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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
Congenital stationary night blindness
Myopia
Hemeralopia
Disease(s) Associated with GRM6
congenital stationary night blindness 1B

Mouse Phenotypes
vision/eye phenotype
impaired pupillary reflex
mydriasis
cataract
abnormal eye physiology
decreased b wave amplitude
abnormal eye electrophysiology
abnormal cone electrophysiology
abnormal rod electrophysiology
Availability Mouse Genotype
Grm6nob3/Grm6nob3 *
Grm6nob4/Grm6nob4
Grm6nob7/Grm6nob7
Grm6nob8/Grm6nob8
Grm6tm1b(EUCOMM)Wtsi/Grm6tm1b(EUCOMM)Wtsi
Grm6tm1Nak/Grm6tm1Nak
Grm6nob3/Grm6nob4
Grm6nob3/Grm6nob7

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory