Gene: DYNC1H1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1778
Gene Symbol: DYNC1H1
DYNC1H1 		0.310 Biomarker group MGD A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease. 29379136 2018
Entrez Id: 1778
Gene Symbol: DYNC1H1
DYNC1H1 		0.310 GeneticVariation group BEFREE Combining linkage analysis and whole-exome sequencing, we identified a novel dominant defect in the DYNC1H1 tail domain (c.1792C>T, p.Arg598Cys) causing axonal HMSN. 25512093 2015
Entrez Id: 1778
Gene Symbol: DYNC1H1
DYNC1H1 		0.310 CausalMutation group CLINVAR