DNA Repair Genes pertinent cancer susceptibility
Gene: ERCC3EnsemblGeneIds (GRCh38): ENSG00000163161
EnsemblGeneIds (GRCh37): ENSG00000163161
OMIM: 133510, Gene2Phenotype
ERCC3 is in 14 panels
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Details
- Sources
-
- Human DNA Repair Genes Database
- Phenotypes
-
- Class: Nucleotide excision repair (NER)
- Activity: 3' to 5' DNA helicase
- OMIM
- 133510
- Clinvar variants
- Variants in ERCC3
- Penetrance
- Complete
- Panels with this gene
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- Adult solid tumours cancer susceptibility
- COVID-19 research
- DDG2P
- Bilateral congenital or childhood onset cataracts
- White matter disorders and cerebral calcification - narrow panel
- Fetal anomalies
- Structural eye disease
- Childhood solid tumours cancer susceptibility
- Childhood solid tumours
- Anophthalmia or microphthalmia
- Monogenic hearing loss
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome
- Intellectual disability
History Filter Activity
Panel promoted to version 1.0
Louise Daugherty (Genomics England Curator)This Cancer Germline 100K panel has been subjected to extensive internal and external review and has been versioned to V1 to enable germline reporting in the Cancer Pipeline.
Created
Ellen McDonagh (Genomics England Curator)ERCC3 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)ERCC3 was added to DNA Repair Genespanel. Sources: Human DNA Repair Genes Database