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Allele : Slc22a3<tm1Dpb> solute carrier family 22 (organic cation transporter), member 3; targeted mutation 1, Denise P Barlow

Primary Identifier  MGI:2388117 Allele Type  Targeted
Attribute String  Null/knockout Gene  Slc22a3
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  Exon 1 and flanking intronic sequences were deleted and replaced with a floxed PGK-neo cassette via homologous recombination. Transient expression of cre recombinase in correctly targeted cells removed the selection cassette leaving behind a single loxP site in place of exon 1. Gene expression was absent in the heart, brain, and skeletal muscle of homozygous mutant animals as determined by Northern blot analysis. However, an aberrant transcript was detected in placentas from homozygous mutant embryos. RT-PCR analysis revealed the mutant transcript results from alternative splicing of intron 2 to exon 3 and does not translate a functional protein product.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Orct3-deficient,
  • Orct3-deficient,
  • Oct3-,
  • Oct3-
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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

17 Publication categories

Trail: Allele