Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 Biomarker disease BEFREE Variants in the dopamine receptor D3 (DRD3) and HCLS1 binding protein 3 (HS1BP3) have been nominated as risk factors for essential tremor (ET). 19524641 2009
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 GeneticVariation disease BEFREE Seven heterozygous A265G variants in the HS1BP3 gene were found in this pedigree, but they did not cosegregate with ET, Parkinson disease, or Bell palsy, supporting the conclusion that this variant is not associated with ET. 17353387 2007
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 GeneticVariation disease BEFREE Two genetic loci have been identified in autosomal dominant (AD) ET and polymorphisms in the DRD3 and HS1-BP3 genes have been proposed as the possible susceptibility factors for ET. 16721753 2006
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 GeneticVariation disease BEFREE The 828C-->G genetic variant in the HS1-BP3 gene occurs relatively frequently in subjects with ET. 16211613 2006
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 GeneticVariation disease BEFREE A rare variant in the HS1-BP3 gene that is associated with essential tremor (ET) in two families is reported. 15699368 2005
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 GeneticVariation disease LHGDN Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease. 16116142 2005
Entrez Id: 64342
Gene Symbol: HS1BP3
HS1BP3
0.060 Biomarker disease LHGDN A variant in the HS1-BP3 gene is associated with familial essential tremor. 15699368 2005