MECP2 regulates neuronal receptors and channels

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Results for "MECP2 regulates neuronal receptors and channels": 1001 gene sets

Name
MECP2 regulates neuronal receptors and channels Gene Set From Reactome Pathways 2024 proteins participating in the MECP2 regulates neuronal receptors and channels pathway from the Reactome Pathways 2024 dataset.
MECP2 regulates transcription of neuronal ligands Gene Set From Reactome Pathways 2024 proteins participating in the MECP2 regulates transcription of neuronal ligands pathway from the Reactome Pathways 2024 dataset.
MECP2 regulates transcription factors Gene Set From Reactome Pathways 2024 proteins participating in the MECP2 regulates transcription factors pathway from the Reactome Pathways 2024 dataset.
MECP2 regulates transcription of genes involved in GABA signaling Gene Set From Reactome Pathways 2024 proteins participating in the MECP2 regulates transcription of genes involved in GABA signaling pathway from the Reactome Pathways 2024 dataset.
TFAP2 (AP-2) family regulates transcription of growth factors and their receptors Gene Set From Reactome Pathways 2024 proteins participating in the TFAP2 (AP-2) family regulates transcription of growth factors and their receptors pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Death Receptors and Ligands Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Death Receptors and Ligands pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 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.
Regulation of MECP2 expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of MECP2 expression and activity pathway from the Reactome Pathways 2024 dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set From Reactome Pathways 2024 proteins participating in the FBXL7 down-regulates AURKA during mitotic entry and in early mitosis pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function pathway from the Reactome Pathways 2024 dataset.
RUNX3 Regulates Immune Response and Cell Migration Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 Regulates Immune Response and Cell Migration pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Caspase Activators and Caspases Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Caspase Activators and Caspases pathway from the Reactome Pathways 2024 dataset.
PU.1-Sin3A-Hdac-MeCP2 complex Gene Set From CORUM Protein Complexes proteins in the PU.1-Sin3A-Hdac-MeCP2 complex protein complex from the CORUM Protein Complexes dataset.
MeCP2-SIN3A-HDAC complex Gene Set From CORUM Protein Complexes proteins in the MeCP2-SIN3A-HDAC complex protein complex from the CORUM Protein Complexes dataset.
Smarcb1/Ini1-Smarca2-Mecp2 complex Gene Set From CORUM Protein Complexes proteins in the Smarcb1/Ini1-Smarca2-Mecp2 complex protein complex from the CORUM Protein Complexes dataset.
Hdac1-Mecp2-Rcor1-Sin3a complex Gene Set From CORUM Protein Complexes proteins in the Hdac1-Mecp2-Rcor1-Sin3a complex protein complex from the CORUM Protein Complexes dataset.
SWI/SNF chromatin-remodeling complex (Mecp2, Smarc) Gene Set From CORUM Protein Complexes proteins in the SWI/SNF chromatin-remodeling complex (Mecp2, Smarc) protein complex from the CORUM Protein Complexes dataset.
SMARCA2/BRM-BAF57-MECP2 complex Gene Set From CORUM Protein Complexes proteins in the SMARCA2/BRM-BAF57-MECP2 complex protein complex from the CORUM Protein Complexes dataset.
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.
mecp2 Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mecp2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Methyl-CpG binding protein MeCP2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Methyl-CpG binding protein MeCP2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
MECP2 Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for MECP2 from the Pathway Commons Protein-Protein Interactions dataset.
MECP2 Gene Set From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the MECP2 gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.
Loss of MECP2 binding ability to 5hmC-DNA Gene Set From Reactome Pathways 2024 proteins participating in the Loss of MECP2 binding ability to 5hmC-DNA pathway from the Reactome Pathways 2024 dataset.
Loss of MECP2 binding ability to 5mC-DNA Gene Set From Reactome Pathways 2024 proteins participating in the Loss of MECP2 binding ability to 5mC-DNA pathway from the Reactome Pathways 2024 dataset.
Loss of MECP2 binding ability to the NCoR/SMRT complex Gene Set From Reactome Pathways 2024 proteins participating in the Loss of MECP2 binding ability to the NCoR/SMRT complex pathway from the Reactome Pathways 2024 dataset.
Loss of function of MECP2 in Rett syndrome Gene Set From Reactome Pathways 2024 proteins participating in the Loss of function of MECP2 in Rett syndrome pathway from the Reactome Pathways 2024 dataset.
Loss of phosphorylation of MECP2 at T308 Gene Set From Reactome Pathways 2024 proteins participating in the Loss of phosphorylation of MECP2 at T308 pathway from the Reactome Pathways 2024 dataset.
Transcriptional Regulation by MECP2 Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional Regulation by MECP2 pathway from the Reactome Pathways 2024 dataset.
Severe congenital encephalopathy due to MECP2 mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital encephalopathy due to MECP2 mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Severe congenital encephalopathy due to MECP2 mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital encephalopathy due to MECP2 mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
PMC6815046-13073_2019_678_MOESM3_ESM.xlsx-MECP2-Unnamed_0_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6815046-13073_2019_678_MOESM3_ESM.xlsx-MECP2-Unnamed_0_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6815046-13073_2019_678_MOESM2_ESM.xlsx-MECP2-Unnamed_0_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6815046-13073_2019_678_MOESM2_ESM.xlsx-MECP2-Unnamed_0_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6815046-13073_2019_678_MOESM4_ESM.xlsx-MECP2-Unnamed_0_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6815046-13073_2019_678_MOESM4_ESM.xlsx-MECP2-Unnamed_0_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Non-metastasis_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Non-metastasis_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Unnamed_1_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Unnamed_1_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Metastasis_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Metastasis_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Unnamed_5_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Unnamed_5_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC11811132-41598_2025_89334_MOESM5_ESM.xlsx-MECP2-fromNode_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC11811132-41598_2025_89334_MOESM5_ESM.xlsx-MECP2-fromNode_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC11811132-41598_2025_89334_MOESM5_ESM.xlsx-MECP2-toNode_MECP2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC11811132-41598_2025_89334_MOESM5_ESM.xlsx-MECP2-toNode_MECP2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
MECP2 Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the MECP2 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
channels Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term channels in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
clustering of voltage-gated sodium channels Gene Set From GO Biological Process Annotations 2015 genes participating in the clustering of voltage-gated sodium channels biological process from the curated GO Biological Process Annotations 2015 dataset.
clustering of voltage-gated potassium channels Gene Set From GO Biological Process Annotations 2015 genes participating in the clustering of voltage-gated potassium channels biological process from the curated GO Biological Process Annotations 2015 dataset.
Shal-type voltage-gated potassium channels Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Shal-type voltage-gated potassium channels protein domain from the InterPro Predicted Protein Domain Annotations dataset.
channels Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term channels in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits Gene Set From Reactome Pathways 2014 proteins participating in the Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits pathway from the Reactome Pathways dataset.
Classical Kir channels Gene Set From Reactome Pathways 2014 proteins participating in the Classical Kir channels pathway from the Reactome Pathways dataset.
Ca2+ activated K+ channels Gene Set From Reactome Pathways 2014 proteins participating in the Ca2+ activated K+ channels pathway from the Reactome Pathways dataset.
HCN channels Gene Set From Reactome Pathways 2014 proteins participating in the HCN channels pathway from the Reactome Pathways dataset.
Potassium Channels Gene Set From Reactome Pathways 2014 proteins participating in the Potassium Channels pathway from the Reactome Pathways dataset.
Activation of G protein gated Potassium channels Gene Set From Reactome Pathways 2014 proteins participating in the Activation of G protein gated Potassium channels pathway from the Reactome Pathways dataset.
Inwardly rectifying K+ channels Gene Set From Reactome Pathways 2014 proteins participating in the Inwardly rectifying K+ channels pathway from the Reactome Pathways dataset.
Tandem pore domain potassium channels Gene Set From Reactome Pathways 2014 proteins participating in the Tandem pore domain potassium channels pathway from the Reactome Pathways dataset.
Tandem of pore domain in a weak inwardly rectifying K+ channels (TWIK) Gene Set From Reactome Pathways 2014 proteins participating in the Tandem of pore domain in a weak inwardly rectifying K+ channels (TWIK) pathway from the Reactome Pathways dataset.
Depolarization of the Presynaptic Terminal Triggers the Opening of Calcium Channels Gene Set From Reactome Pathways 2014 proteins participating in the Depolarization of the Presynaptic Terminal Triggers the Opening of Calcium Channels pathway from the Reactome Pathways dataset.
TRP channels Gene Set From Reactome Pathways 2014 proteins participating in the TRP channels pathway from the Reactome Pathways dataset.
