XRCC2 wt Allele

Preferred Label : XRCC2 wt Allele;

NCIt synonyms : X-Ray Repair Cross Complementing Protein 2 Gene; DNA Repair Protein XRCC2 Gene; DKFZp781P0919; X-Ray Repair, Complementing Defective, in Chinese Hamster, 2 Gene; FANCU; RAD51-Like Gene; X-Ray Repair Complementing Defective Repair in Chinese Hamster Cells 2 Gene; X-Ray Repair Cross Complementing 2 wt Allele;

NCIt definition : Human XRCC2 wild-type allele is located in the vicinity of 7q36.1 and is approximately 30 kb in length. This allele, which encodes DNA-repair protein XRCC2, is involved in homologous recombination between sister chromatids to maintain chromosomal stability and repair DNA damage.;

GenBank Accession Number : NM_005431;

Details

Origin ID

C51013;

UMLS CUI

C1710689;

Automatic exact mappings (from CISMeF team)
- Fanconi anemia complementation group U [DO Concept]
- Fanconi anemia, complementation group u [OMIM Phenotype]
- X-ray repair cross complementing 2 [ORDO Gene]
OMIM relation
- X-ray repair cross complementing 2 [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_associated_with_disease
- Hypersensitivity [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 7q36.1 [NCIt concept]
gene_is_element_in_pathway
- Homologous Recombination Pathway [NCIt concept]
gene_plays_role_in_process
- DNA Maintenance [NCIt concept]
- DNA Repair [NCIt concept]
- Homologous Recombination [NCIt concept]
- Meiosis [NCIt concept]
- Recombination Repair [NCIt concept]

Keyword's position in hierarchy(ies) :

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