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Allele : Pcsk9<m1Bms> proprotein convertase subtilisin/kexin type 9; mutation 1, Bristol Myers Squibb

Primary Identifier  MGI:5516591 Allele Type  Chemically induced (ENU)
Gene  Pcsk9 Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  ENU mutagenesis induced a point mutation that results in the amino acid substitution of a termination codon for tyrosine at position 119 (Y119X). The absence of protein expression was confirmed in the liver and plasma.
  • mutations:
  • Single point mutation
  • synonyms:
  • PCSK9-Y119X,
  • PCSK9-Y119X
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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

3 Publication categories

Trail: Allele