|  Help  |  About  |  Contact Us

Allele : Lmna<tm2.1Gbon> lamin A; targeted mutation 2.1, Gisele Bonne

Primary Identifier  MGI:5306919 Allele Type  Targeted
Attribute String  Hypomorph Gene  Lmna
Transmission  Germline Strain of Origin  129
Is Recombinase  false Is Wild Type  false
molecularNote  A 3 nucleotide (AAG) deletion that removes lysine 32 was introduced into exon 1 and a floxed neo-cre cassette was inserted into intron 1 via homologous recombination. The neo-cre cassette is self-excising in the male germ line. In homozygous mice protein expression of lamin A/C is reduced in skeletal muscles and it fails to relocalize to the nuclear periphery in developing embryos at E17.5.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • Lmna<deltaK32>,
  • Lmna<deltaK32>
Quick Links:
 
Quick Links:
 

1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

9 Publication categories

Trail: Allele