SNPMiner Trials by Shray Alag


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Report for SNP rs7903146

Developed by Shray Alag, 2020.
SNP Clinical Trial Gene

There are 8 clinical trials

Clinical Trials


1 The Role of Newer and Traditional Risk Factors in the Development, Extent and Manifestation of Coronary Artery Disease

In the present study the investigators will measure the extent of coronary artery disease via coronary angiography and the correlating risk factors.

NCT01585948 Patients Undergoing Coronary Angiography
MeSH:Coronary Artery Disease Myocardial Ischemia Coronary Disease
HPO:Coronary artery atherosclerosis Myocardial infarction

The incidence, extent and clinical manifestation of coronary artery disease and the circulating levels of hs-CRP, adipokines and RAGEs.. To associate the incidence, extent and clinical manifestation of coronary artery disease with systemic inflammatory status assessed by hs-CRP levels, circulating adipokines (adiponectin, resistin) and the receptors of advanced glycation end products (sRAGE and esRAGE).. TCF7L2 gene polymorphims and the incidence and extent of coronary artery disease.. To associate the incidence, extent and clinical manifestation of coronary artery disease with the rs7903146 single nucleotide polymorphism of TCF7L2 gene, that has been strongly associated with diabetes mellitus development.. Inclusion Criteria: - Any subject eligible for coronary angiography with or without known CV disease for clinical reasons.

Primary Outcomes

Description: We will investigate the incidence, extent and clinical manifestation of coronary artery disease in diabetics and non-diabetics undergoing coronary angiography for clinical reasons.

Measure: The incidence and extent of coronary artery disease between diabetics and non-diabetic patients.

Time: Up to four years on average.

Secondary Outcomes

Description: To associate the incidence, extent and clinical manifestation of coronary artery disease with classic demographic risk factors (such as smoking, alcohol consumption, physical exercise, arterial hypertension, family history of diabetes mellitus or coronary artery disease) and common biochemical risk factors (such as fasting glucose levels, urea, creatinine, HbA1c%, uric acid, total cholesterol, HDL, LDL, triglycerides, VLDL, glomerular filtration rate - GFR).

Measure: The incidence and extent of coronary artery disease via coronary angiography scores and related biochemical and demographical risk factors.

Time: Up to 4 years on average.

Description: To associate the incidence, extent and clinical manifestation of coronary artery disease with systemic inflammatory status assessed by hs-CRP levels, circulating adipokines (adiponectin, resistin) and the receptors of advanced glycation end products (sRAGE and esRAGE).

Measure: The incidence, extent and clinical manifestation of coronary artery disease and the circulating levels of hs-CRP, adipokines and RAGEs.

Time: Up to 4 years on average.

Description: To associate the incidence, extent and clinical manifestation of coronary artery disease with the rs7903146 single nucleotide polymorphism of TCF7L2 gene, that has been strongly associated with diabetes mellitus development.

Measure: TCF7L2 gene polymorphims and the incidence and extent of coronary artery disease.

Time: Within a maximum period of 4 years.

2 Evaluation of the Enteroinsular Axis in Cystic Fibrosis

Cystic fibrosis related diabetes (CFRD) is associated with worse CF-relevant outcomes. The mechanisms underlying CFRD development are not fully understood, but recent evidence suggests Type 2 Diabetes Mellitus (T2DM) mechanisms may be involved and may involve incretins (gut secreted hormones that augment insulin secretion in response to a nutrient load). This study will examine the prevalence of Genome wide association study (GWAS)-implicated T2DM alleles (including TCF7L2) across the spectrum of glucose abnormalities in CF and will use this information to compare incretin and insulin secretion in non-diabetic children and adults with high risk and low risk alleles.

NCT01852448 Cystic Fibrosis Genetic: Blood or Saliva Sample Collection Other: Glucose -potentiated arginine (GPA) stimulation tests
MeSH:Cystic Fibrosis Fibrosis

SECOND PHASE OF STUDY: Inclusion Criteria 1. Subjects age >8y 2. Diagnosis of Cystic Fibrosis 3. pancreatic insufficient 4. negative urine pregnancy test at enrollment 5. TCF7L2 rs7903146 genotype of T/T or C/C 6.

Primary Outcomes

Description: To examine the prevalence of GWAS-implicated T2DM alleles (including TCF7L2) across the spectrum of glucose abnormalities in children and adults with CF.

Measure: Blood sample for DNA to genotype TCF7L2 and about 10 other GWAS-implicated T2DM genes.

Time: 1 day

Secondary Outcomes

Description: Pancreatic ß-cell function will be evaluated using the GPA test which can be used to measure β-cell secretory capacity and sensitivity to glucose.

Measure: Glucose-Potentiated Arginine Stimulation Test (GPA test)

Time: 1 day

Other Outcomes

Description: Incretin and insulin secretion as well as glucose tolerance will be assessed using the MMTT.

Measure: Mixed Meal Tolerance Testing (MMTT)

Time: 1 day

3 Pathogenesis of Youth Onset Type 2 Diabetes and Prediabetes

Type 2 Diabetes (T2D) in obese youth is often preceded by a prediabetic state called: Impaired Glucose Tolerance (IGT), which is associated with a pre-existing defect in insulin secretion. This study intends to determine if genetic factors are associated with defects in insulin secretion, the incretin system and hepatic insulin resistance in obese adolescents. The long-term goal of this study is to generate information on both the genetics as well as the pathophysiology of Type 2 Diabetes in Youth, which ultimately might guide the investigators towards better preventive and treatment avenues.

NCT03195400 IGT - Impaired Glucose Tolerance T2D Diagnostic Test: Oral Glucose Tolerance Test Diagnostic Test: Hyperglycemic Clamp Diagnostic Test: Isoglycemic Intravenous Glucose Test Diagnostic Test: Hyperinsulinemic Euglycemic Clamp and 2H20
MeSH:Prediabetic State Glucose Intolerance

To delineate the effects of TCF7L2 rs7903146 on functional Beta-Cell Capacity in obese adolescents with Impaired Glucose Tolerance (IGT) and pre-IGT.

Aim 2. To examine the functional effect of the rs7903146 variant in the TCF7L2 gene on a) incretin effect in obese adolescents with IGT and pre-IGT.

Aim 3. To determine the functional effects of TCF7L2 rs7903146 SNP on hepatic glucose fluxes in obese adolescents with IGT and pre-IGT.

Primary Outcomes

Description: An oral glucose tolerance test will be performed to assess glucose tolerance status to determine if subjects are pre-IGT or IGT

Measure: Glucose tolerance status

Time: Baseline

Description: DNA screening to measure whether subject is CC or TT genotype

Measure: Genotype

Time: Baseline

Description: AIRmax stimulation test during the hyperglycemic clamp to ascertain the maximal acute insulin response (AIR) to arginine, which is a measure of functional beta cell capacity.

Measure: Beta cell capacity

Time: Baseline

Description: Subjects will undergo the IsoIVGT test with GLP-1 measurements to measure the incretin effect

Measure: Incretin effect

Time: 3weeks to 1 month post Baseline testing

Description: The AIRmax stimulation test during the hyperglycemic clamp will be repeated at 2 years to determine if genotype TCF7L2 contributes to worsening in beta cell function longitudinally

Measure: Beta cell function (longitudinally)

Time: 2 years post Baseline

Description: Measurements from the Hyperinsulinemic Euglycemic Clamp/ 2H20 Study will be used to assess insulin effects on hepatic glucose production and glycerol kinetics isotopes and the deuterium enrichment at carbons 2 and 5 (C2 and C5) of plasma glucose providing information on glucose fluxes

Measure: Hepatic glucose fluxes

Time: 2 months post baseline testing

4 A Phase I Placebo-controlled Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Globalagliatin Hydrochloride After Multiple Ascending Doses in Patients With Type 2 Diabetes Mellitus

This is a phase I placebo-controlled study to assess safety, tolerability, pharmacokinetics and pharmacodynamics of Globalagliatin Hydrochloride (SY-004) after Multiple Ascending Doses in patients with Type 2 Diabetes Mellitus (T2DM).

NCT03414892 Hyperglycaemia (Diabetic) Type 2 Diabetes Mellitus Drug: Globalagliatin Hydrochloride Drug: Placebo
MeSH:Diabetes Mellitus Diabetes Mellitus, Type 2 Hyperglycemia
HPO:Diabetes mellitus Hyperglycemia Postprandial hyperglycemia Type II diabetes mellitus

Compared with placebo, the mean changes of post-prandial blood glucose from baseline at D7,D14,D21 and D28.. genetic: TCF7L2 ( Transcription factor 7-like 2) rs7903146 and GCKR (glucokinase regulatory protein) rs780094 ).

The genetic(TCF7L2 rs7903146 and GCKR rs780094)effects on response of SY-004 in T2DM patients.. the changes of GA (Glycated albumin) from baseline.

Primary Outcomes

Description: Compared with placebo, the mean change in glucose AUC from baseline at D28.

Measure: the mean change in glucose area under curve (AUC) from baseline.

Time: 28 days

Secondary Outcomes

Description: Compared with placebo, the fasting plasma glucose from baseline at D7,D14,D21 and D28.

Measure: the fasting plasma glucose from baseline

Time: 7, 14, 21, 28 days

Description: Compared with placebo, the changes of MMTT (mixed-meal tolerance test) results from baseline at D28

Measure: the changes of MMTT (mixed-meal tolerance test) results from baseline

Time: 28 days

Description: Compared with placebo, the mean changes of average 7-points blood glucose profiles from baseline at D7,D14,D21 and D28.

Measure: the mean changes of average 7-points blood glucose profiles from baseline

Time: 7, 14, 21, 28 days

Description: Compared with placebo, the mean changes of average 14-points blood glucose profiles from baseline at D7,D14,D21 and D28.

Measure: the mean changes of average 14-points blood glucose profiles from baseline

Time: 7, 14, 21, 28 days

Description: Compared with placebo, the mean changes of post-prandial blood glucose from baseline at D7,D14,D21 and D28.

Measure: the mean changes of post-prandial blood glucose from baseline

Time: 7, 14, 21, 28 days

Other Outcomes

Description: The genetic(TCF7L2 rs7903146 and GCKR rs780094)effects on response of SY-004 in T2DM patients.

Measure: genetic: TCF7L2 ( Transcription factor 7-like 2) rs7903146 and GCKR (glucokinase regulatory protein) rs780094 )

Time: 28 days

Description: Compared with placebo, the changes of GA (Glycated albumin) from baseline at D28.

Measure: the changes of GA (Glycated albumin) from baseline

Time: 28 days

5 The TCF7L2 Gene: Nutrigenomics and Dietary Prevention of Type 2 Diabetes

Nutrients and chemicals in food are able to regulate expression of genetic elements. Gene-nutrient interaction in response specific diets can increase an individual's risk, shifting the individual from health toward the development of chronic disease. The Transcription Factor 7 Like 2 (TCF7L2) gene may either put individuals at risk for or protect from Type 2 diabetes mellitus in the presence of certain foods. The main purpose of this four-week study is to examine diet-induced gene-nutrient interaction, with a focus on glucose, insulin, inflammation (CRP) and the plasma metabolome in individuals who have either the CC or the TT form of the rs7903146 single nucleotide polymorphism (SNP) (C/T) within the TCF7L2 gene. The (2) one-week study diets, one Mediterranean diet (MedDiet) based and the other low-fat based will be separated by a (1) week return to a regular habitual diet.

NCT03458494 Type2 Diabetes Glucose, High Blood Other: Mediterranean Diet Other: Low-fat diet
MeSH:Diabetes Mellitus, Type 2 Hyperglycemia
HPO:Hyperglycemia Postprandial hyperglycemia Type II diabetes mellitus

The main purpose of this four-week study is to examine diet-induced gene-nutrient interaction, with a focus on glucose, insulin, inflammation (CRP) and the plasma metabolome in individuals who have either the CC or the TT form of the rs7903146 single nucleotide polymorphism (SNP) (C/T) within the TCF7L2 gene.

Plasma glucose levels (mg/dl) will be measured in the fasting state during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

Fasting plasma insulin levels (pmol/l) will be measured in the fasting state during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

The response of plasma metabolites to the Mediterranean and low-fat diets diet) will be measured using ultra high-performance liquid chromatography/tandem accurate mass spectrometry (UHPLC/MS/MS) during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

Fasting plasma concentrations of VLDL in mg/dl, assessed by proton nuclear magnetic resonance (NMR) spectroscopy will be measured during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

Fasting plasma concentrations of LDL in mg/dl, assessed by proton nuclear magnetic resonance (NMR) spectroscopy will be measured during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

Fasting plasma concentrations of HDL in mg/dl, assessed by proton nuclear magnetic resonance (NMR) spectroscopy will be measured during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

Plasma C-reactive protein (mg/dl) will be measured in the fasting state during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP.

The rs7903146 single nucleotide polymorphism (SNP) (C/T) within the TCF7L2 gene is the most replicated T2D-associated SNP.

For this purpose, a four-week study will be conducted to examine diet-induced gene-nutrient interaction, with a focus on glucose, insulin, and inflammation (CRP) in individuals who have either the CC or the TT form of the rs7903146 single nucleotide polymorphism (SNP) (C/T) within the TCF7L2 gene.

Primary Outcomes

Description: Plasma glucose levels (mg/dl) will be measured in the fasting state during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: Glucose

Time: 1 week per intervention arm

Secondary Outcomes

Description: Fasting plasma insulin levels (pmol/l) will be measured in the fasting state during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: Insulin

Time: 1 week per intervention arm

Description: The response of plasma metabolites to the Mediterranean and low-fat diets diet) will be measured using ultra high-performance liquid chromatography/tandem accurate mass spectrometry (UHPLC/MS/MS) during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: Metabolomics

Time: 1 week per intervention arm

Description: Fasting plasma concentrations of VLDL in mg/dl, assessed by proton nuclear magnetic resonance (NMR) spectroscopy will be measured during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: Very low density lipoproteins (VLDL)

Time: 1 week per intervention arm

Description: Fasting plasma concentrations of LDL in mg/dl, assessed by proton nuclear magnetic resonance (NMR) spectroscopy will be measured during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: Low-density lipoproteins (LDL)

Time: 1 week per intervention arm

Description: Fasting plasma concentrations of HDL in mg/dl, assessed by proton nuclear magnetic resonance (NMR) spectroscopy will be measured during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: High-density lipoproteins (HDL)

Time: 1 week per intervention arm

Description: Plasma C-reactive protein (mg/dl) will be measured in the fasting state during each one of the intervention phases (the Mediterranean and low-fat diets) in participants with the TT and CC genotypes at the TCF7L2 rs7903146 SNP

Measure: CRP

Time: 1 week per intervention arm

6 Transcription Factor 7 Like 2 Gene Polymorphism and Advanced Glycation End Products as Risk Factors for Diabetic Nephropathy

1. To study genotypic distribution of the TCF7L2 gene polymorphism in Diabetic nephropathy. 2. To assess level of AGEs and Insulin in patients with Diabetic nephropathy. 3. To study correlation between polymorphism of the TCF7L2 gene, AGEs, Insulin and clinical characteristics in patients with diabetic nephropathy

NCT04084886 Diabetic Nephropathies
MeSH:Kidney Diseases Diabetic Nephropathies
HPO:Abnormality of the kidney Nephropathy

TCF7L2 rs7903146 polymorphism is more associated with T2DM which mediated by decreased insulin secretion associated with defects in insulin processing, reduced effects of glucagon-like peptide-1, increased hepatic glucose production and insulin resistance.

Primary Outcomes

Description: find a link between genetic polymorphism of TCF7L2 and the risk of developing nephropathy in diabetic patients. Nephropathy is defined Albumin/creatinine ratio > 30 mg/gm creat.

Measure: value of the odds ratio associated with the relationship between a polymorphism TCF7L2 gene and the occurrence of diabetic nephropathy

Time: one year

Description: the prevalence of TCF7L2, in the diabetic patient, and compared to the values found in the general population. the TCF7L2 genes will be evaluated by PCR-RFLP

Measure: Number of patients with genotype TCF7L2 by PCR

Time: 5 years

7 Effects of an Exercise Program on Physical Functionality and Frailty in Type 2 Diabetic Older Adults. Role of Circulating Concentration of PDEF and Differential Genes

Diabetes is a disease with a high impact in the population older than 65 years old. Some indications suggest that diabetes in the old age aggravate the negative effects of ageing, as the loss of muscle mass and strength, bringing the patients to a situation of vulnerability and elevated risk of disability and death known as "frailty syndrome". Recently, scientists have observed that if older population train with musculation machines emphasising the muscular power, it is possible to have an impact on a disminution of frailty and restoring the physical functionality. This project deeps in the physiological and molecular mechanisms that underlie to improvements in the frail diabetic patients.

NCT04332302 Diabetes Mellitus, Type 2 Frailty Other: Power resistance training
MeSH:Diabetes Mellitus, Type 2 Frailty
HPO:Type II diabetes mellitus

Circulating level of PDEF assessed by Western Blot.. Genotyping of TCF7L2 (rs7903146).

Primary Outcomes

Description: Percentage

Measure: Change from Baseline Glycosylated Hemoglobin (Hemoglobin A1c) at 12 weeks

Time: 0 and 12 weeks.

Description: Percentage

Measure: Change from Baseline Homeostasis Model Assessment - Beta cells (HOMA2-B) at 12 weeks

Time: 0 and 12 weeks.

Description: Percentage

Measure: Change from Baseline Homeostasis Model Assessment - Insuline Resistance (HOMA2-IR) at 12 weeks

Time: 0 and 12 weeks.

Description: Level of frailty assessed by Fried Criteria. Intermediate or prefrail: 1 or 2 criteria present. Positive for frailty phenotype: ≥3 criteria present.

Measure: Change from Baseline Fried frailty score at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: Level of functional capacity assessed by the test SPPB. Scores 0-3: Very low physical function; Scores 4-6: Low physical function; Scores 7-9: Moderate physical function; Scores 10-12: High physical function

Measure: Change from Baseline Functional capacity at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: Level of disability assessed by the Barthel test. A participant scoring 0 points would be dependent in all assessed activities of daily living, whereas a score of 100 would reflect independence in these activities.

Measure: Change from Baseline Disability at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: Level of functional mobility assessed by the Lawton test. A scale from 0 to 8, expressing higher scores better levels of independence.

Measure: Functional mobility at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: Watts.

Measure: Change from Baseline Muscular power at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: Load (kg).

Measure: Change from Baseline Levels of strength at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: g/cm3

Measure: Change from Baseline Bone Mineral Density at 12 weeks

Time: 0 and 12 weeks.

Description: Circulating level of PDEF assessed by Western Blot.

Measure: Change from Baseline Pigment Epitelium Derived Factor (PEDF) at 12 weeks

Time: 0 and 12 weeks.

Description: Assessed by Real-time PCR.

Measure: Genotyping of TCF7L2 (rs7903146)

Time: 0 week.

Description: Assessed by Real-time PCR.

Measure: Genotyping of TM6SF2 (rs10401969)

Time: 0 week.

Description: Assessed by Real-time PCR.

Measure: Genotyping of HLA (rs2854275)

Time: 0 week.

Secondary Outcomes

Description: Kg by square meters.

Measure: Change from Baseline Body Mass Index at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: Meters.

Measure: Change from Baseline Waist circumference at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: mmHg.

Measure: Change from Baseline Blood pressure (systolic and diastolic) at 6 and 12 weeks

Time: 0, 6 and 12 weeks.

Description: mg/dL.

Measure: Change from Baseline Concentration of Triglycerides at 12 weeks

Time: 0 and 12 weeks.

Description: mg/dL.

Measure: Change from Baseline Concentration of Total Cholesterol at 12 weeks

Time: 0 and 12 weeks.

