DNA Repair Genes pertinent cancer susceptibility
Gene: ERCC5EnsemblGeneIds (GRCh38): ENSG00000134899
EnsemblGeneIds (GRCh37): ENSG00000134899
OMIM: 133530, Gene2Phenotype
ERCC5 is in 13 panels
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Details
- Sources
-
- Human DNA Repair Genes Database
- Phenotypes
-
- Class: Nucleotide excision repair (NER)
- Activity: 3' incision
- OMIM
- 133530
- Clinvar variants
- Variants in ERCC5
- Penetrance
- Complete
- Panels with this gene
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- Monogenic hearing loss
- Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome
- Intellectual disability
- Adult solid tumours cancer susceptibility
- Severe microcephaly
- Fetal anomalies
- DDG2P
- Structural eye disease
- White matter disorders and cerebral calcification - narrow panel
- Arthrogryposis
- Childhood solid tumours cancer susceptibility
- Childhood solid tumours
- Anophthalmia or microphthalmia
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)ERCC5 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)ERCC5 was added to DNA Repair Genespanel. Sources: Human DNA Repair Genes Database