| Name |
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Sensitivity To Red Light Reduced-like, SRR1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sensitivity To Red Light Reduced-like, SRR1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
red, far-red light phototransduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the red, far-red light phototransduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
srr1 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term srr1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
red vs non-red hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease red vs non-red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Red vs non-red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Red vs non-red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red vs. non-red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red vs. non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High light scatter reticulocyte percentage of red cells Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High light scatter reticulocyte percentage of red cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
increased cellular sensitivity to uv light Gene SetFrom HPO Gene-Disease Associations genes associated with the increased cellular sensitivity to uv light phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Increased Cellular Sensitivity To Uv Light Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Cellular Sensitivity To Uv Light in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
anemia due to reduced life span of red cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
anemia due to reduced life span of red cells Gene SetFrom HPO Gene-Disease Associations genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reduced Red Cell Adenosine Deaminase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Red Cell Adenosine Deaminase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Red Cell Pyruvate Kinase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Red Cell Pyruvate Kinase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
red nucleus, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in red nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
red nucleus, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in red nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
red nucleus, parvicellular part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in red nucleus, parvicellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Red nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Red nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
red nucleus, magnocellular part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in red nucleus, magnocellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
red nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in red nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Renal tubular acidosis, distal, with normal red cell morphology Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ruthenium Red Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Ruthenium Red from the curated CTD Gene-Chemical Interactions dataset. |
Alizarin Red S Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Alizarin Red S from the curated CTD Gene-Chemical Interactions dataset. |
Allura Red AC Dye Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Allura Red AC Dye from the curated CTD Gene-Chemical Interactions dataset. |
Scarlet Red Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Scarlet Red from the curated CTD Gene-Chemical Interactions dataset. |
Congo Red Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Congo Red from the curated CTD Gene-Chemical Interactions dataset. |
Red-Cell Aplasia, Pure Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Red-Cell Aplasia, Pure from the curated CTD Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset. |
Pyruvate Kinase Deficiency of Red Cells Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Kinase Deficiency of Red Cells from the curated CTD Gene-Disease Associations dataset. |
red color blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease red color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pure red-cell aplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
red-green color blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease red-green color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
black vs red hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease black vs red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
red cell folate concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease red cell folate concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; kidney diseases; red-cell aplasia, pure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
red-cell aplasia, pure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid in plasma and red blood cell folate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid in plasma and red blood cell folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
red Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term red in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
ruthenium red Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the ruthenium red ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
Red blood cell traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Red blood cell traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Black vs. red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Red blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Red blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
red hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the red hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
increased red cell sickling tendency Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased red cell sickling tendency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
cherry red spot of the macula Gene SetFrom HPO Gene-Disease Associations genes associated with the cherry red spot of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
red hair Gene SetFrom HPO Gene-Disease Associations genes associated with the red hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased red cell osmotic fragility Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red cell osmotic fragility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ragged-red muscle fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the ragged-red muscle fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased red cell sickling tendency Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red cell sickling tendency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased red cell osmotic resistance Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red cell osmotic resistance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased red cell hemolysis by shear stress Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red cell hemolysis by shear stress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
red-green dyschromatopsia Gene SetFrom HPO Gene-Disease Associations genes associated with the red-green dyschromatopsia 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. |
Protein RED, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein RED, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Opsin red/green sensitive Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Opsin red/green sensitive protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased spleen red pulp amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased spleen red pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen red pulp morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen red pulp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal red blood cell distribution width Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
intermingled spleen red and white pulp Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased spleen red pulp amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased spleen red pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent red nucleus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent red nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased red blood cell distribution width Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal red blood cell deformability Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal red blood cell deformability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased red blood cell distribution width Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal red nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal red nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[skin/hair/eye pigmentation 2, red hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
pseudohyperkalemia, familial, 2, due to red cell leak Gene SetFrom OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
red bone marrow Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue red bone marrow in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pure Red-Cell Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pure Red-Cell Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Red Cell Adenylate Kinase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Red Cell Adenylate Kinase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Splenic Diffuse Red Pulp Small B-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Splenic Diffuse Red Pulp Small B-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Red Man Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Red Man Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rdw - Red Blood Cell Distribution Width Result Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rdw - Red Blood Cell Distribution Width Result in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Red Blood Cell Count Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Red Blood Cell Count Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Red Cell Distribution Width Determination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Red Cell Distribution Width Determination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ragged-Red Muscle Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ragged-Red Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Red Cell Osmotic Fragility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Osmotic Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cherry Red Spot Of The Macula Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cherry Red Spot Of The Macula 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. |
Increased Level Of Galactitol In Red Blood Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Level Of Galactitol In Red Blood Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Level Of Galactonate In Red Blood Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Level Of Galactonate In Red Blood Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Red Cell Sickling Tendency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Sickling Tendency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Florid Red Complexion (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Florid Red Complexion (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Red Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Red Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Red Cell Hemolysis By Shear Stress Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Hemolysis By Shear Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Red Cell Adenosine Deaminase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Red Cell Adenosine Deaminase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Red Cell Osmotic Resistance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Osmotic Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Red, Cracking, Peeling Skin At Birth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Red, Cracking, Peeling Skin At Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal spleen red pulp morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen red pulp morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased spleen red pulp amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spleen red pulp amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased red blood cell distribution width Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased red blood cell distribution width phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased spleen red pulp amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spleen red pulp amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal red nucleus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal red nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
