Gene: TMCO3

Alternate names for this Gene: C13orf11

Gene Summary: This gene encodes a member of the monovalent cation:proton antiporter 2 (CPA2) family of transporter proteins. Members of this family typically couple the export of monovalent cations, such as potassium or sodium, to the import of protons across cellular membranes. Mutations in this gene have been identified in patients with a rare inherited vision defect, cornea guttata with anterior polar cataract.

Gene is located in Chromosome: 13

Location in Chromosome : 13q34

Description of this Gene: transmembrane and coiled-coil domains 3

Type of Gene: protein-coding