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Egln3tm1Pjr
Targeted Allele Detail
Summary
Symbol: Egln3tm1Pjr
Name: egl-9 family hypoxia-inducible factor 3; targeted mutation 1, Peter J Ratcliffe
MGI ID: MGI:3795244
Synonyms: PHD3-
Gene: Egln3  Location: Chr12:54225767-54250646 bp, - strand  Genetic Position: Chr12, 22.9 cM
Alliance: Egln3tm1Pjr page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:136034
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S/SvEv
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 1 was replaced with a neo cassette. The absence of protein product was confirmed by western blot analysis on mouse embryonic fibroblast extracts. (J:136034)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 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 Egln3 Mutation:  24 strains or lines available
References
Original:  J:136034 Bishop T, et al., Abnormal sympathoadrenal development and systemic hypotension in PHD3-/- mice. Mol Cell Biol. 2008 May;28(10):3386-400
All:  10 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
04/16/2024
MGI 6.23
The Jackson Laboratory