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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 (85 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)
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory