Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55129
Gene Symbol: ANO10
ANO10 		0.300 Biomarker disease CTD_human
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.300 Biomarker disease CTD_human
Entrez Id: 6712
Gene Symbol: SPTBN2
SPTBN2 		0.300 Biomarker disease CTD_human
Entrez Id: 200403
Gene Symbol: VWA3B
VWA3B 		0.300 Biomarker disease CTD_human
Entrez Id: 10273
Gene Symbol: STUB1
STUB1 		0.300 Biomarker disease CTD_human
Entrez Id: 60481
Gene Symbol: ELOVL5
ELOVL5 		0.300 Biomarker disease CTD_human
Entrez Id: 57410
Gene Symbol: SCYL1
SCYL1 		0.300 Biomarker disease CTD_human
Entrez Id: 7222
Gene Symbol: TRPC3
TRPC3 		0.300 Biomarker disease CTD_human
Entrez Id: 9711
Gene Symbol: RUBCN
RUBCN 		0.300 Biomarker disease CTD_human
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: 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: 8913
Gene Symbol: CACNA1G
CACNA1G 		0.300 Biomarker disease CTD_human
Entrez Id: 10725
Gene Symbol: NFAT5
NFAT5 		0.010 GeneticVariation disease BEFREE To investigate sequences or mutations associated with neurodegenerative disorders, we performed analyses for the NFAT5 gene, which is located in the candidate region for the autosomal dominantly inherited spinocerebellar ataxia type 4 (SCA4). 11072102 2000