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Allele : Insr<Rgsc1777> insulin receptor; RIKEN Genomic Sciences Center (GSC), 1777

Primary Identifier  MGI:3818849 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 a T to G transversion in exon 17 that is predicted to result in replacement of leucine by arginine at amino acid position 1105, in the tyrosine kinase domain of the receptor (L1105R).
  • mutations:
  • Single point mutation
  • synonyms:
  • Insr<L1105R>,
  • M101777,
  • M101777,
  • Insr<L1105R>
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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