About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5635067
Allelic
Composition		 Grid2ho-15J/Grid2ho-15J
Genetic
Background		 involves: C3HeB/Fe
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grid2ho-15J mutation (0 available); any Grid2 mutation (87 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
behavior/neurological
abnormal eye movement ( J:220519 )
• larger spontaneous and random eye movements

vision/eye
abnormal eye movement ( J:220519 )
• larger spontaneous and random eye movements

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
autosomal recessive spinocerebellar ataxia 18 DOID:0080042 OMIM:616204
 J:220519

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
09/30/2025
MGI 6.24 		The Jackson Laboratory