Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1287
Gene Symbol: COL4A5
COL4A5 		0.150 Biomarker disease HPO
Entrez Id: 1287
Gene Symbol: COL4A5
COL4A5 		0.150 CausalMutation disease CLINVAR
Entrez Id: 4627
Gene Symbol: MYH9
MYH9 		0.140 Biomarker disease HPO
Entrez Id: 1773
Gene Symbol: DNASE1
DNASE1 		0.130 Biomarker disease HPO
Entrez Id: 2212
Gene Symbol: FCGR2A
FCGR2A 		0.130 Biomarker disease HPO
Entrez Id: 2213
Gene Symbol: FCGR2B
FCGR2B 		0.120 Biomarker disease HPO
Entrez Id: 712
Gene Symbol: C1QA
C1QA 		0.110 Biomarker disease HPO
Entrez Id: 6775
Gene Symbol: STAT4
STAT4 		0.110 Biomarker disease HPO
Entrez Id: 1285
Gene Symbol: COL4A3
COL4A3 		0.110 Biomarker disease HPO
Entrez Id: 6696
Gene Symbol: SPP1
SPP1 		0.110 Biomarker disease HPO
Entrez Id: 1776
Gene Symbol: DNASE1L3
DNASE1L3 		0.100 Biomarker disease HPO
Entrez Id: 1286
Gene Symbol: COL4A4
COL4A4 		0.100 Biomarker disease HPO
Entrez Id: 3654
Gene Symbol: IRAK1
IRAK1 		0.100 Biomarker disease HPO
Entrez Id: 1493
Gene Symbol: CTLA4
CTLA4 		0.100 Biomarker disease HPO
Entrez Id: 715
Gene Symbol: C1R
C1R 		0.100 Biomarker disease HPO
Entrez Id: 11277
Gene Symbol: TREX1
TREX1 		0.100 Biomarker disease HPO
Entrez Id: 26191
Gene Symbol: PTPN22
PTPN22 		0.100 Biomarker disease HPO
Entrez Id: 5340
Gene Symbol: PLG
PLG 		0.100 Biomarker disease HPO
Entrez Id: 7840
Gene Symbol: ALMS1
ALMS1 		0.100 Biomarker disease HPO
Entrez Id: 843
Gene Symbol: CASP10
CASP10 		0.100 Biomarker disease HPO
Entrez Id: 7369
Gene Symbol: UMOD
UMOD 		0.100 Biomarker disease HPO
Entrez Id: 977
Gene Symbol: CD151
CD151 		0.100 Biomarker disease HPO
Entrez Id: 213
Gene Symbol: ALB
ALB 		0.320 Biomarker disease CTD_human Accelerated immune complex nephritis due to mesangial overloading in spontaneous hypertensive (SHR) rats. 161594 1979
Entrez Id: 1287
Gene Symbol: COL4A5
COL4A5 		0.150 GeneticVariation disease BEFREE Three structural aberrations were found in COL4A5, in intragenic deletion, a Pst I site variant, and an uncharacterized abnormality, which appear to cause nephritis and deafness, with allele-specific severity, in three Alport syndrome kindreds in Utah. 2349482 1990
Entrez Id: 7903
Gene Symbol: ST8SIA4
ST8SIA4 		0.010 GeneticVariation disease BEFREE Three structural aberrations were found in COL4A5, in intragenic deletion, a Pst I site variant, and an uncharacterized abnormality, which appear to cause nephritis and deafness, with allele-specific severity, in three Alport syndrome kindreds in Utah. 2349482 1990