ERCC3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 2[15]
- Cytogenetic location
- 2q14.3[20]
- Encodes
- ERCC excision repair 3, TFIIH core complex helicase subunit, TFIIH basal transcription factor complex helicase XPB subunit[12][13]
- Expressed in
- sural nerve, right hemisphere of cerebellum, right uterine tube, gastric mucosa, gonad, granulocyte, ganglionic eminence, body of uterus, anterior pituitary, canal of the cervix[21][22][23][24][25][26][27][28][29][30]
- Found in taxon
- Homo sapiens[14]
- Genetic association
- xeroderma pigmentosum group B, trichothiodystrophy 2, photosensitive, trichothiodystrophy syndromes[16][17][18]
- HomoloGene ID
- 96[3]
- Strand orientation
- reverse strand[19]
🏷️ Also known as
en BTF2
en ERCC3
en ERCC excision repair 3, TFIIH core complex helicase subunit
en excision repair cross-complementation group 3
en GTF2H
en RAD25
en Ssl2
en TFIIH
en TTD2
en XPB
🔖 Identifiers · 9
- Ensembl gene ID
- ENSG00000163161
- Ensembl transcript ID
- ENST00000494464, ENST00000285398, ENST00000426778, ENST00000445889, ENST00000456257, ENST00000460485, ENST00000462306, ENST00000490062, ENST00000491292, ENST00000645736, ENST00000646654, ENST00000647169, ENST00000645467, ENST00000646042, ENST00000642308, ENST00000642972, ENST00000647496, ENST00000644317, ENST00000645504, ENST00000643982, ENST00000645233
- Entrez Gene ID
- 2071
- Exact match
- identifiers.org
- HGNC ID
- 3435
- HGNC gene symbol
- ERCC3
- OMIM ID
- 133510
- RefSeq RNA ID
- XM_011510795, NM_000122, NM_001303416, NM_001303418, XM_011510794
- UMLS CUI
- C1333357
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Summary
ERCC3 is a gene[1].