|  Help  |  About  |  Contact Us

Allele : Fgg<tm1.1Geno> fibrinogen gamma chain; targeted mutation 1.1, Genoway

Primary Identifier  MGI:7511552 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Fgg
Transmission  Germline Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  Glutamine codons 423 and 424 (CAG) in exon 9 were changed to asparagine (p.Q423N, p.Q424N), lysine codon 431 (AAA) to arginine (p.K431R) and a loxP site flanked neomycin resistance gene cassette was inserted into intron 8. The neo cassette was removed through subsequent Cre-mediated recombination. The mutations eliminate the gamma-chain cross-linking sites and recapitulate the same experimentally created mutations in the human ortholog (p.Q398N p.Q399N, p.K406R in the mature peptide) that affect blood clot formation.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • FGG3X,
  • FGG3X
Quick Links:
 
Quick Links:
 

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories