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Allele : Insr<Rgsc824> insulin receptor; RIKEN Genomic Sciences Center (GSC), 824

Primary Identifier  MGI:3812540 Allele Type  Chemically induced (ENU)
Gene  Insr Inheritance Mode  Dominant
Strain of Origin  C57BL/6JJcl Is Recombinase  false
Is Wild Type  false Project Collection  RIKEN GSC ENU Project
molecularNote  This mutation, identified in an ENU mutagenesis screen, comprises an A to G transition in exon 19 that results in replacement of glutamic acid by glycine at amino acid 1196, in the tyrosine kinase domain of the receptor (E1196G).
  • mutations:
  • Single point mutation
  • synonyms:
  • M100824,
  • Insr<E1196G>,
  • M100824,
  • Insr<E1196G>
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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

3 Publication categories