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Allele : Rnaseh2b<tm1Hgu> ribonuclease H2, subunit B; targeted mutation 1, MRC Human Genetics Unit

Primary Identifier  MGI:5431529 Allele Type  Targeted
Attribute String  Null/knockout Gene  Rnaseh2b
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  Exon 7 was replaced with a modified exon 7 in which a G to A point mutation results in the amino acid substitution of threonine for alanine at position 174 (A174T). An additional mutation produces a G to T transversion resulting in a stop codon at position 202 (E202X). A floxed neo cassette was inserted upstream of the modified exon 7. Western blot analysis confirmed the absence of protein expression in E9.5 embryos.
  • mutations:
  • Nucleotide substitutions,
  • Insertion
  • synonyms:
  • Rnaseh2b<E202X>,
  • Rnaseh2b<tm1-hgu-A174T,E202X>,
  • Rnaseh2b<tm1-hgu-A174T,E202X>,
  • Rnaseh2b<E202X>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories

Trail: Allele