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Allele : Flnc<tm1.1Rsdf> filamin C, gamma; targeted mutation 1.1, Rolf Schroder and Dieter O Furst

Primary Identifier  MGI:5907163 Allele Type  Targeted
Attribute String  Conditional ready Gene  Flnc
Transmission  Germline Strain of Origin  C57BL/6
Is Recombinase  false Is Wild Type  false
molecularNote  A stop codon was created by a G to A mutation in exon 48 (W2711X) mimicking the most common myofibrillar myopathy-filaminopathy mutation in man. I addition a loxP site and FRT flanked neo cassette was inserted upstream of exon 47 and a loxP site was inserted the untranslated region of exon 48. Flp mediated recombination removed the neo cassette. RT-PCR analysis indicates mRNA levels are similar to wild-type. Protein levels are also similar to wild-type.
  • mutations:
  • Insertion,
  • Single point mutation
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories

Trail: Allele