Stimuli-sensing channels Gene Set From Reactome Pathways 2014 proteins participating in the Stimuli-sensing channels pathway from the Reactome Pathways dataset.
Voltage gated Potassium channels Gene Set From Reactome Pathways 2014 proteins participating in the Voltage gated Potassium channels pathway from the Reactome Pathways dataset.
ATP sensitive Potassium channels Gene Set From Reactome Pathways 2014 proteins participating in the ATP sensitive Potassium channels pathway from the Reactome Pathways dataset.
Potassium transport channels Gene Set From Reactome Pathways 2014 proteins participating in the Potassium transport channels pathway from the Reactome Pathways dataset.
G protein gated Potassium channels Gene Set From Reactome Pathways 2014 proteins participating in the G protein gated Potassium channels pathway from the Reactome Pathways dataset.
clustering of voltage-gated sodium channels Gene Set From GO Biological Process Annotations 2023 genes participating in the clustering of voltage-gated sodium channels biological process from the curated GO Biological Process Annotations 2023 dataset.
clustering of voltage-gated potassium channels Gene Set From GO Biological Process Annotations 2023 genes participating in the clustering of voltage-gated potassium channels biological process from the curated GO Biological Process Annotations 2023 dataset.
ATP sensitive Potassium channels Gene Set From Reactome Pathways 2024 proteins participating in the ATP sensitive Potassium channels pathway from the Reactome Pathways 2024 dataset.
Activation of G protein gated Potassium channels Gene Set From Reactome Pathways 2024 proteins participating in the Activation of G protein gated Potassium channels pathway from the Reactome Pathways 2024 dataset.
Ca2+ activated K+ channels Gene Set From Reactome Pathways 2024 proteins participating in the Ca2+ activated K+ channels pathway from the Reactome Pathways 2024 dataset.
Classical Kir channels Gene Set From Reactome Pathways 2024 proteins participating in the Classical Kir channels pathway from the Reactome Pathways 2024 dataset.
G protein gated Potassium channels Gene Set From Reactome Pathways 2024 proteins participating in the G protein gated Potassium channels pathway from the Reactome Pathways 2024 dataset.
HCN channels Gene Set From Reactome Pathways 2024 proteins participating in the HCN channels pathway from the Reactome Pathways 2024 dataset.
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits Gene Set From Reactome Pathways 2024 proteins participating in the Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits pathway from the Reactome Pathways 2024 dataset.
Inwardly rectifying K+ channels Gene Set From Reactome Pathways 2024 proteins participating in the Inwardly rectifying K+ channels pathway from the Reactome Pathways 2024 dataset.
Phase 1 - inactivation of fast Na+ channels Gene Set From Reactome Pathways 2024 proteins participating in the Phase 1 - inactivation of fast Na+ channels pathway from the Reactome Pathways 2024 dataset.
Potassium Channels Gene Set From Reactome Pathways 2024 proteins participating in the Potassium Channels pathway from the Reactome Pathways 2024 dataset.
Potassium transport channels Gene Set From Reactome Pathways 2024 proteins participating in the Potassium transport channels pathway from the Reactome Pathways 2024 dataset.
Stimuli-sensing channels Gene Set From Reactome Pathways 2024 proteins participating in the Stimuli-sensing channels pathway from the Reactome Pathways 2024 dataset.
TRP channels Gene Set From Reactome Pathways 2024 proteins participating in the TRP channels pathway from the Reactome Pathways 2024 dataset.
Tandem of pore domain in a weak inwardly rectifying K+ channels (TWIK) Gene Set From Reactome Pathways 2024 proteins participating in the Tandem of pore domain in a weak inwardly rectifying K+ channels (TWIK) pathway from the Reactome Pathways 2024 dataset.
Tandem pore domain potassium channels Gene Set From Reactome Pathways 2024 proteins participating in the Tandem pore domain potassium channels pathway from the Reactome Pathways 2024 dataset.
Voltage gated Potassium channels Gene Set From Reactome Pathways 2024 proteins participating in the Voltage gated Potassium channels pathway from the Reactome Pathways 2024 dataset.
clustering of voltage-gated sodium channels Gene Set From GO Biological Process Annotations 2025 genes participating in the clustering of voltage-gated sodium channels biological process from the curated GO Biological Process Annotations 2025 dataset.
clustering of voltage-gated potassium channels Gene Set From GO Biological Process Annotations 2025 genes participating in the clustering of voltage-gated potassium channels biological process from the curated GO Biological Process Annotations 2025 dataset.
Inflammatory mediator regulation of TRP channels Gene Set From KEGG Pathways 2026 proteins participating in the Inflammatory mediator regulation of TRP channels pathway from the KEGG Pathways 2026 dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
Lysosphingolipid and LPA receptors Gene Set From Reactome Pathways 2014 proteins participating in the Lysosphingolipid and LPA receptors pathway from the Reactome Pathways dataset.
Formyl peptide receptors bind formyl peptides and many other ligands Gene Set From Reactome Pathways 2014 proteins participating in the Formyl peptide receptors bind formyl peptides and many other ligands pathway from the Reactome Pathways dataset.
Binding and Uptake of Ligands by Scavenger Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Binding and Uptake of Ligands by Scavenger Receptors pathway from the Reactome Pathways dataset.
Glutamate Binding, Activation of AMPA Receptors and Synaptic Plasticity Gene Set From Reactome Pathways 2014 proteins participating in the Glutamate Binding, Activation of AMPA Receptors and Synaptic Plasticity pathway from the Reactome Pathways dataset.
Nuclear receptors in lipid metabolism and toxicity(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nuclear receptors in lipid metabolism and toxicity(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
miRNA targets in ECM and membrane receptors Gene Set From WikiPathways Pathways 2024 proteins participating in the miRNA targets in ECM and membrane receptors pathway from the WikiPathways Pathways 2024 dataset.
Nuclear receptors in lipid metabolism and toxicity Gene Set From WikiPathways Pathways 2024 proteins participating in the Nuclear receptors in lipid metabolism and toxicity pathway from the WikiPathways Pathways 2024 dataset.
Major receptors targeted by epinephrine and norepinephrine Gene Set From WikiPathways Pathways 2024 proteins participating in the Major receptors targeted by epinephrine and norepinephrine pathway from the WikiPathways Pathways 2024 dataset.
Activation of NMDA receptors and postsynaptic events Gene Set From Reactome Pathways 2024 proteins participating in the Activation of NMDA receptors and postsynaptic events pathway from the Reactome Pathways 2024 dataset.
Assembly and cell surface presentation of NMDA receptors Gene Set From Reactome Pathways 2024 proteins participating in the Assembly and cell surface presentation of NMDA receptors pathway from the Reactome Pathways 2024 dataset.
Binding and Uptake of Ligands by Scavenger Receptors Gene Set From Reactome Pathways 2024 proteins participating in the Binding and Uptake of Ligands by Scavenger Receptors pathway from the Reactome Pathways 2024 dataset.
Diseases of signal transduction by growth factor receptors and second messengers Gene Set From Reactome Pathways 2024 proteins participating in the Diseases of signal transduction by growth factor receptors and second messengers pathway from the Reactome Pathways 2024 dataset.
Expression and translocation of olfactory receptors Gene Set From Reactome Pathways 2024 proteins participating in the Expression and translocation of olfactory receptors pathway from the Reactome Pathways 2024 dataset.
Formyl peptide receptors bind formyl peptides and many other ligands Gene Set From Reactome Pathways 2024 proteins participating in the Formyl peptide receptors bind formyl peptides and many other ligands pathway from the Reactome Pathways 2024 dataset.
Glutamate binding, activation of AMPA receptors and synaptic plasticity Gene Set From Reactome Pathways 2024 proteins participating in the Glutamate binding, activation of AMPA receptors and synaptic plasticity pathway from the Reactome Pathways 2024 dataset.
Lysosphingolipid and LPA receptors Gene Set From Reactome Pathways 2024 proteins participating in the Lysosphingolipid and LPA receptors pathway from the Reactome Pathways 2024 dataset.
Neurotransmitter receptors and postsynaptic signal transmission Gene Set From Reactome Pathways 2024 proteins participating in the Neurotransmitter receptors and postsynaptic signal transmission pathway from the Reactome Pathways 2024 dataset.
Unblocking of NMDA receptors, glutamate binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the Unblocking of NMDA receptors, glutamate binding and activation pathway from the Reactome Pathways 2024 dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
Lissencephaly gene (LIS1) in neuronal migration and development Gene Set From PID Pathways proteins participating in the Lissencephaly gene (LIS1) in neuronal migration and development pathway from the PID Pathways dataset.
Complement system in neuronal development and plasticity Gene Set From WikiPathways Pathways 2024 proteins participating in the Complement system in neuronal development and plasticity pathway from the WikiPathways Pathways 2024 dataset.
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes Gene Set From Reactome Pathways 2024 proteins participating in the FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes pathway from the Reactome Pathways 2024 dataset.
Multinodular and vacuolating neuronal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multinodular and vacuolating neuronal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
sumoylation by ranbp2 regulates transcriptional repression Gene Set From Biocarta Pathways proteins participating in the sumoylation by ranbp2 regulates transcriptional repression pathway from the Biocarta Pathways dataset.
sonic hedgehog receptor ptc1 regulates cell cycle Gene Set From Biocarta Pathways proteins participating in the sonic hedgehog receptor ptc1 regulates cell cycle pathway from the Biocarta Pathways dataset.
phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway Gene Set From Biocarta Pathways proteins participating in the phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway pathway from the Biocarta Pathways dataset.
Sumoylation by RanBP2 regulates transcriptional repression Gene Set From PID Pathways proteins participating in the Sumoylation by RanBP2 regulates transcriptional repression pathway from the PID Pathways dataset.
p75NTR negatively regulates cell cycle via SC1 Gene Set From Reactome Pathways 2014 proteins participating in the p75NTR negatively regulates cell cycle via SC1 pathway from the Reactome Pathways dataset.
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription Gene Set From Reactome Pathways 2014 proteins participating in the SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription pathway from the Reactome Pathways dataset.
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion Gene Set From Reactome Pathways 2014 proteins participating in the Glucagon-like Peptide-1 (GLP1) regulates insulin secretion pathway from the Reactome Pathways dataset.
NOTCH1 Intracellular Domain Regulates Transcription Gene Set From Reactome Pathways 2014 proteins participating in the NOTCH1 Intracellular Domain Regulates Transcription pathway from the Reactome Pathways dataset.
NOTCH2 intracellular domain regulates transcription Gene Set From Reactome Pathways 2014 proteins participating in the NOTCH2 intracellular domain regulates transcription 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.
PERK regulates gene expression Gene Set From Reactome Pathways 2014 proteins participating in the PERK regulates gene expression pathway from the Reactome Pathways dataset.
p75NTR regulates axonogenesis Gene Set From Reactome Pathways 2014 proteins participating in the p75NTR regulates axonogenesis pathway from the Reactome Pathways dataset.
SIRT1 negatively regulates rRNA Expression Gene Set From Reactome Pathways 2014 proteins participating in the SIRT1 negatively regulates rRNA Expression pathway from the Reactome Pathways dataset.
Vasopressin regulates renal water homeostasis via Aquaporins Gene Set From Reactome Pathways 2014 proteins participating in the Vasopressin regulates renal water homeostasis via Aquaporins pathway from the Reactome Pathways dataset.
NoRC negatively regulates rRNA expression Gene Set From Reactome Pathways 2014 proteins participating in the NoRC negatively regulates rRNA expression pathway from the Reactome Pathways 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.
B-WICH complex positively regulates rRNA expression Gene Set From Reactome Pathways 2024 proteins participating in the B-WICH complex positively regulates rRNA expression pathway from the Reactome Pathways 2024 dataset.
ERBB2 Regulates Cell Motility Gene Set From Reactome Pathways 2024 proteins participating in the ERBB2 Regulates Cell Motility pathway from the Reactome Pathways 2024 dataset.
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion Gene Set From Reactome Pathways 2024 proteins participating in the Glucagon-like Peptide-1 (GLP1) regulates insulin secretion pathway from the Reactome Pathways 2024 dataset.
Intracellular metabolism of fatty acids regulates insulin secretion Gene Set From Reactome Pathways 2024 proteins participating in the Intracellular metabolism of fatty acids regulates insulin secretion pathway from the Reactome Pathways 2024 dataset.
NFE2L2 regulates pentose phosphate pathway genes Gene Set From Reactome Pathways 2024 proteins participating in the NFE2L2 regulates pentose phosphate pathway genes pathway from the Reactome Pathways 2024 dataset.
