Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
CUI: C3553951
Disease: PEROXISOME BIOGENESIS DISORDER 7B
PEROXISOME BIOGENESIS DISORDER 7B 		0.700 Biomarker GENOMICS_ENGLAND Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. 28944237

2017
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
CUI: C3553951
Disease: PEROXISOME BIOGENESIS DISORDER 7B
PEROXISOME BIOGENESIS DISORDER 7B 		0.700 Biomarker GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308

2016
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
CUI: C3553951
Disease: PEROXISOME BIOGENESIS DISORDER 7B
PEROXISOME BIOGENESIS DISORDER 7B 		0.700 Biomarker GENOMICS_ENGLAND A practical approach to diagnosing adult onset leukodystrophies. 24357685

2014
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
CUI: C3553951
Disease: PEROXISOME BIOGENESIS DISORDER 7B
PEROXISOME BIOGENESIS DISORDER 7B 		0.700 Biomarker GENOMICS_ENGLAND The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum. 15542397

2004