About   Help   FAQ
Symbol
Name
ID
Grm1
glutamate receptor, metabotropic 1
MGI:1351338
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Fatigue
Disease(s) Associated with GRM1
autosomal recessive spinocerebellar ataxia 13

Mouse Phenotypes
behavior/neurological phenotype
abnormal contextual conditioning behavior
decreased exploration in new environment
abnormal spatial learning
impaired righting response
limb grasping
tremors
ataxia
impaired balance
impaired limb coordination
weakness
hunched posture
abnormal gait
decreased locomotor activity
abnormal maternal nurturing
abnormal sexual interaction
Availability Mouse Genotype
Grm1crv4/Grm1crv4
Grm1m1Btlr/Grm1m1Btlr
Grm1nmf373/Grm1nmf373
Grm1rcw-2J/Grm1rcw-2J
Grm1rcw-3J/Grm1rcw-3J
Grm1rcw-4J/Grm1rcw-4J
Grm1rcw/Grm1rcw
Grm1tm1Crpl/Grm1tm1Crpl
Grm1tm1Dgen/Grm1tm1Dgen
Grm1tm1Kyo/Grm1tm1Kyo *
Grm1tm1Stl/Grm1tm1Stl
Grm1tvrm84/Grm1tvrm84
Grm1wobl/Grm1wobl

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/14/2024
MGI 6.23
The Jackson Laboratory