Gene: PEX26 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55670
Gene Symbol: PEX26
PEX26 		0.510 Biomarker disease CTD_human Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities. 26319495 2015
Entrez Id: 55670
Gene Symbol: PEX26
PEX26 		0.510 GeneticVariation disease BEFREE To the best of our knowledge, this is the first successful PGD for ZS caused by mutation in PEX26 gene, with the subsequent delivery of a homozygous normal baby. 17336976 2007
Entrez Id: 55670
Gene Symbol: PEX26
PEX26 		0.510 Biomarker disease CTD_human Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. 12851857 2003
Entrez Id: 55670
Gene Symbol: PEX26
PEX26 		0.510 Biomarker disease GENOMICS_ENGLAND