Egln1^tm1Fong
Targeted Allele Detail

Summary

• Symbol: Egln1^tm1Fong
• Name: egl-9 family hypoxia-inducible factor 1; targeted mutation 1, Guo-Hua Fong
• MGI ID: MGI:3690045
• Synonyms: Phd2^-
• Gene: Egln1 Location: Chr8:125635326-125676063 bp, - strand Genetic Position: Chr8, 72.86 cM
• Alliance: Egln1^tm1Fong page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:114669
• Parent Cell Line: G4 (ES Cell)
• Strain of Origin: (129S6/SvEvTac x C57BL/6NCrl)F1

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: Exon 2 removed via cre mediated recombination. A neo remained downstream of the deleted sequence. RT-PCR confirmed absence of wild-type transcript. (J:114669)

Expression

In Structures Affected by this Mutation:

9 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Egln1 Mutation: 22 strains or lines available

References

• Original: J:114669 Takeda K, et al., Placental but Not Heart Defects Are Associated with Elevated Hypoxia-Inducible Factor {alpha} Levels in Mice Lacking Prolyl Hydroxylase Domain Protein 2. Mol Cell Biol. 2006 Nov;26(22):8336-46
• All: 8 reference(s)