abnormality of lysosomal metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A major lysosomal function is the breakdown and recycling of macromolecules and organelles into basic precursors. (Human Phenotype Ontology, HP_0004356)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004356
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7 genes associated with the abnormality of lysosomal metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CA2 carbonic anhydrase II
CLCN7 chloride channel, voltage-sensitive 7
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
OCRL oculocerebrorenal syndrome of Lowe
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b