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Symbol
Name
ID
Egln1
egl-9 family hypoxia-inducible factor 1
MGI:1932286
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations

Mouse Phenotypes
muscle phenotype
abnormal myocardium layer morphology
increased myocardial fiber size
myocardial fiber degeneration
abnormal trabecula carnea morphology
thin ventricle myocardium compact layer
dilated cardiomyopathy
decreased ventricle muscle contractility
decreased cardiomyocyte apoptosis
Availability Mouse Genotype
Egln1tm1Fong/Egln1tm1Fong
Egln1tm1Fong/Egln1+ *
Egln1tm1.1Brei/Egln1tm1.1Brei
Myl2tm1(cre)Krc/Myl2+  (conditional)
Egln1tm1Kael/Egln1tm1Kael
Tg(CAG-cre/Esr1*)5Amc/0  (conditional)
Egln1tm1Kael/Egln1tm1Kael
Tg(Myh6-cre)2182Mds/0  (conditional)

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
04/30/2024
MGI 6.23
The Jackson Laboratory