×
Entrez Id: 57410
Gene Symbol: SCYL1
SCYL1
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 200403
Gene Symbol: VWA3B
VWA3B
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 440193
Gene Symbol: CCDC88C
CCDC88C
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 10273
Gene Symbol: STUB1
STUB1
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 2911
Gene Symbol: GRM1
GRM1
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 6712
Gene Symbol: SPTBN2
SPTBN2
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 10528
Gene Symbol: NOP56
NOP56
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 9711
Gene Symbol: RUBCN
RUBCN
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 51567
Gene Symbol: TDP2
TDP2
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 79876
Gene Symbol: UBA5
UBA5
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 4311
Gene Symbol: MME
MME
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 7222
Gene Symbol: TRPC3
TRPC3
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: 60481
Gene Symbol: ELOVL5
ELOVL5
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 55129
Gene Symbol: ANO10
ANO10
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 343641
Gene Symbol: TGM6
TGM6
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 255928
Gene Symbol: SYT14
SYT14
0.300
Biomarker
disease
CTD_human
×
Entrez Id: 6314
Gene Symbol: ATXN7
ATXN7
0.800
Biomarker
disease
MGD
SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity.12575948 2003
×
Entrez Id: 6314
Gene Symbol: ATXN7
ATXN7
0.800
GeneticVariation
disease
BEFREE
SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity.12575948 2003
×
Entrez Id: 6314
Gene Symbol: ATXN7
ATXN7
0.800
Biomarker
disease
BEFREE
Spinocerebellar ataxia type 7 (SCA7 ) is one of the nine diseases that are grouped in this family and is caused by polyglutamine expansion of the ataxin-7 protein, which is a component of the GCN5-containing human SAGA histone acetyltransferase complex.20621284 2010
×
Entrez Id: 2648
Gene Symbol: KAT2A
KAT2A
0.020
AlteredExpression
disease
BEFREE
Spinocerebellar ataxia type 7 (SCA7) is one of the nine diseases that are grouped in this family and is caused by polyglutamine expansion of the ataxin-7 protein, which is a component of the GCN5 -containing human SAGA histone acetyltransferase complex.20621284 2010