652, 230108_at, 2080_s_at, 35043_at, ENST00000374129, 207347_at, g4557564_3p_at, ENST00000462247, ENST00000355832, ENST00000542458 |
| Search EB-eye |
ENSG00000225830
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