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Symbol
Name
ID

Grm6
glutamate receptor, metabotropic 6
MGI:1351343

Phenotype annotations related to vision/eye

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Bone spicule pigmentation of the retina	Congenital stationary night blindness	Horizontal nystagmus	Myopia	Hemeralopia	Nyctalopia
Disease(s) Associated with GRM6
congenital stationary night blindness 1B

Mouse Phenotypes		vision/eye phenotype	impaired pupillary reflex	abnormal eye morphology	mydriasis	cataract	abnormal eye physiology	decreased b-wave amplitude	abnormal eye electrophysiology	abnormal cone electrophysiology	abnormal rod electrophysiology
Availability	Mouse Genotype	vision/eye phenotype	impaired pupillary reflex	abnormal eye morphology	mydriasis	cataract	abnormal eye physiology	decreased b-wave amplitude	abnormal eye electrophysiology	abnormal cone electrophysiology	abnormal rod electrophysiology
	Grm6^nob3/Grm6^nob3	*
	Grm6^nob4/Grm6^nob4
	Grm6^nob7/Grm6^nob7
	Grm6^nob8/Grm6^nob8
	Grm6^{tm1b(EUCOMM)Wtsi}/Grm6^{tm1b(EUCOMM)Wtsi}
	Grm6^tm1Nak/Grm6^tm1Nak
	Grm6^nob3/Grm6^nob4
	Grm6^nob3/Grm6^nob7

Contributing Projects: 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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