Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency

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Results for "Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency": 1003 gene sets

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Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, congenital, associated with episodic apnea Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with episodic apnea phenotype from the curated OMIM Gene-Disease Associations dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myasthenic syndrome, acetazolamide-responsive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myasthenic syndrome, acetazolamide-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myasthenic syndrome with episodic apnea Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset.
Congenital myasthenic syndrome ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome ib from the curated CTD Gene-Disease Associations dataset.
Myasthenic syndrome, congenital, postsynaptic slow-channel Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic syndrome, congenital, postsynaptic slow-channel from the curated CTD Gene-Disease Associations dataset.
Myasthenic Syndrome, Congenital, Fast-Channel Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic Syndrome, Congenital, Fast-Channel from the curated CTD Gene-Disease Associations dataset.
congenital myasthenic syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital myasthenic syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital myasthenic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital myasthenic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myasthenic syndrome, fast-channel congenital Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, fast-channel congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, slow-channel congenital Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, slow-channel congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Gene Set From Reactome Pathways 2014 proteins participating in the Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) pathway from the Reactome Pathways dataset.
Congenital Myasthenic Syndrome Ib Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myasthenic Syndrome Ib in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital myasthenic syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myasthenic syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myasthenic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 3B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 3B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 3A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 4C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 4C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 4B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 4B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myasthenic syndrome 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myasthenic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myasthenic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Presynaptic congenital myasthenic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Presynaptic congenital myasthenic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Myasthenic Syndromes, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic Syndromes, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Myasthenic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myasthenic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myopathy With Myasthenic-Like Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myopathy With Myasthenic-Like Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synaptic congenital myasthenic syndromes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Synaptic congenital myasthenic syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lambert-eaton myasthenic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lambert-eaton myasthenic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung cancer; lambert-eaton myasthenic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer; lambert-eaton myasthenic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Lambert-Eaton Myasthenic Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lambert-Eaton Myasthenic Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
myasthenic syndrome, acetazolamide-responsive Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, acetazolamide-responsive phenotype from the curated OMIM Gene-Disease Associations dataset.
Lambert-Eaton Myasthenic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lambert-Eaton Myasthenic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lambert-Eaton myasthenic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lambert-Eaton myasthenic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myasthenic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myasthenic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GFPT1-related myasthenic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GFPT1-related myasthenic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
g-protein coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the g-protein coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
adenylate cyclase-inhibiting g-protein coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the adenylate cyclase-inhibiting g-protein coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
phospholipase c-activating g-protein coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating g-protein coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine receptor regulator activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine receptor regulator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
g-protein coupled acetylcholine receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the g-protein coupled acetylcholine receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine receptor activator activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine receptor activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine receptor binding Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Nicotinic acetylcholine receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nicotinic acetylcholine receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor M3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscarinic acetylcholine receptor M3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor M2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscarinic acetylcholine receptor M2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor M5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscarinic acetylcholine receptor M5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor M4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscarinic acetylcholine receptor M4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nicotinic acetylcholine-gated receptor, transmembrane domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nicotinic acetylcholine-gated receptor, transmembrane domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscarinic acetylcholine receptor family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor M1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscarinic acetylcholine receptor M1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Muscarinic acetylcholine receptor 2 and 4 signaling pathway Gene Set From PANTHER Pathways proteins participating in the Muscarinic acetylcholine receptor 2 and 4 signaling pathway pathway from the PANTHER Pathways dataset.
Nicotinic acetylcholine receptor signaling pathway Gene Set From PANTHER Pathways proteins participating in the Nicotinic acetylcholine receptor signaling pathway pathway from the PANTHER Pathways dataset.
Muscarinic acetylcholine receptor 1 and 3 signaling pathway Gene Set From PANTHER Pathways proteins participating in the Muscarinic acetylcholine receptor 1 and 3 signaling pathway pathway from the PANTHER Pathways dataset.
G protein-coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine receptor binding Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acetylcholine receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
G protein-coupled acetylcholine receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the G protein-coupled acetylcholine receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acetylcholine receptor regulator activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine receptor regulator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acetylcholine receptor activator activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine receptor activator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acetylcholine receptor inhibitor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine receptor inhibitor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
G protein-coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine receptor activator activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine receptor activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
G protein-coupled acetylcholine receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the G protein-coupled acetylcholine receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine receptor regulator activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine receptor regulator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine receptor inhibitor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine receptor inhibitor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein 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.
congenital heart defects; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
TNF receptor-associated periodic fever syndrome (TRAPS) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the TNF receptor-associated periodic fever syndrome (TRAPS) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
tumor necrosis factor receptor-associated periodic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease tumor necrosis factor receptor-associated periodic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Tnf Receptor-Associated Periodic Fever Syndrome (Traps) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tnf Receptor-Associated Periodic Fever Syndrome (Traps) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tumor Necrosis Factor Receptor Associated Periodic Syndrome [Traps] Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tumor Necrosis Factor Receptor Associated Periodic Syndrome [Traps] in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
TNF receptor-associated periodic fever syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TNF receptor-associated periodic fever syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
myasthenic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term myasthenic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Myasthenic Crisis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenic Crisis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vesicle-associated membrane protein-associated protein B Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein B protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vesicle-associated membrane protein-associated protein A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vesicle-associated membrane-protein-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane-protein-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
chronic ulcerative colitis (CUC), ulcerative colitis?associated dysplasia (UCD), colitis-associated cancer (CAC) Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease chronic ulcerative colitis (CUC), ulcerative colitis?associated dysplasia (UCD), colitis-associated cancer (CAC) from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
autoimmune-associated congenital heart block. Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune-associated congenital heart block. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Other Congenital Malformations Of Spine, Not Associated With Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformations Of Spine, Not Associated With Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Channelopathy-associated congenital insensitivity to pain Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Channelopathy-associated congenital insensitivity to pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Plcg2-Associated Antibody Deficiency And Immune Dysregulation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Plcg2-Associated Antibody Deficiency And Immune Dysregulation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
role of nicotinic acetylcholine receptors in the regulation of apoptosis Gene Set From Biocarta Pathways proteins participating in the role of nicotinic acetylcholine receptors in the regulation of apoptosis pathway from the Biocarta Pathways dataset.
clathrin-sculpted acetylcholine transport vesicle Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the clathrin-sculpted acetylcholine transport vesicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
acetylcholine-gated channel complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the acetylcholine-gated channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
clathrin-sculpted acetylcholine transport vesicle membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the clathrin-sculpted acetylcholine transport vesicle membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
acetylcholine-gated channel complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the acetylcholine-gated channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Acetylcholine Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Acetylcholine from the curated CTD Gene-Chemical Interactions dataset.
Acetylcholine Gene Set From DrugBank Drug Targets interacting proteins for the Acetylcholine drug from the curated DrugBank Drug Targets dataset.
acetylcholine responsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease acetylcholine responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acetylcholine Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term acetylcholine in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2015 genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine transport Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine transport biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2015 dataset.
vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2015 genes participating in the vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine catabolic process in synaptic cleft Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine catabolic process in synaptic cleft biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the acetylcholine catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
acetylcholine-gated channel complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the acetylcholine-gated channel complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
clathrin-sculpted acetylcholine transport vesicle membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the clathrin-sculpted acetylcholine transport vesicle membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
acetylcholine-activated cation-selective channel activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine-activated cation-selective channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine binding Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine-gated cation channel activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acetylcholine-gated cation channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acetylcholine Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the acetylcholine ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
Acetylcholine Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Acetylcholine metabolite from the curated HMDB Metabolites of Enzymes dataset.
abnormal synaptic acetylcholine release Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal synaptic acetylcholine release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Acetylcholine Neurotransmitter Release Cycle Gene Set From Reactome Pathways 2014 proteins participating in the Acetylcholine Neurotransmitter Release Cycle pathway from the Reactome Pathways dataset.
Highly sodium permeable acetylcholine nicotinic receptors Gene Set From Reactome Pathways 2014 proteins participating in the Highly sodium permeable acetylcholine nicotinic receptors pathway from the Reactome Pathways dataset.
Highly calcium permeable nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Highly calcium permeable nicotinic acetylcholine receptors pathway from the Reactome Pathways dataset.
Muscarinic acetylcholine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Muscarinic acetylcholine receptors pathway from the Reactome Pathways dataset.
Postsynaptic nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Postsynaptic nicotinic acetylcholine receptors pathway from the Reactome Pathways dataset.
Highly calcium permeable postsynaptic nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Highly calcium permeable postsynaptic nicotinic acetylcholine receptors pathway from the Reactome Pathways dataset.
Acetylcholine regulates insulin secretion Gene Set From Reactome Pathways 2014 proteins participating in the Acetylcholine regulates insulin secretion pathway from the Reactome Pathways dataset.
Activation of Nicotinic Acetylcholine Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Activation of Nicotinic Acetylcholine Receptors pathway from the Reactome Pathways dataset.
Presynaptic nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Presynaptic nicotinic acetylcholine receptors pathway from the Reactome Pathways dataset.
Acetylcholine Binding And Downstream Events Gene Set From Reactome Pathways 2014 proteins participating in the Acetylcholine Binding And Downstream Events pathway from the Reactome Pathways dataset.
