mucopolysaccharidosis i 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 enzyme alpha-L-iduronidase. (Human Disease Ontology, DOID_12802)
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Genes

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

Symbol Name Standardized Value
IDUA iduronidase, alpha-L- 3.47974
SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), member 1 1.21955
GAA glucosidase, alpha; acid 1.05934
M6PR mannose-6-phosphate receptor (cation dependent) 0.890898
GUSB glucuronidase, beta 0.817565
IDS iduronate 2-sulfatase 0.770027
B4GALNT1 beta-1,4-N-acetyl-galactosaminyl transferase 1 0.740299
GALC galactosylceramidase 0.698313
NAGLU N-acetylglucosaminidase, alpha 0.619834
MMP12 matrix metallopeptidase 12 0.595233
HEXA hexosaminidase A (alpha polypeptide) 0.571107
MID2 midline 2 0.561004
ARSA arylsulfatase A 0.548971
MCOLN1 mucolipin 1 0.48893
CTSS cathepsin S 0.481705
SLC6A7 solute carrier family 6 (neurotransmitter transporter), member 7 0.436778
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5 0.407172
CLDN5 claudin 5 0.374068
DCT dopachrome tautomerase 0.334681
ARSH arylsulfatase family, member H 0.30848
CTLA4 cytotoxic T-lymphocyte-associated protein 4 0.301254
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal 0.244696
C6ORF25 chromosome 6 open reading frame 25 0.225573
GLA galactosidase, alpha 0.225229
LCAT lecithin-cholesterol acyltransferase 0.207578
GBA glucosidase, beta, acid 0.200006
SMAD3 SMAD family member 3 0.164571