Description: mg/dL.

Measure: Change from Baseline Concentration of HDL Cholesterol at 12 weeks

Time: 0 and 12 weeks.

Description: mg/dL.

Measure: Change from Baseline Concentration of LDL Cholesterol at 12 weeks

Time: 0 and 12 weeks.

Description: Level of quality of life assessed by the test EuroQoL index, EQ-5D-5L. The score is the time trade-off (TTO). Scale from 11111 to 55555 being the higher the best health related quality of life.

Measure: Change from Baseline Subjective level of quality of life at 12 weeks

Time: 0 and 12 weeks.

Description: Accelerometry, counts/min.

Measure: Change from Baseline Physical activity at 12 weeks

Time: 0 and 12 weeks.

Description: Level of balance assessed in a force platform. Newtons.

Measure: Change from Baseline Balance at 12 weeks

Time: 0 and 12 weeks.

8 The Association Between TCF7L2 rs7903146, Diet and Type 2 Diabetes Mellitus Risk

This study investigates the association of genetic effects of rs7903146 and dietary intake on type 2 Diabetes Mellitus (T2DM) risk in a healthy population. T2DM risk was assessed through glycated haemoglobin (HbA1c) concentration in 73 subjects. Dietary intake was assessed using a validated food frequency questionnaire (FFQ).

NCT04446754 Health Behavior Blood Glucose, High Diet Habit Genetic Predisposition
MeSH:Diabetes Mellitus Diabetes Mellitus, Type 2 Hyperglycemia Disease Susceptibility Genetic Predisposition to Disease
HPO:Diabetes mellitus Hyperglycemia Postprandial hyperglycemia Type II diabetes mellitus

The Association Between TCF7L2 rs7903146, Diet and Type 2 Diabetes Mellitus Risk.

The Genetic Effects of rs7903146 and Dietary Intake on Type 2 Diabetes Mellitus Risk in a Healthy Population This study investigates the association of genetic effects of rs7903146 and dietary intake on type 2 Diabetes Mellitus (T2DM) risk in a healthy population.

salivary (1-ml) DNA for genotype TCF7L2 gene (rs7903146 SNP).

Genome-wide association studies identify the transcription factor 7-like 2 (TCF7L2) rs7903146 (C/T) gene as one of the most important associated with T2DM-risk.

However, most studies associating genetic effects of dietary intake on rs7903146 and T2DM-risk utilised volatile instantaneous measures of glucose(5) and focussed on individual macronutrients.

Understanding the association of rs7903146 and overall macronutrient intake using a stable blood homeostasis marker may provide a fuller insight into T2DM-risk.

Primary Outcomes

Description: salivary (1-ml) DNA for genotype TCF7L2 gene (rs7903146 SNP)

Measure: DNA

Time: 3 months

Description: capillary blood collected (via the ears or fingers) using a Microvette CB Lithium Heparin tube (SARSTEDT AG & C0., Nümbrecht, Germany)

Measure: Hba1c

Time: 3 months

Description: Dietary intake estimated using The European Prospective Investigation into Cancer and Nutrition (EPIC)-Norfolk (food frequency questionnaire)

Measure: Diet intake

Time: 3 months

Secondary Outcomes

Description: Body weight in kg measured by bioelectrical impedance analysis using a 0.5kg clothing offset

Measure: Body weight

Time: 3 months

Description: Waist measurement was taken midway between iliac crest and lowest rib

Measure: Waist

Time: 3 months

Description: Hip circumference was measured over the greater trochanters at their widest point (nearest 0.1cm)

Measure: Hip

Time: 3 months

Description: Subject height was recorded to the nearest 0.1-cm via stadiometer

Measure: Height

Time: 3 months

Description: Assessed through Physical Activity Readiness Questionnaire (PAR-Q)

Measure: Physical activity

Time: 3 months

Description: Measured in kg and percentage (%) measured by bioelectrical impedance analysis

Measure: Fat mass

Time: 3 months

Description: Measured in kg and percentage (%) measured by bioelectrical impedance analysis

