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 		0.320 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 		0.320 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 		0.320 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 		0.320 GeneticVariation disease BEFREE Nine ataxic adults having the following molecular genetic diagnoses underwent ophthalmic examination and ocular motility recordings: four with spinocerebellar ataxia type 6 (SCA-6), three with SCA-3, one with SCA-1, and one with episodic ataxia type 2 (EA-2). 11992880 2002
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.320 Biomarker disease CTD_human Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro. 11719269 2002
Entrez Id: 6310
Gene Symbol: ATXN1
ATXN1 		0.320 GeneticVariation disease BEFREE They were genetically analysed as two spinocerebellar ataxia type 6 (SCA 6), one SCA 1, and one SCA 7. 10674722 1999