beta-mannosidosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A lysosomal storage disease that has_material_basis_in deficiency of the beta-A-manosidase enzyme resulting in the disruption of N-linked glycoprotein oligosaccharide catabolism. (Human Disease Ontology, DOID_3633)
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Genes

19 genes co-occuring with the disease beta-mannosidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MANBA mannosidase, beta A, lysosomal 3.7934
MGAT4C MGAT4 family, member C 1.6525
MAN2B1 mannosidase, alpha, class 2B, member 1 1.35725
SGSH N-sulfoglucosamine sulfohydrolase 1.21089
CNP 2',3'-cyclic nucleotide 3' phosphodiesterase 1.20569
NAGA N-acetylgalactosaminidase, alpha- 1.18841
SYCP3 synaptonemal complex protein 3 1.06816
PRAMEF20 PRAME family member 20 1.02524
GCNT4 glucosaminyl (N-acetyl) transferase 4, core 2 0.949519
GCNT1 glucosaminyl (N-acetyl) transferase 1, core 2 0.898282
MAG myelin associated glycoprotein 0.787213
GCNT2 glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) 0.778204
HEXDC hexosaminidase (glycosyl hydrolase family 20, catalytic domain) containing 0.773296
AGA aspartylglucosaminidase 0.698313
TSKU tsukushi, small leucine rich proteoglycan 0.684692
MBP myelin basic protein 0.60303
GAA glucosidase, alpha; acid 0.406051
MAOA monoamine oxidase A 0.397471
HEXA hexosaminidase A (alpha polypeptide) 0.355235