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Egln2tm1Pec
Targeted Allele Detail
Summary
Symbol: Egln2tm1Pec
Name: egl-9 family hypoxia-inducible factor 2; targeted mutation 1, Peter Carmeliet
MGI ID: MGI:3776872
Synonyms: Phd1-
Gene: Egln2  Location: Chr7:26858083-26866227 bp, - strand  Genetic Position: Chr7, 15.83 cM
Alliance: Egln2tm1Pec page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:132630
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExons 2 and 3 were replaced with a neo cassette. The absence of protein product was confirmed by western blot analysis on mouse embryonic fibroblast extracts. (J:132630)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Egln2 Mutation:  18 strains or lines available
References
Original:  J:132630 Aragones J, et al., Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism. Nat Genet. 2008 Feb;40(2):170-80
All:  14 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory