ERCC2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 19[15]
- Cytogenetic location
- 19q13.32[19]
- Encodes
- ERCC excision repair 2, TFIIH core complex helicase subunit, TFIIH basal transcription factor complex helicase XPD subunit[12][13]
- Expressed in
- stromal cell of endometrium, right adrenal gland, left adrenal gland, right adrenal cortex, ganglionic eminence, left adrenal cortex, ventricular zone, right testis, left testis, prefrontal cortex[20][21][22][23][24][25][26][27][28][29]
- Found in taxon
- Homo sapiens[14]
- Genetic association
- xeroderma pigmentosum group D, trichothiodystrophy syndromes[16][17]
- HomoloGene ID
- 344[3]
- Strand orientation
- reverse strand[18]
🏷️ Also known as
en COFS2
en EM9
en ERCC2
en ERCC excision repair 2, TFIIH core complex helicase subunit
en excision repair cross-complementation group 2
en TFIIH
en TTD
en TTD1
en XPD
🔖 Identifiers · 10
- CIViC gene ID
- 1736
- Ensembl gene ID
- ENSG00000104884
- Ensembl transcript ID
- ENST00000591309, ENST00000391941, ENST00000391942, ENST00000391944, ENST00000391945, ENST00000485403, ENST00000586131, ENST00000586441, ENST00000586737, ENST00000586856, ENST00000587376, ENST00000588652, ENST00000646507, ENST00000684264, ENST00000684218, ENST00000684407, ENST00000684458, ENST00000682414, ENST00000684468, ENST00000682508
- Entrez Gene ID
- 2068
- Exact match
- identifiers.org
- HGNC ID
- 3434
- HGNC gene symbol
- ERCC2
- OMIM ID
- 126340
- RefSeq RNA ID
- NM_000400, NM_001130867, XM_011526611, XR_001753633, XM_047438393, XR_007066680
- UMLS CUI
- C1333356
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