Gene: PEX19 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5824
Gene Symbol: PEX19
PEX19 		0.510 Biomarker group GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 5824
Gene Symbol: PEX19
PEX19 		0.510 Biomarker group CTD_human A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder. 20683989 2010
Entrez Id: 5824
Gene Symbol: PEX19
PEX19 		0.510 Biomarker group BEFREE These results demonstrate that PEX19 is the causative gene for CG-J PBD and suggest that the C-terminal part, including the CAAX homology box, is required for the biological function of Pex19p. 10051604 1999