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Allele : Egln3<tm1.1Jifan> egl-9 family hypoxia-inducible factor 3; targeted mutation 1.1, Jing Fang

Primary Identifier  MGI:7624036 Allele Type  Targeted
Attribute String  Conditional ready Gene  Egln3
Transmission  Germline Strain of Origin  C57BL/6
Is Recombinase  false Is Wild Type  false
molecularNote  A loxP site was inserted into intron 2 and a loxP2272 site, in inverted copy of exon 3 (where histidine codon 196 (CAT) was changed to alanine (GCT) (p.H196A)), a second loxP site, a second loxP2272 site, and an FRT site flanked neomycin resistance gene cassette, were inserted into intron 3. The neo cassette was removed through subsequent Cre-mediated recombination. This allele expresses the wildtype peptide. Only after Cre-mediated removal of the endogenous exon 3 and flipping of the mutated copy, will it express the mutated peptide. The mutation abolishes the prolyl hydroxylase activity of the encoded peptide.
  • mutations:
  • Insertion
  • synonyms:
  • PHD3-H196A<F>,
  • PHD3-H196A<F>
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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

4 Publication categories