ATXN8OS, ATXN8 opposite strand lncRNA, 6315

N. diseases: 91; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.030 GeneticVariation disease BEFREE We analyzed the ATXN8OS gene in 150 Japanese patients with ataxia and 76 patients with Parkinson's disease or related disorders. 29916049 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.030 Biomarker disease BEFREE SCA6 and SCA8 have also been reported with a PD-like phenotype. 25866756 2015
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.030 GeneticVariation disease LHGDN This study appears to be the first report describing the PD phenotype in association with an expanded allele in the TATA-binding protein gene and suggests that SCA8 may also be a cause of typical PD. 14756671 2004
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.030 Biomarker disease BEFREE This study appears to be the first report describing the PD phenotype in association with an expanded allele in the TATA-binding protein gene and suggests that SCA8 may also be a cause of typical PD. 14756671 2004