intermingled spleen red and white pulp Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent red nucleus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent red nucleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal red blood cell deformability Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal red blood cell deformability phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased red blood cell distribution width Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased red blood cell distribution width phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal red blood cell distribution width Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal red blood cell distribution width phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased red blood cell distribution width Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased red blood cell distribution width phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased red blood cell distribution width Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased red blood cell distribution width phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal red blood cell distribution width Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal red blood cell distribution width phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Red blood cell (erythrocyte)_Airway_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Plasma_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Plasma_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Blood_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Blood_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red pulp macrophage_Bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red pulp macrophage_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Bone marrow_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Brain_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Breast_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Breast_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Skeletal muscle_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Skeletal muscle_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Heart_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Ovary_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Ovary_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Placenta_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Placenta_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Salivary gland_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Salivary gland_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Blood vessel_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Blood vessel_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Red blood cell (erythrocyte)_Ectocervix_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Red blood cell (erythrocyte)_Ectocervix_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Spleen_CT2_Splenic Red Pulp Stromal Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Spleen_CT2_Splenic Red Pulp Stromal Cell cell type from the HuBMAP ASCT+B dataset. |
Spleen_CT2_Splenic Red Pulp Stromal Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spleen_CT2_Splenic Red Pulp Stromal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Pure red-cell aplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pure red-cell aplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Pyruvate kinase deficiency of red cells Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pyruvate kinase deficiency of red cells from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Pure red-cell aplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
red-green color blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease red-green color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Red color blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Red color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pyruvate kinase deficiency of red cells Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pyruvate kinase deficiency of red cells in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Red bone marrow Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Red bone marrow in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
red.1 Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue red.1 in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Pyruvate kinase deficiency of red cells Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyruvate kinase deficiency of red cells phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Red blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Reticulocyte fraction of red cells Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reticulocyte fraction of red cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red cell distribution width Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red cell distribution width phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red blood cell density in sickle cell anemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red blood cell density in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red blood cell traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red blood cell traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red wine liking Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red wine liking phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alloimmunization response to red blood cell transfusion in sickle cell anemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alloimmunization response to red blood cell transfusion in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red blood cell fatty acid levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red blood cell fatty acid levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red blood cell folate levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red blood cell folate levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Black vs. red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Interleukin-6 (red blood cell fatty acid level interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Interleukin-6 (red blood cell fatty acid level interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intercellular adhesion molecule 1 (red blood cell fatty acid level interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intercellular adhesion molecule 1 (red blood cell fatty acid level interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Monocyte chemoattractant protein-1 (red blood cell fatty acid level interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Monocyte chemoattractant protein-1 (red blood cell fatty acid level interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Tumor necrosis factor receptor II (red blood cell fatty acid level interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tumor necrosis factor receptor II (red blood cell fatty acid level interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
C-reactive protein (red blood cell fatty acid level interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the C-reactive protein (red blood cell fatty acid level interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red vs. brown/black hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red vs. brown/black hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
CONGO RED FREE ACID Gene Setinteracting proteins for the CONGO RED FREE ACID drug from theDGIdb Drug Targets 2026 dataset. |
PYROGALLOL RED Gene Setinteracting proteins for the PYROGALLOL RED drug from theDGIdb Drug Targets 2026 dataset. |
NILE RED Gene Setinteracting proteins for the NILE RED drug from theDGIdb Drug Targets 2026 dataset. |
SCARLET RED Gene Setinteracting proteins for the SCARLET RED drug from theDGIdb Drug Targets 2026 dataset. |
RUTHENIUM RED Gene Setinteracting proteins for the RUTHENIUM RED drug from theDGIdb Drug Targets 2026 dataset. |
TETRAZOLIUM RED Gene Setinteracting proteins for the TETRAZOLIUM RED drug from theDGIdb Drug Targets 2026 dataset. |
BROMOPYROGALLOL RED Gene Setinteracting proteins for the BROMOPYROGALLOL RED drug from theDGIdb Drug Targets 2026 dataset. |
light-harvesting complex, core complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the light-harvesting complex, core complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
thylakoid light-harvesting complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the thylakoid light-harvesting complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
psi associated light-harvesting complex i Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the psi associated light-harvesting complex i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
plasma membrane light-harvesting complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plasma membrane light-harvesting complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
psii associated light-harvesting complex ii Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the psii associated light-harvesting complex ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
light-harvesting complex, peripheral complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
light-harvesting complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the light-harvesting complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
light Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term light in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
cellular response to blue light Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to blue light biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of visible light Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of visible light biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of light stimulus involved in sensory perception Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of light stimulus involved in sensory perception biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to low light intensity stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to low light intensity stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to high light intensity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to high light intensity biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of myosin light chain kinase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of myosin-light-chain-phosphatase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of myosin-light-chain-phosphatase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to light intensity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to light intensity biological process from the curated GO Biological Process Annotations 2015 dataset. |
blue light signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the blue light signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of light stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of light stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
phototransduction, visible light Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phototransduction, visible light biological process from the curated GO Biological Process Annotations 2015 dataset. |
sensory perception of light stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the sensory perception of light stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to light stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to light stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of myosin light chain kinase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of light stimulus involved in visual perception Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to blue light Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to blue light biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to light stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to light stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
