Gene: DCAF8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 50717
Gene Symbol: DCAF8
DCAF8 		0.110 GeneticVariation group BEFREE Our results indicate that DCAF8 p.R317C mutation is responsible for this specific variety of HMSN2 with infrequent giant axons and mild cardiomyopathy. 24500646 2014
Entrez Id: 50717
Gene Symbol: DCAF8
DCAF8 		0.110 Biomarker group HPO