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Gene BrowserrightADGRV1

ADGRV1

adhesion G protein-coupled receptor V1

HCNC Approved Symbol
ADGRV1 (HGNC:17416)
Genomic Coordinates
5:90,558,797 - 91,164,437 (5q14.3)
Synonyms
DKFZp761P0710, KIAA0686, FEB4, VLGR1, USH2C, MASS1, GPR98
Disease Associations
This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

24Patients

Total 24 patients were diagnosed with a variant in the ADGRV1 gene.

Frequently observed phenotypes (Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

024
Patient count
Hearing impairment
 8(33.3%)
Patient Count: 8 (33.3%)

% of total patients presenting each phenotype is shown in parentheses.

 8(33.3%)
Retinitis pigmentosa
 7(29.2%)
Patient Count: 7 (29.2%)

% of total patients presenting each phenotype is shown in parentheses.

 7(29.2%)
Hearing loss
 5(20.8%)
Patient Count: 5 (20.8%)

% of total patients presenting each phenotype is shown in parentheses.

 5(20.8%)
Decreased visual acuity
 5(20.8%)
Patient Count: 5 (20.8%)

% of total patients presenting each phenotype is shown in parentheses.

 5(20.8%)
Night blindness
 5(20.8%)
Patient Count: 5 (20.8%)

% of total patients presenting each phenotype is shown in parentheses.

 5(20.8%)
No Results
• Last updated: 2024-06-30
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Your variant of interest may already be in ClinVar.