myosin light chain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the myosin light chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mitochondrial light strand promoter anti-sense binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mitochondrial light strand promoter anti-sense binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mitochondrial light strand promoter sense binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mitochondrial light strand promoter sense binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
clathrin light chain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the clathrin light chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
myosin-light-chain-phosphatase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the myosin-light-chain-phosphatase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
blue light photoreceptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the blue light photoreceptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
myosin light chain kinase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the myosin light chain kinase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
myosin vi light chain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the myosin vi light chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
dynein light intermediate chain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the dynein light intermediate chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
dynein light chain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the dynein light chain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
abnormal pupillary light reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Neurofilament light polypeptide Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Neurofilament light polypeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinesin light chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinesin light chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myosin light chain kinase-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin light chain kinase-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Telokin/Myosin light chain kinase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Telokin/Myosin light chain kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinesin light chain repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinesin light chain repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Thrombin light chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thrombin light chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynein light chain, type 1/2, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein light chain, type 1/2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Axonemal dynein light chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Axonemal dynein light chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynein light chain, roadblock-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein light chain, roadblock-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynein light chain, type 1/2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein light chain, type 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Clathrin light chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Clathrin light chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynein family light intermediate chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein family light intermediate chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Obscurin-myosin light chain kinase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Obscurin-myosin light chain kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynein light chain-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein light chain-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynein 1 light intermediate chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein 1 light intermediate chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Microtubule-associated protein 1A/1B light chain 3C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 1A/1B light chain 3C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased corneal light-scattering Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased corneal light-scattering phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to light Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to light phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immunoglobulin light chain v-j recombination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin light chain v-j recombination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, dark/light hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/light eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[kappa light chain deficiency] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [kappa light chain deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Light Fixation Seizure Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Light Fixation Seizure Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Light Chain Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Light Chain Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Light Chain Myeloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Light Chain Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Light Chain (Al) Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Light Chain (Al) Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Difficulty Adjusting From Light To Dark Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Difficulty Adjusting From Light To Dark in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polymorphous Light Eruption Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Light Eruption in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Light Induced Retinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Light Induced Retinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fetal Malnutrition Without Mention Of Light-For-Dates Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition Without Mention Of Light-For-Dates in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Decreased Light- And Dark-Adapted Electroretinogram Amplitude Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Light- And Dark-Adapted Electroretinogram Amplitude in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Visual Acuity, No Light Perception Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity, No Light Perception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Light- And Dark-Adapted Electroretinogram Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Light- And Dark-Adapted Electroretinogram in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slow Pupillary Light Response Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow Pupillary Light Response in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impairment, Light Touch Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impairment, Light Touch Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Visual Acuity Light Perception With Projection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity Light Perception With Projection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Pupillary Light Reflex Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Pupillary Light Reflex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Light Complexion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Light Complexion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Light-Adapted Electroretinogram Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Light-Adapted Electroretinogram in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
detection of light stimulus involved in visual perception Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of myosin-light-chain-phosphatase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of myosin-light-chain-phosphatase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of myosin-light-chain-phosphatase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of myosin-light-chain-phosphatase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of visible light Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of visible light biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to light intensity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to light intensity biological process from the curated GO Biological Process Annotations 2023 dataset. |
sensory perception of light stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the sensory perception of light stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of myosin light chain kinase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
phototransduction, visible light Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phototransduction, visible light biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to light stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to light stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to blue light Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to blue light biological process from the curated GO Biological Process Annotations 2023 dataset. |
blue light signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the blue light signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to light stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to light stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to high light intensity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to high light intensity biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of light stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of light stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of light stimulus involved in sensory perception Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of light stimulus involved in sensory perception biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of myosin light chain kinase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of myosin light chain kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to blue light Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to blue light biological process from the curated GO Biological Process Annotations 2023 dataset. |
clathrin light chain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the clathrin light chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
myosin light chain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the myosin light chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
myosin-light-chain-phosphatase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the myosin-light-chain-phosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
myosin light chain kinase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the myosin light chain kinase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
blue light photoreceptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the blue light photoreceptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
myosin VI light chain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the myosin VI light chain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
increased corneal light-scattering Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased corneal light-scattering phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibuloocular light reflex Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibuloocular light reflex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immunoglobulin light chain V-J recombination Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin light chain V-J recombination phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal behavioral response to light Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal behavioral response to light phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - PBMC - L3 - Intermediate B cell, kappa light chain Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - Intermediate B cell, kappa light chain cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - Intermediate B cell, lambda light chain Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - Intermediate B cell, lambda light chain cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - Memory B cell, kappa light chain Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - Memory B cell, kappa light chain cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - Memory B cell, lambda light chain Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - Memory B cell, lambda light chain cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - Naive B cell, kappa light chain Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - Naive B cell, kappa light chain cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - Naive B cell, lambda light chain Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - Naive B cell, lambda light chain cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Tonsil - L2 - Light Zone GCBC Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Light Zone GCBC cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Tonsil - L2 - PC committed Light Zone GCBC Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - PC committed Light Zone GCBC cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Light zone cell_Palatine tonsil_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Light zone cell_Palatine tonsil_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Light zone Follicular dendritic cell (LZ-FDCs)_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Light zone Follicular dendritic cell (LZ-FDCs)_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
detection of light stimulus involved in visual perception Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of visible light Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of visible light biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to light intensity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to light intensity biological process from the curated GO Biological Process Annotations 2025 dataset. |
sensory perception of light stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the sensory perception of light stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
phototransduction, visible light Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phototransduction, visible light biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to light stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to light stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to blue light Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to blue light biological process from the curated GO Biological Process Annotations 2025 dataset. |
blue light signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the blue light signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to light stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to light stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to high light intensity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to high light intensity biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of light stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of light stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of light stimulus involved in sensory perception Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of light stimulus involved in sensory perception biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to blue light Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to blue light biological process from the curated GO Biological Process Annotations 2025 dataset. |
clathrin light chain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the clathrin light chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
myosin light chain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the myosin light chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
myosin-light-chain-phosphatase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the myosin-light-chain-phosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
myosin light chain kinase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the myosin light chain kinase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
blue light photoreceptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the blue light photoreceptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
myosin VI light chain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the myosin VI light chain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Immunoglobulin light chain amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin light chain amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin heavy-and-light chain Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin heavy-and-light chain in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
PSII associated light-harvesting complex II Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the PSII associated light-harvesting complex II cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Thylakoid light-harvesting complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Thylakoid light-harvesting complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
light-harvesting complex, peripheral complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
light-harvesting complex, core complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the light-harvesting complex, core complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Plasma membrane light-harvesting complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Plasma membrane light-harvesting complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
PSI associated light-harvesting complex I Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the PSI associated light-harvesting complex I cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Light complexion Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Light complexion phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High light scatter reticulocyte count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High light scatter reticulocyte count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (heavy vs. light/non-drinkers) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (heavy vs. light/non-drinkers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Light vs. dark hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Light vs. dark hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Smoking status (heavy vs light) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Smoking status (heavy vs light) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Plasma neurofilament light levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma neurofilament light levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cerebrospinal fluid neurofilament light levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal fluid neurofilament light levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Facial pigmentation measurement (UV light) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial pigmentation measurement (UV light) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Facial pigmentation measurement (polar light) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial pigmentation measurement (polar light) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (liver involvement) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (liver involvement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Change in neurofilament light levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Change in neurofilament light levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LIGHT Gene Setinteracting proteins for the LIGHT drug from theDGIdb Drug Targets 2026 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. |
Severe combined immunodeficiency with sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
DSIF complex (DRB sensitivity-inducing factor complex) Gene Setproteins in the DSIF complex (DRB sensitivity-inducing factor complex) protein complex from the CORUM Protein Complexes dataset. |
Ragweed Sensitivity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ragweed Sensitivity from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset. |
Echo Virus 11 Sensitivity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Echo Virus 11 Sensitivity from the curated CTD Gene-Disease Associations dataset. |
ALCOHOL SENSITIVITY, ACUTE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ALCOHOL SENSITIVITY, ACUTE from the curated CTD Gene-Disease Associations dataset. |
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Multiple Chemical Sensitivity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Chemical Sensitivity from the curated CTD Gene-Disease Associations dataset. |
Severe combined immunodeficiency with sensitivity to ionizing radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency with sensitivity to ionizing radiation from the curated CTD Gene-Disease Associations dataset. |
dentin sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentin sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple chemical sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
radiation, uv, sensitivity to Gene SetFrom GAD Gene-Disease Associations genes associated with the disease radiation, uv, sensitivity to in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin release and insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin release and insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
warfarin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease warfarin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased antilipolytic insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased antilipolytic insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta-cell function; insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta-cell function; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
human taste sensitivity to sucrose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease human taste sensitivity to sucrose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
salt sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behavioral traits; tryptophan depletion sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behavioral traits; tryptophan depletion sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
interpersonal sensitivity; paranoid ideation; psychoticism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease interpersonal sensitivity; paranoid ideation; psychoticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
1,3-butadiene sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease 1,3-butadiene sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
baroflex sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease baroflex sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucocorticoid sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucocorticoid sensitivity 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. |
insulin sensitivity; glucose disposal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin sensitivity; glucose disposal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mutagen sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mutagen sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple chemical sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple chemical sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sensitivity to tzt-1027 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sensitivity to tzt-1027 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; cholesterol, total; insulin sensitivity; hyperinsulinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; cholesterol, total; insulin sensitivity; hyperinsulinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; insulin sensitivity; fatty acid Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; insulin sensitivity; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute sensitivity to anti-acetylcholinesterases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute sensitivity to anti-acetylcholinesterases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
skin sensitivity to sun Gene SetFrom GAD Gene-Disease Associations genes associated with the disease skin sensitivity to sun in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; nitric oxide production; salt sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
radiation, ionizing, sensitivity to Gene SetFrom GAD Gene-Disease Associations genes associated with the disease radiation, ionizing, sensitivity to in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sensitivity to beta(1)-adrenergic blockade Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sensitivity to beta(1)-adrenergic blockade in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
5-fluorouracil sensitivity. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease 5-fluorouracil sensitivity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased sensitivity to glucocorticoids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased sensitivity to glucocorticoids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acenocoumarol, sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acenocoumarol, sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
radiation sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease radiation sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin sensitivity; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin sensitivity; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
phenylthiocarbamide sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease phenylthiocarbamide sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
radiotherapy sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease radiotherapy sensitivity 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. |
insulin sensitivity and body composition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin sensitivity and body composition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sensitivity Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term sensitivity in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Skin sensitivity to sun Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Skin sensitivity to sun phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Opioid sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Opioid sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Contrast sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Contrast sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Capecitabine sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Capecitabine sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
increased sensitivity to ionizing radiation Gene SetFrom HPO Gene-Disease Associations genes associated with the increased sensitivity to ionizing radiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired thermal sensitivity Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired thermal sensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased sensitivity to hypoxemia Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased sensitivity to hypoxemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Multiple Chemical Sensitivity Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Chemical Sensitivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
increased cellular sensitivity to gamma-irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to gamma-irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased sensitivity to induced cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased sensitivity to xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased physiological sensitivity to xenobiotic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased physiological sensitivity to xenobiotic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to alkylating agents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to alkylating agents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased insulin sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased insulin sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased sensitivity to induced cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to ultraviolet irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to ultraviolet irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased sensitivity to induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to gamma-irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to gamma-irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased physiological sensitivity to xenobiotic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased physiological sensitivity to xenobiotic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sour taste sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sour taste sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to oxidative stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased sensitivity to skin irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to skin irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal taste sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal taste sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to x-ray irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to x-ray irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to ionizing radiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to ionizing radiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to hydrogen peroxide Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to hydrogen peroxide phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to oxidative stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased sensitivity to induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased sensitivity to skin irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to skin irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to hydroxyurea Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to hydroxyurea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to methylmethanesulfonate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to methylmethanesulfonate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bitter taste sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bitter taste sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to ionizing radiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to ionizing radiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to x-ray irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to x-ray irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to methylmethanesulfonate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to methylmethanesulfonate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal umami taste sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal umami taste sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sweet taste sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sweet taste sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to alkylating agents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to alkylating agents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal salty taste sensitivity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal salty taste sensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to ultraviolet irradiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to ultraviolet irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to hydrogen peroxide Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to hydrogen peroxide phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased sensitivity to xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensitivity to induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{organophosphate poisoning, sensitivity to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {organophosphate poisoning, sensitivity to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
?ragweed sensitivity Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?ragweed sensitivity phenotype from the curated OMIM Gene-Disease Associations dataset. |
warfarin sensitivity Gene SetFrom OMIM Gene-Disease Associations genes associated with the warfarin sensitivity phenotype from the curated OMIM Gene-Disease Associations dataset. |
{codeine sensitivity} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {codeine sensitivity} phenotype from the curated OMIM Gene-Disease Associations dataset. |
alcohol sensitivity, acute Gene SetFrom OMIM Gene-Disease Associations genes associated with the alcohol sensitivity, acute phenotype from the curated OMIM Gene-Disease Associations dataset. |
radiation sensitivity/chromosome instability syndrome, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the radiation sensitivity/chromosome instability syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset. |
{debrisoquine sensitivity} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {debrisoquine sensitivity} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{warfarin sensitivity} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {warfarin sensitivity} phenotype from the curated OMIM Gene-Disease Associations dataset. |
6-mercaptopurine sensitivity Gene SetFrom OMIM Gene-Disease Associations genes associated with the 6-mercaptopurine sensitivity phenotype from the curated OMIM Gene-Disease Associations dataset. |
Scotopic Sensitivity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scotopic Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dentin Sensitivity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dentin Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gluten Sensitivity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gluten Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Solvent Sensitivity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Solvent Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
6 Alpha Mercaptopurine Sensitivity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease 6 Alpha Mercaptopurine Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Impaired Thermal Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Thermal Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Insulin Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Insulin Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Insulin Sensitivity Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Insulin Sensitivity Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Sensitivity, Acute Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Sensitivity, Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sound Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sound Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Suxamethonium Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Suxamethonium Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Chemical Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Chemical Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aspirin Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aspirin Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Warfarin Sensitivity (Disorder) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Warfarin Sensitivity (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Coumarin Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coumarin Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Sensitivity To Hypoxemia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sensitivity To Hypoxemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Contrast Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Contrast Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Sensitivity To Ionizing Radiation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Sensitivity To Ionizing Radiation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to gamma-irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to gamma-irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to ionizing radiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to ionizing radiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased sensitivity to induced cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to gamma-irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to gamma-irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to ultraviolet irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to ultraviolet irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased sensitivity to induced cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased insulin sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased insulin sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased physiological sensitivity to xenobiotic Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased physiological sensitivity to xenobiotic phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to ionizing radiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to ionizing radiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to ultraviolet irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to ultraviolet irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased physiological sensitivity to xenobiotic Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased physiological sensitivity to xenobiotic phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to hydrogen peroxide Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to hydrogen peroxide phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to methylmethanesulfonate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to methylmethanesulfonate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to oxidative stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal taste sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal taste sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bitter taste sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bitter taste sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sweet taste sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sweet taste sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to alkylating agents Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to alkylating agents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased sensitivity to skin irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased sensitivity to skin irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to methylmethanesulfonate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to methylmethanesulfonate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to X-ray irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to X-ray irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal umami taste sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal umami taste sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to hydrogen peroxide Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to hydrogen peroxide phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to oxidative stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to X-ray irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to X-ray irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal salty taste sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal salty taste sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sour taste sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sour taste sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased sensitivity to skin irradiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sensitivity to skin irradiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to alkylating agents Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to alkylating agents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to hydroxyurea Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to hydroxyurea phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to DNA damaging agents Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to DNA damaging agents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal visual contrast sensitivity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual contrast sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Warfarin sensitivity Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Warfarin sensitivity from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Warfarin sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Warfarin sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple chemical sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe combined immunodeficiency with sensitivity to ionizing radiation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe combined immunodeficiency with sensitivity to ionizing radiation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dentin sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dentin sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Warfarin sensitivity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Warfarin sensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alcohol sensitivity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alcohol sensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PAIN SENSITIVITY QUANTITATIVE TRAIT LOCUS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PAIN SENSITIVITY QUANTITATIVE TRAIT LOCUS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
prednisolone sensitivity in B-cell precursor acute lymphoblastic leukaemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the prednisolone sensitivity in B-cell precursor acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
dexamethasone sensitivity in B-cell precursor acute lymphoblastic leukaemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the dexamethasone sensitivity in B-cell precursor acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gestational insulin sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational insulin sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pancreatic beta-cell glucose sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pancreatic beta-cell glucose sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Skin sensitivity to sun Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Skin sensitivity to sun phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Impaired insulin sensitivity in response to n-3 PUFA supplementation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Impaired insulin sensitivity in response to n-3 PUFA supplementation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Opioid sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Opioid sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Contrast sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Contrast sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High-sensitivity C-reactive protein levels in HIV infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High-sensitivity C-reactive protein levels in HIV infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Initial alcohol sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Initial alcohol sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
HIgh-sensitivity cardiac troponin T levels (high vs low) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIgh-sensitivity cardiac troponin T levels (high vs low) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High-sensitivity cardiac troponin T levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High-sensitivity cardiac troponin T levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Capecitabine sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Capecitabine sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corrected insulin response adjusted for insulin sensitivity index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corrected insulin response adjusted for insulin sensitivity index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Insulin sensitivity index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Insulin sensitivity index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Modified Stumvoll Insulin Sensitivity Index (BMI interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Modified Stumvoll Insulin Sensitivity Index (BMI interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Modified Stumvoll Insulin Sensitivity Index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Modified Stumvoll Insulin Sensitivity Index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Modified Stumvoll Insulin Sensitivity Index (model adjusted for BMI) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Modified Stumvoll Insulin Sensitivity Index (model adjusted for BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Stress sensitivity (neuroticism score x major depressive disorder status interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stress sensitivity (neuroticism score x major depressive disorder status interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Reduced zinc in breast milk Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Reduced zinc in breast milk phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leucine - Reduced Carbonyl Gene Setinteracting proteins for the Leucine - Reduced Carbonyl drug from the curated DrugBank Drug Targets dataset. |
reduced level of rnfrom the dmwd allele adjacent to the expanded repeat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced level of rnfrom the dmwd allele adjacent to the expanded repeat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced cerebrospinal fluid pterins Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced cerebrospinal fluid pterins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced muscle mrna levels and insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced muscle mrna levels and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced gene expression and lower plasma levels of beta2-glycoprotein i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced gene expression and lower plasma levels of beta2-glycoprotein i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced insulin secretion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced risk of osteoporotic fractures case control study Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced risk of osteoporotic fractures case control study in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced plasma concentrations of repaglinide Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced plasma concentrations of repaglinide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease reduced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease reduced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type 2 diabetes; reduced prostate cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type 2 diabetes; reduced prostate cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced serum c-peptide and insulin responses to an oral glucose challenge Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced serum c-peptide and insulin responses to an oral glucose challenge in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced expression of the apolipoprotein a-i gene and resolution of disputed paternity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced expression of the apolipoprotein a-i gene and resolution of disputed paternity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease-reduced risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease-reduced risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced dopamine d2 receptor binding Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced dopamine d2 receptor binding in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wegener's granulomatosis- reduced risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wegener's granulomatosis- reduced risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced kidney allograft survival Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced kidney allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced beta-cell function Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced beta-cell function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced early insulin response to oral glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced levels of von willebrand factor messenger rna Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced levels of von willebrand factor messenger rna in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced coronary artery calcification Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced coronary artery calcification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced trans-activation impaired sperm production and male infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced trans-activation impaired sperm production and male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced intrapartum blood loss--a possible evolutionary selection mechanism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced hdl cholesterol and lpa-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced hdl cholesterol and lpa-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced low-density lipoprotein particle size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced low-density lipoprotein particle size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced risk of lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced risk of lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced beta(3)-adrenoceptor function Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced beta(3)-adrenoceptor function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced cbs activity and elevated post-load homocysteine levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced cbs activity and elevated post-load homocysteine levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced energy expenditure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced risk of restenosis after coronary stenting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced risk of restenosis after coronary stenting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term reduced in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
reduced factor viii activity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the reduced factor viii activity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
reduced bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the reduced bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
reduced number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the reduced number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
Riboflavin reduced Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Riboflavin reduced metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Reduced Vitamin K (phylloquinone) Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Reduced Vitamin K (phylloquinone) metabolite from the curated HMDB Metabolites of Enzymes dataset. |
reduced amplitude of pattern visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced protein s activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced protein s activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced pancreatic beta cells Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced pancreatic beta cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced beta/alpha synthesis ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced beta/alpha synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mitochondrial malic enzyme reduced Gene SetFrom HPO Gene-Disease Associations genes associated with the mitochondrial malic enzyme reduced phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced number of intrahepatic bile ducts Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced number of intrahepatic bile ducts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced amplitude of b-wave (erg) Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced amplitude of b-wave (erg) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced subcutaneous adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor xiii activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor xiii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced von willebrand factor activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced von willebrand factor activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced protein c activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced protein c activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced catalase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced catalase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced natural killer cell activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced natural killer cell activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced prothrombin activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced prothrombin activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor x activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor x activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor xii activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor xii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mildly reduced visual acuity Gene SetFrom HPO Gene-Disease Associations genes associated with the mildly reduced visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal stenosis with reduced interpedicular distance Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal stenosis with reduced interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced quantity of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced quantity of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor vii activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor vii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced vital capacity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced vital capacity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor viii activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor viii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced phenylalanine hydroxylase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced phenylalanine hydroxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced tendon reflexes Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced tendon reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced consciousness/confusion Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced consciousness/confusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced lymphocyte surface expression of cd43 (sialophorin) Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced lymphocyte surface expression of cd43 (sialophorin) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced thyroxin-binding globulin Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced thyroxin-binding globulin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced prothrombin consumption Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced prothrombin consumption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced activity of n-acetylglucosaminyltransferase ii Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced activity of n-acetylglucosaminyltransferase ii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced number of corneal endothelial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced number of corneal endothelial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced alpha/beta synthesis ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced alpha/beta synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced bone mineral density Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced dihydropyrimidine dehydrogenase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced dihydropyrimidine dehydrogenase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced orotidine 5-prime phosphate decarboxylase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced orotidine 5-prime phosphate decarboxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced delayed hypersensitivity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced delayed hypersensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced antithrombin iii activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced antithrombin iii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor v activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor v activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor ix activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor ix activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced factor xi activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor xi activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced systolic function Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced systolic function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
markedly reduced t cell function Gene SetFrom HPO Gene-Disease Associations genes associated with the markedly reduced t cell function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced xanthine dehydrogenase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced xanthine dehydrogenase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced number of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reduced folate carrier Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Reduced folate carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Reduced growth phenotype protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Reduced growth phenotype protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
reduced nmda-mediated synaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced nmda-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced male fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced ampa-mediated synaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced ampa-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced enamel thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced enamel thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced hyperactivated sperm motility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced hyperactivated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced thrombolysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced thrombolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced male mating frequency Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced male mating frequency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced linear vestibular evoked potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced cerebellar foliation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced sensorimotor gating Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced sensorimotor gating phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced female fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced nmda receptor mediated synaptic activity in barrel cortex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced nmda receptor mediated synaptic activity in barrel cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced hair shaft melanin granule number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced kindling response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced kindling response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced activated sperm motility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced activated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
leukemia, acute myeloid, reduced survival in Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukemia, acute myeloid, reduced survival in phenotype from the curated OMIM Gene-Disease Associations dataset. |
{macular degeneration, age-related, 14, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 14, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{colonic adenoma recurrence, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {colonic adenoma recurrence, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{macular degeneration, age-related, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome, acquired, reduced susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malaria, cerebral, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malaria, cerebral, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
beta-2-adrenoreceptor agonist, reduced response to Gene SetFrom OMIM Gene-Disease Associations genes associated with the beta-2-adrenoreceptor agonist, reduced response to phenotype from the curated OMIM Gene-Disease Associations dataset. |
dopamine receptor d2, reduced brain density of Gene SetFrom OMIM Gene-Disease Associations genes associated with the dopamine receptor d2, reduced brain density of phenotype from the curated OMIM Gene-Disease Associations dataset. |
Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reduced Facial Expression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reduced Facial Expression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Markedly Reduced Food Intake Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Markedly Reduced Food Intake in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reduced Fetal Movement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Fetal Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Concentration Span Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Concentration Span in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Visual Acuity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Pancreatic Beta Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Pancreatic Beta Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Leukocyte Alkaline Phosphatase Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Leukocyte Alkaline Phosphatase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Tendon Reflexes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Tendon Reflexes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Forced Vital Capacity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Forced Vital Capacity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Vital Capacity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Vital Capacity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Number Of Teeth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Number Of Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Intraabdominal Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Intraabdominal Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Intrathoracic Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Intrathoracic Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Subcutaneous Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Subcutaneous Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor Vii Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor Vii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Bone Mineral Density Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Bone Mineral Density in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Aldolase Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Aldolase Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor Xi Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor Xi Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Ejection Fraction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Ejection Fraction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Alpha/Beta Synthesis Ratio Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Alpha/Beta Synthesis Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor Xiii Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor Xiii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Renal Corticomedullary Differentiation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Renal Corticomedullary Differentiation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Amplitude Of Dark-Adapted Bright Flash Electroretinogram A-Wave Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Amplitude Of Dark-Adapted Bright Flash Electroretinogram A-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain N-Acetyl Aspartate Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain N-Acetyl Aspartate Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Delayed Hypersensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Delayed Hypersensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Catalase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Catalase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Beta/Alpha Synthesis Ratio Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Beta/Alpha Synthesis Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Activity Of N-Acetylglucosaminyltransferase Ii Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Activity Of N-Acetylglucosaminyltransferase Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Mhc Ii Surface Expression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Mhc Ii Surface Expression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Muscle Collagen Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Muscle Collagen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Muscle Fiber Alpha Dystroglycan Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Muscle Fiber Alpha Dystroglycan in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Systolic Function Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Systolic Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Natural Killer Cell Count Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Natural Killer Cell Count in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Protein S Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Protein S Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Dihydropyrimidine Dehydrogenase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Dihydropyrimidine Dehydrogenase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor X Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor X Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Prothrombin Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Prothrombin Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Prothrombin Antigen Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Prothrombin Antigen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor Viii Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor Viii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor Ix Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor Ix Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spinal Stenosis With Reduced Interpedicular Distance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Stenosis With Reduced Interpedicular Distance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Muscle Fiber Merosin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Muscle Fiber Merosin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Proportion Of Cd4-Negative, Cd8-Negative, Alpha-Beta Regulatory T Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Proportion Of Cd4-Negative, Cd8-Negative, Alpha-Beta Regulatory T Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mildly Reduced Visual Acuity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mildly Reduced Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mitochondrial Malic Enzyme Reduced Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mitochondrial Malic Enzyme Reduced in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain Creatine Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain Creatine Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Prothrombin Consumption Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Prothrombin Consumption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Number Of Intrahepatic Bile Ducts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Number Of Intrahepatic Bile Ducts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Amygdala Volume Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Amygdala Volume in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Proportion Of Naive T Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Proportion Of Naive T Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Xanthine Dehydrogenase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Xanthine Dehydrogenase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain Choline Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain Choline Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Maximal Inspiratory Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Maximal Inspiratory Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced C-Peptide Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced C-Peptide Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Quantity Of Von Willebrand Factor Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Quantity Of Von Willebrand Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Von Willebrand Factor Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Von Willebrand Factor Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain Glutamine Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain Glutamine Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Phenylalanine Hydroxylase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Phenylalanine Hydroxylase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Erythrocyte 2,3-Diphosphoglycerate Concentration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Erythrocyte 2,3-Diphosphoglycerate Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Antigen-Specific T Cell Proliferation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Antigen-Specific T Cell Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Granulocyte Cd59 Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Granulocyte Cd59 Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Thyroxin-Binding Globulin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Thyroxin-Binding Globulin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Exercise Tolerance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Exercise Tolerance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Antithrombin Antigen Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Antithrombin Antigen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Euglobulin Clot Lysis Time Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Euglobulin Clot Lysis Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Natural Killer Cell Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Natural Killer Cell Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Muscle Carnitine Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Muscle Carnitine Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Orotidine 5-Prime Phosphate Decarboxylase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Orotidine 5-Prime Phosphate Decarboxylase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Lymphocyte Surface Expression Of Cd43 Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Lymphocyte Surface Expression Of Cd43 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
reduced female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced male fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced male fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced male mating frequency Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced male mating frequency phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced NMDA-mediated synaptic currents Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced NMDA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced enamel thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced enamel thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced cerebellar foliation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced linear vestibular evoked potential Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced sensorimotor gating Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced sensorimotor gating phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced thrombolysis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced thrombolysis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced hair shaft melanin granule number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced NMDA receptor mediated synaptic activity in barrel cortex Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced NMDA receptor mediated synaptic activity in barrel cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced AMPA-mediated synaptic currents Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced AMPA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced sympathetic cervical ganglion size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced sympathetic cervical ganglion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Reduced quantity of Von Willebrand factor Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced quantity of Von Willebrand factor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced von Willebrand factor activity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced von Willebrand factor activity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced protein C activity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced protein C activity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced delayed hypersensitivity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced delayed hypersensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced eye contact Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced eye contact phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced bone mineral density Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced bone mineral density phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced muscle fiber perlecan Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced muscle fiber perlecan phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced left ventricular ejection fraction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced left ventricular ejection fraction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced sperm motility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced sperm motility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Beta blocker survival benefit in heart failure with reduced ejection fraction (time to all cause mortality x beta blocker interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Beta blocker survival benefit in heart failure with reduced ejection fraction (time to all cause mortality x beta blocker interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |