Symbol Name ID |
Grk1
G protein-coupled receptor kinase 1 MGI:1345146 |
Darker colors indicate more annotations |
Human Phenotypes | Congenital stationary night blindness |
Mizuo phenomenon |
Disease(s) Associated with GRK1 | ||
Oguchi disease-2 |
Mouse Phenotypes | abnormal retina apoptosis |
short retina rod cell outer segment |
abnormal retina rod cell morphology |
retina photoreceptor degeneration |
decreased total retina thickness |
retina spots |
abnormal electroretinogram waveform feature |
abnormal rod electrophysiology |
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Availability | Mouse Genotype | ||||||||
Grk1tm1Citb/Grk1tm1Citb | |||||||||
Grk1tvrm207/Grk1tvrm207 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 03/19/2024 MGI 6.23 |
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