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Allele : Il12rb2<Ifnm-d> interleukin 12 receptor, beta 2; interferon response to microorgansisms, defective

Primary Identifier  MGI:2156401 Allele Type  Spontaneous
Gene  Il12rb2 Inheritance Mode  Recessive
Strain of Origin  C57BL/10ScCr Is Recombinase  false
Is Wild Type  false
molecularNote  The defective IL-12 response in C57BL/10ScCr mice has been attributed to a point mutation in the Il12rb2 gene. The substitution of a C to G at coding nucleotide 2331 creates a premature stop codon at tyrosine amino acid position 778 (p.Y778*). The resulting truncated protein lacks the C-terminal 96 amino acids of cytosplasmic domain.
  • mutations:
  • Single point mutation
  • synonyms:
  • Ifnm,
  • Ifnm
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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

8 Publication categories

Trail: Allele