about
P688
Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice.Auditory deficits associated with the frings mgr1 (mass1) mutation in miceA novel gene causing a mendelian audiogenic mouse epilepsyA novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cellsA forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell functionMolecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioningWhirlin replacement restores the formation of the USH2 protein complex in whirlin knockout photoreceptorsDeficiency of Vlgr1 resulted in deafness and susceptibility to audiogenic seizures while the degree of hearing impairment was not correlated with seizure severity in C57BL/6- and 129-backcrossed lines of Vlgr1 knockout miceVlgr1 is required for proper stereocilia maturation of cochlear hair cellsThe very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2Very large G protein-coupled receptor 1 regulates myelin-associated glycoprotein via Gαs/Gαq-mediated protein kinases A/C.Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss.Constitutive Gαi coupling activity of very large G protein-coupled receptor 1 (VLGR1) and its regulation by PDZD7 protein.Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein networkGPR98/Gpr98 gene is involved in the regulation of human and mouse bone mineral density
P921
Q27308986-F9495EAD-6497-40CB-BC19-86F53095BB8FQ28504635-3CA26FF8-735F-4E1B-A4EC-0067CBDCE130Q28507622-EE7C4E4C-8C9D-450C-8A0F-29C2B7503C7AQ28507828-F4658985-11AE-4015-B304-320BC497DE23Q28509513-DFA7D47A-7EE3-4080-8E01-EB34D40C5554Q28510477-536B4DF2-3610-4941-AB64-993DBC83C74DQ28510685-70D6501A-5F2E-4B95-A8A8-708895DE5629Q28513848-D0F8AD5D-1DAA-495D-9D0B-7512C7406562Q28585236-64EE6254-B666-4F64-8480-8C18A3100990Q28588359-32F8A4CF-7F59-4F37-A95D-A105438813F0Q28588493-87894052-8D5B-4656-BD1A-EB7C27F24B6EQ28589815-7865197D-4FD2-4429-A46A-5E86BE34B3E9Q28590110-D07345A6-6B10-4020-A4AD-70F4CF78F035Q28594174-246FA454-689E-41C7-98BA-586337AAA6AFQ33587467-72CA1D28-B43E-4C04-85A2-0A66F5823736Q34107213-1C6748C4-C7C6-4DBF-94FB-3BCE4472E429Q36456242-B85E3C0E-12C4-4734-9473-B6F3370AF8F4Q83656297-FC55087A-E75C-4403-9D97-6D42A9A43D7E
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Adhesion G protein-coupled receptor V1
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Adhesion G protein-coupled receptor V1
@en
type
label
Adhesion G protein-coupled receptor V1
@en
altLabel
Adgrv1
@en
G-protein coupled receptor 98
@en
Very large G-protein coupled receptor 1
@en
adhesion G-protein coupled receptor V1
@en
monogenic audiogenic seizure susceptibility protein 1
@en
monogenic, audiogenic seizure susceptibility 1
@en
neurepin
@en
very large G protein-coupled receptor 1
@en
prefLabel
Adhesion G protein-coupled receptor V1
@en
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ENSMUSP00000093245
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