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Gene : GRK1 Homo sapiens

Name  ? G protein-coupled receptor kinase 1 Cytological Location  13q34
Brief Description  G protein-coupled receptor kinase 1
Description  This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates rhodopsin and initiates its deactivation. Defects in GRK1 are known to cause Oguchi disease 2 (also known as stationary night blindness Oguchi type-2). [provided by RefSeq, Jul 2008]
  • synonyms:
  • rhodopsin kinase,
  • RK,
  • NM_002929,
  • RHOK,
  • OTTHUMG00000185528,
  • RK,
  • GPRK1,
  • GRK1,
  • uc010tkf.3,
  • HGNC:10013,
  • RHOK,
  • GPRK1
  • identifiers:
  • 6011,
  • ENSG00000185974,
  • GRK1

Genome feature

Region: gene ? Length: 91966  
Location: 13:113645771-113737736 Cyto location: 13q34

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Proteins.


Gene Report --> GWAS hit


1 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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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3753 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results