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Allele : Nr3c1<em1Clib> nuclear receptor subfamily 3, group C, member 1; endonuclease-mediated mutation 1, Claude Libert

Primary Identifier  MGI:6512048 Allele Type  Endonuclease-mediated
Gene  Nr3c1 Strain of Origin  FVB/NJ
Is Recombinase  false Is Wild Type  false
molecularNote  Using an sgRNA (targeting GCTATGCTTTGCTCCTGA) and ssODN template (G GCATTTGCCCTGGGTTGGAGATCATACAGACAAGCAAGTGGAAACCTGCTATGCTTTGCTCCTGATCTGATTATTAATGAGTAAGTTACATGGCCTTAACCCTCCACAAAGAACTA) with CRISPR/Cas9 technology, isoleucine codon 643 (ATT) in exon 6 was changed to alanine (GCT) (p.I643A). Targeting was performed in Nr3c1tm3Gsc heterozygote zygotes to produce mice with either p.I643A only (this allele) or p.I643A plus p.A474T in cis (Nr3c1em2Clib). Peptide coordinates are in reference to canonical sequence SW:P06537-1 with the full complement of polyQ at the N-terminal end.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • GR<I634A>,
  • GR<I634A>,
  • GR<dim2>,
  • GR<L>,
  • GR<dim2>,
  • GR<L>
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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

3 Publication categories