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Allele : Slc23a2<tm1Nbm> solute carrier family 23 (nucleobase transporters), member 2; targeted mutation 1, Robert L Nussbaum

Primary Identifier  MGI:2180333 Allele Type  Targeted
Attribute String  Null/knockout Gene  Slc23a2
Transmission  Germline Strain of Origin  129S6/SvEvTac
Is Recombinase  false Is Wild Type  false
molecularNote  532 nucleotides of the gene spanning exons 10-12 were replaced with a neomycin resistance cassette via homologous recombination resulting in a deletion and frameshift. RT-PCR verified the presence of mutant transcript in brain of homozygous mutant animals. Disruption of protein function was verified via ascorbic-acid uptake assay. Mouse embryonic fibroblasts from homozygous mutant animals exhibit less than 5% of normal ascorbic-acid uptake compared to wild-type.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • Slc23a1<-/->,
  • SVCT2<->,
  • SVCT2<->,
  • Slc23a1<-/->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

17 Publication categories