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Symbol
Name
ID
Etfdh
electron transferring flavoprotein, dehydrogenase
MGI:106100
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Developmental cataract
Disease(s) Associated with ETFDH
multiple acyl-CoA dehydrogenase deficiency

Mouse Phenotypes
abnormal retinal vasculature morphology
abnormal retinal blood vessel morphology
Availability Mouse Genotype
Etfdhtm1b(EUCOMM)Hmgu/Etfdh+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/16/2019
MGI 6.13
The Jackson Laboratory