Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 GeneticVariation LHGDN R1615P: a novel mutation in ABCA1 associated with low levels of HDL and type II diabetes mellitus. 16055210

2006

Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.200 GeneticVariation LHGDN Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood. 17446535

2007

Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.200 GeneticVariation LHGDN We identified one ABCC8 and four KCNJ11 mutation carriers, of whom four were successfully transferred to SU, dramatically improving their diabetes control and quality of life. 17213273

2007

Entrez Id: 9370
Gene Symbol: ADIPOQ
ADIPOQ
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.400 Biomarker LHGDN Obesity, adiponectin and inflammation as predictors of new-onset diabetes mellitus after kidney transplantation. 17229078

2007

Entrez Id: 9370
Gene Symbol: ADIPOQ
ADIPOQ
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.400 GeneticVariation LHGDN Genetic variation of the adiponectin gene is associated with obesity, MetS, and diabetes mellitus in the elderly. 17684226

2007

Entrez Id: 9370
Gene Symbol: ADIPOQ
ADIPOQ
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.400 GeneticVariation LHGDN The adiponectin rs17300539 G>A variant and nephropathy risk. 18974768

2008

Entrez Id: 177
Gene Symbol: AGER
AGER
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 Biomarker LHGDN Distribution of the receptor for advanced glycation end products in the human male reproductive tract: prevalence in men with diabetes mellitus. 17588956

2007

Entrez Id: 197
Gene Symbol: AHSG
AHSG
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 Biomarker LHGDN Participants with fetuin-A levels within the highest tertile (> 0.97 g/L) had an increased risk of incident diabetes (13.3 cases/1000 person-years) compared with participants in the lowest tertile (< or = 0.76 g/L) (6.5 cases/1000 person-years) in models adjusted for age, sex, race, waist circumference, body weight, physical activity, blood pressure level, fasting glucose level, high-density lipoprotein cholesterol concentration, triglyceride concentration, and C-reactive protein level (adjusted hazard ratio, 2.41; 95% confidence interval, 1.28-4.53; P = .007). 18612115

2008

Entrez Id: 231
Gene Symbol: AKR1B1
AKR1B1
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 AlteredExpression LHGDN Upregulation of aldose reductase during foam cell formation as possible link among diabetes, hyperlipidemia, and atherosclerosis. 18451330

2008

Entrez Id: 208
Gene Symbol: AKT2
AKT2
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.040 GeneticVariation LHGDN Here we describe a mutation in the gene encoding the protein kinase AKT2/PKBbeta in a family that shows autosomal dominant inheritance of severe insulin resistance and diabetes mellitus. 15166380

2004

Entrez Id: 8862
Gene Symbol: APLN
APLN
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.070 Biomarker LHGDN Dysregulation of apelin might be involved in the mechanism of establishment of overt diabetes mellitus as well as associated atherosclerotic complications. 18484561

2008

Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.190 GeneticVariation LHGDN The frequency of the APOA5-1131C allele in DM patients was significantly higher than that of the control group (0.430 vs 0.296, P = 0.006). 17548321

2007

Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 GeneticVariation LHGDN Variant K of butyrylcholinesterase and types 1 and 2 of diabetes mellitus. 16429499

2005

Entrez Id: 632
Gene Symbol: BGLAP
BGLAP
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 AlteredExpression LHGDN Impaired gamma carboxylation of osteocalcin in elderly women with type II diabetes mellitus: relationship between increase in undercarboxylated osteocalcin levels and low bone mineral density. 15108065

2004

Entrez Id: 11132
Gene Symbol: CAPN10
CAPN10
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 Biomarker LHGDN A novel 111/121 diplotype in the Calpain-10 gene is associated with type 2 diabetes. 16721485

2006

Entrez Id: 847
Gene Symbol: CAT
CAT
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.400 GeneticVariation LHGDN The C111T polymorphism may implicate a very weak effect on blood catalase activity in different types of diabetes mellitus. 17577741

2007

Entrez Id: 847
Gene Symbol: CAT
CAT
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.400 GeneticVariation LHGDN Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus. 15800961

2005

Entrez Id: 6347
Gene Symbol: CCL2
CCL2
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 AlteredExpression LHGDN Our data suggest that elevated serum MCP-1 levels and increased monocyte CCR2, CD36, CD68 expression correlate with poor blood glucose control and potentially contribute to increased recruitment of monocytes to the vessel wall in diabetes mellitus. 16631114

2006

Entrez Id: 9332
Gene Symbol: CD163
CD163
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.020 GeneticVariation LHGDN Among DM individuals, the Hp 2-2 genotype was associated with a decrease in the percentage of PBMs expressing CD163 (2.3+/-0.5% versus 5.6+/-1.3%, P=0.01) and an increase in plasma soluble CD163 (3.0+/-0.2 microg/mL versus 2.3+/-0.2 microg/mL, P=0.04). 17525367

2007

Entrez Id: 948
Gene Symbol: CD36
CD36
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 AlteredExpression LHGDN Monocyte CD36 expression (by laser flow cytometry), plasma LDL diene conjugates, plasma LDL hydroxyoctadecadienoic acid-13 (a peroxisome proliferator activator receptor gamma agonist) were measured at 0, 2 and 4 h. Mean monocyte CD36 expression at baseline was 34% higher in the diabetes group (P=0.01), did not change during acute hyperglycaemia and plasma LDL conjugated diene concentration was the only variable directly related to CD36 expression (F=4.53; P=0.05; r=0.51). 12618277

2003

Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 GeneticVariation LHGDN Taq1B polymorphism of CETP gene on lipid abnormalities in patients with type II diabetes mellitus. 15138631

2004

Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.460 GeneticVariation LHGDN Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus. 17013908

2006

Entrez Id: 1401
Gene Symbol: CRP
CRP
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 AlteredExpression LHGDN Previous epidemiologic studies have demonstrated a positive association between serum C-reactive protein (CRP) level and diabetes mellitus. 18924263

2008

Entrez Id: 1401
Gene Symbol: CRP
CRP
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 Biomarker LHGDN The association of C-reactive protein with an oxidative metabolite of LDL and its implication in atherosclerosis. 17261875

2007

Entrez Id: 1559
Gene Symbol: CYP2C9
CYP2C9
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.040 GeneticVariation LHGDN Patients with diabetes mellitus who are carriers of a CYP2C9*3 allele require lower doses of tolbutamide to regulate their serum glucose levels compared to patients with the wild-type genotype. 17597710

2008