Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 Biomarker disease GENOMICS_ENGLAND A novel APOA1 mutation in a patient with renal amyloidosis: unveiling amyloid by next-generation sequencing. 31482740 2019
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 Biomarker disease GENOMICS_ENGLAND A case report of hereditary apolipoprotein A-I amyloidosis associated with a novel APOA1 mutation and variable phenotype. 27240838 2016
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 2243
Gene Symbol: FGA
FGA 		0.700 Biomarker disease GENOMICS_ENGLAND Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency. 25427968 2015
Entrez Id: 2243
Gene Symbol: FGA
FGA 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary amyloidosis caused by R554L fibrinogen Aα-chain mutation in a Spanish family and review of the literature. 23551149 2013
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary lysozyme amyloidosis -- phenotypic heterogeneity and the role of solid organ transplantation. 21988333 2012
Entrez Id: 567
Gene Symbol: B2M
B2M 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin. 22693999 2012
Entrez Id: 567
Gene Symbol: B2M
B2M 		0.700 GeneticVariation disease UNIPROT Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin. 22693999 2012
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.700 Biomarker disease GENOMICS_ENGLAND Nonneuropathic amyloidoses (Ostertag type amyloidosis) include those due to abnormalities in lysozyme, fibrinogen Aalpha-chain, and apolipoprotein A-I and A-II. 16523055 2006
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 Biomarker disease GENOMICS_ENGLAND Organ transplantation in hereditary apolipoprotein AI amyloidosis. 16925563 2006
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 GeneticVariation disease UNIPROT Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. 8208902 1994
Entrez Id: 2243
Gene Symbol: FGA
FGA 		0.700 GeneticVariation disease UNIPROT Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. 8097946 1993
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.700 GeneticVariation disease UNIPROT Human lysozyme gene mutations cause hereditary systemic amyloidosis. 8464497 1993
Entrez Id: 2243
Gene Symbol: FGA
FGA 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. 8097946 1993
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 GeneticVariation disease UNIPROT Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. 1502149 1992
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.700 Biomarker disease GENOMICS_ENGLAND Familial nephropathic non-neuropathic amyloidosis: clinical features, immunohistochemistry and chemistry. 1808634 1991
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 GeneticVariation disease UNIPROT A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. 2123470 1990
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 GeneticVariation disease UNIPROT Variant apolipoprotein AI as a major constituent of a human hereditary amyloid. 3142462 1988
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.700 Biomarker disease CTD_human
Entrez Id: 567
Gene Symbol: B2M
B2M 		0.700 CausalMutation disease CLINVAR
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 CausalMutation disease CLINVAR
Entrez Id: 2243
Gene Symbol: FGA
FGA 		0.700 Biomarker disease CTD_human
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 567
Gene Symbol: B2M
B2M 		0.700 Biomarker disease CTD_human
Entrez Id: 335
Gene Symbol: APOA1
APOA1 		0.700 Biomarker disease CTD_human