Harmonizome 3.0

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> <strong>proteinstrong> s activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> <strong>Proteinstrong> S Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> iron-sulfur <strong>proteinstrong> as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> <strong>proteinstrong> c activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> iron-sulfur <strong>proteinstrong> as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> iron-sulfur <strong>proteinstrong> as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> <strong>proteinstrong> C activity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the <strong>Reducedstrong> growth phenotype <strong>proteinstrong> 1 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Insulin Like Growth Factor Binding <strong>Proteinstrong> Acid Labile Subunit Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> cbs activity and elevated post-load homocysteine levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> flavin or flavo<strong>proteinstrong> as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the <strong>reducedstrong> factor viii activity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor xiii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> von willebrand factor activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> catalase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> natural killer cell activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> prothrombin activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor x activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor xii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor vii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor viii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> phenylalanine hydroxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> activity of n-acetylglucosaminyltransferase ii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> dihydropyrimidine dehydrogenase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> orotidine 5-prime phosphate decarboxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> antithrombin iii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor v activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor ix activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> factor xi activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> xanthine dehydrogenase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> nmda receptor mediated synaptic activity in barrel cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Red Cell Adenosine Deaminase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Factor Vii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Factor Xi Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Factor Xiii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Catalase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Activity Of N-Acetylglucosaminyltransferase Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Dihydropyrimidine Dehydrogenase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Factor X Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Prothrombin Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Factor Viii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Factor Ix Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Xanthine Dehydrogenase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Von Willebrand Factor Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Phenylalanine Hydroxylase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Red Cell Pyruvate Kinase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Natural Killer Cell Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Orotidine 5-Prime Phosphate Decarboxylase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> flavin or flavo<strong>proteinstrong> as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> NMDA receptor mediated synaptic activity in barrel cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> flavin or flavo<strong>proteinstrong> as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, <strong>reducedstrong> ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> von Willebrand factor activity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From GAD Gene-Disease Associations

genes associated with the disease activated <strong>proteinstrong> c resistance; blood coagulation disorders; liver diseases; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease activated <strong>proteinstrong> c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From ClinVar Gene-Phenotype Associations

genes associated with the <strong>Reducedstrong> zinc in breast milk phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

From DrugBank Drug Targets

interacting <strong>proteinstrong>s for the Leucine - <strong>Reducedstrong> Carbonyl drug from the curated DrugBank Drug Targets dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> 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.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> cerebrospinal fluid pterins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> muscle mrna levels and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> gene expression and lower plasma levels of beta2-glyco<strong>proteinstrong> i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> risk of osteoporotic fractures case control study in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> plasma concentrations of repaglinide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease <strong>reducedstrong> in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes; <strong>reducedstrong> prostate cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> 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.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> expression of the apolipo<strong>proteinstrong> a-i gene and resolution of disputed paternity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease-<strong>reducedstrong> risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> dopamine d2 receptor binding in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease wegener's granulomatosis- <strong>reducedstrong> risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> kidney allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> 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.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> beta-cell function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> levels of von willebrand factor messenger rna in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> coronary artery calcification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> trans-activation impaired sperm production and male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> hdl cholesterol and lpa-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> low-density lipo<strong>proteinstrong> particle size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> risk of lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> beta(3)-adrenoceptor function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>reducedstrong> risk of restenosis after coronary stenting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term <strong>reducedstrong> in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the <strong>reducedstrong> bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to <strong>reducedstrong> life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From GWASdb SNP-Phenotype Associations

genes associated with the <strong>reducedstrong> number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

From HMDB Metabolites of Enzymes

interacting <strong>proteinstrong>s for the Riboflavin <strong>reducedstrong> metabolite from the curated HMDB Metabolites of Enzymes dataset.

From HMDB Metabolites of Enzymes

interacting <strong>proteinstrong>s for the <strong>Reducedstrong> Vitamin K (phylloquinone) metabolite from the curated HMDB Metabolites of Enzymes dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> pancreatic beta cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> beta/alpha synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the anemia due to <strong>reducedstrong> life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the mitochondrial malic enzyme <strong>reducedstrong> phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> number of intrahepatic bile ducts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> amplitude of b-wave (erg) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the mildly <strong>reducedstrong> visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the spinal stenosis with <strong>reducedstrong> interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> quantity of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> vital capacity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> tendon reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> consciousness/confusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> lymphocyte surface expression of cd43 (sialophorin) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> thyroxin-binding globulin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> prothrombin consumption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> number of corneal endothelial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> alpha/beta synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> delayed hypersensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> systolic function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the markedly <strong>reducedstrong> t cell function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From HPO Gene-Disease Associations

