ERCC excision repair 2, TFIIH core complex helicase subunit

Preferred Label : ERCC excision repair 2, TFIIH core complex helicase subunit;

Approved symbol HGNC : ERCC2;

Name synonyms HGNC : TFIIH basal transcription factor complex helicase XPB subunit; complementation group 2 protein; excision repair cross-complementing rodent repair deficiency;

Alias symbols HGNC : EM9; MAG; MGC102762; MGC126218; MGC126219;

Chromosome HGNC : 19q13.32;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000104884;

Details

Origin ID

HGNC:3434;

UMLS CUI

C1333356;

Automatic exact mappings (from CISMeF team)
- ERCC excision repair 2, TFIIH core complex helicase subunit [ORDO Gene]
- Ercc excision repair 2, tfiih core complex helicase subunit [OMIM gene]
- Myelin-associated glycoprotein [OMIM gene]
- TFIIH Basal Transcription Factor Complex Helicase XPB Subunit [NCIt concept]
NCIt concept
- ERCC2 Gene [NCIt concept]
OMIM gene
- Ercc excision repair 2, tfiih core complex helicase subunit [OMIM gene]
Orphanet gene
- ERCC excision repair 2, TFIIH core complex helicase subunit [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ERCC2 Gene [NCIt concept]
- Ercc excision repair 2, tfiih core complex helicase subunit [OMIM gene]

Keyword's position in hierarchy(ies) :

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