Inherited ovarian cancer (without breast cancer)
Gene: EPCAMEnsemblGeneIds (GRCh38): ENSG00000119888
EnsemblGeneIds (GRCh37): ENSG00000119888
OMIM: 185535, Gene2Phenotype
EPCAM is in 13 panels
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Details
- Sources
-
- Emory Genetics Laboratory
- Phenotypes
-
- Breast and Ovarian Cancer
- OMIM
- 185535
- Clinvar variants
- Variants in EPCAM
- Penetrance
- Complete
- Panels with this gene
-
- Gastrointestinal epithelial barrier disorders
- Intestinal failure or congenital diarrhoea
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Inherited polyposis and early onset colorectal cancer - germline testing
- Adult solid tumours for rare disease
- Inherited ovarian cancer (without breast cancer)
- Familial breast cancer
- Adult solid tumours cancer susceptibility
- GI tract tumours
- DDG2P
- Primary immunodeficiency or monogenic inflammatory bowel disease
- COVID-19 research
- Inherited MMR deficiency (Lynch syndrome)
History Filter Activity
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)31/07/2017: Promoted panel to version 1, after checking against the original list sent by Clare Turnbull for this panel.
Created
Ellen McDonagh (Genomics England Curator)EPCAM was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)EPCAM was added to Familial ovarian cancerpanel. Sources: Emory Genetics Laboratory