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Gene : ADGRV1 Homo sapiens

Name  ? adhesion G protein-coupled receptor V1 Cytological Location  5q14.3
Brief Description  adhesion G protein-coupled receptor V1
Description  This gene encodes a member of the G-protein coupled receptor superfamily. The encoded protein contains a 7-transmembrane receptor domain, binds calcium and is expressed in the central nervous system. Mutations in this gene are associated with Usher syndrome 2 and familial febrile seizures. Several alternatively spliced transcripts have been described. [provided by RefSeq, Jul 2008]
  • synonyms:
  • MASS1,
  • MASS1,
  • GPR98,
  • GPR98,
  • USH2B,
  • monogenic, audiogenic seizure susceptibility 1 homolog (mouse),
  • KIAA0686,
  • DKFZp761P0710,
  • NM_032119,
  • FEB4,
  • AB014586,
  • USH2C,
  • VLGR1,
  • VLGR1,
  • OTTHUMG00000162668,
  • G protein-coupled receptor 98,
  • FEB4,
  • ADGRV1,
  • USH2C,
  • HGNC:17416,
  • VLGR1b
  • identifiers:
  • 84059,
  • ENSG00000164199,
  • ADGRV1

Genome feature

Region: gene ? Length: 605642  
Location: 5:90558796-91164437 Cyto location: 5q14.3

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2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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3740 SNPs

5 Cross References

18 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results