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Allele : Iapp<tm2(IAPP*S53G)Nole> islet amyloid polypeptide; targeted mutation 2, Norman L Eberhardt

Primary Identifier  MGI:7620150 Allele Type  Targeted
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Iapp
Transmission  Germline Strain of Origin  129S/SvEv
Is Recombinase  false Is Wild Type  false
molecularNote  A 102 bp part of exon 3 was replaced with the equivalent sequence from a mutated human IAPP cDNA with an A>G (UniProt:P10997:p.S53G) mutation and a loxP site flanked neomycin resistance gene cassette was inserted downstream of the gene. This mutation is associated with premature onset type 2 diabetes in the Asian population.
  • mutations:
  • Insertion
  • synonyms:
  • hIAPP<S20G>,
  • hIAPP<S20G>
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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