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Allele : Rarg<tm1Ipc> retinoic acid receptor, gamma; targeted mutation 1, Pierre Chambon

Primary Identifier  MGI:1931079 Allele Type  Targeted
Attribute String  Null/knockout Gene  Rarg
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
description  Homozygous mutants show growth deficiency and increased post-natal early lethality. Mutants also show a variety of homeotic transformations of the axial skeleton.
molecularNote  Insertion of a neomycin resistance cassette into exon 8 at the position corresponding to amino acid 75 of the gamma1 isoform disrupted Rarg in the B region common to all isoforms. This disruption is predicted to prevent the synthesis of all RARG isoforms. RNase protection analysis of E13.5 embryos indicated that the mRNAs encoding the both the gamma1 and the gamma2 isoforms were mutated in this allele, and did not detect the wild-type transcript for either isoform.
  • mutations:
  • Insertion
  • synonyms:
  • Agamma,
  • RARgamma<->,
  • RARgamma<->,
  • Agamma
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

36 Publication categories