mucopolysaccharidosis iv Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzymes galactose 6-sulfate sulfatase (Type A) or beta-galactosidase (Type B) needed to break down the keratan sulfate sugar chain. (Human Disease Ontology, DOID_12804)
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Genes

22 genes co-occuring with the disease mucopolysaccharidosis iv in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GALNS galactosamine (N-acetyl)-6-sulfatase 3.70974
SUMF1 sulfatase modifying factor 1 1.635
ARSH arylsulfatase family, member H 1.62605
LGSN lengsin, lens protein with glutamine synthetase domain 1.31624
CRTAP cartilage associated protein 1.24863
PEX6 peroxisomal biogenesis factor 6 0.890898
APRT adenine phosphoribosyltransferase 0.855677
PEX2 peroxisomal biogenesis factor 2 0.84585
P3H1 prolyl 3-hydroxylase 1 0.834788
GLB1 galactosidase, beta 1 0.793361
ACAT1 acetyl-CoA acetyltransferase 1 0.724502
PPIB peptidylprolyl isomerase B (cyclophilin B) 0.65565
PTK2B protein tyrosine kinase 2 beta 0.636708
ARSB arylsulfatase B 0.59952
M6PR mannose-6-phosphate receptor (cation dependent) 0.529994
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.484744
IDUA iduronidase, alpha-L- 0.419517
CYBA cytochrome b-245, alpha polypeptide 0.34384
SOX9 SRY (sex determining region Y)-box 9 0.264077
COL1A1 collagen, type I, alpha 1 0.210253
ACAN aggrecan 0.18651
COL1A2 collagen, type I, alpha 2 0.165435