abnormality of glycosaminoglycan metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of glycosaminoglycan metabolism. (Human Phenotype Ontology, HP_0004371)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004371
Similar Terms
Downloads & Tools

Genes

17 genes associated with the abnormality of glycosaminoglycan 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