C1QTNF5 wt Allele

Preferred Label : C1QTNF5 wt Allele;

NCIt synonyms : LORD; UNQ303/PRO344; C1q TNF-Alpha-Related Protein 5 Gene; Myonectin Gene; CTRP5; C1q and TNF Related 5 wt Allele; DKFZp586B0621;

NCIt definition : Human C1QTNF5 wild-type allele is located in the vicinity of 11q23.3 and is approximately 8 kb in length. This allele, which encodes complement C1q tumor necrosis factor-related protein 5, may play a role in cell adhesion to basement membranes. Mutations in the gene are associated with late-onset retinal degeneration.;

NCIt note : The C1QTNF5 gene is located within the 3' untranslated region of exon 13 of the MFRP gene. It can be transcribed as a bicistronic transcript including sequences from the MFRP gene or as a monocistronic transcript expressed from an internal promoter. (EntrezGene, OMIM and UniProt);

GenBank Accession Number : AF329841;

Détails

Origin ID

C215331;

OMIM relation
- C1q- and tumor necrosis factor-related protein 5 [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 11q23.3 [NCIt concept]
gene_plays_role_in_process
- Cell-Cell Adhesion Process [NCIt concept]
- Cell-Matrix Adhesion Process [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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