aspartylglucosaminuria Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050461)
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Genes

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

Symbol Name Standardized Value
AGA aspartylglucosaminidase 4.27279
IGLV1-51 immunoglobulin lambda variable 1-51 1.28828
M6PR mannose-6-phosphate receptor (cation dependent) 1.24254
NAGA N-acetylgalactosaminidase, alpha- 0.97254
MFSD8 major facilitator superfamily domain containing 8 0.926279
TEAD2 TEA domain family member 2 0.844211
GAA glucosidase, alpha; acid 0.788442
HEXA hexosaminidase A (alpha polypeptide) 0.732596
SGPL1 sphingosine-1-phosphate lyase 1 0.691495
SEMA6C sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C 0.638676
CLN5 ceroid-lipofuscinosis, neuronal 5 0.626103
PPT1 palmitoyl-protein thioesterase 1 0.556732
NAGLU N-acetylglucosaminidase, alpha 0.536957
ADH4 alcohol dehydrogenase 4 (class II), pi polypeptide 0.513033
KIR2DL3 killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3 0.469197
KIR2DL1 killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1 0.433021
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.416896
NBPF10 neuroblastoma breakpoint family, member 10 0.375179
CLN3 ceroid-lipofuscinosis, neuronal 3 0.346777
ADH1B alcohol dehydrogenase 1B (class I), beta polypeptide 0.345308
ARSH arylsulfatase family, member H 0.296211
BGN biglycan 0.287593
LGALS7 lectin, galactoside-binding, soluble, 7 0.284728
CP ceruloplasmin (ferroxidase) 0.27153
LAMP1 lysosomal-associated membrane protein 1 0.247852
DCN decorin 0.194232
ARSA arylsulfatase A 0.187415