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Allele : Slc26a5<tm1Xen> solute carrier family 26, member 5; targeted mutation 1, Taconic Biosciences

Primary Identifier  MGI:7413898 Allele Type  Targeted
Attribute String  Null/knockout Gene  Slc26a5
Transmission  Germline Strain of Origin  129S1/Sv-Oca2<+> Tyr<+> Kitl<+>
Is Recombinase  false Is Wild Type  false
molecularNote  A genomic region including exons 5 through 8 was replaced with a pgk-neo cassette via homologous recombination. Western blot analysis confirmed the absence of protein expression in cochlea from homozygous mice.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • prestin<Hsk>,
  • prestin<Hsk>
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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