Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5195
Gene Symbol: PEX14
PEX14
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.520 Biomarker CTD_human Identification of a novel PEX14 mutation in Zellweger syndrome. 18285423

2008
Entrez Id: 5195
Gene Symbol: PEX14
PEX14
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.520 Biomarker CTD_human Indeed, human PEX14 rescues the import of a PTS1-dependent as well as a PTS2-dependent protein into the peroxisomes in fibroblasts from a patient with Zellweger syndrome belonging to the new complementation group. 15146459

2004
Entrez Id: 5195
Gene Symbol: PEX14
PEX14
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.520 Biomarker GENOMICS_ENGLAND