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Mmachc tm1.1/tm1.1 cblC mouse (exons 3-4 lacZ replacement)

Mmachc tm1.1/tm1.1 mice survive until approximately E9.5-E15.5 and reproduce features of cblC-type methylmalonic acidemia.

Model identity

Model name
Mmachc tm1.1/tm1.1 cblC mouse (exons 3-4 lacZ replacement)
Species
mouse
Genotype / zygosity
Mmachc tm1.1/tm1.1
Allele
exons 3-4 replaced by lacZ cassette

Biological characteristics

Research questions
What genetically engineered animal models exist for cblC methylmalonic acidemia and how do they reproduce embryonic disease features.
Limitations
Embryonic lethality between E9.5 and E15.5 prevents postnatal study of the homozygous null state.

References

  1. Genetically engineered animal models of methylmalonic acidemia review (PMID:41239408)
  2. ARRIVE 2.0 guidelines