FANCF wt Allele

Preferred Label : FANCF wt Allele;

NCIt synonyms : MGC126856; FAF; FA Complementation Group F wt Allele; Fanconi Anemia, Complementation Group F Gene; Fanconi Anemia Complementation Group F Gene;

NCIt definition : Human FANCF wild-type allele is located in the vicinity of 11p15 and is approximately 3 kb in length. This allele, which encodes Fanconi anemia group F protein, may play a role in the modulation of both cell cycle progression and DNA repair. Mutation of the gene is associated with Fanconi anemia.;

GenBank Accession Number : NM_022725;

Details

Origin ID

C86554;

UMLS CUI

C2828056;

OMIM relation
- Fancf 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
- 11p15 [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Fanconi Anemia, Complementation Group F [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) :

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