Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9829
Gene Symbol: DNAJC6
DNAJC6
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.130 GeneticVariation BEFREE Although DNAJC6 (Auxilin), DNAJC12, and DNAJC5 (CSPα) exhibit strong genetic association with disease, DNAJC26 (GAK), DNAJC13 (RME-8), and DNAJC10 (Erdj5) require additional evidence to definitively link reported variants to parkinsonism. 31120186

2019
Entrez Id: 9829
Gene Symbol: DNAJC6
DNAJC6
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.130 GeneticVariation BEFREE The SYNJ1 gene is a compelling candidate for Parkinsonism; mutations in the functionally linked protein auxilin cause a similar early-onset phenotype, and other findings implicate endosomal dysfunctions in the pathogenesis. 23804577

2013
Entrez Id: 9829
Gene Symbol: DNAJC6
DNAJC6
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.130 Biomarker BEFREE Our findings further establish DNAJC6 as a juvenile parkinsonism gene, and expand the spectrums of the parkinsonism phenotype and DNAJC6 mutation. 23211418

2013
Entrez Id: 9829
Gene Symbol: DNAJC6
DNAJC6
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.130 Biomarker HPO