infantile onset spinocerebellar ataxia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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18 genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
C10ORF2 chromosome 10 open reading frame 2 2.56554
FAM178A family with sequence similarity 178, member A 2.04596
ATCAY ataxia, cerebellar, Cayman type 1.30882
PDLIM3 PDZ and LIM domain 3 1.29265
POLG polymerase (DNA directed), gamma 1.19143
SACS sacsin molecular chaperone 1.19014
ACTN2 actinin, alpha 2 1.14857
SPTBN2 spectrin, beta, non-erythrocytic 2 1.01216
SIL1 SIL1 nucleotide exchange factor 0.824948
TTPA tocopherol (alpha) transfer protein 0.801154
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) 0.715215
INA internexin neuronal intermediate filament protein, alpha 0.663181
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae) 0.633169
LDB3 LIM domain binding 3 0.590558
PAX2 paired box 2 0.391141
SULT2A1 sulfotransferase family, cytosolic, 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 0.345308
MGAM maltase-glucoamylase 0.168381
SHBG sex hormone-binding globulin 0.161912