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Allele : Rarb<tm1Ipc> retinoic acid receptor, beta; targeted mutation 1, Pierre Chambon

Primary Identifier  MGI:1857623 Allele Type  Targeted
Attribute String  Null/knockout Gene  Rarb
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
molecularNote  Ablation of the expression of the most abundant isoform, Rarbeta2, encoded by this locus was achieved in two steps. First, all of the in-frame start codons for the Rarbeta2 isoform were eliminated by site-specific mutagenesis of nucleotides 459 through 491. Second, a neomycin resistance gene was inserted into the first exon of the Rarbeta2 isoform, exon 4. RT-PCR and Western blot analysis, using isoform specific primers and antibodies, showed a lack of Rarbeta2 mRNA and protein, as well as normal levels of transcript and protein corresponding to the other isoforms.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Rarb2-,
  • Abeta,
  • RARbeta2<->,
  • Rarb2-,
  • RARbeta2<->,
  • Abeta
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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

18 Publication categories

Trail: Allele