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Allele : Nr3c2<tm2.1Gsc> nuclear receptor subfamily 3, group C, member 2; targeted mutation 2.1, Gunther Schutz
Primary Identifier  MGI:3613035 Allele Type  Targeted
Attribute String  Null/knockout Gene  Nr3c2
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  Cre mediated excision was used to remove exon 3, which which encode the first zinc finger of the mineralocorticoid receptor DNA binding domain.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • MR<null>,
  • MR<null>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele




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