ADAM9 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human ADAM9 wild-type allele is located in the vicinity of 8p11.22 and is approximately 108 kb in length. This allele, which encodes disintegrin and metalloproteinase domain-containing protein 9, plays a role in the cleavage and solubilzation of many biologically active membrane-bound proteins. Mutation of the gene is associated with cone-rod dystrophy type 9.
**Synonyms:** - A Disintegrin and Metalloproteinase Domain 9 (Meltrin Gamma) Gene - A Disintegrin and Metalloproteinase Domain 9 Gene - ADAM Metallopeptidase Domain 9 (Meltrin Gamma) Gene - ADAM Metallopeptidase Domain 9 wt Allele - CORD9 - Cone Rod Dystrophy 9 Gene - KIAA0021 - MCMP - MDC9 - MLTNG - Mltng
/api/v1/systems/nci_thesaurus/nodes/C179211Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.