B6.129P2-Unc13ctm1Bros/Ph

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EMMA IDEM:11617
Citation informationRRID:IMSR_EM:11617 

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International strain nameB6.129P2-Unc13ctm1Bros/Ph
Alternative nameUnc13c tm1Bros
Strain typeTargeted Mutant Strains : Knock-out
Allele/Transgene symbolUnc13ctm1Bros
Gene/Transgene symbolUnc13c

Information from provider

ProviderNils Brose
Provider affiliationDepartment of Molecular Neurobiology, Max Planck Institute of Experimental Medicine
Genetic informationIn the targeting vector, two exons representing bp 3108 –3265 of the rat Munc13-3 cDNA (GenBank accession number U24072) were replaced by a neomycin resistance cassette. The vector also contained two copies of the herpes simplex virus thymidine kinase gene. Upon homologous recombination of the targeting vector with the Munc13-3 gene, the insertion of the neomycin resistance cassette results in a deletion that represents amino acid residues 1014 –1066 (upstream of the C1 domain) and a shift in the open reading frame in the mature mRNA.
Phenotypic informationHomozygous:
Munc 13-3 KOs exhibit no obvious abnormalities and have a normal life expectancy. Both male and female Munc13-3 KOs are fertile. Litter sizes resulting from interbreeding of homozygous Munc13-3 KOs are indistinguishable from those obtained with wild-type controls. KOs have an impaired ability to learn complex motor tasks.

Heterozygous:
Heterozygous mice are normal and show no obvious alterations in comparison to wild-type controls.
Breeding historyHomologous recombination in 129/Sv embryonic stem cells, consecutive backcrosses with C57BL/6J animals.
References
  • The cerebellum-specific Munc13 isoform Munc13-3 regulates cerebellar synaptic transmission and motor learning in mice.;Augustin I, Korte S, Rickmann M, Kretzschmar H A, Südhof T C, Herms J W, Brose N, ;2001;The Journal of neuroscience : the official journal of the Society for Neuroscience;21;10-7; 11150314
Homozygous fertileyes
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreInstitute of Molecular Genetics, Prague, Czech Republic
Animals used for archivinghomozygous 129/Sv x C57BL/6J males
Breeding at archiving centre17 backcrosses to C57BL/6J

Disease and phenotype information

IMPC phenotypes (gene matching)
  • increased circulating creatinine level / IMPC
  • increased circulating phosphate level / IMPC
MGI phenotypes (allele matching)
  • abnormal CNS synaptic transmission / MGI
  • abnormal motor learning / MGI
  • enhanced paired-pulse facilitation / MGI
  • nervous system phenotype / MGI
MGI phenotypes (gene matching)
  • abnormal CNS synaptic transmission / MGI
  • abnormal motor learning / MGI
  • enhanced paired-pulse facilitation / MGI
  • no phenotypic analysis / MGI
  • nervous system phenotype / MGI

Literature references

  • The cerebellum-specific Munc13 isoform Munc13-3 regulates cerebellar synaptic transmission and motor learning in mice.;Augustin I, Korte S, Rickmann M, Kretzschmar H A, Südhof T C, Herms J W, Brose N, ;2001;The Journal of neuroscience : the official journal of the Society for Neuroscience;21;10-7; 11150314

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