3-methylglutaconic aciduria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003535
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Genes

8 genes associated with the 3-methylglutaconic aciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGK acylglycerol kinase
ATP5E ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit
ATPAF2 ATP synthase mitochondrial F1 complex assembly factor 2
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase
POLG polymerase (DNA directed), gamma
SERAC1 serine active site containing 1
TMEM70 transmembrane protein 70