Gene: DCTN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1639
Gene Symbol: DCTN1
DCTN1 		0.040 GeneticVariation disease BEFREE DCTN1 F52L mutation case of Perry syndrome with progressive supranuclear palsy-like tauopathy. 29499916 2018
Entrez Id: 1639
Gene Symbol: DCTN1
DCTN1 		0.040 Biomarker disease BEFREE A DCTN1/PSP phenotype case showed increased binding in putamen, parietal lobe, and GP. 28568506 2017
Entrez Id: 1639
Gene Symbol: DCTN1
DCTN1 		0.040 GeneticVariation disease BEFREE One of the variants, DCTN1 p.K56R, was present in two patients with progressive supranuclear palsy (PSP) with a shared minimal 2.2 Mb haplotype. 27132499 2016
Entrez Id: 1639
Gene Symbol: DCTN1
DCTN1 		0.040 GeneticVariation disease BEFREE Sequencing of the DCTN1 gene in familial forms of PSP at a referral center among 21 patients with familial PSP-like phenotypes. 24343258 2014