abnormality of polysaccharide metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the metabolism of polysaccharide. (Human Phenotype Ontology, HP_0011012)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011012
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Genes

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

Symbol Name
ARSB arylsulfatase B
FUCA1 fucosidase, alpha-L- 1, tissue
GALNS galactosamine (N-acetyl)-6-sulfatase
GLB1 galactosidase, beta 1
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GNS glucosamine (N-acetyl)-6-sulfatase
GUSB glucuronidase, beta
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
HYAL1 hyaluronoglucosaminidase 1
IDS iduronate 2-sulfatase
IDUA iduronidase, alpha-L-
MCOLN1 mucolipin 1
NAGLU N-acetylglucosaminidase, alpha
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SGSH N-sulfoglucosamine sulfohydrolase
SUMF1 sulfatase modifying factor 1