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Allele : Insr<tm1.1Shlm> insulin receptor; targeted mutation 1.1, Gerald Shulman

Primary Identifier  MGI:5881945 Allele Type  Targeted
Gene  Insr Transmission  Germline
Strain of Origin  C57BL/6J-A<w-J>/J Is Recombinase  false
Is Wild Type  false
description  ES cell line = B6Aw6
molecularNote  Exon 19 was replaced with a copy containing an engineered mutation changing Thr1150 codon ACA to alanine codon GCC. This mutation prevents phosphorylation of the peptide at that residue and creates a kinase dead version of the peptide. It is the equivalent of a recombinant engineered Thr1160Ala mutation in human thought to protect the peptide from inhibition by PRKCE. The FRT site flanked neomycin resistance gene cassette that was inserted into intron 18 was removed through flp-mediated recombination.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Insr<T1150A>,
  • Insr<T1150A>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories

Trail: Allele