CENPX wt Allele

Preferred Label : CENPX wt Allele;

NCIt synonyms : Retinoic Acid-Inducible Gene D9; CENP-X; STRA13; D9; Stimulated By Retinoic Acid 13 Gene; MHF2; FAAP10; Centromere Protein X wt Allele; Stimulated By Retinoic Acid 13 Homolog (Mouse) Gene; Stimulated By Retinoic Acid 13 Homolog Gene; Fanconi Anemia-Associated Polypeptide, 10-kD Gene;

NCIt definition : Human CENPX wild-type allele is located in the vicinity of 17q25.3 and is approximately 5 kb in length. This allele, which encodes centromere protein X, is involved in DNA binding, DNA repair and the resolution of DNA replication forks.;

GenBank Accession Number : BC009571;

Details

Origin ID

C116632;

UMLS CUI

C3889647;

Automatic exact mappings (from CISMeF team)
- Centromeric protein X [OMIM gene]
OMIM relation
- Centromeric protein X [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
- 17q25.3 [NCIt concept]
gene_plays_role_in_process
- DNA Binding [NCIt concept]
- DNA Maintenance [NCIt concept]
- DNA Repair [NCIt concept]
- Mitosis [NCIt concept]
- Monoubiquitination [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients