Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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
Entrez Id: 2243
Gene Symbol: FGA
FGA
0.700 CausalMutation disease CLINVAR
Entrez Id: 335
Gene Symbol: APOA1
APOA1
0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4069
Gene Symbol: LYZ
LYZ
0.700 CausalMutation disease CLINVAR
Entrez Id: 104326055
Gene Symbol: APOA1-AS
APOA1-AS
0.100 CausalMutation disease CLINVAR
Entrez Id: 2934
Gene Symbol: GSN
GSN
0.300 Biomarker disease GENOMICS_ENGLAND Three forms of dominant amyloid neuropathy. 6975851 1981
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: 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: 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 Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. 1502149 1992
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 Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. 8208902 1994
Entrez Id: 952
Gene Symbol: CD38
CD38
0.010 Biomarker disease BEFREE In this study, we analyzed blood mononuclear cells (BMNCs) from 16 patients with MGUS, 2 with amyloidosis, 8 with smoldering MM (SMM), 2 with indolent MM (IMM), and 15 with active MM using three different methods to detect and quantitate clonal cells, ie, immunofluorescence microscopy (IM) for monoclonal plasma cells, three-color flow cytometry (FC) for CD38(+)CD45- CD45(dim) cells, and the allele-specific oligonucleotide polymerase chain reaction (ASO-PCR). 8704185 1996
Entrez Id: 5788
Gene Symbol: PTPRC
PTPRC
0.010 Biomarker disease BEFREE In this study, we analyzed blood mononuclear cells (BMNCs) from 16 patients with MGUS, 2 with amyloidosis, 8 with smoldering MM (SMM), 2 with indolent MM (IMM), and 15 with active MM using three different methods to detect and quantitate clonal cells, ie, immunofluorescence microscopy (IM) for monoclonal plasma cells, three-color flow cytometry (FC) for CD38(+)CD45- CD45(dim) cells, and the allele-specific oligonucleotide polymerase chain reaction (ASO-PCR). 8704185 1996
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: 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