Measure: Lean mass

Time: 3 months


HPO Nodes


HP:0000819: Diabetes mellitus
Genes 528
PLIN1 ABCC8 CASR PRSS1 ELMO2 LIMK1 SOX3 PDX1 SLC2A2 PDX1 PDX1 HNF1A HYMAI SPINK1 GNAS COX1 REEP6 PRPF6 STAT3 ND2 SPINK1 KLF11 KIAA1549 WRN KCNJ11 LIG4 ARL6 EDA2R ELN KCNJ11 FOXH1 WFS1 PWAR1 HMGA1 RRM2B GPR35 LIPE PRSS2 WRAP53 STAT3 HAMP TRNC PPP1R3A ATM PAX4 MMP14 RDH12 CP ZNF408 BRAF TRNK TRNL1 ND4 TTC7A NDUFS3 NDUFV2 AEBP1 SPINK1 PSTPIP1 HMGA2 LRP6 LIPE PALLD TCF4 TRNQ CDKN2A TRNK TTPA INS NDUFB11 GJA1 PAX4 CEL PTCH1 PRSS2 XRCC4 BSCL2 SLC7A14 LMNB2 BBS2 PALB2 INSR TIMMDC1 NDUFAF8 NDUFB10 SIX3 AGBL5 WRN GAS1 COX3 PLAGL1 TREX1 PDX1 SMAD4 SLC19A2 LMNA CORIN PDE8B IL6 BEST1 CRX PRKAR1A WFS1 TGIF1 MST1 NDN GCK NDUFS6 CFTR RETN FOXRED1 RBP3 CNGB1 LIPC ZNF513 GPD2 UBR1 NDUFAF4 WFS1 FOS ABCC8 CISD2 TRNQ IFT140 HFE HYMAI IRS1 HNF4A RNASEH2B FGF8 ARMC5 APOA5 LEMD3 DCAF17 PPARG EDA TP53 DCAF17 AGPAT2 GLRX5 OFD1 TINF2 TRNS1 MAGEL2 APPL1 MAPK8IP1 ARL6 GTF2IRD1 PPARG TRNH NDUFS8 NDUFAF3 TDGF1 CDHR1 SNORD115-1 ZFYVE26 TMEM126B CP IGF2BP2 PTPN22 CAV1 CNGA1 DHDDS RFC2 KIZ MEN1 HBB XRCC4 TRNW PRPF8 FOXP1 ABCC8 LMNA NEK2 SNRPN LMNA MAK FGFR1 MMP2 CLIP2 GCK BBS2 HESX1 KCNJ11 ZFP57 PRKACA GLIS3 HNF1A VANGL1 NDUFS2 NEUROD1 NDUFV1 ABCA4 C8ORF37 TRNS2 DMPK LEP BRCA1 ADAR IFIH1 GCK CERKL NRL COX1 CTRC INS GJB4 WFS1 AIP RAC1 GJB3 SBDS ND5 PTF1A LMNA ITCH PROM1 PRSS1 PIK3R1 NEUROD1 HBB GCK CISD2 ND6 IMPDH1 TERT LEPR ALMS1 BRCA2 PRCD BMP2 CAT ELN KCNJ11 TRNL1 PNPLA6 PAX4 NDUFAF2 FOXP3 GATA6 PRPF4 PLAGL1 NODAL HNF1A CA4 TUB CAV1 RNASEH2C TTC8 POLR3A PIK3R1 NR2E3 HNF4A NDUFB3 POLA1 PWRN1 PRKACA PCARE AR INSR COX2 STOX1 IL2RA PDE4D BSCL2 HGSNAT CTNS DNAJC3 IGF1R KLF11 IPW GJA1 GCK DLL1 PEX10 HNF1B CTC1 DNM1L ND6 ARHGEF18 RP1 SLC25A4 NSMCE2 TRNL1 CLRN1 AHR STAT1 NDUFS7 ND1 OPA1 DNAJC3 NDUFAF5 ABCC8 AMACR NOP10 EIF2AK3 MKKS ABCC8 PPARG TRNF ALMS1 GUCA1B PDE6G CTNNB1 CCDC28B ND3 INSR LHX1 CDON APOE HNF4A CPA1 SLC29A3 DMXL2 TOPORS IDH3B NEUROG3 HFE SCAPER ND1 ARL2BP PDE6B BLK TRNE HNF1B HNF1B SAMHD1 PEX6 NEUROD1 NPAP1 COX3 GPR101 CNOT1 EIF2S3 PRPF3 IL2RA HLA-DRB1 ZIC2 NDUFS1 SPATA7 TRMT10A BLM CYP19A1 FUZ PRKAR1A CYTB PTRH2 LMNA TRNV FBN1 MLXIPL ZFP57 AIP KCNJ11 KCNJ11 KRAS FLT1 FXN PLIN1 INS WFS1 TWNK RPGR HNF4A DISP1 BLK PNPLA2 POLG MC4R POLG2 BAZ1B NSMCE2 RTEL1 TRNS2 PROKR2 ND1 PPARG NDP AHI1 SOX2 SAG SLC29A3 HERC2 UBR1 IER3IP1 KCTD1 ABCC8 CFTR CNBP CAVIN1 SLC12A3 MKRN3-AS1 FOXP3 SLC16A2 TWNK PROK2 PCNT EYS COX2 TRNF RGR GTF2I STAT1 PAX4 DHX38 IDH3A ZMPSTE24 PPP1R15B XRCC4 PTPN1 CLCNKB HJV ERGIC1 LEPR RHO SHH NPM1 ZBTB20 ATM NDUFA6 INS AIRE RP9 PTF1A TCF7L2 KLHL7 DNAJC21 AKT2 RLBP1 AKT2 TP53 PLCD1 NKX2-5 CDH23 NDUFS4 FOXC2 HNF1A LMNA LMNA MTNR1B HNF1A TRNW MKRN3 SRP54 GLI2 NDUFA1 IRS2 NDUFA11 TERC USH2A CTRC POC1A RP2 ITPR3 MOG PDX1 IFT172 APPL1 ARNT2 ATP6 ND5 SNORD116-1 CIDEC BBS1 NDUFAF1 PDE11A FAM161A RPE65 PDE4D PARN INS PRPH2 ROM1 TBL2 OTX2 POLD1 MAFA HNF4A KDSR CEP19 GCK SEMA4A ARL3 CEL LRAT HNF1A GATA6 TULP1 SNRNP200 IFT88 AGPAT2 TRNE FSCN2 TRNS1 NDUFB9 GATA3 STUB1 ENPP1 MERTK RNASEH2A KCNJ11 HLA-DQB1 NHP2 FXN IMPG2 SUFU POMGNT1 EIF2AK3 SARS2 HYMAI GCK TKT USB1 ZMPSTE24 PRPF31 HNF1B PDX1 SLC30A8 PNPLA2 SLC19A2 DKC1 PDE6A USP8 EFL1 FGFR1 CRB1 PEX1 NUBPL
HP:0000077: Abnormality of the kidney
Genes 1719
