Preferred Label : CHCHD2 wt Allele;
NCIt synonyms : Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 2 wt Allele; MNRR1; Mitochondria Nuclear Retrograde Regulator 1 Gene; C7orf17; MIX17 Homolog B Gene; Mitochondrial Nuclear Retrograde Regulator 1 Gene; Coiled-Coil-Helix-Coiled-Coil-Helix Domain-Containing Protein 2, Mitochondrial Gene; MIX17B; Aging-Associated Gene 10; Chromosome 7 Open Reading Frame 17 Gene; AAG10; NS2TP; PARK22;
NCIt definition : Human CHCHD2 wild-type allele is located in the vicinity of 7p11.2 and is approximately
12 kb in length. This allele, which encodes coiled-coil-helix-coiled-coil-helix domain-containing
protein 2, is involved in transcriptional regulation via binding to oxygen responsive
elements of target genes. Mutations in the gene are associated with autosomal dominant
Parkinson disease 22.;
GenBank Accession Number : AF078845;
Origin ID : C215440;
OMIM relation
- gene_found_in_organism
- gene_plays_role_in_process
