Phenotypes Associated with This Genotype

Genotype
MGI:4949279

• Allelic Composition: Grid2^tm1(cre)Mwa/Grid2^tm1(cre)Mwa
• Genetic Background: involves: C57BL/6N

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

vision/eye

abnormal eye movement ( J:220519 )

• larger spontaneous eye movements

nervous system

nervous system phenotype ( J:170673 )

N • mice exhibit normal parallel fiber-interneuron synapses

behavior/neurological

abnormal eye movement ( J:220519 )

• larger spontaneous 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