Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3251
Gene Symbol: HPRT1
HPRT1
0.130 Biomarker disease HPO
Entrez Id: 6928
Gene Symbol: HNF1B
HNF1B
0.110 Biomarker disease HPO
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
0.100 GeneticVariation disease CLINVAR
Entrez Id: 2038
Gene Symbol: EPB42
EPB42
0.100 Biomarker disease HPO
Entrez Id: 4040
Gene Symbol: LRP6
LRP6
0.100 Biomarker disease HPO
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
0.100 Biomarker disease HPO
Entrez Id: 1188
Gene Symbol: CLCNKB
CLCNKB
0.100 Biomarker disease HPO
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
0.100 Biomarker disease HPO
Entrez Id: 2538
Gene Symbol: G6PC
G6PC
0.100 Biomarker disease HPO
Entrez Id: 5631
Gene Symbol: PRPS1
PRPS1
0.100 Biomarker disease HPO
Entrez Id: 4582
Gene Symbol: MUC1
MUC1
0.100 Biomarker disease HPO
Entrez Id: 6521
Gene Symbol: SLC4A1
SLC4A1
0.100 Biomarker disease HPO
Entrez Id: 2542
Gene Symbol: SLC37A4
SLC37A4
0.100 Biomarker disease HPO
Entrez Id: 348
Gene Symbol: APOE
APOE
0.100 Biomarker disease HPO
Entrez Id: 5213
Gene Symbol: PFKM
PFKM
0.100 Biomarker disease HPO
Entrez Id: 286
Gene Symbol: ANK1
ANK1
0.100 Biomarker disease HPO
Entrez Id: 6710
Gene Symbol: SPTB
SPTB
0.100 Biomarker disease HPO
Entrez Id: 55157
Gene Symbol: DARS2
DARS2
0.100 CausalMutation disease CLINVAR
Entrez Id: 29927
Gene Symbol: SEC61A1
SEC61A1
0.100 Biomarker disease HPO
Entrez Id: 6708
Gene Symbol: SPTA1
SPTA1
0.100 Biomarker disease HPO
Entrez Id: 3251
Gene Symbol: HPRT1
HPRT1
0.130 GeneticVariation disease BEFREE Although these 'evolutionary conserved' amino acids account for only 32% of the amino acids in the human hprt protein, they are involved in 76% of the missense mutations at the hprt locus in human T-lymphocytes, 67% in Lesch-Nyhan patients (with severe hprt-deficiency), but only 43% in gout patients (with partial hprt deficiency). 1306134 1992
Entrez Id: 3251
Gene Symbol: HPRT1
HPRT1
0.130 GeneticVariation disease BEFREE A C-to-A substitution at base 73 in exon 2, which predicted proline 25 to threonine, was detected in the gout patient (designated HPRT Yonago). 8112742 1994
Entrez Id: 596
Gene Symbol: BCL2
BCL2
0.010 AlteredExpression disease BEFREE Synovial T cells from rheumatoid arthritis and gout patients could be rescued from spontaneous apoptosis in vitro either by IL-2R gamma chain signaling cytokines (which upregulate Bcl-2 and Bcl-XL) or by interaction with synovial fibroblasts (which upregulates Bcl-xL but not Bcl-2). 9022077 1997
Entrez Id: 6928
Gene Symbol: HNF1B
HNF1B
0.110 GeneticVariation disease LHGDN Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation. 12675839 2003
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.310 GeneticVariation disease BEFREE Results of the present study suggest that polymorphisms of the IL-1beta promoter and IL-1beta exon 5 are not related to gout patients in central Taiwan. 14661113 2005