NOTCH1 Intracellular Domain Regulates Transcription Gene Set From Reactome Pathways 2024 proteins participating in the NOTCH1 Intracellular Domain Regulates Transcription pathway from the Reactome Pathways 2024 dataset.
NOTCH2 intracellular domain regulates transcription Gene Set From Reactome Pathways 2024 proteins participating in the NOTCH2 intracellular domain regulates transcription pathway from the Reactome Pathways 2024 dataset.
NOTCH3 Intracellular Domain Regulates Transcription Gene Set From Reactome Pathways 2024 proteins participating in the NOTCH3 Intracellular Domain Regulates Transcription pathway from the Reactome Pathways 2024 dataset.
NOTCH4 Intracellular Domain Regulates Transcription Gene Set From Reactome Pathways 2024 proteins participating in the NOTCH4 Intracellular Domain Regulates Transcription pathway from the Reactome Pathways 2024 dataset.
NPAS4 regulates expression of target genes Gene Set From Reactome Pathways 2024 proteins participating in the NPAS4 regulates expression of target genes pathway from the Reactome Pathways 2024 dataset.
NoRC negatively regulates rRNA expression Gene Set From Reactome Pathways 2024 proteins participating in the NoRC negatively regulates rRNA expression pathway from the Reactome Pathways 2024 dataset.
PERK regulates gene expression Gene Set From Reactome Pathways 2024 proteins participating in the PERK regulates gene expression pathway from the Reactome Pathways 2024 dataset.
PI5P Regulates TP53 Acetylation Gene Set From Reactome Pathways 2024 proteins participating in the PI5P Regulates TP53 Acetylation pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates Cell Cycle Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates Cell Cycle pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates Proteins Involved in RNA Processing Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates Proteins Involved in RNA Processing pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates estrogen receptor mediated transcription Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates estrogen receptor mediated transcription pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates expression of components of tight junctions Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates expression of components of tight junctions pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates transcription of genes involved in BCR signaling Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates transcription of genes involved in BCR signaling pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates transcription of genes involved in WNT signaling Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates transcription of genes involved in WNT signaling pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates transcription of genes involved in differentiation of HSCs Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates transcription of genes involved in differentiation of HSCs pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates transcription of genes involved in differentiation of keratinocytes Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates transcription of genes involved in differentiation of keratinocytes pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates transcription of genes involved in differentiation of myeloid cells Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates transcription of genes involved in differentiation of myeloid cells pathway from the Reactome Pathways 2024 dataset.
RUNX1 regulates transcription of genes involved in interleukin signaling Gene Set From Reactome Pathways 2024 proteins participating in the RUNX1 regulates transcription of genes involved in interleukin signaling pathway from the Reactome Pathways 2024 dataset.
RUNX2 regulates bone development Gene Set From Reactome Pathways 2024 proteins participating in the RUNX2 regulates bone development pathway from the Reactome Pathways 2024 dataset.
RUNX2 regulates chondrocyte maturation Gene Set From Reactome Pathways 2024 proteins participating in the RUNX2 regulates chondrocyte maturation pathway from the Reactome Pathways 2024 dataset.
RUNX2 regulates genes involved in cell migration Gene Set From Reactome Pathways 2024 proteins participating in the RUNX2 regulates genes involved in cell migration pathway from the Reactome Pathways 2024 dataset.
RUNX2 regulates genes involved in differentiation of myeloid cells Gene Set From Reactome Pathways 2024 proteins participating in the RUNX2 regulates genes involved in differentiation of myeloid cells pathway from the Reactome Pathways 2024 dataset.
RUNX2 regulates osteoblast differentiation Gene Set From Reactome Pathways 2024 proteins participating in the RUNX2 regulates osteoblast differentiation pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates BCL2L11 (BIM) transcription Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates BCL2L11 (BIM) transcription pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates CDKN1A transcription Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates CDKN1A transcription pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates NOTCH signaling Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates NOTCH signaling pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates RUNX1-mediated transcription Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates RUNX1-mediated transcription pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates WNT signaling Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates WNT signaling pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates YAP1-mediated transcription Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates YAP1-mediated transcription pathway from the Reactome Pathways 2024 dataset.
RUNX3 regulates p14-ARF Gene Set From Reactome Pathways 2024 proteins participating in the RUNX3 regulates p14-ARF pathway from the Reactome Pathways 2024 dataset.
