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Allele : Rnf2<tm1.1Hgu> ring finger protein 2; targeted mutation 1.1, MRC Human Genetics Unit
Primary Identifier  MGI:6414568 Allele Type  Targeted
Attribute String  Not Specified Gene  Rnf2
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  Gap repair produced the amino acid substitution of alanine for isoleucine at position 53 (53A) as well as introducing two silent restriction sites (SacI and XbaI) into exon 3. A floxed neomycin resistance cassette was introduced into intron 3 and removed by cre-mediated recombination.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Ring1B<I53A>,
  • Ring1B<I53A>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

5 Publication categories





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