genes associated with the <strong>reducedstrong> number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the <strong>Reducedstrong> folate carrier <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Sensitivity To Red Light <strong>Reducedstrong>-like, SRR1 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> nmda-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> ampa-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> enamel thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> hyperactivated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> thrombolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> male mating frequency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> sensorimotor gating phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> hair shaft melanin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> kindling response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From MPO Gene-Phenotype Associations

gene mutations causing the <strong>reducedstrong> activated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the leukemia, acute myeloid, <strong>reducedstrong> survival in phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the {macular degeneration, age-related, 14, <strong>reducedstrong> risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the {colonic adenoma recurrence, <strong>reducedstrong> risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the {macular degeneration, age-related, <strong>reducedstrong> risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the {long qt syndrome, acquired, <strong>reducedstrong> susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the {malaria, cerebral, <strong>reducedstrong> risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the beta-2-adrenoreceptor agonist, <strong>reducedstrong> response to phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the dopamine receptor d2, <strong>reducedstrong> brain density of phenotype from the curated OMIM Gene-Disease Associations dataset.

From DisGeNET Gene-Disease Associations

genes associated with the disease Acute Encephalopathy With Biphasic Seizures And Late <strong>Reducedstrong> Diffusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

From DisGeNET Gene-Disease Associations

genes associated with the disease <strong>Reducedstrong> Facial Expression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

From DisGeNET Gene-Disease Associations

genes associated with the disease Markedly <strong>Reducedstrong> Food Intake in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Fetal Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Concentration Span in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Pancreatic Beta Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Leukocyte Alkaline Phosphatase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Tendon Reflexes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Forced Vital Capacity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Vital Capacity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Number Of Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Intraabdominal Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Intrathoracic Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Subcutaneous Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Bone Mineral Density in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Aldolase Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Ejection Fraction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Alpha/Beta Synthesis Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Renal Corticomedullary Differentiation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Amplitude Of Dark-Adapted Bright Flash Electroretinogram A-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Brain N-Acetyl Aspartate Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Delayed Hypersensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Beta/Alpha Synthesis Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Mhc Ii Surface Expression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Muscle Collagen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Muscle Fiber Alpha Dystroglycan in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Systolic Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Natural Killer Cell Count in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Prothrombin Antigen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Spinal Stenosis With <strong>Reducedstrong> Interpedicular Distance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Muscle Fiber Merosin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> 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.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Mildly <strong>Reducedstrong> Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Mitochondrial Malic Enzyme <strong>Reducedstrong> in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Brain Creatine Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Prothrombin Consumption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Number Of Intrahepatic Bile Ducts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Amygdala Volume in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Proportion Of Naive T Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Brain Choline Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Maximal Inspiratory Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> C-Peptide Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Quantity Of Von Willebrand Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Brain Glutamine Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Erythrocyte 2,3-Diphosphoglycerate Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Antigen-Specific T Cell Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Granulocyte Cd59 Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Thyroxin-Binding Globulin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Exercise Tolerance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Antithrombin Antigen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Euglobulin Clot Lysis Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Muscle Carnitine Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype <strong>Reducedstrong> Lymphocyte Surface Expression Of Cd43 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> male fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> male mating frequency phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> NMDA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> enamel thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> sensorimotor gating phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> thrombolysis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> hair shaft melanin granule number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> AMPA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From MGI Mouse Phenotype Associations 2023

gene mutations causing the <strong>reducedstrong> sympathetic cervical ganglion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> quantity of Von Willebrand factor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> delayed hypersensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> eye contact phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> bone mineral density phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> muscle fiber perlecan phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> left ventricular ejection fraction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> sperm motility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Beta blocker survival benefit in heart failure with <strong>reducedstrong> ejection fraction (time to all cause mortality x beta blocker interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the <strong>Reducedstrong> foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (<strong>reducedstrong> eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (<strong>reducedstrong> 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.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of <strong>proteinstrong> kinase activity by regulation of <strong>proteinstrong> phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the activation of signaling <strong>proteinstrong> activity involved in unfolded <strong>proteinstrong> response biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2023

genes participating in the negative regulation of <strong>proteinstrong> kinase activity by regulation of <strong>proteinstrong> phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.

From GO Biological Process Annotations 2025

genes participating in the negative regulation of <strong>proteinstrong> kinase activity by regulation of <strong>proteinstrong> phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; pre-eclampsia; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease factor v deficiency; hypoprothrombinemias; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease activated <strong>proteinstrong> c resistance; <strong>proteinstrong> s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; <strong>proteinstrong> c deficiency; <strong>proteinstrong> s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of <strong>proteinstrong> ubiquitination involved in ubiquitin-dependent <strong>proteinstrong> catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> modification by small <strong>proteinstrong> conjugation biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of g-<strong>proteinstrong> coupled receptor <strong>proteinstrong> signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> maturation by <strong>proteinstrong> folding biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> targeting to vacuole involved in ubiquitin-dependent <strong>proteinstrong> catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of <strong>proteinstrong> modification by small <strong>proteinstrong> conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of <strong>proteinstrong> processing involved in <strong>proteinstrong> targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of g-<strong>proteinstrong> coupled receptor <strong>proteinstrong> signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of <strong>proteinstrong> processing involved in <strong>proteinstrong> targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the desensitization of g-<strong>proteinstrong> coupled receptor <strong>proteinstrong> signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of <strong>proteinstrong> modification by small <strong>proteinstrong> conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> ubiquitination involved in ubiquitin-dependent <strong>proteinstrong> catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of <strong>proteinstrong> ubiquitination involved in ubiquitin-dependent <strong>proteinstrong> catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> deubiquitination involved in ubiquitin-dependent <strong>proteinstrong> catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of g-<strong>proteinstrong> coupled receptor <strong>proteinstrong> signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of <strong>proteinstrong> ubiquitination involved in ubiquitin-dependent <strong>proteinstrong> catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> processing involved in <strong>proteinstrong> targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of <strong>proteinstrong> modification by small <strong>proteinstrong> conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> kinase c-activating g-<strong>proteinstrong> coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the desensitization of g-<strong>proteinstrong> coupled receptor <strong>proteinstrong> signaling pathway by arrestin biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> modification by small <strong>proteinstrong> removal biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the <strong>proteinstrong> modification by small <strong>proteinstrong> conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the <strong>proteinstrong> binding involved in <strong>proteinstrong> folding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Vacuolar <strong>proteinstrong> sorting-associated <strong>proteinstrong> 54 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Myelin <strong>proteinstrong> zero-like <strong>proteinstrong> 1 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Myelin <strong>proteinstrong> zero-like <strong>proteinstrong> 2 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Myelin <strong>proteinstrong> zero-like <strong>proteinstrong> 3 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Tumour <strong>proteinstrong> p53-inducible nuclear <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the ADP-ribosylation factor-like <strong>proteinstrong> 6-interacting <strong>proteinstrong> 6 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Dyslexia-associated <strong>proteinstrong> KIAA0319-like <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Small proline-rich <strong>proteinstrong>/late cornified envelope <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the <strong>Proteinstrong> kinase A anchor <strong>proteinstrong>, RI-RII subunit-binding domain <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Guanine nucleotide binding <strong>proteinstrong> (G-<strong>proteinstrong>), alpha subunit <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the <strong>Proteinstrong> transport <strong>proteinstrong> SecG/Sec61-beta/Sbh <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the <strong>Proteinstrong> of unknown function DUF3669, zinc finger <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the 50S ribosomal <strong>proteinstrong> L18Ae/60S ribosomal <strong>proteinstrong> L20 and L18a <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Cleft lip and palate transmembrane <strong>proteinstrong> 1-like <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Pre-rRNA-processing <strong>proteinstrong> IPI1/Testis-expressed sequence 10 <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Tumor <strong>proteinstrong> p53-inducible <strong>proteinstrong> 11 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the V-set and transmembrane domain-containing <strong>proteinstrong> 2-like <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Actin-related <strong>proteinstrong> 2/3 complex subunit 5-like <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the GTP-binding <strong>proteinstrong> TrmE/Glycine cleavage system T <strong>proteinstrong>, domain 1 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Insulin-like growth factor binding <strong>proteinstrong>-related <strong>proteinstrong> (IGFBP-rP), MAC25 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Vacuolar <strong>proteinstrong> sorting-associated <strong>proteinstrong> 13 domain <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the EH domain-binding <strong>proteinstrong> 1-like <strong>proteinstrong> 1 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the SWR1-complex <strong>proteinstrong> 5/Craniofacial development <strong>proteinstrong> <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the DMRT/<strong>proteinstrong> doublesex/<strong>proteinstrong> male abnormal 3 <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

<strong>proteinstrong>s predicted to have the Vacuolar <strong>proteinstrong> sorting <strong>proteinstrong> 36, GLUE domain <strong>proteinstrong> domain from the InterPro Predicted <strong>Proteinstrong> Domain Annotations dataset.