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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cacna1atg-la
leaner
MGI:1856210
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cacna1atg-la/Cacna1atg-la B6.Cg-Os +/+ Cacna1atg-la/J MGI:3721273
ht2
Cacna1atg-la/Cacna1a+ involves: AKR/J * C3H/HeJ * C57BL/6J MGI:3710961
ht3
Cacna1atg-la/Cacna1aWb involves: AKR/J * C3H/HeJ * C57BL/6J MGI:3706705


Genotype
MGI:3721273
hm1
Allelic
Composition
Cacna1atg-la/Cacna1atg-la
Genetic
Background
B6.Cg-Os +/+ Cacna1atg-la/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacna1atg-la mutation (1 available); any Cacna1a mutation (118 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• activation threshold and conduction velocity of L5 dorsal root evoked by electrical stimulation of the sciatic nerve are not significantly different from those of wild-type
• the dose-repsonse curves for opioid peptide impact on dorsal root-evokes slow ventral root potential is normal
• although the capsaicin-sensitive component in C-fiber response is not significantly afffected, homozygotes are less sensitive to inhibition of femoral nerve-evoked slow ventral root potential by tachykinin NK1 receptor agonist GR82334
• femoral nerve-evoked peak amplitudes of dorsal root potentials are smaller than in wild-type controls but are inhibited by GABAa receptor antagonist bucuculline to a similar extent. The slow component of the dorsal root potential is smaller and does not increase with increased pulse width
• tachykinin receptor antagonist GR82334 is less inhibitory of the femoral nerve-evoked slow verntral root depolarization than in wild-type controls
• electrical stimulation of dorsal roots at C-fiber strength yileds a slightly smaller amplitude of monosynaptic reflux and integrated area of slow ventral root potential than in wild-type mice
• electrical stimulation of a dorsal root at C-fiber strength gives slow ventral root potentials and monosynaptic reflexes that are not diminished by a P/Q-type channel blocker but are diminished by an N-type channel blocker indicating an absence of a P/Q-type channel component in the response

behavior/neurological
• decreased frequency of foot withdrawals in response to a defined mechanical stimulus with calebrated Von Frey hairs
• enhanced thermal responses are found in paw flick and tail flick assays compared with wild-type and heterozygotes




Genotype
MGI:3710961
ht2
Allelic
Composition
Cacna1atg-la/Cacna1a+
Genetic
Background
involves: AKR/J * C3H/HeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacna1atg-la mutation (1 available); any Cacna1a mutation (118 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• genotyping of phenotypically normal progeny from a cross between mice heterozygous for Cacna1aWb and for Cacna1atg-la demonstrated that all were either wild-type (Cacna1a+/Cacna1a+) or heterozygous for Cacna1atg-la




Genotype
MGI:3706705
ht3
Allelic
Composition
Cacna1atg-la/Cacna1aWb
Genetic
Background
involves: AKR/J * C3H/HeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacna1atg-la mutation (1 available); any Cacna1a mutation (118 available)
Cacna1aWb mutation (0 available); any Cacna1a mutation (118 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice having both mutant alleles are said to exhibit a severe ataxic/dystonic phenotype similar to that of homozygous wobbly mice, in contrast with the mild ataxia of wobbly heterozygotes
• mice having both mutant alleles are said to exhibit a severe ataxic/dystonic phenotype similar to that of homozygous wobbly mice, in contrast with the mild ataxia of wobbly heterozygotes
• in the hindlimb extension reflex test, mice with both mutant alleles exhibit spasmodic movements and flexion of the hindlimbs
• these compound mutant mice perform poorly in the inclined-plane test
• in the narrow-beam cross, mice with both mutant alleles are unable to cross a narrow beam toward a platform, indicating poor fine motor control
• in the rotarod test, these compound mutant mice cannot maintain purchase on even a stationary rod
• the grip strength of mice with both mutant alleles is significantly weaker than that of wild-type controls

muscle
• mice having both mutant alleles are said to exhibit a severe ataxic/dystonic phenotype similar to that of homozygous wobbly mice, in contrast with the mild ataxia of wobbly heterozygotes





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