Gene: APOA5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 GermlineCausalMutation disease ORPHANET "Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an ""FCS score""." 29980054 2018
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 GeneticVariation disease BEFREE We report a novel homozygous apolipoprotein A5 (APOA5) frameshift mutation (c.G425del-C, p.Arg143AlafsTer57) identified in a 12-year-old boy of Pakistani origin with severe hypertriglyceridemia (up to 35 mmol/L) and type V hyperlipoproteinemia. 27678447 2017
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 GermlineCausalMutation disease ORPHANET Chylomicronaemia--current diagnosis and future therapies. 25732519 2015
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 GeneticVariation disease BEFREE Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment. 16200213 2005
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 Biomarker disease GENOMICS_ENGLAND Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment. 16200213 2005
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 Biomarker disease CTD_human
Entrez Id: 116519
Gene Symbol: APOA5
APOA5 		0.720 CausalMutation disease CLINVAR