FANCC wt Allele

Preferred Label : FANCC wt Allele;

NCIt synonyms : FACC; FAC; FA3; FLJ14675; Fanconi Anemia Complementation Group C Gene; FA Complementation Group C wt Allele; Fanconi Anemia, Complementation Group C Gene;

NCIt definition : Human FANCC wild-type allele is located in the vicinity of 9q22.3 and is approximately 219 kb in length. This allele, which encodes Fanconi anemia group C protein, may be involved in the mediation of both DNA repair and cell cycle progression. Mutation of the gene is associated with Fanconi anemia.;

GenBank Accession Number : BC006303;

Details

Origin ID

C86028;

UMLS CUI

C2828029;

OMIM relation
- Fancc gene [OMIM gene]
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
- 9q22.3 [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Fanconi Anemia, Complementation Group C [NCIt concept]
gene_is_element_in_pathway
- BARD1 Pathway [NCIt concept]
- BARD1 Signaling Pathway [NCIt concept]
- Cancer Susceptibility Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Cycle Regulation Process [NCIt concept]
- DNA Maintenance [NCIt concept]
- DNA Repair [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients