KCNV2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human KCNV2 wild-type allele is located in the vicinity of 9p24.2 and is approximately 13 kb in length. This allele, which encodes potassium voltage-gated channel subfamily V member 2 protein, is involved in the regulation of voltage-gated potassium channel activity. Mutation of the gene is associated with autosomal recessive retinal cone dystrophy 3B.

**Synonyms:** - KV11.1 - KV8.2 - Kv8.2 - Potassium Channel, Subfamily V, Member 2 Gene - Potassium Channel, Voltage Gated Modifier Subfamily V, Member 2 Gene - Potassium Channel, Voltage-Gated, Subfamily V, Member 2 Gene - Potassium Voltage-Gated Channel Modifier Subfamily V Member 2 wt Allele - RCD3B