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Allele : Nr1h2<em3Gpt> nuclear receptor subfamily 1, group H, member 2; endonuclease-mediated mutation 3, GemPharmatech Co., Ltd
Primary Identifier  MGI:7303202 Allele Type  Endonuclease-mediated
Attribute String  Null/knockout Gene  Nr1h2
Inheritance Mode  Not Specified Strain of Origin  C57BL/6JGpt
Is Recombinase  false Is Wild Type  false
molecularNote  CRISPR-targeting introduced a coding region modification (del2344).
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Nr1h2<em3Cd2344>,
  • Nr1h2<em3Cd2344>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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Trail: Allele

0 Driven By

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Trail: Allele




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