ADGRV1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ADGRV1 wild-type allele is located in the vicinity of 5q14.3 and is approximately 635 kb in length. This allele, which encodes adhesion G-protein coupled receptor V1 protein, is involved in signaling and the development of hearing and vision. Mutations in the gene are associated with familial febrile seizures 4 and Usher syndrome 2C.

**Synonyms:** - Adhesion G Protein-Coupled Receptor V1 wt Allele - DKFZp761P0710 - FEB4 - G Protein-Coupled Receptor 98 Gene - GPR98 - KIAA0686 - KIAA1943 - MASS1 - Monogenic Audiogenic Seizure Susceptibility 1, Mouse, Homolog of Gene - Monogenic Audiogenic Seizure Susceptibility Protein 1 Homolog Gene - Monogenic, Audiogenic Seizure Susceptibility 1 Homolog (Mouse) Gene - USH2B - USH2C - VLGR1 - VLGR1b