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Allele : Nppc<lbab> natriuretic peptide type C; long bone abnormality

Primary Identifier  MGI:2388899 Allele Type  Spontaneous
Gene  Nppc Inheritance Mode  Recessive
Strain of Origin  PL/J Is Recombinase  false
Is Wild Type  false
molecularNote  lbab is a spontaneous mutation identified at The Jackson Laboratory. A C-to-G transversion mutation in exon 2 results in the substitution of arginine with glycine at position 117 (p.R117G) in a conserved domain of the encoded protein.
  • mutations:
  • Single point mutation
  • synonyms:
  • lbab,
  • lbab
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

11 Publication categories