WT1 SMARCAL1 SLC34A1 SDCCAG8 KCNJ1 MICOS13 INSR ELP1 IL17F AMMECR1 KCNAB2 NF1 STIL CASP10 KCNJ11 CC2D2A GPR35 MYLK TMEM138 DYNC2LI1 RAG2 SLC9A3R1 NSD1 CYP11B2 GNA11 KRT17 SF3B4 GLA WDR35 CC2D2A CCR1 CEP41 CCR6 NDUFS3 NUP133 ANOS1 PIK3CA MOCOS INS GBA CDK6 CFI FGFR3 TRNT XRCC4 CLCNKB BSCL2 PIEZO2 BCOR LMNB2 IFT43 PHYH SLX4 DICER1 INSR OCLN KMT2D NUP93 BBS4 ABCG8 BUB3 DHODH LRP5 AQP2 ATRX AKT3 SCARB2 ABCA12 GLA FANCI FGFR1 BRF1 RAI1 RAB18 FOXF1 EDNRB CLCN5 FLRT3 SLC25A11 EVC2 SI TBC1D20 DICER1 WNT4 DICER1 WT1 NUP133 PHC1 SOX9 FGF8 SALL4 LZTFL1 LTBP4 IFT80 UFD1 NDUFAF3 TDGF1 TMEM126B SDHD SEC61A1 LPIN2 IRF5 PTPRJ FANCE KITLG WIPF1 DLST COX6B1 HBB GANAB PKHD1 FGFR2 DCC COX14 ATP7B EP300 POU3F4 FREM1 SLC5A2 COL4A3 KIF14 EXTL3 DEAF1 COL4A3 PYGM WDPCP SLC34A1 HESX1 PIGP WAS ZFP57 IL23R FANCL CFH DIS3L2 PEX12 NCAPD3 DCHS1 ITGA3 SMAD4 MAFB NDUFV1 CFH PEX5 USP8 PCK1 TGM1 CFHR1 CREBBP PLG PKD1 PREPL IRAK1 ATRX ND6 AKT1 DNMT3A NSD2 C8ORF37 PEX2 MAD2L2 WDR19 PPP2R1A FOXP3 APC TRNL1 NODAL MSH6 DYNC2H1 KCNA1 PRDX1 PEX13 SMARCE1 ALPL NEK1 MEOX1 NDUFB3 PBX1 KCNJ10 CDKN1C PTEN RFWD3 PIGN PIGT KCNQ1OT1 COL5A2 NDUFAF3 H19 LEMD3 FGA PYGL MITF CHRM3 FAT4 TAPT1 MMUT DLL1 C3 KIF1B PALB2 NDUFS7 PDE6D SDHD CAMKMT WNT4 ACSL4 RTTN VHL ABCC8 KEAP1 SC5D SDHB STXBP1 STRADA EIF2AK3 NPHP3 MKKS FKRP ABCC6 TACO1 MCPH1 NEK8 SMARCD1 TRNF ALMS1 C1QA CDK5RAP2 TRPC6 CCDC28B ND3 PIGL C4A AVPR2 APOE AURKA AMER1 VHL FGFR3 CYP4F22 PRDM16 MRPS22 AP2S1 TP53 SLC7A9 ITGB4 COLEC11 PRKCSH APRT GDNF MBTPS2 RREB1 IFT140 TMEM237 CAD TSC2 NPHP3 PAH C1QBP WASHC5 SCN2A PC TMEM216 CYB561 TMCO1 MMUT PEX19 CFTR NDUFS1 ITGA2 NXN BBS12 LMOD1 MKS1 COL4A3 SOX10 NUP205 ZBTB16 COA8 SRY DYNC2I1 KCNJ11 FLT1 SMARCB1 RECQL4 PPP2R3C WT1 POR FAS MMACHC MBTPS2 DISP1 ROBO2 PDGFRL AXIN2 FLNA PTPN22 ASPM NRAS KYNU NAA10 TLR2 CENPF CCBE1 CDC73 WT1 GATA4 WDPCP SLC2A9 F8 FGFR2 TREX1 UBR1 GBA EBP KCTD1 TRIM28 GP1BB BBS12 SBDS SLC12A3 MAP11 REN TNXB RAD51 EMP2 NRIP1 ATN1 COL4A4 HNF1B PEX11B KLLN WT1 FH SLC17A5 ADAT3 C3 LIG4 TRNS1 IFT27 INPP5E FGFR2 EXT2 KYNU MAP2K2 UMOD APC CLCNKB ESCO2 CDC73 BRAF STAT4 PALB2 BBS7 PIGO HRAS SNAP29 TBX22 COL4A1 PLCD1 ADAMTS3 PIGL RAD51C CDH23 NDUFS4 FOXC2 LMNA SDHB SOX9 CDC42 GLMN SLC3A1 TBX1 CD96 DPH1 PTPN12 OFD1 RPGRIP1L SETD5 CCDC22 APPL1 COL14A1 IL2RG COQ8B ALOX12B ND4 WDR19 SLC6A17 PIGW SERPINF2 HELLPAR HNF1A NR0B1 DMRT3 PEX6 COPB2 NDUFB9 WDR19 ITGA8 HLA-DRB1 TRNV NPHP4 CD46 HPRT1 TP63 IFT172 CACNA1D WDR19 BUB1B RPL11 WNT4 CCN2 FAT4 SLC30A9 ANTXR1 SLC34A3 KDM6A CFHR3 OSGEP NUBPL SMS DYNC2LI1 PIGY TMEM231 LIMK1 GRHPR MINPP1 PDX1 LPIN1 NARS2 MAGI2 AFF4 LYZ NPHP4 AMMECR1 ARL6 ELN NADK2 NUP160 CEP55 IFT27 POLE H19 GBE1 TSC1 FUT8 ALDH18A1 HABP2 TBX1 SALL4 WDR4 SAA1 ADGRG2 UMOD NSDHL ZNF592 CEP135 KANSL1 NDUFV2 KNL1 ERCC8 PLG ROR2 HMGA2 GPC4 TRNQ XYLT2 NLRP3 KMT2A DSTYK ITGA8 FOXI1 CA2 WDR4 MYD88 LMAN1 LRP2 PEX1 DZIP1L GCM2 NDUFB10 SIX3 FRAS1 GP1BB CORIN AGGF1 RPGRIP1L NOD2 NUMA1 RERE UQCC2 H19-ICR MASP1 B9D1 CTU2 AGTR1 FANCB SLC1A1 FIBP PIK3CA UBR1 TRIM28 FOS PTPRO CCDC141 WT1 CPLANE1 PUS3 PAX2 CCDC141 PTPN22 RAI1 SPP1 ARMC5 IGF2 LEMD3 TRAF3IP1 HLA-DPB1 TMEM216 DHDDS MEN1 LMX1B TRNS1 CSPP1 TMEM216 TRNH PIGV HGD PEX14 IL12A WT1 ERCC4 DMXL2 FCGR2B REST SGPL1 MOCS2 CAV1 CC2D2A BBS10 SRP54 DHCR24 ABCC8 ARNT2 PCK2 BBS9 CD2AP DNASE1L3 NABP1 PDE6D HPSE2 AR ALG1 SKIV2L COA3 G6PC CFI PDGFRB INF2 ENPP1 NEUROD1 LZTFL1 ARL6 C1QC UMPS DNAJB11 CTNS BRCA2 CEP55 STXBP1 NELFA CD151 COX1 TBX1 TBL1XR1 CCND1 NSUN2 PAX2 TRRAP RPGRIP1L RAD51C LMNA BRCA1 ATP7A PRTN3 CSPP1 WDR35 ZEB2 HOXD13 TCTN2 SNAI2 SASS6 ALMS1 ETFDH ELN FGFR2 PLVAP PNPLA6 SULT2B1 F10 SON WDR19 NUP107 FAT4 LCAT KCNQ1OT1 FGF17 PIK3C2A CAV1 STRA6 IL17RA COQ6 CDKL5 NSD1 BUB1 YAP1 ARL6 ABCC6 COX2 WNT4 RET STOX1 COX20 HPRT1 USP9X INTU HDAC4 SPECC1L PPM1B IARS1 CTNS PEX3 MGME1 FAS CCND1 H19-ICR ARX ODC1 HNF1B PEX2 HSD11B2 SON NPHP1 RAG1 PRCC CEP120 SCO1 PHGDH G6PC3 SLC36A2 FGFR1 IFT80 SEC63 RBM8A MYMK GDF6 MAP3K1 SRCAP CPT2 MDM2 WWOX RAB3GAP2 HOGA1 MYH11 PET100 GLI3 PML SLC29A3 GP1BA WDR11 SCNN1B HSPG2 FBLN5 SCNN1B TMEM231 ZNF148 FRAS1 BLK SDHC SEMA3E FANCF IFT140 TBX3 KCNJ10 CHD7 CC2D2A SHH TCTN2 LMX1B CPT2 CEP290 ZIC2 MYO5B PGK1 PLEC KAT6A VDR CCND1 FANCG PPP3CA FUZ NIPBL YY1 IL7R ITGA2B FBN1 COQ7 CDKL5 NLRP3 KIAA0753 APOE ALDOB LETM1 INS FANCI PIGN GABBR2 APC2 EYA1 PIGA ACP5 ZAP70 TPRKB BUB1 MCM5 TMEM231 EPAS1 SPECC1L TFE3 SIX5 RPGRIP1L TRIM8 ASXL1 ETFA SF3B4 ALOXE3 PKD2 TRNN SMO TSC2 FGF10 BAX THOC6 TRAF3IP2 CLCN5 CEP290 ZNF423 DPF2 RPGRIP1L VPS33A NOTCH2 SLC4A4 DACT1 KLLN GANAB INPP5E WT1 PRKAR1A LMX1B CEP83 LRP4 WDR62 ANKS6 WAS OCRL CASP10 PIGT CA2 DHCR7 B9D2 RASGRP1 POGZ ANTXR1 LDLRAP1 IGF2 TMEM67 TMEM237 KIF7 EHMT1 KIAA0753 GNB1 MLH3 NOTCH3 DACT1 HNF4A INVS PQBP1 SLC3A1 FLCN ITGB4 VIPAS39 RARB CEP290 GRIP1 GLI2 WDR73 TMEM127 KAT6B BBIP1 AAGAB PACS1 PIK3CA TP53RK NDUFAF1 FBXL4 PEX13 COL1A1 FLNA HMBS TREX1 DNASE1 NOTCH2 MAX WT1 GPC3 VAC14 KIF1B USF3 DNAJC21 CCNQ USP9X BBIP1 NBN CWC27 PEX3 C1QB CHD7 CD109 EIF2AK3 ENG TKT MBTPS2 CLEC7A APC TALDO1 BSND RPL26 CIT TRIP11 USP8 WDR73 PGM3 FGFR1 FLNA SOX18 GNB1 PROKR2 KMT2D GATM FGFR3 GLI3 BCS1L HAAO TSC2 LRP4 POMT1 FAN1 B4GAT1 ARID1B PTEN STK11 CLCN5 SOX9 GPC3 MEFV OSTM1 CTLA4 BRIP1 INSL3 HOGA1 ATRX GATA3 MED25 TTC37 SALL4 YAP1 FXYD2 CHD7 MTRR PEX1 REN ND4 GPC3 MSH3 NCAPG2 STX3 TRIM32 CFH GRHPR TCF4 ALG8 BCOR TRNK NPHS1 CFI SLC7A7 HRAS SETBP1 IRF2BP2 RAI1 SLC35A2 SLC37A4 TFAP2A PTCH1 SEMA3E PIGQ CHST14 RPGRIP1 CEP120 XDH PDSS2 KCNH1 GALNT3 CLDN16 PEX10 ESCO2 NUP107 WT1 WRN DVL1 GCM2 COX8A BRAF NRAS POU6F2 RAD21 C4A MNX1 CEP290 GREB1L IL6 FLCN INF2 CTNNB1 SLC25A20 FANCA DSTYK KLHL7 RET WFS1 MST1 PEX12 DSE NDUFS6 NPHS2 SLC2A2 MET RAB23 GEMIN4 SCNN1A XRCC2 KISS1R TMEM67 WDR19 OFD1 FAM20A NTNG1 B2M CRTAP OCRL PIK3R2 WNT5A ALX4 AGPAT2 HSD17B4 DCLRE1C NPHP1 PMM2 GTF2IRD1 ND5 NDUFS8 FANCB FAS GPKOW SLC22A12 PIGY CEP57 FANCM LDLR ERCC6 CPT1A GPC4 CTLA4 MUC1 HPSE2 DIS3L2 OFD1 SDHB CLIP2 GCK COG6 COMT POR DCDC2 SFTPC XYLT1 STAT4 SLC4A1 GP1BA RMRP SLITRK6 GLIS3 SIX1 ERAP1 MAFB NDUFS2 ENPP1 BICC1 CFHR5 PDSS2 HIRA DKC1 TBCK AKT1 NPHP1 PAX6 SRY WFS1 GNAO1 TMEM107 PGAM2 SEC23B DYNC2I2 CHRM3 CYP24A1 KIF14 MDH2 GSN PLA2G2A TBC1D24 HLA-B CYTB WNT3 MKS1 TTC8 PROKR2 TRNL1 SLC6A20 PAX4 IQCB1 MEFV TMEM67 BCS1L PLAGL1 PRKCD HNF1A ADAMTS13 ND3 ARL3 CEP164 SLC12A1 STRA6 ND6 CLDN19 KMT2A COL4A1 RPS26 TTC21B ACTG2 AGXT LAMB2 CILK1 BBS10 MKS1 ARID2 SLC7A7 KCNQ1 EYA1 GCK ERBB3 ACTN4 IFT122 ADA2 FGFR2 SRC PMM2 RET TRNL1 HDAC8 LIPN THOC6 SDR9C7 PIK3CA DHCR7 RAB3GAP1 TREX1 IL17RC NPHP1 IFT172 NDUFB8 VHL TCTN3 RECQL4 PEX16 MITF SETBP1 KRAS TFAP2A CLCNKA ATP6V0A4 CPLANE1 RNU4ATAC ZIC3 B3GLCT RAI1 SALL1 CDKN1B F2 BBS5 PUF60 GREB1L DHX37 ND1 SDHD SLC26A4 TXNL4A HS6ST1 MSH2 ALDOB TRNE ND1 LAGE3 COQ2 HNF1B ATP1A1 LMNA COX10 MKKS THBD F5 LRIG2 TRIM37 HLA-DRB1 ALG9 FOXE1 FANCC H19-ICR SLC6A19 LIG4 TCTN3 COG1 MAP3K7 TBX15 H19 CFB MECP2 MFSD2A FANCB HNF4A PKD1 FANCD2 LARGE1 ADCY10 ZIC3 ADA PLCE1 CEP63 B9D1 BAZ1B TRNS2 PAFAH1B1 PCSK9 BCOR LRP5 