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Allele : Lmna<tm11Lgf> lamin A; targeted mutation 11, Loren G Fong

Primary Identifier  MGI:5752218 Allele Type  Targeted
Gene  Lmna Transmission  Germline
Strain of Origin  129P2/OlaHsd Is Recombinase  false
Is Wild Type  false
molecularNote  Introns 10 and 11 and the last 150 nucleotides of exon 11 were deleted, thereby abolishing production of lamin C and producing a mutated prelamin A that precludes wild-type Lmna synthesis. The lamin C 3' UTR replaced the endogenous prelamin A 3' UTR and a floxed neomycin resistance cassette was inserted downstream of the modified 3' UTR. Absence of a Mir9 binding site results in expression in neurons. High levels of expression are detected in the CNS and peripheral tissues.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • Lmna<HG-C>,
  • Lmna<HG-C>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories