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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cacna1asmrl
small roller
MGI:5499996
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cacna1asmrl/Cacna1asmrl CXB10/HiAJ-Cacna1asmrl/GrsrJ MGI:5500085


Genotype
MGI:5500085
hm1
Allelic
Composition
Cacna1asmrl/Cacna1asmrl
Genetic
Background
CXB10/HiAJ-Cacna1asmrl/GrsrJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacna1asmrl mutation (1 available); any Cacna1a mutation (118 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cacna1asmrl/Cacna1asmrl mouse (right) showing smaller body size and rolling on its side when walking compared to heterozygous control (left)

behavior/neurological
• as soon as pups begin to try to walk there is clear weakness and difficulty in locomotion characterized as having ataxia with a severe side-to-side gait with swaying hindquarters, splaying hind legs, and the body held close to the ground, and homozygotes often fall over and have difficulty righting

mortality/aging
• diminished litter size, fewer than expected homozygotes born, and stillborn and postnatal lethality of what are likely homozygotes
• heterozygous intercrosses also produce fewer homozygotes than expected and have a higher than normal percent of stillborn and pups dying in the first week after birth
• a high percentage of stillborn, which are thought to be homozygotes due to having fewer than expected homozygotes at phenotypic onset
• a high percentage of pups predicted to be homozygotes are found dead or missing prior to phenotypic assessment at approximately 1 week of age

reproductive system
• homozygous females bred to heterozygous males have an average litter size less than 3, and when bred to wildtype males have an average litter size of 3.8, still smaller than normal

vision/eye
N
• ophthalmoscopic examination of 2 males at approximately 25 weeks of age found no abnormalities

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
spinocerebellar ataxia type 6 DOID:0050956 OMIM:183086
J:222308





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory