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Symbol
Name
ID
Adgrv1
adhesion G protein-coupled receptor V1
MGI:1274784
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Congenital sensorineural hearing impairment
Disease(s) Associated with ADGRV1
Usher syndrome type 2C

Mouse Phenotypes
abnormal cochlear hair cell stereociliary bundle morphology
abnormal cochlear hair cell inter-stereocilial links morphology
absent cochlear hair bundle ankle links
abnormal inner hair cell stereociliary bundle morphology
abnormal orientation of outer hair cell stereociliary bundles
abnormal outer hair cell stereociliary bundle morphology
cochlear inner hair cell degeneration
cochlear outer hair cell degeneration
cochlear hair cell degeneration
pillar cell degeneration
organ of Corti degeneration
abnormal cochlear outer hair cell physiology
abnormal hair cell mechanoelectric transduction
increased or absent threshold for auditory brainstem response
absent distortion product otoacoustic emissions
increased susceptibility to age-related hearing loss
deafness
Availability Mouse Genotype
Adgrv1frings/Adgrv1frings
Adgrv1mpc188H/Adgrv1mpc188H
Adgrv1rueda/Adgrv1rueda
Adgrv1tm1.1(KOMP)Vlcg/Adgrv1tm1.1(KOMP)Vlcg
Adgrv1tm1Msat/Adgrv1tm1Msat
Adgrv1tm1Pwh/Adgrv1tm1Pwh
Adgrv1tm2Msat/Adgrv1tm2Msat

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory