hypermethioninemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body. (Human Disease Ontology, DOID_0050544)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003235
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Genes

7 genes associated with the hypermethioninemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADK adenosine kinase
AHCY adenosylhomocysteinase
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
GNMT glycine N-methyltransferase
MAT1A methionine adenosyltransferase I, alpha
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
TTC37 tetratricopeptide repeat domain 37