Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 53947
Gene Symbol: A4GALT
A4GALT
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 23461
Gene Symbol: ABCA5
ABCA5
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 23460
Gene Symbol: ABCA6
ABCA6
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
0.100 GeneticVariation phenotype GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
Entrez Id: 23456
Gene Symbol: ABCB10
ABCB10
0.100 GeneticVariation phenotype GWASCAT Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease. 30111768 2018
Entrez Id: 89845
Gene Symbol: ABCC10
ABCC10
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 28
Gene Symbol: ABO
ABO
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 28
Gene Symbol: ABO
ABO
0.100 GeneticVariation phenotype GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
Entrez Id: 28
Gene Symbol: ABO
ABO
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 84129
Gene Symbol: ACAD11
ACAD11
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 2532
Gene Symbol: ACKR1
ACKR1
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 1238
Gene Symbol: ACKR2
ACKR2
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 26027
Gene Symbol: ACOT11
ACOT11
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 26027
Gene Symbol: ACOT11
ACOT11
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 52
Gene Symbol: ACP1
ACP1
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 52
Gene Symbol: ACP1
ACP1
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 51205
Gene Symbol: ACP6
ACP6
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 84532
Gene Symbol: ACSS1
ACSS1
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 89
Gene Symbol: ACTN3
ACTN3
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 89
Gene Symbol: ACTN3
ACTN3
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 98
Gene Symbol: ACYP2
ACYP2
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 51816
Gene Symbol: ADA2
ADA2
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
Entrez Id: 51816
Gene Symbol: ADA2
ADA2
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
Entrez Id: 8038
Gene Symbol: ADAM12
ADAM12
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018