|  Help  |  About  |  Contact Us

Allele : Rxra<tm1.1Pcn> retinoid X receptor alpha; targeted mutation 1.1, Pierre Chambon

Primary Identifier  MGI:3839151 Allele Type  Targeted
Attribute String  Null/knockout Gene  Rxra
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
molecularNote  Most of exon 2, all of intron 2 and 102 bp of exon 3, encoding for amino acids 11-132, were deleted in an ES cell line that carried Rxratm1Ipc . A floxed hygro cassette (between exons 2 and 4) and a floxed neo cassette (between exons 9 and 10) were removed by Cre mediated recombination. The final mutant allele lacks both transcriptional activating function 1 and 2. Northern and Western blot analysis confirmed the expression of a truncated mRNA and protein in homozygous and heterozygous embryos. Expression levels of both the truncated mRNA and protein are lower than those for the wild-type mRNA and protein.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • Rxra<afo>,
  • Rxra<afo>
Quick Links:
 
Quick Links:
 

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories