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Allele : Insr<Rgsc294> insulin receptor; RIKEN Genomic Sciences Center (GSC), 294

Primary Identifier  MGI:3811869 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 mutatation, identified in an ENU mutagenesis screen, comprises an A to G transition in exon 18 that results in the substitution of serine for asparagine at amino acid position 1154 (N1154S), in the tyrosine kinase domain of the receptor.
  • mutations:
  • Single point mutation
  • synonyms:
  • M100294,
  • M100294,
  • Insr<N1154S>,
  • Insr<N1154S>
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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

4 Publication categories

Trail: Allele