Acetylcholine Synthesis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Acetylcholine Synthesis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Acetylcholine Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Acetylcholine Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Favorable Response Of Weakness To Acetylcholine Esterase Inhibitors Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Favorable Response Of Weakness To Acetylcholine Esterase Inhibitors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unfavorable Response Of Muscle Weakness To Acetylcholine Esterase Inhibitors Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unfavorable Response Of Muscle Weakness To Acetylcholine Esterase Inhibitors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.
skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2023 genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine transport Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine transport biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to acetylcholine Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to acetylcholine biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset.
response to acetylcholine Gene Set From GO Biological Process Annotations 2023 genes participating in the response to acetylcholine biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine catabolic process in synaptic cleft Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine catabolic process in synaptic cleft biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine uptake Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine uptake biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of acetylcholine uptake Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of acetylcholine uptake biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of systemic arterial blood pressure by acetylcholine Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by acetylcholine biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the acetylcholine metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
acetylcholine-gated channel complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the acetylcholine-gated channel complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
clathrin-sculpted acetylcholine transport vesicle membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the clathrin-sculpted acetylcholine transport vesicle membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
clathrin-sculpted acetylcholine transport vesicle Gene Set From GO Cellular Component Annotations 2023 proteins localized to the clathrin-sculpted acetylcholine transport vesicle cellular component from the curated GO Cellular Component Annotations 2023 dataset.
acetylcholine transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acetylcholine-gated monoatomic cation-selective channel activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine-gated monoatomic cation-selective channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acetylcholine:proton antiporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acetylcholine:proton antiporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal synaptic acetylcholine release Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synaptic acetylcholine release phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased acetylcholine level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased acetylcholine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased acetylcholine level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased acetylcholine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Acetylcholine Gene Set From MW Enzyme Metabolite Associations interacting proteins for Acetylcholine metabolite from the MW Gene Metabolite Associations dataset.
Acetylcholine synthesis Gene Set From WikiPathways Pathways 2024 proteins participating in the Acetylcholine synthesis pathway from the WikiPathways Pathways 2024 dataset.
Acetylcholine Neurotransmitter Release Cycle Gene Set From Reactome Pathways 2024 proteins participating in the Acetylcholine Neurotransmitter Release Cycle pathway from the Reactome Pathways 2024 dataset.
Acetylcholine binding and downstream events Gene Set From Reactome Pathways 2024 proteins participating in the Acetylcholine binding and downstream events pathway from the Reactome Pathways 2024 dataset.
Acetylcholine inhibits contraction of outer hair cells Gene Set From Reactome Pathways 2024 proteins participating in the Acetylcholine inhibits contraction of outer hair cells pathway from the Reactome Pathways 2024 dataset.
Acetylcholine regulates insulin secretion Gene Set From Reactome Pathways 2024 proteins participating in the Acetylcholine regulates insulin secretion pathway from the Reactome Pathways 2024 dataset.
Highly calcium permeable nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Highly calcium permeable nicotinic acetylcholine receptors pathway from the Reactome Pathways 2024 dataset.
Highly calcium permeable postsynaptic nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Highly calcium permeable postsynaptic nicotinic acetylcholine receptors pathway from the Reactome Pathways 2024 dataset.
Highly sodium permeable postsynaptic acetylcholine nicotinic receptors Gene Set From Reactome Pathways 2024 proteins participating in the Highly sodium permeable postsynaptic acetylcholine nicotinic receptors pathway from the Reactome Pathways 2024 dataset.
Muscarinic acetylcholine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Muscarinic acetylcholine receptors pathway from the Reactome Pathways 2024 dataset.
Postsynaptic nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Postsynaptic nicotinic acetylcholine receptors pathway from the Reactome Pathways 2024 dataset.
Presynaptic nicotinic acetylcholine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Presynaptic nicotinic acetylcholine receptors pathway from the Reactome Pathways 2024 dataset.
regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.
skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2025 genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine transport Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine transport biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to acetylcholine Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to acetylcholine biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset.
response to acetylcholine Gene Set From GO Biological Process Annotations 2025 genes participating in the response to acetylcholine biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine catabolic process in synaptic cleft Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine catabolic process in synaptic cleft biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of acetylcholine secretion, neurotransmission Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of acetylcholine secretion, neurotransmission biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine uptake Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine uptake biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of acetylcholine uptake Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of acetylcholine uptake biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of systemic arterial blood pressure by acetylcholine Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by acetylcholine biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the acetylcholine metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
acetylcholine-gated channel complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the acetylcholine-gated channel complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
clathrin-sculpted acetylcholine transport vesicle membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the clathrin-sculpted acetylcholine transport vesicle membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
clathrin-sculpted acetylcholine transport vesicle Gene Set From GO Cellular Component Annotations 2025 proteins localized to the clathrin-sculpted acetylcholine transport vesicle cellular component from the curated GO Cellular Component Annotations 2025 dataset.
acetylcholine transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine-gated monoatomic cation-selective channel activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine-gated monoatomic cation-selective channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine binding Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine:proton antiporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acetylcholine:proton antiporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acetylcholine-gated channel complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the acetylcholine-gated channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
clathrin-sculpted acetylcholine transport vesicle Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the clathrin-sculpted acetylcholine transport vesicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
clathrin-sculpted acetylcholine transport vesicle membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the clathrin-sculpted acetylcholine transport vesicle membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
acetylcholine-gated channel complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the acetylcholine-gated channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart Defects, Congenital, And Other Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interleukin-1 receptor-associated kinase 1-binding protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interleukin-1 receptor-associated kinase 1-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Trace amine associated receptor family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Trace amine associated receptor family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Alpha-2-macroglobulin receptor-associated protein, domain 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha-2-macroglobulin receptor-associated protein, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Trace amine associated receptor 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Trace amine associated receptor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
T-cell receptor-associated transmembrane adapter 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the T-cell receptor-associated transmembrane adapter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interleukin-1 receptor-associated kinase 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interleukin-1 receptor-associated kinase 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thyroid hormone receptor-associated protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thyroid hormone receptor-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Receptor tyrosine-protein phosphatase C-associated protein CD45-AP Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor tyrosine-protein phosphatase C-associated protein CD45-AP protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor TRAF Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor TRAF protein domain from the InterPro Predicted Protein Domain Annotations dataset.
B-cell receptor-associated protein 29/31 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the B-cell receptor-associated protein 29/31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TNF receptor-associated factor 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TNF receptor-associated factor 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Angiotensin II, type I receptor-associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Angiotensin II, type I receptor-associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myeloid And/Or Lymphoid Neoplasm Associated With Platelet Derived Growth Factor Receptor Alpha Rearrangement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myeloid And/Or Lymphoid Neoplasm Associated With Platelet Derived Growth Factor Receptor Alpha Rearrangement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prothrombin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamine deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Lactase Deficiency, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Sucrase-isomaltase deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sucrase-isomaltase deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
PROTHROMBIN DEFICIENCY, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROTHROMBIN DEFICIENCY, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Glutamine deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutamine deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
congenital intrinsic factor deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital intrinsic factor deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital intrinsic factor deficiency. Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital intrinsic factor deficiency. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital haptoglobin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital haptoglobin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to itga7 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
[lpa deficiency, congenital] Gene Set From OMIM Gene-Disease Associations genes associated with the [lpa deficiency, congenital] phenotype from the curated OMIM Gene-Disease Associations dataset.
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
lactase deficiency, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the lactase deficiency, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoaldosteronism, congenital, due to cmo i deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
glutamine deficiency, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the glutamine deficiency, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
sucrase-isomaltase deficiency, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the sucrase-isomaltase deficiency, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Deficiency Of Pulmonary Surfactant Protein B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Deficiency Of Pulmonary Surfactant Protein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sucrase-Isomaltase Deficiency, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sucrase-Isomaltase Deficiency, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Leukocyte Adherence Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Leukocyte Adherence Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Deficiency Of Intrinsic Factor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Deficiency Of Intrinsic Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glutamine Deficiency, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glutamine Deficiency, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Leptin Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Leptin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lp(A) Deficiency, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lp(A) Deficiency, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Isolated Thyroid Stimulating Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Isolated Thyroid Stimulating Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Thrombotic Disease, Due To Protein C Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Thrombotic Disease, Due To Protein C Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anti-Plasmin Deficiency, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Plasmin Deficiency, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lactase Deficiency, Congenital Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lactase Deficiency, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Congenital leptin deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital leptin deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital sucrase-isomaltase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital sucrase-isomaltase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital leptin deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital leptin deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital lactase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital lactase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital sucrase-isomaltase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital sucrase-isomaltase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to integrin alpha-7 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital intrinsic factor deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital intrinsic factor deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital factor V deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital factor V deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary thrombophilia due to congenital protein C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital protein C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital isolated adrenocorticotropic hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital isolated adrenocorticotropic hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital factor VII deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital factor VII deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital prothrombin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital prothrombin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital plasminogen activator inhibitor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital plasminogen activator inhibitor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to integrin alpha-7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to CSF3R deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital brain dysgenesis due to glutamine synthetase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital brain dysgenesis due to glutamine synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to congenital leptin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to congenital leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated congenital growth hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated congenital growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital NAD deficiency disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital NAD deficiency disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sucrose-isomaltase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sucrose-isomaltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary thrombophilia due to congenital protein S deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital protein S deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lymphoproliferative syndrome, ebv-associated, autosomal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lymphoproliferative syndrome, ebv-associated, autosomal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HIV-Associated Lipodystrophy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HIV-Associated Lipodystrophy Syndrome from the curated CTD Gene-Disease Associations dataset.
Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 from the curated CTD Gene-Disease Associations dataset.
hemochromatosis; hiv infections; hiv-associated lipodystrophy syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; hiv infections; hiv-associated lipodystrophy syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; hiv-associated lipodystrophy syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; hiv-associated lipodystrophy syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x associated tremor/ataxia syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; hiv-associated lipodystrophy syndrome; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; hiv-associated lipodystrophy syndrome; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nevoid basal cell carcinoma syndrome associated Gene Set From GAD Gene-Disease Associations genes associated with the disease nevoid basal cell carcinoma syndrome associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x-associated tremor/ataxia syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x-associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv-associated lipodystrophy syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv-associated lipodystrophy syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslipidemias; hiv infections; hiv-associated lipodystrophy syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslipidemias; hiv infections; hiv-associated lipodystrophy syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
HIV-Associated Lipodystrophy Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the HIV-Associated Lipodystrophy Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Joubert syndrome-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Joubert syndrome-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
turner syndrome-associated neurocognitive phenotype Gene Set From OMIM Gene-Disease Associations genes associated with the turner syndrome-associated neurocognitive phenotype phenotype from the curated OMIM Gene-Disease Associations dataset.
Hiv-Associated Lipodystrophy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv-Associated Lipodystrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proteasome-Associated Autoinflammatory Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proteasome-Associated Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myeloid Leukemia Associated With Down Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myeloid Leukemia Associated With Down Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Behavioral Syndrome Associated With Physiological Disturbance And Physical Factors Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Behavioral Syndrome Associated With Physiological Disturbance And Physical Factors in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myeloid Proliferations Associated With Down Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myeloid Proliferations Associated With Down Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
MECP2 and associated Rett syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the MECP2 and associated Rett syndrome pathway from the WikiPathways Pathways 2024 dataset.
SATB2-associated syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease SATB2-associated syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease proteosome-associated autoinflammatory syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
proteasome-associated autoinflammatory syndrome 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease proteasome-associated autoinflammatory syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fragile X-associated tremor/ataxia syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fragile X-associated tremor/ataxia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteasome-associated autoinflammatory syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteasome-associated autoinflammatory syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
SATB2-associated syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SATB2-associated syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteasome-associated autoinflammatory syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteasome-associated autoinflammatory syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
proteosome-associated autoinflammatory syndrome 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease proteosome-associated autoinflammatory syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myeloid leukemia associated with Down Syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid leukemia associated with Down Syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cryopyrin associated periodic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cryopyrin associated periodic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proteasome-associated autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proteasome-associated autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proteosome-associated autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proteosome-associated autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fragile X-associated tremor/ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fragile X-associated tremor/ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MECOM-associated syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MECOM-associated syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
UBR4-associated neurodevelopmental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the UBR4-associated neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PUM1-associated developmental disability-ataxia-seizure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PUM1-associated developmental disability-ataxia-seizure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SIM1-associated metabolic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SIM1-associated metabolic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TNK2-associated Epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TNK2-associated Epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
EEF1D-associated Neurodevelopmental Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the EEF1D-associated Neurodevelopmental Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FBRSL1-associated neurodevelopmental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FBRSL1-associated neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuraminidase deficiency with beta-galactosidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choline deficiency; dna damage; folic acid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
protein c deficiency; protein s deficiency; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Set From Reactome Pathways 2024 proteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset.
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Interferon gamma receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interferon gamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interleukin 2 Receptor, Alpha, Deficiency of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Interleukin 2 Receptor, Alpha, Deficiency of from the curated CTD Gene-Disease Associations dataset.
interleukin-7 receptor alpha deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease interleukin-7 receptor alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obesity, morbid, due to leptin receptor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
interleukin 1 receptor antagonist deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the interleukin 1 receptor antagonist deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
[igg receptor i, phagocytic, familial deficiency of] Gene Set From OMIM Gene-Disease Associations genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset.
interleukin-2 receptor, alpha chain, deficiency of Gene Set From OMIM Gene-Disease Associations genes associated with the interleukin-2 receptor, alpha chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.
Glucocorticoid Receptor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucocorticoid Receptor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Androgen Receptor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Androgen Receptor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Receptor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Receptor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interleukin 2 Receptor, Alpha, Deficiency Of Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interleukin 2 Receptor, Alpha, Deficiency Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ifn-Gamma Receptor 1 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ifn-Gamma Receptor 1 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interferon Gamma Receptor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interferon Gamma Receptor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interferon Gamma, Receptor 1, Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interferon Gamma, Receptor 1, Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interleukin 1 Receptor Antagonist Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interleukin 1 Receptor Antagonist Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Melanocortin 4 Receptor Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Melanocortin 4 Receptor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Igg Receptor I, Phagocytic, Familial Deficiency Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Igg Receptor I, Phagocytic, Familial Deficiency Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebral folate receptor alpha deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral folate receptor alpha deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral folate receptor alpha deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral folate receptor alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
interleukin-7 receptor alpha deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease interleukin-7 receptor alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature due to growth hormone secretagogue receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone secretagogue receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to leptin receptor gene deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to leptin receptor gene deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to melanocortin 4 receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to melanocortin 4 receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
IFN-gamma receptor 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the IFN-gamma receptor 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Interferon gamma receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Interferon gamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal Congenital Contracture Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Congenital central hypoventilation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.
Lethal congenital contracture syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.
RETT SYNDROME, CONGENITAL VARIANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RETT SYNDROME, CONGENITAL VARIANT from the curated CTD Gene-Disease Associations dataset.
Lethal Congenital Contractural Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Congenital Contractural Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set From GAD Gene-Disease Associations genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital central hypoventilation syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital central hypoventilation syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
limb deformities, congenital; rothmund-thomson syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease limb deformities, congenital; rothmund-thomson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital sick sinus syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital sick sinus syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital nephrotic syndrome Gene Set From HPO Gene-Disease Associations genes associated with the congenital nephrotic syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rett syndrome, congenital variant Gene Set From OMIM Gene-Disease Associations genes associated with the rett syndrome, congenital variant phenotype from the curated OMIM Gene-Disease Associations dataset.
central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.
lethal congenital contracture syndrome 5 Gene Set From OMIM Gene-Disease Associations genes associated with the lethal congenital contracture syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
lethal congenital contracture syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lethal congenital contracture syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
lethal congenital contracture syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the lethal congenital contracture syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital short bowel syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
central hypoventilation syndrome, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
melanocytic nevus syndrome, congenital, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the melanocytic nevus syndrome, congenital, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
lethal congenital contractural syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the lethal congenital contractural syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
lethal congenital contractural syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the lethal congenital contractural syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Varicella Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Varicella Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Malformation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lethal Congenital Contractural Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lethal Congenital Contractural Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Kidneys Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Kidneys Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Junctional Epidermolysis Bullosa-Pyloric Atresia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Junctional Epidermolysis Bullosa-Pyloric Atresia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Finnish Congenital Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Finnish Congenital Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Long Qt Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Hypertrophy-Cerebral Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Hypertrophy-Cerebral Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Lipodystrophy, Congenital Cataracts, And Neurodegeneration Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Lipodystrophy, Congenital Cataracts, And Neurodegeneration Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Rubella Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Rubella Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lethal Congenital Contracture Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lethal Congenital Contracture Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Zika Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Zika Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interstitial Lung Disease, Nephrotic Syndrome, And Epidermolysis Bullosa, Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interstitial Lung Disease, Nephrotic Syndrome, And Epidermolysis Bullosa, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Neutropenia, Myelofibrosis, Nephromegaly Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Neutropenia, Myelofibrosis, Nephromegaly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progeroid Syndrome, Congenital, Petty Type Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progeroid Syndrome, Congenital, Petty Type in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Congenital central hypoventilation syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital central hypoventilation syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital central hypoventilation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital central hypoventilation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lethal congenital contracture syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lethal congenital contracture syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital limbs-face contractures-hypotonia-developmental delay syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital limbs-face contractures-hypotonia-developmental delay syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Zika virus congenital syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Zika virus congenital syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lethal congenital contracture syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lethal congenital contracture syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lethal congenital contracture syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lethal congenital contracture syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lethal congenital contracture syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lethal congenital contracture syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lethal congenital contracture syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lethal congenital contracture syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pancreatic hypoplasia-diabetes-congenital heart disease syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataracts-facial dysmorphism-neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataracts-facial dysmorphism-neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal congenital contracture syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal congenital contracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal congenital contractural syndrome Finnish Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal congenital contractural syndrome Finnish phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Slow-Channel Congenital Myasthenia Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Slow-Channel Congenital Myasthenia Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancreatic hypoplasia-diabetes-congenital heart disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Porencephaly-microcephaly-bilateral congenital cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Porencephaly-microcephaly-bilateral congenital cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KAT6B-related multiple congenital anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KAT6B-related multiple congenital anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital short bowel syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital short bowel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital neutropenia-myelofibrosis-nephromegaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital neutropenia-myelofibrosis-nephromegaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies/dysmorphic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies/dysmorphic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital heart defects and skeletal malformations syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital heart defects and skeletal malformations syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital bilateral perisylvian syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bilateral perisylvian syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital insensitivity to pain-hypohidrosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital insensitivity to pain-hypohidrosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital anomalies of kidney and urinary tract syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital anomalies of kidney and urinary tract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies-neurodevelopmental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
neuroregulin receptor degredation protein-1 controls erbb3 receptor recycling Gene Set From Biocarta Pathways proteins participating in the neuroregulin receptor degredation protein-1 controls erbb3 receptor recycling pathway from the Biocarta Pathways dataset.
toll-like receptor 2-toll-like receptor 6 protein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
toll-like receptor 1-toll-like receptor 2 protein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
TGF-beta receptor II-TGF-beta receptor I-TGF-beta3 complex Gene Set From CORUM Protein Complexes proteins in the TGF-beta receptor II-TGF-beta receptor I-TGF-beta3 complex protein complex from the CORUM Protein Complexes dataset.
TGF-beta receptor II-TGF-beta receptor I-TGF-beta1 complex Gene Set From CORUM Protein Complexes proteins in the TGF-beta receptor II-TGF-beta receptor I-TGF-beta1 complex protein complex from the CORUM Protein Complexes dataset.
epidermal growth factor-activated receptor transactivation by g-protein coupled receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the epidermal growth factor-activated receptor transactivation by g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
toll-like receptor 2-toll-like receptor 6 protein complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
toll-like receptor 1-toll-like receptor 2 protein complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
receptor tyrosine kinase-like orphan receptor binding Gene Set From GO Molecular Function Annotations 2015 genes performing the receptor tyrosine kinase-like orphan receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
G protein-coupled receptor 40-related receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the G protein-coupled receptor 40-related receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein-tyrosine phosphatase, receptor/non-receptor type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-tyrosine phosphatase, receptor/non-receptor type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Gamma-aminobutyric acid A receptor/Glycine receptor alpha Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Gamma-aminobutyric acid A receptor/Glycine receptor alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Oestrogen receptor/oestrogen-related receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Oestrogen receptor/oestrogen-related receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Receptor-ligand binding initiates the second proteolytic cleavage of Notch receptor Gene Set From Reactome Pathways 2014 proteins participating in the Receptor-ligand binding initiates the second proteolytic cleavage of Notch receptor pathway from the Reactome Pathways dataset.
cross-receptor inhibition within G protein-coupled receptor heterodimer Gene Set From GO Biological Process Annotations 2023 genes participating in the cross-receptor inhibition within G protein-coupled receptor heterodimer biological process from the curated GO Biological Process Annotations 2023 dataset.
Toll-like receptor 1-Toll-like receptor 2 protein complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the Toll-like receptor 1-Toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
Toll-like receptor 2-Toll-like receptor 6 protein complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the Toll-like receptor 2-Toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
receptor-receptor interaction Gene Set From GO Molecular Function Annotations 2023 genes performing the receptor-receptor interaction molecular function from the curated GO Molecular Function Annotations 2023 dataset.
receptor tyrosine kinase-like orphan receptor binding Gene Set From GO Molecular Function Annotations 2023 genes performing the receptor tyrosine kinase-like orphan receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
cross-receptor inhibition within G protein-coupled receptor heterodimer Gene Set From GO Biological Process Annotations 2025 genes participating in the cross-receptor inhibition within G protein-coupled receptor heterodimer biological process from the curated GO Biological Process Annotations 2025 dataset.
Toll-like receptor 1-Toll-like receptor 2 protein complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the Toll-like receptor 1-Toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Toll-like receptor 2-Toll-like receptor 6 protein complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the Toll-like receptor 2-Toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
receptor-receptor interaction Gene Set From GO Molecular Function Annotations 2025 genes performing the receptor-receptor interaction molecular function from the curated GO Molecular Function Annotations 2025 dataset.
receptor tyrosine kinase-like orphan receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the receptor tyrosine kinase-like orphan receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Toll-like receptor 1-Toll-like receptor 2 protein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Toll-like receptor 1-Toll-like receptor 2 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Toll-like receptor 2-Toll-like receptor 6 protein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Toll-like receptor 2-Toll-like receptor 6 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Toll-like receptor 1-Toll-like receptor 2 protein complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Toll-like receptor 1-Toll-like receptor 2 protein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Toll-like receptor 2-Toll-like receptor 6 protein complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Toll-like receptor 2-Toll-like receptor 6 protein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glut1 deficiency syndrome 1, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex II deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucose transporter type 1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome caused by tenascin-X deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos syndrome caused by tenascin-X deficiency from the curated CTD Gene-Disease Associations dataset.
Growth mental deficiency syndrome of Myhre Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth mental deficiency syndrome of Myhre from the curated CTD Gene-Disease Associations dataset.
GLUT1 DEFICIENCY SYNDROME 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLUT1 DEFICIENCY SYNDROME 2 from the curated CTD Gene-Disease Associations dataset.
Leukocyte-Adhesion Deficiency Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte-Adhesion Deficiency Syndrome from the curated CTD Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
leukocyte-adhesion deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leukocyte-adhesion deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral creatine deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral creatine deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rh deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rh deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leigh syndrome and cytochrome c oxidase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease leigh syndrome and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
magnesium deficiency; wasting syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease magnesium deficiency; wasting syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; hemoglobinuria; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hemoglobinuria; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral creatine deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to mitochondrial complex i deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome, due to cox deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome, due to cox deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
glut1 deficiency syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the glut1 deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
glut1 deficiency syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the glut1 deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
autoinflammation, antibody deficiency, and immune dysregulation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the autoinflammation, antibody deficiency, and immune dysregulation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to mitochondrial cox4 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral creatine deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral creatine deficiency syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral creatine deficiency syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to cytochrome c oxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to mitochondrial complex 1 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
Polyglandular Deficiency Syndrome, Persian-Jewish Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglandular Deficiency Syndrome, Persian-Jewish Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iodine Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iodine Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glut1 Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glut1 Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bjornstad Syndrome With Mild Mitochondrial Complex Iii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bjornstad Syndrome With Mild Mitochondrial Complex Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leigh Syndrome Due To Mitochondrial Complex I Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leigh Syndrome Due To Mitochondrial Complex I Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antibody Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Factor Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Constitutional Mismatch Repair Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Constitutional Mismatch Repair Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Immunodeficiency Syndrome Due To P14 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Immunodeficiency Syndrome Due To P14 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercoagulability Syndrome Due To Glycosylphosphatidylinositol Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercoagulability Syndrome Due To Glycosylphosphatidylinositol Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rh Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rh Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) pathway from the Reactome Pathways 2024 dataset.
Cerebral creatine deficiency syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral creatine deficiency syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dopamine transporter deficiency syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dopamine transporter deficiency syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral creatine deficiency syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral creatine deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
IGSF1 deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease IGSF1 deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dopamine transporter deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dopamine transporter deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rh deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rh deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diphthamide deficiency syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diphthamide deficiency syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diphthamide deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diphthamide deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Classic dopamine transporter deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Classic dopamine transporter deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atypical dopamine transporter deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atypical dopamine transporter deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diphthamide deficiency syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diphthamide deficiency syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral creatine deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral creatine deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ehlers-Danlos syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ehlers-Danlos syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leigh syndrome due to mitochondrial complex IV deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leigh syndrome due to mitochondrial complex IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GLUT1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GLUT1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood onset GLUT1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset GLUT1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Classic dopamine transporter deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Classic dopamine transporter deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Coagulation factor deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Coagulation factor deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Creatine deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Creatine deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NTHL1-deficiency tumor predisposition syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NTHL1-deficiency tumor predisposition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
AP-4 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the AP-4 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary immunodeficiency syndrome due to p14 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary immunodeficiency syndrome due to p14 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Triokinase and FMN cyclase deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Triokinase and FMN cyclase deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
er associated degradation (erad) pathway Gene Set From Biocarta Pathways proteins participating in the er associated degradation (erad) pathway pathway from the Biocarta Pathways dataset.
phospholipase c delta in phospholipid associated cell signaling Gene Set From Biocarta Pathways proteins participating in the phospholipase c delta in phospholipid associated cell signaling pathway from the Biocarta Pathways dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pulmonary hypertension, primary, fenfluramine-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, fenfluramine-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYH-associated polyposis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MYH-associated polyposis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial platelet disorder with associated myeloid malignancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypobetalipoproteinemia, familial, associated with apob32 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sting-associated vasculopathy, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
senescence-associated heterochromatin focus Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the senescence-associated heterochromatin focus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
nascent polypeptide-associated complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nascent polypeptide-associated complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
dystrophin-associated glycoprotein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dystrophin-associated glycoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
golgi-associated vesicle Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the golgi-associated vesicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
spectrin-associated cytoskeleton Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the spectrin-associated cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
golgi-associated vesicle membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the golgi-associated vesicle membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
microtubule associated complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the microtubule associated complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
microtubule associated complex Gene Set From COMPARTMENTS Experimental Protein Localization Evidence Scores proteins localized to the microtubule associated complex cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
seh1-associated complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the seh1-associated complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
senescence-associated heterochromatin focus Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the senescence-associated heterochromatin focus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
lysp100-associated nuclear domain Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lysp100-associated nuclear domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
nascent polypeptide-associated complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nascent polypeptide-associated complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
dystrophin-associated glycoprotein complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dystrophin-associated glycoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
hemidesmosome associated protein complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the hemidesmosome associated protein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
golgi-associated vesicle Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the golgi-associated vesicle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
spectrin-associated cytoskeleton Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the spectrin-associated cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
psi associated light-harvesting complex i Gene Set From 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.
nucleolus-associated heterochromatin Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nucleolus-associated heterochromatin cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
golgi-associated vesicle membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the golgi-associated vesicle membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
psii associated light-harvesting complex ii Gene Set From 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.
microtubule associated complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the microtubule associated complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
presequence translocase-associated import motor Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the presequence translocase-associated import motor cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
CENP-A nucleosome associated complex Gene Set From CORUM Protein Complexes proteins in the CENP-A nucleosome associated complex protein complex from the CORUM Protein Complexes dataset.
Brm-associated complex Gene Set From CORUM Protein Complexes proteins in the Brm-associated complex protein complex from the CORUM Protein Complexes dataset.
(ER)-localized multiprotein complex, Ig heavy chains associated Gene Set From CORUM Protein Complexes proteins in the (ER)-localized multiprotein complex, Ig heavy chains associated protein complex from the CORUM Protein Complexes dataset.
HDAC1-associated core complex cI Gene Set From CORUM Protein Complexes proteins in the HDAC1-associated core complex cI protein complex from the CORUM Protein Complexes dataset.
p400-associated complex Gene Set From CORUM Protein Complexes proteins in the p400-associated complex protein complex from the CORUM Protein Complexes dataset.
Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Set From CORUM Protein Complexes proteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset.
DMAP1-associated complex Gene Set From CORUM Protein Complexes proteins in the DMAP1-associated complex protein complex from the CORUM Protein Complexes dataset.
HDAC1-associated core complex cII Gene Set From CORUM Protein Complexes proteins in the HDAC1-associated core complex cII protein complex from the CORUM Protein Complexes dataset.
Nop56p-associated pre-rRNA complex Gene Set From CORUM Protein Complexes proteins in the Nop56p-associated pre-rRNA complex protein complex from the CORUM Protein Complexes dataset.
Brg1-associated complex I Gene Set From CORUM Protein Complexes proteins in the Brg1-associated complex I protein complex from the CORUM Protein Complexes dataset.
Brg1-associated complex II Gene Set From CORUM Protein Complexes proteins in the Brg1-associated complex II protein complex from the CORUM Protein Complexes dataset.
HDAC1-associated protein complex Gene Set From CORUM Protein Complexes proteins in the HDAC1-associated protein complex protein complex from the CORUM Protein Complexes dataset.
Menin-associated histone methyltransferase complex Gene Set From CORUM Protein Complexes proteins in the Menin-associated histone methyltransferase complex protein complex from the CORUM Protein Complexes dataset.
Death-inducing signaling complex DISC (type I cells associated), stimulated Gene Set From CORUM Protein Complexes proteins in the Death-inducing signaling complex DISC (type I cells associated), stimulated protein complex from the CORUM Protein Complexes dataset.
BASC (Ab 80) complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC (Ab 80) complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
PU.1-associated protein complex Gene Set From CORUM Protein Complexes proteins in the PU.1-associated protein complex protein complex from the CORUM Protein Complexes dataset.
FCP1-associated protein complex Gene Set From CORUM Protein Complexes proteins in the FCP1-associated protein complex protein complex from the CORUM Protein Complexes dataset.
Splicing-associated factors complex Gene Set From CORUM Protein Complexes proteins in the Splicing-associated factors complex protein complex from the CORUM Protein Complexes dataset.
Cyclin D1-associated protein complex Gene Set From CORUM Protein Complexes proteins in the Cyclin D1-associated protein complex protein complex from the CORUM Protein Complexes dataset.
SRCAP-associated chromatin remodeling complex Gene Set From CORUM Protein Complexes proteins in the SRCAP-associated chromatin remodeling complex protein complex from the CORUM Protein Complexes dataset.
Parvulin-associated pre-rRNP complex Gene Set From CORUM Protein Complexes proteins in the Parvulin-associated pre-rRNP complex protein complex from the CORUM Protein Complexes dataset.
BRG1-associated complex Gene Set From CORUM Protein Complexes proteins in the BRG1-associated complex protein complex from the CORUM Protein Complexes dataset.
SAP complex (Sin3-associated protein complex) Gene Set From CORUM Protein Complexes proteins in the SAP complex (Sin3-associated protein complex) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.
LARC complex (LCR-associated remodeling complex) Gene Set From CORUM Protein Complexes proteins in the LARC complex (LCR-associated remodeling complex) protein complex from the CORUM Protein Complexes dataset.
FIB-associated protein complex Gene Set From CORUM Protein Complexes proteins in the FIB-associated protein complex protein complex from the CORUM Protein Complexes dataset.
BASC (Ab C-20) complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC (Ab C-20) complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.
BASC (Ab 81) complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC (Ab 81) complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
Membrane-associated multicomponent signaling complex, anti-CD40 stimulated (Cd40, Ikbkg, Map3k1, Traf2, Ube2n) Gene Set From CORUM Protein Complexes proteins in the Membrane-associated multicomponent signaling complex, anti-CD40 stimulated (Cd40, Ikbkg, Map3k1, Traf2, Ube2n) protein complex from the CORUM Protein Complexes dataset.
BASC complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.
Pantothenate Kinase-Associated Neurodegeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pantothenate Kinase-Associated Neurodegeneration from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.
Primary Ovarian Insufficiency, Fragile X-Associated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Primary Ovarian Insufficiency, Fragile X-Associated from the curated CTD Gene-Disease Associations dataset.
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis from the curated CTD Gene-Disease Associations dataset.
BREAST CANCER, 11-22 TRANSLOCATION-ASSOCIATED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST CANCER, 11-22 TRANSLOCATION-ASSOCIATED from the curated CTD Gene-Disease Associations dataset.
Cryopyrin-Associated Periodic Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cryopyrin-Associated Periodic Syndromes from the curated CTD Gene-Disease Associations dataset.
Heterotopia, Periventricular, associated with Chromosome 5p Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heterotopia, Periventricular, associated with Chromosome 5p Anomalies from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.
Heterotopia, Periventricular, Associated With Chromosome 5q Deletion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heterotopia, Periventricular, Associated With Chromosome 5q Deletion from the curated CTD Gene-Disease Associations dataset.
pantothenate kinase-associated neurodegeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pantothenate kinase-associated neurodegeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
respiratory bronchiolitis-associated interstitial lung disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease respiratory bronchiolitis-associated interstitial lung disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pantothenate kinase-associated neurodegeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pantothenate kinase-associated neurodegeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
isolated colobomas or colobomas associated Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated colobomas or colobomas associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
post-coital associated preterm births Gene Set From GAD Gene-Disease Associations genes associated with the disease post-coital associated preterm births in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thyroid associated orbitopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease thyroid associated orbitopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anti-neutrophil cytoplasmic antibody-associated vasculitis; Gene Set From GAD Gene-Disease Associations genes associated with the disease anti-neutrophil cytoplasmic antibody-associated vasculitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mucosa-associated lymphoid tissue lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease mucosa-associated lymphoid tissue lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
betel-associated oral carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease betel-associated oral carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
desmin-associated restrictive cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease desmin-associated restrictive cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asbestos-associated pulmonary disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease asbestos-associated pulmonary disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity- associated hypertension ??????? Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity- associated hypertension ??????? in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; pneumonia, ventilator-associated; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; pneumonia, ventilator-associated; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antineutrophil cytoplasmic antibody; (anca)-associated vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease antineutrophil cytoplasmic antibody; (anca)-associated vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hla-associated diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hla-associated diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
prolonged survival associated Gene Set From GAD Gene-Disease Associations genes associated with the disease prolonged survival associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cores and rods is associated Gene Set From GAD Gene-Disease Associations genes associated with the disease cores and rods is associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pancreaticobiliary maljunction-associated biliary tract tumors Gene Set From GAD Gene-Disease Associations genes associated with the disease pancreaticobiliary maljunction-associated biliary tract tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thyroid-associated ophthalmopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease thyroid-associated ophthalmopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-1 associated myelopathy/tropical spastic; paraparesis Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-1 associated myelopathy/tropical spastic; paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulonephritis, hepatitis b virus-associated Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, hepatitis b virus-associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
5-fluorouracil-associated toxicity Gene Set From GAD Gene-Disease Associations genes associated with the disease 5-fluorouracil-associated toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol associated symptoms; alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol associated symptoms; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-i-associated myelopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i-associated myelopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage associated with exposure to air pollution Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage associated with exposure to air pollution in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelopathy, htlv-1 associated Gene Set From GAD Gene-Disease Associations genes associated with the disease myelopathy, htlv-1 associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
herpes-associated recurrent lymphocytic meningitis Gene Set From GAD Gene-Disease Associations genes associated with the disease herpes-associated recurrent lymphocytic meningitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes-associated autoantibodies Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes-associated autoantibodies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
defective heparin binding associated Gene Set From GAD Gene-Disease Associations genes associated with the disease defective heparin binding associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves ophthalmopathy; thyroid associated opthalmopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease graves ophthalmopathy; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-associated memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease age-associated memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aids-associated nephropathy; focal segmental glomsclerosis; glomerulosclerosis, focal segmental Gene Set From GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; focal segmental glomsclerosis; glomerulosclerosis, focal segmental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
soluble cytotoxic t lymphocyte-associated antigen-4 Gene Set From GAD Gene-Disease Associations genes associated with the disease soluble cytotoxic t lymphocyte-associated antigen-4 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anti neutrophil cytoplasmic antibody; (anca)-associated vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease anti neutrophil cytoplasmic antibody; (anca)-associated vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy-associated venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy-associated venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hpv-associated cervical dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease hpv-associated cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anti-myeloperoxidase subtypes of anca-associated systemic vasculitides Gene Set From GAD Gene-Disease Associations genes associated with the disease anti-myeloperoxidase subtypes of anca-associated systemic vasculitides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-associated memory impairment (aami) Gene Set From GAD Gene-Disease Associations genes associated with the disease age-associated memory impairment (aami) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel Gene Set From GAD Gene-Disease Associations genes associated with the disease vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinoblastoma is associated Gene Set From GAD Gene-Disease Associations genes associated with the disease retinoblastoma is associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial alzheimer's disease associated Gene Set From GAD Gene-Disease Associations genes associated with the disease familial alzheimer's disease associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphomas of mucosa-associated lymphoid tissue. Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphomas of mucosa-associated lymphoid tissue. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary heart disease, transplant associated Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary heart disease, transplant associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
areca quid chewing-associated oral squamous cell carcinomas Gene Set From GAD Gene-Disease Associations genes associated with the disease areca quid chewing-associated oral squamous cell carcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; pneumonia, ventilator-associated; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; pneumonia, ventilator-associated; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma, b-cell, marginal zone; mucosa-associated lymphoid tissue lymphoma; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, b-cell, marginal zone; mucosa-associated lymphoid tissue lymphoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
externalizing behavior problems and associated temperament traits Gene Set From GAD Gene-Disease Associations genes associated with the disease externalizing behavior problems and associated temperament traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
transplant associated vasculopathy after cardiac transplantation Gene Set From GAD Gene-Disease Associations genes associated with the disease transplant associated vasculopathy after cardiac transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vasospastic angina associated Gene Set From GAD Gene-Disease Associations genes associated with the disease vasospastic angina associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Ventilator-associated lung injury_Lung Tissue_GSE2411 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Ventilator-associated lung injury_Lung Tissue_GSE2411 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
cytoplasm-associated proteasomal ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the cytoplasm-associated proteasomal ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of er-associated ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of er-associated ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of er-associated ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of er-associated ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
guanylate kinase-associated protein clustering Gene Set From GO Biological Process Annotations 2015 genes participating in the guanylate kinase-associated protein clustering biological process from the curated GO Biological Process Annotations 2015 dataset.
senescence-associated heterochromatin focus assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the senescence-associated heterochromatin focus assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
lung-associated mesenchyme development Gene Set From GO Biological Process Annotations 2015 genes participating in the lung-associated mesenchyme development biological process from the curated GO Biological Process Annotations 2015 dataset.
mucosal-associated lymphoid tissue development Gene Set From GO Biological Process Annotations 2015 genes participating in the mucosal-associated lymphoid tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.
er-associated ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the er-associated ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
er-associated misfolded protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the er-associated misfolded protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
antigen transcytosis by m cells in mucosal-associated lymphoid tissue Gene Set From GO Biological Process Annotations 2015 genes participating in the antigen transcytosis by m cells in mucosal-associated lymphoid tissue biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of er-associated ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of er-associated ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
senescence-associated heterochromatin focus Gene Set From GO Cellular Component Annotations 2015 proteins localized to the senescence-associated heterochromatin focus cellular component from the curated GO Cellular Component Annotations 2015 dataset.
dystrophin-associated glycoprotein complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the dystrophin-associated glycoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
golgi-associated vesicle Gene Set From GO Cellular Component Annotations 2015 proteins localized to the golgi-associated vesicle cellular component from the curated GO Cellular Component Annotations 2015 dataset.
spectrin-associated cytoskeleton Gene Set From GO Cellular Component Annotations 2015 proteins localized to the spectrin-associated cytoskeleton cellular component from the curated GO Cellular Component Annotations 2015 dataset.
golgi-associated vesicle membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the golgi-associated vesicle membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
microtubule associated complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the microtubule associated complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
presequence translocase-associated import motor Gene Set From GO Cellular Component Annotations 2015 proteins localized to the presequence translocase-associated import motor cellular component from the curated GO Cellular Component Annotations 2015 dataset.
krueppel-associated box domain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the krueppel-associated box domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Lipoprotein-associated phospholipase A2 activity change in response to statin therapy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to statin therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
HIV-associated dementia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the HIV-associated dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Lipoprotein-associated phospholipase A2 activity and mass Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Antineutrophil cytoplasmic antibody-associated vasculitis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Antineutrophil cytoplasmic antibody-associated vasculitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
rhythm disturbances associated with pheochromocytoma Gene Set From HPO Gene-Disease Associations genes associated with the rhythm disturbances associated with pheochromocytoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypertension associated with pheochromocytoma Gene Set From HPO Gene-Disease Associations genes associated with the hypertension associated with pheochromocytoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Lymphoma, Mucosa-Associated Lymphoid Tissue Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, Mucosa-Associated Lymphoid Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cryopyrin-associated Periodic Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cryopyrin-associated Periodic Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pneumonia, Ventilator-Associated Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pneumonia, Ventilator-Associated phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Microtubule-associated protein, MAP65/Ase1/PRC1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein, MAP65/Ase1/PRC1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen 2/12 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen 2/12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nuclear RNA-splicing-associated protein, SR-25 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear RNA-splicing-associated protein, SR-25 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 54 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 54 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Signal-induced proliferation-associated 1-like protein, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Signal-induced proliferation-associated 1-like protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RelA-associated inhibitor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RelA-associated inhibitor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Centrosome-associated, FAM110, N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Centrosome-associated, FAM110, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Axin interactor dorsalization-associated protein, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Axin interactor dorsalization-associated protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Stress-associated endoplasmic reticulum protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Stress-associated endoplasmic reticulum protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lysosomal-associated transmembrane protein 4B Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysosomal-associated transmembrane protein 4B protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BRCA1-associated 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BRCA1-associated 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytoskeleton-associated protein 2, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytoskeleton-associated protein 2, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
S-phase kinase-associated protein 1-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the S-phase kinase-associated protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
HSPB1-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the HSPB1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adaptin ear-binding coat-associated protein 1 NECAP-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adaptin ear-binding coat-associated protein 1 NECAP-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cation channel sperm-associated protein subunit beta Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation channel sperm-associated protein subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.
MOFRL-associated domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the MOFRL-associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
NADH:ubiquinone oxidoreductase intermediate-associated protein 30 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the NADH:ubiquinone oxidoreductase intermediate-associated protein 30 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RNA polymerase II-associated protein 1, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA polymerase II-associated protein 1, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peptidase M43, pregnancy-associated plasma-A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase M43, pregnancy-associated plasma-A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Motilin/ghrelin-associated peptide Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Motilin/ghrelin-associated peptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spermatid-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatid-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dyslexia-associated protein KIAA0319-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dyslexia-associated protein KIAA0319-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sin3 associated polypeptide p18 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sin3 associated polypeptide p18 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RalBP1-associated Eps domain-containing protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RalBP1-associated Eps domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Heavy-metal-associated, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Heavy-metal-associated, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Krueppel-associated box-related Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Krueppel-associated box-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytoskeleton-associated protein 2 family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytoskeleton-associated protein 2 family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adenylate cyclase-associated CAP, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenylate cyclase-associated CAP, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PX-associated, sorting nexin 13 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PX-associated, sorting nexin 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Topoisomerase II-associated protein PAT1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Topoisomerase II-associated protein PAT1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
E3 ubiquitin ligase EDD, ubiquitin-associated domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the E3 ubiquitin ligase EDD, ubiquitin-associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adenylate cyclase-associated CAP Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenylate cyclase-associated CAP protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated serine/threonine-protein kinase, pre-PK domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated serine/threonine-protein kinase, pre-PK domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
MHC class II-associated invariant chain, trimerisation Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the MHC class II-associated invariant chain, trimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.
NACHT-associated domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the NACHT-associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma associated antigen, MAGE, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma associated antigen, MAGE, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PCI/PINT associated module Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PCI/PINT associated module protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PTIP-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PTIP-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adenylyl cyclase-associated protein CAP2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenylyl cyclase-associated protein CAP2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adenylyl cyclase-associated protein CAP1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenylyl cyclase-associated protein CAP1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule associated protein 1A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule associated protein 1A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Calmodulin-regulated spectrin-associated protein, CH domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Calmodulin-regulated spectrin-associated protein, CH domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Centrosome-associated protein CEP250 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Centrosome-associated protein CEP250 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transmembrane Fragile-X-F-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transmembrane Fragile-X-F-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lamina-associated polypeptide 2 alpha Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lamina-associated polypeptide 2 alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF hand associated, type-2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF hand associated, type-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EF hand associated, type-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EF hand associated, type-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinoblastoma-associated protein, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinoblastoma-associated protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sperm-associated antigen 17 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sperm-associated antigen 17 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transmembrane protein adipocyte-associated 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transmembrane protein adipocyte-associated 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ewing's tumour-associated antigen 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ewing's tumour-associated antigen 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Helicase-associated putative binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Helicase-associated putative binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cation channel sperm-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation channel sperm-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cation channel sperm-associated protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation channel sperm-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cation channel sperm-associated protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation channel sperm-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cation channel sperm-associated protein 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation channel sperm-associated protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BTB/Kelch-associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BTB/Kelch-associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lysosome-associated membrane glycoprotein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysosome-associated membrane glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Rho-associated protein kinase 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Rho-associated protein kinase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Rho-associated protein kinase 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Rho-associated protein kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
S-phase kinase-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the S-phase kinase-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PDZ-associated domain of NMDA receptors Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PDZ-associated domain of NMDA receptors protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule associated protein, tubulin-binding repeat Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule associated protein, tubulin-binding repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spermatogenesis-associated serine-rich protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated serine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen B5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen B5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Domain of unknown function DUF1981, Sec7 associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF1981, Sec7 associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Fanconi anemia-associated protein of 24kDa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Fanconi anemia-associated protein of 24kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Proliferation-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Proliferation-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Keratin-associated protein, PMG type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Keratin-associated protein, PMG type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PAS-associated, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PAS-associated, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
SMN complex, gem-associated protein 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the SMN complex, gem-associated protein 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Actin filament-associated protein 1-like 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin filament-associated protein 1-like 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Actin filament-associated protein 1-like 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin filament-associated protein 1-like 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
MORF4 family-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the MORF4 family-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen D1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen D1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen D4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen D4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Major facilitator superfamily associated domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Major facilitator superfamily associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cation channel sperm-associated protein, subunit gamma Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation channel sperm-associated protein, subunit gamma protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytoplasmic activation/proliferation-associated protein-1 C term Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytoplasmic activation/proliferation-associated protein-1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 13 domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synaptobrevin/Vesicle-associated membrane protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptobrevin/Vesicle-associated membrane protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RyR/IP3R Homology associated domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RyR/IP3R Homology associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RNA-polymerase II-associated protein 3-like, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA-polymerase II-associated protein 3-like, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane-associated diazepam binding inhibitor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated diazepam binding inhibitor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Kinesin-associated microtubule-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinesin-associated microtubule-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lamina-associated polypeptide 1C Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lamina-associated polypeptide 1C protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PAP/25A-associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the PAP/25A-associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Keratin-associated protein, type6/8/16/19/20 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Keratin-associated protein, type6/8/16/19/20 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Kinetochore-associated protein Dsn1/Mis13 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore-associated protein Dsn1/Mis13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
JNK/Rab-associated protein-1, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the JNK/Rab-associated protein-1, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Galanin message associated peptide (GMAP) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Galanin message associated peptide (GMAP) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Contactin-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Contactin-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
SIT4 phosphatase-associated protein family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the SIT4 phosphatase-associated protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Exosome-associated factor Rrp6, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Exosome-associated factor Rrp6, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Translation machinery-associated protein 16 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Translation machinery-associated protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Axin interactor, dorsalization-associated protein, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Axin interactor, dorsalization-associated protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein 1B Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein 1B protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dynein associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynein associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Hypoxia-inducible lipid droplet-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Hypoxia-inducible lipid droplet-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Junctional protein associated with coronary artery disease Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Junctional protein associated with coronary artery disease protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Phox-associated domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Phox-associated domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thyroid transcription factor 1-associated protein 26 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thyroid transcription factor 1-associated protein 26 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Actin-filament associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-filament associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Centrosome and spindle pole associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Centrosome and spindle pole associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Contactin-associated protein-like 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Contactin-associated protein-like 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Contactin-associated protein-like 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Contactin-associated protein-like 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Contactin-associated protein-like 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Contactin-associated protein-like 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Contactin-associated protein-like 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Contactin-associated protein-like 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Keratin-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Keratin-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nck-associated protein 5-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nck-associated protein 5-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen B2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen B2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule associated protein MAP2/MAP4/Tau Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule associated protein MAP2/MAP4/Tau protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Learning associated protein 18-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Learning associated protein 18-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
MHC class II-associated invariant chain/CLIP, MHC II-interacting Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the MHC class II-associated invariant chain/CLIP, MHC II-interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Haem NO binding associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Haem NO binding associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U3 small nucleolar RNA-associated protein 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cyclase-associated protein CAP/septum formation inhibitor MinC, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cyclase-associated protein CAP/septum formation inhibitor MinC, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 2/4, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane associated eicosanoid/glutathione metabolism-like domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane associated eicosanoid/glutathione metabolism-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
F-box associated (FBA) domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the F-box associated (FBA) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Translocon-associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Translocon-associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cancer-associated antigen RCAS1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cancer-associated antigen RCAS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U6 snRNA-associated Sm-like protein LSm2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U6 snRNA-associated Sm-like protein LSm2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spermatogenesis-associated protein 16 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Fanconi anemia-associated protein of 100kDa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Fanconi anemia-associated protein of 100kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nascent polypeptide-associated complex subunit alpha Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nascent polypeptide-associated complex subunit alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated, VPS28 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated, VPS28 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lysosome-associated membrane glycoprotein, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysosome-associated membrane glycoprotein, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
GidA associated domain 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the GidA associated domain 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Centrosome-associated, FAM110, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Centrosome-associated, FAM110, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cilia/flagella-associated protein 20/WDR90/C3orf67 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cilia/flagella-associated protein 20/WDR90/C3orf67 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Heavy metal-associated domain, HMA Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Heavy metal-associated domain, HMA protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Disheveled-associated activator of morphogenesis 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Disheveled-associated activator of morphogenesis 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TFIID subunit, WD40-associated region Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TFIID subunit, WD40-associated region protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spermatogenesis-associated protein 32 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 32 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spermatogenesis-associated protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sperm-associated antigen 4 protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sperm-associated antigen 4 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 13A N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13A N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Adenylate cyclase-associated CAP, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenylate cyclase-associated CAP, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Kidney-associated antigen 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kidney-associated antigen 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Translocation associated membrane protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Translocation associated membrane protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar membrane-associated protein Iml1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar membrane-associated protein Iml1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lysosomal-associated transmembrane protein, 4A/5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysosomal-associated transmembrane protein, 4A/5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TATA box-binding protein-associated factor 1D Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TATA box-binding protein-associated factor 1D protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated protein Tau Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated protein Tau protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated serine/threonine-protein kinase 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated serine/threonine-protein kinase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Microtubule-associated serine/threonine-protein kinase 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated serine/threonine-protein kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spindle associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U3 small nucleolar RNA-associated protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ubiquitin-associated/translation elongation factor EF1B, N-terminal, eukaryote Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-associated/translation elongation factor EF1B, N-terminal, eukaryote protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 41 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 41 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Regulatory associated protein of TOR Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulatory associated protein of TOR protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cyclin-dependent kinase 2-associated protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cyclin-dependent kinase 2-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Nascent polypeptide-associated complex NAC domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Nascent polypeptide-associated complex NAC domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
GRIP1-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the GRIP1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Keratin-associated protein 21-2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Keratin-associated protein 21-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Exosome-associated factor Rrp47/DNA strand repair C1D Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Exosome-associated factor Rrp47/DNA strand repair C1D protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sperm acrosome-associated protein 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sperm acrosome-associated protein 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
E2F-associated phosphoprotein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the E2F-associated phosphoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Surfactant-associated protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Surfactant-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Heavy metal-associated domain, copper ion-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Heavy metal-associated domain, copper ion-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
SPRY-associated Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the SPRY-associated protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Soluble lamin-associated protein of 75kDa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Soluble lamin-associated protein of 75kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small ribonucleoprotein associated, SmB/SmN Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ribonucleoprotein associated, SmB/SmN protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mss4/translationally controlled tumour-associated TCTP Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mss4/translationally controlled tumour-associated TCTP protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinoblastoma-associated protein, B-box Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinoblastoma-associated protein, B-box protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sperm-associated antigen 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sperm-associated antigen 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cyclin-dependent kinase 2-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cyclin-dependent kinase 2-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Fragile site-associated protein, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Fragile site-associated protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen D2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen D2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Melanoma-associated antigen 3/6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Melanoma-associated antigen 3/6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DDB1- and CUL4-associated factor 16 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DDB1- and CUL4-associated factor 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
HEAT repeat associated with sister chromatid cohesion protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the HEAT repeat associated with sister chromatid cohesion protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Harmonizome 3.0

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set

myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set

myasthenic syndrome, congenital, associated with episodic apnea Gene Set

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

Myasthenic syndrome, congenital, fast-channel Gene Set

Myasthenic syndrome, slow-channel congenital Gene Set

Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

Congenital myasthenic syndrome, acetazolamide-responsive Gene Set

Congenital myasthenic syndrome with episodic apnea Gene Set

Congenital myasthenic syndrome ib Gene Set

Myasthenic syndrome, congenital, postsynaptic slow-channel Gene Set

Myasthenic Syndrome, Congenital, Fast-Channel Gene Set

congenital myasthenic syndrome Gene Set

congenital myasthenic syndrome Gene Set

myasthenic syndrome, fast-channel congenital Gene Set

myasthenic syndrome, slow-channel congenital Gene Set

myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Gene Set

Congenital Myasthenic Syndrome Ib Gene Set

Congenital myasthenic syndrome Gene Set

Congenital myasthenic syndrome Gene Set

Congenital myasthenic syndrome 3B Gene Set

Congenital myasthenic syndrome 3A Gene Set

Congenital myasthenic syndrome 5 Gene Set

Congenital myasthenic syndrome 14 Gene Set

Congenital myasthenic syndrome 13 Gene Set

Congenital myasthenic syndrome 6 Gene Set

Congenital myasthenic syndrome 10 Gene Set

Congenital myasthenic syndrome 15 Gene Set

Congenital myasthenic syndrome 19 Gene Set

Congenital myasthenic syndrome 12 Gene Set

Congenital myasthenic syndrome 22 Gene Set

Congenital myasthenic syndrome 8 Gene Set

Congenital myasthenic syndrome 21 Gene Set

Congenital myasthenic syndrome 1B Gene Set

Congenital myasthenic syndrome 1A Gene Set

Congenital myasthenic syndrome 20 Gene Set

Congenital myasthenic syndrome 16 Gene Set

Congenital myasthenic syndrome 17 Gene Set

Congenital myasthenic syndrome 18 Gene Set

Congenital myasthenic syndrome 2C Gene Set

Congenital myasthenic syndrome 9 Gene Set

Congenital myasthenic syndrome 4C Gene Set

Congenital myasthenic syndrome 4B Gene Set

Congenital myasthenic syndrome 11 Gene Set

Congenital myasthenic syndrome Gene Set

Presynaptic congenital myasthenic syndrome Gene Set

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

Myasthenic Syndromes, Congenital Gene Set

Congenital Myasthenic Syndromes Gene Set

Congenital Myopathy With Myasthenic-Like Onset Gene Set

Synaptic congenital myasthenic syndromes Gene Set

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

lambert-eaton myasthenic syndrome Gene Set

lung cancer; lambert-eaton myasthenic syndrome Gene Set

Lambert-Eaton Myasthenic Syndrome Gene Set

myasthenic syndrome, acetazolamide-responsive Gene Set

Lambert-Eaton Myasthenic Syndrome Gene Set

Myasthenic Syndrome Gene Set

Lambert-Eaton myasthenic syndrome Gene Set

Myasthenic syndrome Gene Set

GFPT1-related myasthenic syndrome Gene Set

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

g-protein coupled acetylcholine receptor signaling pathway Gene Set

adenylate cyclase-inhibiting g-protein coupled acetylcholine receptor signaling pathway Gene Set

phospholipase c-activating g-protein coupled acetylcholine receptor signaling pathway Gene Set

acetylcholine receptor regulator activity Gene Set

acetylcholine receptor activity Gene Set

g-protein coupled acetylcholine receptor activity Gene Set

acetylcholine receptor activator activity Gene Set

acetylcholine receptor binding Gene Set

Nicotinic acetylcholine receptor Gene Set