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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Itpr1wblo
wobbly locomotion
MGI:4437432
Summary 2 genotypes


Genotype
MGI:4441291
cx1
Allelic
Composition
Glatm1Kul/Glatm1Kul
Itpr1wblo/Itpr1wblo
Genetic
Background
B6;129-Glatm1Kul Itpr1wblo/GrsrJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Glatm1Kul mutation (3 available); any Gla mutation (16 available)
Itpr1wblo mutation (1 available); any Itpr1 mutation (180 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• a wobbly gait from impaired coordination of movement is first observed at approximately 5 weeks of age and becomes less severe in the adult

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
spinocerebellar ataxia type 15 DOID:0050965 OMIM:606658
J:222308




Genotype
MGI:4441292
cx2
Allelic
Composition
Glatm1Kul/Y
Itpr1wblo/Itpr1wblo
Genetic
Background
B6;129-Glatm1Kul Itpr1wblo/GrsrJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Glatm1Kul mutation (3 available); any Gla mutation (16 available)
Itpr1wblo mutation (1 available); any Itpr1 mutation (180 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• a wobbly gait from impaired coordination of movement is first observed at approximately 5 weeks of age and becomes less severe in the adult

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
spinocerebellar ataxia type 15 DOID:0050965 OMIM:606658
J:222308





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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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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory