Gene: ATXN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 AlteredExpression disease BEFREE Except for individuals with spinocerebellar ataxia type 1, age at onset was also influenced by other (CAG)n-containing genes: ATXN7 in spinocerebellar ataxia type 2; ATXN2, ATN1 and HTT in spinocerebellar ataxia type 3; ATXN1 and ATXN3 in spinocerebellar ataxia type 6; and ATXN3 and TBP in spinocerebellar ataxia type 7. 24972706 2014
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 Biomarker disease BEFREE SCA1 and SCA7 patients had African ancestry. 19659750 2010
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 Biomarker disease CTD_human Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1. 18337722 2008
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 Biomarker disease CTD_human Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes. 17322884 2007
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 Biomarker disease CTD_human The AXH domain of Ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/Senseless proteins. 16122429 2005
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 Biomarker disease CTD_human Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro. 11719269 2002
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.330 GeneticVariation disease BEFREE Thirty-five patients belonged to the ADCA type I group (SCA1, 12; SCA2, 10; SCA3, 13) and five to the ADCA type II group. 10366224 1999