abnormality of glycolipid metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of glycolipid metabolism. (Human Phenotype Ontology, HP_0010969)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010969
Similar Terms
Downloads & Tools

Genes

8 genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GBA glucosidase, beta, acid
GM2A GM2 ganglioside activator
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
HEXA hexosaminidase A (alpha polypeptide)
HEXB hexosaminidase B (beta polypeptide)
MCOLN1 mucolipin 1
PSAP prosaposin