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Allele : Irf8<myls> interferon regulatory factor 8; myeloproliferative syndrome
Primary Identifier  MGI:3578920 Allele Type  Spontaneous
Gene  Irf8 Inheritance Mode  Recessive
Strain of Origin  BXH2/TyJ Is Recombinase  false
Is Wild Type  false
molecularNote  Sequencing revealed a C-to-T transition at coding nucleotide 880, creating an arginine to cysteine substitution at codon 294 (p.R294C) within the putative IAD domain.
  • mutations:
  • Single point mutation
  • synonyms:
  • Irf8<R294C>,
  • Irf8<BXH2>,
  • Irf8<R294C>,
  • IRF-8<C294>,
  • Irf8<BXH2>,
  • Icsbp1<C294>,
  • Irf8<m>,
  • Irf8<m>,
  • IRF-8<C294>,
  • Icsbp1<C294>
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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

22 Publication categories





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