Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.300 Biomarker disease CTD_human Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. 19430480 2009
Entrez Id: 29949
Gene Symbol: IL19
IL19 		0.300 Biomarker disease CTD_human Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. 19430480 2009
Entrez Id: 50604
Gene Symbol: IL20
IL20 		0.300 Biomarker disease CTD_human Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. 19430480 2009
Entrez Id: 246778
Gene Symbol: IL27
IL27 		0.300 Biomarker disease CTD_human Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. 19430480 2009
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA 		0.300 Biomarker disease CTD_human Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes. 30224649 2018
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA 		0.300 Biomarker disease CTD_human Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource. 19701192 2009
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA 		0.300 Biomarker disease CTD_human Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes. 17676041 2007
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA 		0.300 Biomarker disease CTD_human IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production. 19119414 2009
Entrez Id: 3569
Gene Symbol: IL6
IL6 		0.300 Biomarker disease CTD_human
Entrez Id: 3630
Gene Symbol: INS
INS 		0.500 Biomarker disease CTD_mouse Inhibition of SREBP With Fatostatin Does Not Attenuate Early Diabetic Nephropathy in Male Mice. 29420703 2018
Entrez Id: 3630
Gene Symbol: INS
INS 		0.500 Biomarker disease CTD_mouse A sensitized screen of N-ethyl-N-nitrosourea-mutagenized mice identifies dominant mutants predisposed to diabetic nephropathy. 17151334 2007
Entrez Id: 3630
Gene Symbol: INS
INS 		0.500 Therapeutic disease CTD_human Cortical and hippocampal mitochondria bioenergetics and oxidative status during hyperglycemia and/or insulin-induced hypoglycemia. 20620209 2010
Entrez Id: 3710
Gene Symbol: ITPR3
ITPR3 		0.300 Biomarker disease CTD_human
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		0.300 Biomarker disease CTD_human Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes. 18025464 2007
Entrez Id: 4842
Gene Symbol: NOS1
NOS1 		0.300 Biomarker disease CTD_human Chronic resveratrol treatment restores vascular responsiveness of cerebral arterioles in type 1 diabetic rats. 21666113 2011
Entrez Id: 4846
Gene Symbol: NOS3
NOS3 		0.300 Biomarker disease CTD_human Chronic resveratrol treatment restores vascular responsiveness of cerebral arterioles in type 1 diabetic rats. 21666113 2011
Entrez Id: 5078
Gene Symbol: PAX4
PAX4 		0.300 Biomarker disease CTD_human
Entrez Id: 5588
Gene Symbol: PRKCQ
PRKCQ 		0.300 Biomarker disease CTD_human Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. 18978792 2008
Entrez Id: 26191
Gene Symbol: PTPN22
PTPN22 		0.300 Biomarker disease CTD_human Inhibition of lymphoid tyrosine phosphatase by benzofuran salicylic acids. 21190368 2011
Entrez Id: 26191
Gene Symbol: PTPN22
PTPN22 		0.300 Biomarker disease CTD_human Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes. 30224649 2018
Entrez Id: 10019
Gene Symbol: SH2B3
SH2B3 		0.300 Biomarker disease CTD_human Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes. 30224649 2018
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1 		0.300 Biomarker disease CTD_human Iron and infection: effects of host iron status and the iron-regulatory genes haptoglobin and NRAMP1 (SLC11A1) on host-pathogen interactions in tuberculosis and HIV. 16597321 2006
Entrez Id: 55315
Gene Symbol: SLC29A3
SLC29A3 		0.300 Biomarker disease CTD_human SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway. 19336477 2009
Entrez Id: 55315
Gene Symbol: SLC29A3
SLC29A3 		0.300 Biomarker disease CTD_human Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease. 20140240 2010
Entrez Id: 6774
Gene Symbol: STAT3
STAT3 		0.300 Biomarker disease CTD_human Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease. 25038750 2014