CLCNKB FREM1 POMT2 DYNC2LI1 SMOC1 APRT COL4A5 SDHD ARX COA8 ITGB3 ACTG1 CLPB FLCN CAVIN1 PIGA FLNA ARID1B NPHP4 JAG1 FAM20A MMUT FAH ZNF423 STAT1 IFNG SDCCAG8 TBX18 YWHAE MED25 FGFR3 DYNC2I2 GLIS2 HYLS1 TACR3 TTC21B RNU4ATAC NPHS1 PIGL NDUFA6 PIK3R2 AIRE SF3B4 NPHP3 MEFV PIGV FH DPH1 SMC1A PIK3CA KAT6B CEP164 HMOX1 MEFV PLCD1 PUF60 DIS3L2 BTNL2 SPART PGM3 DUSP6 KANK2 NDUFA1 PLD1 TBC1D24 CHD7 BBS1 NDUFA11 ALG9 CASR FLII JAM3 SMARCAL1 PNKP NSMF BBS1 EP300 LEMD3 GLI3 EXT2 TSC1 ARL6IP6 SERPINH1 AMMECR1 HIC1 C8ORF37 FOXF1 BAP1 NPHP1 GP1BB F8 GDF6 TRNK DYNC2I2 PEX7 GABRD ABCC6 AGPAT2 POU6F2 PEX10 WDR73 MARS1 CSPP1 FANCA ATRX CDC73 OFD1 CLDN19 KCNJ10 NUP133 SPINK5 SLX4 HPRT1 IFIH1 SNRPB PRKCD SETD2 RPS19 SCN1B FCGR2A LAGE3 SLC26A1 CTH FEZF1 TP63 CDC73 TMEM231 TTR PDX1 STS FANCL FGF20 SOX17 GNAS DDX59 STAT5B ND2 KLF11 ARX OCRL MAP3K7 COG7 PEX7 SIX5 APOA1 IL12A-AS1 FOXH1 CASR PORCN STAT3 KIF14 COL4A4 FGF8 DLC1 CTNNB1 TRNT1 IFT43 CDK4 FKTN ITGA6 AKT1 SOX11 PRKCSH DDX59 CLCN5 KLRC4 TRIP13 PIEZO2 EVC CRB2 PEX6 TELO2 AGXT LRIG2 IFT172 DNA2 HLA-B DCHS1 FIBP NOD2 CEP290 HPRT1 SHANK3 SCO2 NDUFS2 NDUFB11 SLC25A22 VPS33A HSPA9 ADCY10 TP53 FLI1 NF1 CD46 GPC4 LIPT2 TIMMDC1 NDUFAF8 RAD21 BRCA2 GAS1 TMEM70 FASLG COX3 FANCB STRADA FAM20C ROR2 SDHA SNRPB MCTP2 PIGN ARVCF KIAA0586 INVS OPLAH TGIF1 FOXRED1 PTPN11 IQSEC2 SKI SDHC VPS33B MAPKBP1 MKKS NDUFAF4 CEP290 CISD2 B3GLCT AQP2 ZAP70 UBE2T BNC2 NPM1 SMC1A PEX1 AVPR2 PPARG STAG1 TRIM32 CCND2 TTC21B RBM10 EFEMP2 PRODH PORCN FLCN MYH9 FREM2 PTPN22 RBM10 PREPL PHEX RET GSN RFC2 IQCB1 OGG1 DCC RAF1 TSC1 CCNQ NDUFAF3 FOXP1 SOX10 EYA1 ANOS1 ERCC4 PTPN11 BBS2 VAMP7 CASR JMJD1C VANGL1 GRIA3 HBB MAFB NLRP3 PKD2 OSGEP FLNA TRIP13 SIX1 CACNA1S CENPJ PAX1 CDKN1B NAA10 TMEM126B ND5 NFIA SDHB BUB1B CLDN10 ATP6V1B1 EPG5 EHMT1 BMPER SOX4 ELP1 NR5A1 MKKS YY1AP1 NDUFAF2 LMNB2 HNF1A ARID1A RNF139 TCTN3 BRAF AIP TMEM67 POLR3A CPT2 TRNW TBX1 SPRY2 CCBE1 CPT1A HNF4A PPP1R15B SLC4A1 TRAF3IP1 CEP290 TNXB TMEM67 SEC24C BSCL2 DYNC2H1 NEUROD2 CDKN1C ANKLE2 BMP4 MAX TMEM107 SPRY4 PRMT7 COL7A1 TPRKB GPC3 PGAP2 ALG8 TTC8 PAX2 RSPO2 FANCE SHANK3 NPHP3 NDUFAF5 TMEM237 NOTCH2 TMEM67 SMARCC2 SDHAF2 PEX19 CD81 CHST14 RFWD3 PGK1 WDR35 CTNS ZFPM2 SURF1 LHX1 TMEM127 CDON NIPBL HNF4A CHD4 PHYH ACE ENPP1 RRM2B SCARB2 COQ2 DYNC2I1 NPHP1 APOB PEX5 ACVRL1 INTS1 FLCN GDF3 FH IL17RD SLC34A1 HNF1B PEX26 TRIP13 NUP85 TP53RK BRCA2 ITGA2B RIPK4 FIG4 VHL SMC3 B9D2 MAGED2 ANLN CASK XPNPEP3 TTC37 ZNF687 RERE TMEM67 TAF13 KRAS NIPAL4 MLXIPL HOXA13 RBBP8 KCNJ11 FREM2 SALL1 ATP6 NUP107 LAMB2 IKZF1 UBAC2 RARA LMX1B APC TMEM138 AGT SSR4 TCN2 MAP2K1 CHN1 DGKE VHL ND1 SMARCA4 APOL1 FIP1L1 MOCS1 NPHP3 HLA-DPA1 NEK8 SHPK ABCC8 TLR4 DVL3 RMND1 ADA DMP1 DYNC2H1 WNT3 TMEM216 MLH1 COPA PKHD1 FANCD2 BICC1 CPT2 ETFB FAM149B1 TBC1D8B SC5D GTF2I GDF2 BMPER FLNA MCC STXBP1 DNASE1L3 KCNE5 PYCR2 IL10 METTL5 SHH CRB2 SLC37A4 PTCH1 SH2B1 IGF2 CDC42 REST STAT3 TMEM260 AHI1 PRPS1 GNA11 GLI1 COL5A1 CACNA1D PTPN22 BBS4 TRNW ABCG5 AFF4 SDCCAG8 FN1 WT1 ADAMTSL1 FN1 HPS1 PROK2 WASHC5 SERPINA1 ITPR3 CEP152 MYO1E SLC12A3 PHF21A CYP27A1 SLC3A1 HNRNPU BUB1B FANCC ITGB3 DLL4 RAD54B SIK1 TBL2 SDHB TMEM216 DZIP1L RYR1 FLNB KYNU RBM8A IGF2 CEL SDCCAG8 MME ND2 CC2D2A PTH1R ARHGDIA KCTD1 GATA3 SEMA3A GP9 KCNJ5 ACTG2 LDHA TMEM231 CASR UMOD SUFU SARS2 HYMAI FLNA FLNB HMGA2 KDM6A PGAP3 SCNN1G VHL MCFD2 ACTB PUF60 COL3A1 CD96 CIT
Protein Mutations 4
C282T C677T K55R Y93H