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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cacna1btm1Ttan
targeted mutation 1, Tsutomu Tanabe
MGI:2387803
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cacna1btm1Ttan/Cacna1btm1Ttan involves: 129S4/SvJae * C57BL/6 MGI:3625851


Genotype
MGI:3625851
hm1
Allelic
Composition
Cacna1btm1Ttan/Cacna1btm1Ttan
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacna1btm1Ttan mutation (1 available); any Cacna1b mutation (103 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• ~30% of the homozygous mice were lost prior to weaning age
• surviving mice appear normal and survive to adulthood without any apparent motor dysfunction

nervous system
N
• measures of sympathetic nervous system function did not differ between mutant and control mice; peripheral body temperature, resting heart rate and blood pressure are similar in mutant and control mice
• field EPSPs at Schaffer collateral-CA1 synapses in hippocampal slices are depressed by halothane in mutants; depression is concentration dependent, reversible and greater in mutants than wild-type

behavior/neurological
• when halothane is used, homozygotes show a lower EC50 for the minimum alveolar concentration (MAC) for loss of the righting reflex; EC50 for the MAC needed for loss of tail pinch response is also lower in mutants
• sleep time after intravenous injection of propofol is shorter in mutants than in wild-type
• in an elevated plus-maze test, mutant mice enter and spend more time in the open arms than controls
• sin an open-field test, mutant mice travel a longer total distance than controls
• mutant mice show a prolonged latency in a tail flick test compared to controls
• no differences in latency is detectable in a paw flick or hot plate test between the mutant and control mice
• responses to acute mechanical stimuli by the tail pressure test or using von Frey filaments were not different between the mutant and control mice
• at acoustic stimuli of 115 and 120 dB, mutant mice exhibit reduced responses compared to controls
• the biphasic pain response of mutant mice exhibit significantly attenuated response in the early part of Phase 2, but normal pain behaviors are seen in Phase 1 when hindpaws are injected with 2% formalin; the level of swelling associated with injection of formalin is similar in mutant mice and controls, indicating that reduced pain responses are not due to reduced inflammation
• the stretching/writhing motion response to visceral inflammatory pain caused by injection of 0.6% acetic acid into the peritoneal cavity is reduced in similar in control and mutant mice





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory