| Name |
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fat-free mass and sarcopenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fat-free mass and sarcopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Leg fat mass and leg lean mass (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Leg fat mass and leg lean mass (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
body mass; leptin; fat mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; leptin; fat mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Trunk fat mass adjusted for trunk lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trunk fat mass adjusted for trunk lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
bmi. fat mass. and leptin levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bmi. fat mass. and leptin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Hip bone mineral density and total body fat mass (bivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip bone mineral density and total body fat mass (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sarcopenia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sarcopenia from the curated CTD Gene-Disease Associations dataset. |
muscle testing; sarcopenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscle testing; sarcopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcopenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcopenia Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term sarcopenia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Sarcopenia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sarcopenia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Age-Related Sarcopenia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Sarcopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sarcopenia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sarcopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
fat mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fat mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leptin; fat mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leptin; fat mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; insulin; glucose; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; insulin; glucose; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Fat body mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Fat body mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormal body fat mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body fat mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased body fat mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased body fat mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased body fat mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased body fat mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal body fat mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal body fat mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal body fat mass Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal body fat mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Leg fat mass (lean adjusted) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Leg fat mass (lean adjusted) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Leg lean mass (fat adjusted) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Leg lean mass (fat adjusted) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Trunk fat mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trunk fat mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fat body mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fat body mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fat content (MRI proton density fat fraction measure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fat content (MRI proton density fat fraction measure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat distribution (trunk fat ratio) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat distribution (trunk fat ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat distribution (leg fat ratio) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat distribution (leg fat ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat distribution (arm fat ratio) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat distribution (arm fat ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension and left ventricular mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension and left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index and waist circumference Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index and waist circumference in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipid levels and body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipid levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma cholesterol levels and body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma cholesterol levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index, blood pressure and cholesterol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index, blood pressure and cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Comprehensive strength and appendicular lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Comprehensive strength and appendicular lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index and cholesterol (psychopharmacological treatment) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index and cholesterol (psychopharmacological treatment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Lipoprotein-associated phospholipase A2 activity and mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index and systolic blood pressure (bivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and systolic blood pressure (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and diastolic blood pressure (bivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and diastolic blood pressure (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and HDL-C (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and HDL-C (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and LDL-C (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and LDL-C (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and triglycerides (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and triglycerides (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and fasting insulin (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and fasting insulin (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and fasting glucose (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and fasting glucose (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and type 2 diabetes (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and type 2 diabetes (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and systole blood pressure (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and systole blood pressure (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and coronary artery disease (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and coronary artery disease (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein-associated phospholipase A2 activity and mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Comprehensive strength and appendicular lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Comprehensive strength and appendicular lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lean body mass and age at menarche (combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lean body mass and age at menarche (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and cholesterol (psychopharmacological treatment) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and cholesterol (psychopharmacological treatment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and waist-hip ratio (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and waist-hip ratio (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (joint analysis main effects and physical activity interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (joint analysis main effects and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (joint analysis main effects and smoking interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and body mass index (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and body mass index (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
increased fatty acid binding increased fat oxidation and insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased fatty acid binding increased fat oxidation and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fat level and partitioning Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fat level and partitioning in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased fat oxidation and hyperinsulinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased fat oxidation and hyperinsulinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance and intra-abdominal fat thickness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance and intra-abdominal fat thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
absence of subcutaneous fat over entire body except buttocks, hips, and thighs Gene SetFrom HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat over entire body except buttocks, hips, and thighs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Body fat percentage and type 2 diabetes (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and type 2 diabetes (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage and triglycerides (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and triglycerides (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage and HDL-C (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and HDL-C (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage and fasting glucose (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and fasting glucose (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage and LDL-C (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and LDL-C (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage and fasting insulin (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and fasting insulin (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage and coronary artery disease (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage and coronary artery disease (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Visceral fat, circulating phospholipid PC(16:0/2:0) and white matter microstructure (shared variance) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Visceral fat, circulating phospholipid PC(16:0/2:0) and white matter microstructure (shared variance) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fat digestion and absorption Gene SetFrom KEGG Pathways 2026 proteins participating in the Fat digestion and absorption pathway from the KEGG Pathways 2026 dataset. |
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
High bone mass Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MASS syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MASS syndrome from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 from the curated CTD Gene-Disease Associations dataset. |
Body Mass Index Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Mass Index in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
higher body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease higher body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucocorticoids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucocorticoids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass diabetes, type 2 glucose insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass diabetes, type 2 glucose insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, ldl; cholesterol, total; insulin; apob Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, ldl; cholesterol, total; insulin; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; left ventricular function; blood pressure; left ventricular structure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; insulin; glucose; hba(1c) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; insulin; glucose; hba(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; leptin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
larger body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease larger body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hemoglobin a(1c) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hemoglobin a(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipids; left ventricular mass; aortic gradient; aortic valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipids; left ventricular mass; aortic gradient; aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; triglycerides; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular mass; left ventricular wall thickness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular mass; left ventricular wall thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; height; weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; height; weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; left ventricular mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lower body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lower body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; schizophrenia; body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; schizophrenia; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; adiposity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass (lean) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass (lean) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
combined bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease combined bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular mass; renin activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular mass; renin activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; glucose; nervous system activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; glucose; nervous system activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; muscle testing; igf-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; muscle testing; igf-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; energy expenditure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hypertension; insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hypertension; insulin; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; birth weight; height Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; birth weight; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose; insulin secretion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index in women. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index in women. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; muscle testing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; muscle testing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, hdl; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
minimum lifetime body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease minimum lifetime body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
very low bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease very low bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; glucose tolerance; insulin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; glucose tolerance; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass (bwt, weight gain, bmi); fertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass (bwt, weight gain, bmi); fertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; body mass; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased bone mass in patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased bone mass in patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; glucose; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mass; osteoporotic fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mass; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, hdl; insulin; folate; homocysteine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; insulin; folate; homocysteine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular mass in male athletes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular mass in male athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; diabetes, type 2; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; diabetes, type 2; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peak bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peak bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; hypertension; albuminuria; glycohemoglobin a1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; hypertension; albuminuria; glycohemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; obesity; glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; obesity; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; triglycerides; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; triglycerides; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mass Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term mass in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
inner cell mass cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cellular morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cellular morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Body mass (lean) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass (lean) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Bipolar disorder (body mass index interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder (body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index (education interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (education interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Left ventricular mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Left ventricular mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass in chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index (non-asthmatics) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (non-asthmatics) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index (interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass index (asthmatics) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass index (asthmatics) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
decreased muscle mass Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased muscle mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased red blood cell mass Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red blood cell mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pancreatic beta cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic beta cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inner cell mass degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner cell mass proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased body mass index Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased trabecular bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lean body mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased inner cell mass proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lean body mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner cell mass proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreatic beta cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic beta cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner cell mass apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal trabecular bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal total tissue mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased total tissue mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased trabecular bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased total tissue mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal compact bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body mass index Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased body mass index Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeletal muscle mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased skeletal muscle mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner cell mass morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner cell mass morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased skeletal muscle mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased compact bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased lean body mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pancreatic beta cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic beta cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased compact bone mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased inner cell mass apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[body mass index qtl 15] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl 15] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl1] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl1] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl3] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl3] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl5] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl5] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl16] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl16] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl14] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl14] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl2] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl2] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[lean body mass qtl 1] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [lean body mass qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl6] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl6] phenotype from the curated OMIM Gene-Disease Associations dataset. |
mass syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the mass syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
[body mass index qtl13] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [body mass index qtl13] phenotype from the curated OMIM Gene-Disease Associations dataset. |
