FANCI wt Allele

Preferred Label : FANCI wt Allele;

NCIt synonyms : FLJ10719; KIAA1794; Fanconi Anemia Complementation Group I Gene; FA Complementation Group I wt Allele; Fanconi Anemia, Complementation Group I Gene;

NCIt definition : Human FANCI wild-type allele is located in the vicinity of 15q26.1 and is approximately 73 kb in length. This allele, which encodes Fanconi anemia group I protein, is involved in the modulation of DNA repair. Mutation of the gene is associated with Fanconi anemia complementation group I.;

GenBank Accession Number : BC004277;

Details

Origin ID

C92475;

UMLS CUI

C2985126;

OMIM relation
- Fanci 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
- 15q26.1 [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Fanconi Anemia, Complementation Group I [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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