RAD51C wt Allele

Preferred Label : RAD51C wt Allele;

NCIt synonyms : RAD51 Homolog C Gene; RAD51L2; RAD51 Paralog C wt Allele; FANCO; RAD51, S. cerevisiae, Homolog of, C Gene; R51H3; BROVCA3; RAD51 (S. cerevisiae) Homolog C Gene; RAD51 Homolog C (S. cerevisiae) Gene;

NCIt definition : Human RAD51C wild-type allele is located within 17q22-q23 and is approximately 3 kb in length. This allele, which encodes DNA repair protein RAD51 homolog 3 protein, may play a role in meiotic recombination and repair of damaged DNA.;

NCIt note : RAD51C has three alternative variants have been observed with highest expression in testis, heart muscle, spleen, and prostate.;

GenBank Accession Number : NM_002876; AF029669;

Details

Origin ID

C51005;

UMLS CUI

C1706140;

OMIM relation
- Rad51 paralog C [OMIM gene]
See also inter- (CISMeF)
- Breast-ovarian cancer, familial, susceptibility to, 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17q22-q23 [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Fanconi Anemia, Complementation Group O [NCIt concept]
gene_is_element_in_pathway
- Homologous Recombination Pathway [NCIt concept]
gene_plays_role_in_process
- DNA Binding [NCIt concept]
- DNA Repair [NCIt concept]
- Homologous Recombination [NCIt concept]
- Meiotic Recombination [NCIt concept]
- Recombination Repair [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients