Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51741
Gene Symbol: WWOX
WWOX 		0.300 Biomarker disease CTD_human
Entrez Id: 2895
Gene Symbol: GRID2
GRID2 		0.300 Biomarker disease CTD_human
Entrez Id: 23152
Gene Symbol: CIC
CIC 		0.300 Biomarker disease CTD_human Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1. 18337722 2008
Entrez Id: 6311
Gene Symbol: ATXN2
ATXN2 		0.300 Biomarker disease CTD_human Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease. 19224595 2009
Entrez Id: 2296
Gene Symbol: FOXC1
FOXC1 		0.300 Biomarker disease CTD_human FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation. 19668217 2009
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A 		0.300 Biomarker disease CTD_human Efficacy and tolerability of acetazolamide in migraine prophylaxis: a randomised placebo-controlled trial. 11985388 2002
Entrez Id: 255928
Gene Symbol: SYT14
SYT14 		0.300 Biomarker disease CTD_human
Entrez Id: 10528
Gene Symbol: NOP56
NOP56 		0.300 Biomarker disease CTD_human
Entrez Id: 4311
Gene Symbol: MME
MME 		0.300 Biomarker disease CTD_human
Entrez Id: 57231
Gene Symbol: SNX14
SNX14 		0.300 Biomarker disease CTD_human
Entrez Id: 84991
Gene Symbol: RBM17
RBM17 		0.300 Biomarker disease CTD_human Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1. 18337722 2008
Entrez Id: 146057
Gene Symbol: TTBK2
TTBK2 		0.300 Biomarker disease CTD_human Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11. 18037885 2007
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.300 Biomarker disease CTD_human Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro. 11719269 2002
Entrez Id: 10939
Gene Symbol: AFG3L2
AFG3L2 		0.300 Biomarker disease CTD_human Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. 20208537 2010
Entrez Id: 8913
Gene Symbol: CACNA1G
CACNA1G 		0.300 Biomarker disease CTD_human
Entrez Id: 5521
Gene Symbol: PPP2R2B
PPP2R2B 		0.300 Biomarker disease CTD_human The spinocerebellar ataxia 12 gene product and protein phosphatase 2A regulatory subunit Bbeta2 antagonizes neuronal survival by promoting mitochondrial fission. 18940801 2008
Entrez Id: 342371
Gene Symbol: ATXN1L
ATXN1L 		0.300 Therapeutic disease CTD_human Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes. 17322884 2007