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
-
- Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome
- Childhood solid tumours cancer susceptibility
- White matter disorders and cerebral calcification - childhood onset
- Anophthalmia or microphthalmia
- Adult solid tumours cancer susceptibility
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Intellectual disability
- Fetal anomalies
- Monogenic hearing loss
- Bilateral congenital or childhood onset cataracts
- Structural eye disease
- COVID-19 research
- Childhood solid tumours
- DDG2P
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