Gene: SYNJ1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8867
Gene Symbol: SYNJ1
SYNJ1 		0.320 GeneticVariation disease BEFREE A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson's Disease Associated with Epilepsy. 30187305 2018
Entrez Id: 8867
Gene Symbol: SYNJ1
SYNJ1 		0.320 Biomarker disease GENOMICS_ENGLAND Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline. 27435091 2016
Entrez Id: 8867
Gene Symbol: SYNJ1
SYNJ1 		0.320 Biomarker disease GENOMICS_ENGLAND Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism. 27496670 2016
Entrez Id: 8867
Gene Symbol: SYNJ1
SYNJ1 		0.320 GeneticVariation disease BEFREE Here, I first outline the evolution of the research strategies to find PD-related genes, and then focus on recent advances in the field of the monogenic forms, including VPS35 mutations in autosomal dominant PD, and DNAJC6 and SYNJ1 mutations in recessive forms of juvenile parkinsonism. 24262182 2014
Entrez Id: 8867
Gene Symbol: SYNJ1
SYNJ1 		0.320 Biomarker disease GENOMICS_ENGLAND Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. 23804577 2013
Entrez Id: 8867
Gene Symbol: SYNJ1
SYNJ1 		0.320 Biomarker disease GENOMICS_ENGLAND The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures. 23804563 2013