Gene: PEX13 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5194
Gene Symbol: PEX13
PEX13 		0.310 Biomarker disease BEFREE Here we used mice with brain-restricted inactivation of the peroxisome biogenesis gene PEX13 to model the pathophysiological features of ZS, and determine the impact of peroxisome dysfunction on neurogenesis and cell maturation in ZS. 29187321 2018
Entrez Id: 5194
Gene Symbol: PEX13
PEX13 		0.310 Biomarker disease CTD_human Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. 19449432 2009
Entrez Id: 5194
Gene Symbol: PEX13
PEX13 		0.310 Biomarker disease CTD_human Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders. 10332040 1999