Gene: TEX14
Alternate names for this Gene: CT113|SPGF23
Gene Summary: The protein encoded by this gene is necessary for intercellular bridges in germ cells, which are required for spermatogenesis. Three transcript variants encoding different isoforms have been found for this gene.
Gene is located in Chromosome: 17
Location in Chromosome : 17q22
Description of this Gene: testis expressed 14, intercellular bridge forming factor
Type of Gene: protein-coding
Gene: RAD51C
Alternate names for this Gene: BROVCA3|FANCO|R51H3|RAD51L2
Gene Summary: This gene is a member of the RAD51 family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51 and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with other RAD51 paralogs and is reported to be important for Holliday junction resolution. Mutations in this gene are associated with Fanconi anemia-like syndrome. This gene is one of four localized to a region of chromosome 17q23 where amplification occurs frequently in breast tumors. Overexpression of the four genes during amplification has been observed and suggests a possible role in tumor progression. Alternative splicing results in multiple transcript variants.
Gene is located in Chromosome: 17
Location in Chromosome : 17q22
Description of this Gene: RAD51 paralog C
Type of Gene: protein-coding
rs587780840 in
TEX14;RAD51C gene and
FANCONI ANEMIA, COMPLEMENTATION GROUP O
PMID 26270727 2015 Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
PMID 20400964 2010 Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
PMID 21990120 2012 Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.
PMID 24800917 2014 Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.