visceral mass Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue visceral mass in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Adnexal Mass Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adnexal Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adrenal Mass Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adrenal Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mass Lesion Of Brain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mass Lesion Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mass Of Thyroid Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mass Of Thyroid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retroperitoneal Mass Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retroperitoneal Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracardiac Mass Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracardiac Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Mass Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flank Mass Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Flank Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Body Mass Index Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Body Mass Index in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lean Body Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lean Body Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Liver Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Liver Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mass Of Body Region Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mass Of Body Region in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mass Lesion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mass Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Body Mass Index Procedure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Body Mass Index Procedure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Body Mass Index Quantitative Trait Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Body Mass Index Quantitative Trait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finding Of Body Mass Index Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finding Of Body Mass Index in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Muscle Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Muscle Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Soft Tissue Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Soft Tissue Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Left Ventricular Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Ventricular Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Body Mass Index Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Body Mass Index in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Body Mass Index Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Body Mass Index in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Red Blood Cell Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Blood Cell Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Bone Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Bone Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Body Mass Index, Modifier Of Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Body Mass Index, Modifier Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
inner cell mass cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
increased trabecular bone mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased trabecular bone mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inner cell mass proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased lean body mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased lean body mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased skeletal muscle mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased skeletal muscle mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner cell mass proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner cell mass proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner cell mass proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner cell mass proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased inner cell mass apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased inner cell mass apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner cell mass morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner cell mass morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
inner cell mass degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased bone mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased bone mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pancreatic beta cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pancreatic beta cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased bone mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased bone mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased skeletal muscle mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased skeletal muscle mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner cell mass apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner cell mass apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased lean body mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased lean body mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased trabecular bone mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased trabecular bone mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased compact bone mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased compact bone mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white adipose tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown adipose tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreatic beta cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreatic beta cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased body mass index Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased body mass index phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased body mass index Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased body mass index phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreatic alpha cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreatic alpha cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased compact bone mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased compact bone mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brown adipose tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brown adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic alpha cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic alpha cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pancreatic alpha cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pancreatic alpha cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lean body mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lean body mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skeletal muscle mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skeletal muscle mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased total tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased total tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased total tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased total tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown adipose tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white adipose tissue mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white adipose tissue mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal body mass index Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal body mass index phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased lean body mass Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased lean body mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased lean body mass Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased lean body mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal lean body mass Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal lean body mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased skeletal muscle mass Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased skeletal muscle mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased skeletal muscle mass Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased skeletal muscle mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Inner cell mass cell_Embryo_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner cell mass cell_Embryo_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner cell mass cell_Inner cell mass_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner cell mass cell_Inner cell mass_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
inner cell mass cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Visceral mass Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Visceral mass in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Buccal mass Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Buccal mass in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
High bone mass Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Body mass index quantitative trait locus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Body mass index quantitative trait locus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MASS syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MASS syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Normal body mass index vs. thin Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Normal body mass index vs. thin phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist-to-hip ratio adjusted for body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist circumference adjusted for body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist circumference adjusted for body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (age interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in gastrointestinal cancer or chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in gastrointestinal cancer or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in cancer or chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in cancer or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in gastrointestinal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in gastrointestinal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in lung cancer or chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in lung cancer or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) in cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lean body mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lean body mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bipolar disorder or body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder or body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bipolar disorder (body mass index interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder (body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass (lean) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass (lean) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (change over time) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (SNP x SNP interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (SNP x SNP interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (dietary energy interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (dietary energy interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (recreational physical activity interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (recreational physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (ever vs never smoking interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (ever vs never smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (smoking years interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (smoking years interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular mass to end-diastolic volume ratio (MTAG) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular mass to end-diastolic volume ratio (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular mass (MTAG) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular mass (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular mass to end-diastolic volume ratio Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular mass to end-diastolic volume ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass in chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index in non-asthmatics Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index in non-asthmatics phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index in asthmatics Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index in asthmatics phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (adult) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (adult) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Appendicular lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Appendicular lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (physical activity interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index in physically active individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index in physically active individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index in physically inactive individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index in physically inactive individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (age <50) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (age <50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index x age interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index x age interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (age>50) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (age>50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index x sex x age interaction (4df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index x sex x age interaction (4df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular mass x antihypertensive treatment interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular mass x antihypertensive treatment interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index variance Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index variance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Abdominal Fat Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Abdominal Fat in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Fat Distribution Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Fat Distribution in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Subcutaneous Fat Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Subcutaneous Fat in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Intra-Abdominal Fat Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Intra-Abdominal Fat in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
intra-abdominal fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intra-abdominal fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; body fat; lipid metabolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; body fat; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
subcutaneous fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease subcutaneous fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
subcutaneous fat accumulation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease subcutaneous fat accumulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
energy intake; fat intake Gene SetFrom GAD Gene-Disease Associations genes associated with the disease energy intake; fat intake in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose tolerance; insulin; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body fat; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body fat; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; body fat; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; body fat; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; body fat; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; body fat; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body fat distribution Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body fat distribution in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperinsulinemia; fat oxidation; intestinal fatty acid absorption Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperinsulinemia; fat oxidation; intestinal fatty acid absorption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, response to; dietary fat, response to Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, response to; dietary fat, response to in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
regional fat distribution Gene SetFrom GAD Gene-Disease Associations genes associated with the disease regional fat distribution in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
excessive fat accumulation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease excessive fat accumulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fat Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fat in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
positive regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
white fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
fat-soluble vitamin catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fat-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
fat pad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fat pad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
fat-soluble vitamin biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fat-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of brown fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of brown fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
fat-soluble vitamin metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fat-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
mammary gland fat development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mammary gland fat development biological process from the curated GO Biological Process Annotations 2015 dataset. |
brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of brown fat cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of brown fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Fat distribution (HIV) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Fat distribution (HIV) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Renal sinus fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Renal sinus fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Visceral fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Visceral fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
minimal subcutaneous fat Gene SetFrom HPO Gene-Disease Associations genes associated with the minimal subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased intraabdominal fat Gene SetFrom HPO Gene-Disease Associations genes associated with the increased intraabdominal fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absence of subcutaneous fat Gene SetFrom HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of subcutaneous fat tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of subcutaneous fat tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased intramuscular fat Gene SetFrom HPO Gene-Disease Associations genes associated with the increased intramuscular fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased subcutaneous fat Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fat malabsorption Gene SetFrom HPO Gene-Disease Associations genes associated with the fat malabsorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Fat storage-inducing transmembrane protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fat storage-inducing transmembrane protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial brown fat uncoupling protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial brown fat uncoupling protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Focal adhesion kinase, targeting (FAT) domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Focal adhesion kinase, targeting (FAT) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PIK-related kinase, FAT Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PIK-related kinase, FAT protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased brown fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased white fat cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brown fat cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parametrial fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parametrial fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased percent body fat Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased gonadal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased retroperitoneal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased retroperitoneal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal femoral fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal femoral fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased interscapular fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased interscapular fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mesenteric fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mesenteric fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fat cell differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fat cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased percent body fat Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased total fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased omental fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased omental fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat lipid droplet number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased renal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased renal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased total body fat amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased total body fat amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal epididymal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal epididymal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal omental fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal omental fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased omental fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased omental fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interscapular fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interscapular fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased uterine fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased uterine fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retroperitoneal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retroperitoneal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hypodermis fat layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hypodermis fat layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fat-soluble vitamin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fat-soluble vitamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased white fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterine fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterine fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased abdominal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased abdominal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased renal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased renal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inguinal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inguinal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent epididymal fat pad Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent epididymal fat pad phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat lipid droplet number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fat cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fat cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased total fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased retroperitoneal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased retroperitoneal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mesenteric fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mesenteric fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased interscapular fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased interscapular fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mesenteric fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mesenteric fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased gonadal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased epididymal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased epididymal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gonadal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gonadal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased white fat cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell differentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell differentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mammary fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mammary fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased parametrial fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased parametrial fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased femoral fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased inguinal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased inguinal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal total fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased total body fat amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased total body fat amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased epididymal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased epididymal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal abdominal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal abdominal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased inguinal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased inguinal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mammary fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mammary fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal percent body fat Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased parametrial fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased parametrial fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased white fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fat Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term fat in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
fat pad Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue fat pad from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
fat pad Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fat pad in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
fat body Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fat body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Fat-endothelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-fibroblast Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-fibroblast relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-leucocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-leucocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-macrophage Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-macrophage relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-mast cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-mast cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-mesenchymal stem cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-mesenchymal stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-myofibroblast cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-myofibroblast cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-neutrophil Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-neutrophil relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-nk cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-nk cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-plasma cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-plasma cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-smooth muscle cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-smooth muscle cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Fat-t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Fat-t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pulmonary Fat Embolism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fat Embolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intestinal Malabsorption Of Fat Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intestinal Malabsorption Of Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Body Fat Distribution Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Body Fat Distribution in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Subcutaneous Fat Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Subcutaneous Fat Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Body Fat Percentage (Physical Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Body Fat Percentage (Physical Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Subcutaneous Fat Tissue Distribution Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Subcutaneous Fat Tissue Distribution in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Intraabdominal Fat Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Intraabdominal Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fat Redistribution Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fat Redistribution in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fat Intolerance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fat Intolerance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absence Of Subcutaneous Fat Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Subcutaneous Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lack Of Facial Subcutaneous Fat Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lack Of Facial Subcutaneous Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Oval Fat Body Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oval Fat Body in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Intramuscular Fat Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Intramuscular Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Minimal Subcutaneous Fat Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Minimal Subcutaneous Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
white fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of fat cell apoptotic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of fat cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
fat pad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fat pad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
fat-soluble vitamin metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fat-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
fat-soluble vitamin catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fat-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
fat-soluble vitamin biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fat-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
decreased total body fat amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased total body fat amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fat-soluble vitamin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fat-soluble vitamin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased percent body fat/body weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased gonadal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased gonadal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased uterine fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased uterine fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased epididymal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased epididymal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased renal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased renal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white fat cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased inguinal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased inguinal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased parametrial fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased parametrial fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inguinal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inguinal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal abdominal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased epididymal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased epididymal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased total body fat amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased total body fat amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fat cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fat cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased abdominal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased abdominal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased total fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased total fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased percent body fat/body weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal epididymal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal epididymal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased gonadal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased gonadal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mammary fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mammary fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retroperitoneal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retroperitoneal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal interscapular fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interscapular fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal white fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased total fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased total fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased interscapular fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased interscapular fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased abdominal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased abdominal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased retroperitoneal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retroperitoneal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gonadal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gonadal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal white fat cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mesenteric fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mesenteric fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inguinal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inguinal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased retroperitoneal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased retroperitoneal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mesenteric fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mesenteric fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal percent body fat/body weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brown fat cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brown fat cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased interscapular fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased interscapular fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white fat cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat lipid droplet number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat lipid droplet number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent epididymal fat pad Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent epididymal fat pad phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fat cell differentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fat cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal renal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brown fat cell differentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brown fat cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased parametrial fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased parametrial fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased renal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased renal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased mesenteric fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mesenteric fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased mammary fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mammary fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased femoral fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased omental fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased omental fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hypodermis fat layer morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hypodermis fat layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal white fat cell differentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell differentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased omental fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased omental fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal beige fat cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal beige fat cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal beige fat cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal beige fat cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat lipid droplet number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat lipid droplet number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased total body fat amount Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased total body fat amount phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased total body fat amount Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased total body fat amount phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Fetal Development - L1 - Epicardial fat cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Epicardial fat cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Heart-Epicardial fat cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Epicardial fat cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Brown adipocyte_Abdominal fat pad_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Brown adipocyte_Abdominal fat pad_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Fat cell (adipocyte)_Adipose tissue_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Fat cell (adipocyte)_Adipose tissue_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Fat cell (adipocyte)_Adipose tissue_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Fat cell (adipocyte)_Adipose tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Brown fat cell_Adipose tissue_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Brown fat cell_Adipose tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Beige fat cell_Adipose tissue_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Beige fat cell_Adipose tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
White fat cell_Adipose tissue_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the White fat cell_Adipose tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Fat cell_Heart_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Fat cell_Heart_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
White fat cell differentiation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the White fat cell differentiation pathway from the WikiPathways Pathways 2024 dataset. |
Metabolism of fat-soluble vitamins Gene Setproteins participating in the Metabolism of fat-soluble vitamins pathway from the Reactome Pathways 2024 dataset. |
fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
white fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of fat cell apoptotic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of fat cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of brown fat cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
fat pad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fat pad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of fat cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
fat-soluble vitamin metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fat-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
fat-soluble vitamin catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fat-soluble vitamin catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of white fat cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
fat-soluble vitamin biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fat-soluble vitamin biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
Fat necrosis of breast Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fat necrosis of breast in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fat pad Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Fat pad from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Fat pad Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Fat pad in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Fat body Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Fat body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Parametrial fat pad Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Parametrial fat pad in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Serum C-reactive protein concentration in low fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum C-reactive protein concentration in low fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Serum C-reactive protein concentration in high fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum C-reactive protein concentration in high fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Dietary fat liking Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dietary fat liking phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Postprandial triglyceride response to high fat diet meal Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Postprandial triglyceride response to high fat diet meal phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LDL peak particle diameter (total fat intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL peak particle diameter (total fat intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pericardial fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pericardial fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Relative fat intake Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relative fat intake phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Delta-5 desaturase activity response to n3-polyunsaturated fat supplement Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Delta-5 desaturase activity response to n3-polyunsaturated fat supplement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Delta-6 desaturase activity response to n3-polyunsaturated fat supplement Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Delta-6 desaturase activity response to n3-polyunsaturated fat supplement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Visceral fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Visceral fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hyperglycemia in more-fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hyperglycemia in more-fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Homeostasis model assessment of insulin resistance in less-fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance in less-fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hyperinsulinemia in less-fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hyperinsulinemia in less-fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Renal sinus fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Renal sinus fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fat distribution (HIV) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fat distribution (HIV) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body fat percentage variance Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body fat percentage variance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Percent liver fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Percent liver fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pancreas fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pancreas fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
FAT EMULSION Gene Setinteracting proteins for the FAT EMULSION drug from theDGIdb Drug Targets 2026 dataset. |
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene SetFrom Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset. |
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coloboma, uveal, with cleft lip and palate and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset. |
anxiety and hostility and depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vitamins and metabolites in pregnant women and neonates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on amino acids and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset. |
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset. |
Synthesis and interconversion of nucleotide di- and triphosphates Gene Setproteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SRF and miRs in smooth muscle differentiation and proliferation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset. |
ApoE and miR 146 in inflammation and atherosclerosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset. |
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset. |
Somatroph axis GH and its relationship to dietary restriction and aging Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset. |
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Setproteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset. |
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Setproteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset. |
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Setproteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset. |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Setproteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset. |
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Setproteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset. |
Transport of bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Regulation of gene expression and signal transduction in immune and stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Basic cell groups and regions Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
head and face region of M1 Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
telomeres telomerase cellular aging and immortality Gene SetFrom Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset. |
mcalpain and friends in cell motility Gene SetFrom Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset. |
role of ppar-gamma coactivators in obesity and thermogenesis Gene SetFrom Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset. |
il12 and stat4 dependent signaling pathway in th1 development Gene SetFrom Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset. |
hypoxia and p53 in the cardiovascular system Gene SetFrom Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset. |
lissencephaly gene (lis1) in neuronal migration and development Gene SetFrom Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset. |
role of erbb2 in signal transduction and oncology Gene SetFrom Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset. |
corticosteroids and cardioprotection Gene SetFrom Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset. |
cyclins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
mechanism of acetaminophen activity and toxicity Gene SetFrom Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset. |
nfat and hypertrophy of the heart Gene SetFrom Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset. |
acetylation and deacetylation of rela in nucleus Gene SetFrom Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset. |
thrombin signaling and protease-activated receptors Gene SetFrom Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset. |
antigen processing and presentation Gene SetFrom Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset. |
stathmin and breast cancer resistance to antimicrotubule agents Gene SetFrom Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset. |
role of ß-arrestins in the activation and targeting of map kinases Gene SetFrom Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset. |
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene SetFrom Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset. |
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene SetFrom Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset. |
btg family proteins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene SetFrom Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset. |
endocytotic role of ndk phosphins and dynamin Gene SetFrom Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset. |
regulation of eif-4e and p70s6 kinase Gene SetFrom Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset. |
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene SetFrom Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset. |
vegf hypoxia and angiogenesis Gene SetFrom Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset. |
yaci and bcma stimulation of b cell immune responses Gene SetFrom Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset. |
lck and fyn tyrosine kinases in initiation of tcr activation Gene SetFrom Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset. |
hiv-1 nef: negative effector of fas and tnf Gene SetFrom Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset. |
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene SetFrom Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset. |
ucalpain and friends in cell spread Gene SetFrom Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset. |
ionomycin and phorbal ester signaling pathway Gene SetFrom Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset. |
carm1 and regulation of the estrogen receptor Gene SetFrom Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset. |
phosphoinositides and their downstream targets Gene SetFrom Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset. |
melanocyte development and pigmentation pathway Gene SetFrom Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset. |
akap95 role in mitosis and chromosome dynamics Gene SetFrom Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset. |
transcription factor creb and its extracellular signals Gene SetFrom Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset. |
the igf-1 receptor and longevity Gene SetFrom Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset. |
cdc25 and chk1 regulatory pathway in response to dna damage Gene SetFrom Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset. |
human cytomegalovirus and map kinase pathways Gene SetFrom Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset. |
influence of ras and rho proteins on g1 to s transition Gene SetFrom Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset. |
proteolysis and signaling pathway of notch Gene SetFrom Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset. |
apoptotic dna-fragmentation and tissue homeostasis Gene SetFrom Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset. |
ion channels and their functional role in vascular endothelium Gene SetFrom Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset. |
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
fosb gene expression and drug abuse Gene SetFrom Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset. |
links between pyk2 and map kinases Gene SetFrom Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset. |
opposing roles of aif in apoptosis and cell survival Gene SetFrom Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset. |
degradation of the rar and rxr by the proteasome Gene SetFrom Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset. |
cadmium induces dna synthesis and proliferation in macrophages Gene SetFrom Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset. |
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset. |
role of brca1 brca2 and atr in cancer susceptibility Gene SetFrom Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset. |
chrebp regulation by carbohydrates and camp Gene SetFrom Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset. |
pten dependent cell cycle arrest and apoptosis Gene SetFrom Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset. |
induction of apoptosis through dr3 and dr4/5 death receptors Gene SetFrom Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset. |
CIITA-18437201-Raji B cells and iDC-human Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
VDR-23401126-LCL-AND-THP1-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Hypothyroidism, central, and testicular enlargement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, mental retardation, and seizures Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vater association with macrocephaly and ventriculomegaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal hamartomas nephroblastomatosis and fetal gigantism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microtia, hearing impairment, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, spastic quadriplegia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined cellular and humoral immune defects with granulomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined d-2- and l-2-hydroxyglutaric aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation with language impairment and autistic features Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, anterior maxillary protrusion, and strabismus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile convulsions and paroxysmal choreoathetosis, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Cutaneous and Mucosal Venous Malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy hereditary sensory and autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly with mental retardation and digital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth retardation, developmental delay, coarse facies, and early death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anemia sideroblastic and spinocerebellar ataxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, congenital heart defects, and posterior embryotoxon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rigidity and multifocal seizure syndrome, lethal neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alopecia, neurologic defects, and endocrinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Knuckle pads, deafness AND leukonychia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multicentric osteolysis, nodulosis and arthropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stapes ankylosis with broad thumb and toes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, short stature, and impaired glucose metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination and Congenital Cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair and keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, microphthalmia and nystagmus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas and Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Band-like calcification with simplified gyration and polymicrogyria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, epilepsy, and diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia and hypogonadotropic hypogonadism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, juvenile, with microcornea and glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, deafness, and narcolepsy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte and dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, hiatal hernia and nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis and congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined malonic and methylmalonic aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis Gyrata syndrome of Beare and Stevenson Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aniridia, cerebellar ataxia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor and sensory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniosynostosis and dental anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, hyperphagia, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebroretinal microangiopathy with calcifications and cysts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Generalized epilepsy and paroxysmal dyskinesia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alacrima, achalasia, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, normal intelligence and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Calcification of joints and arteries Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis and recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pineal hyperplasia AND diabetes mellitus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Morbid obesity and spermatogenic failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Striatal necrosis, bilateral, and progressive polyneuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sensory and autonomic neuropathy type IIA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopia, high, with cataract and vitreoretinal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V and factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Camptodactyly, tall stature, and hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum and acne Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth deficiency and mental retardation with facial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, cochlear, with myopia and intellectual impairment Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of sialidase AND beta galactosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Setproteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset. |
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Setproteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset. |
6S methyltransferase and RG-containing Sm proteins complex Gene Setproteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset. |
Remodeling and spacing factor (RSF) complex Gene Setproteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset. |
PBAF complex (Polybromo- and BAF containing complex) Gene Setproteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset. |
Cleavage and polyadenylation factor (CPSF) Gene Setproteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Nucleic and chromatin Fanconi complex Gene Setproteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset. |
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Setproteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset. |
20S methylosome and RG-containing Sm protein complex Gene Setproteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset. |
Amino Acids, Peptides, and Proteins Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset. |