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Allele : Txnip<Hyplip1> thioredoxin interacting protein; hyperlipidemia 1

Primary Identifier  MGI:2687368 Allele Type  Spontaneous
Attribute String  Hypomorph Gene  Txnip
Inheritance Mode  Dominant Strain of Origin  HcB19/Dem
Is Recombinase  false Is Wild Type  false
molecularNote  A T-to-A transversion mutation at coding nucleotide 291 in the 1,456-bp cDNA results in a tyrosine (TAT) to a stop codon (TAA) alteration at amino acid 97 (p.Y97*) in the encoded protein. This mutation was absent in the C3H parental strain and all other strains observed. A decreased level of mutant transcript was expressed from this allele.
  • mutations:
  • Single point mutation
  • synonyms:
  • txnip<hcb>,
  • txnip<hcb>,
  • Txnip<->,
  • Txnip<->
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

15 Publication categories

Trail: Allele