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Allele : Fbn1<tm2.1Hcd> fibrillin 1; targeted mutation 2.1, Harry C Dietz

Primary Identifier  MGI:5558867 Allele Type  Targeted
Gene  Fbn1 Transmission  Germline
Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+> Is Recombinase  false
Is Wild Type  false
molecularNote  Exon 38 was replaced with a floxed neomycin resistance cassette and a modified exon 38 in which nucleotide substitutions result in the amino acid substitution of glutamic acid for aspartic acid at position 1545 (D1545E). This mutation destroys the integrin binding site. Cre-mediated recombination removed the selection cassette.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Fbn1<D1545E>,
  • Fbn1<D1545E>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele