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Egln3tm1Vlcg
Targeted Allele Detail
Nomenclature
Symbol: Egln3tm1Vlcg
Name: egl-9 family hypoxia-inducible factor 3; targeted mutation 1, Velocigene
MGI ID: MGI:5304712
Synonyms: Phd3-
Gene: Egln3  Location: Chr12:54178981-54203860 bp, - strand  Genetic Position: Chr12, 22.9 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:179490
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Not Specified
    No details provided.
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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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:  16 strains or lines available
References
Original:  J:179490 Moslehi J, et al., Loss of hypoxia-inducible factor prolyl hydroxylase activity in cardiomyocytes phenocopies ischemic cardiomyopathy. Circulation. 2010 Sep 7;122(10):1004-16
All:  4 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
04/06/2021
MGI 6.16
The Jackson Laboratory