SIRT1 negatively regulates rRNA expression Gene Set From Reactome Pathways 2024 proteins participating in the SIRT1 negatively regulates rRNA expression pathway from the Reactome Pathways 2024 dataset.
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription Gene Set From Reactome Pathways 2024 proteins participating in the SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription pathway from the Reactome Pathways 2024 dataset.
TFAP2 (AP-2) family regulates transcription of cell cycle factors Gene Set From Reactome Pathways 2024 proteins participating in the TFAP2 (AP-2) family regulates transcription of cell cycle factors pathway from the Reactome Pathways 2024 dataset.
TFAP2 (AP-2) family regulates transcription of other transcription factors Gene Set From Reactome Pathways 2024 proteins participating in the TFAP2 (AP-2) family regulates transcription of other transcription factors pathway from the Reactome Pathways 2024 dataset.
TGFBR3 regulates FGF2 signaling Gene Set From Reactome Pathways 2024 proteins participating in the TGFBR3 regulates FGF2 signaling pathway from the Reactome Pathways 2024 dataset.
TGFBR3 regulates TGF-beta signaling Gene Set From Reactome Pathways 2024 proteins participating in the TGFBR3 regulates TGF-beta signaling pathway from the Reactome Pathways 2024 dataset.
TGFBR3 regulates activin signaling Gene Set From Reactome Pathways 2024 proteins participating in the TGFBR3 regulates activin signaling pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Metabolic Genes Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Metabolic Genes pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Cell Cycle Genes Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Cell Cycle Genes pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Cell Death Genes Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Cell Death Genes pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of DNA Repair Genes Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of DNA Repair Genes pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Genes Involved in Cytochrome C Release pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest pathway from the Reactome Pathways 2024 dataset.
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain Gene Set From Reactome Pathways 2024 proteins participating in the TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain pathway from the Reactome Pathways 2024 dataset.
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain Gene Set From Reactome Pathways 2024 proteins participating in the TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain pathway from the Reactome Pathways 2024 dataset.
Vasopressin regulates renal water homeostasis via Aquaporins Gene Set From Reactome Pathways 2024 proteins participating in the Vasopressin regulates renal water homeostasis via Aquaporins pathway from the Reactome Pathways 2024 dataset.
p75NTR negatively regulates cell cycle via SC1 Gene Set From Reactome Pathways 2024 proteins participating in the p75NTR negatively regulates cell cycle via SC1 pathway from the Reactome Pathways 2024 dataset.
p75NTR regulates axonogenesis Gene Set From Reactome Pathways 2024 proteins participating in the p75NTR regulates axonogenesis pathway from the Reactome Pathways 2024 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cbl mediated ligand-induced downregulation of egf receptors pathway Gene Set From Biocarta Pathways proteins participating in the cbl mediated ligand-induced downregulation of egf receptors pathway pathway from the Biocarta Pathways dataset.
activation of pkc through g-protein coupled receptors Gene Set From Biocarta Pathways proteins participating in the activation of pkc through g-protein coupled receptors pathway from the Biocarta Pathways dataset.
regulation of ck1/cdk5 by type 1 glutamate receptors Gene Set From Biocarta Pathways proteins participating in the regulation of ck1/cdk5 by type 1 glutamate receptors pathway from the Biocarta Pathways 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.
Receptors, IgG Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Receptors, IgG from the curated CTD Gene-Chemical Interactions dataset.
Receptors, IgE Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Receptors, IgE from the curated CTD Gene-Chemical Interactions dataset.
Receptors, Tumor Necrosis Factor Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Receptors, Tumor Necrosis Factor in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Receptors, Interleukin-6 Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Receptors, Interleukin-6 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Receptors, Leptin Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Receptors, Leptin in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Receptors, Transferrin Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Receptors, Transferrin in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Receptors, Tumor Necrosis Factor, Type II Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Receptors, Tumor Necrosis Factor, Type II in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
receptors, tumor necrosis factor, type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease receptors, tumor necrosis factor, type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
receptors, leptin Gene Set From GAD Gene-Disease Associations genes associated with the disease receptors, leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
receptors, interleukin-6 Gene Set From GAD Gene-Disease Associations genes associated with the disease receptors, interleukin-6 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
receptors, transferrin Gene Set From GAD Gene-Disease Associations genes associated with the disease receptors, transferrin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
receptors, tumor necrosis factor Gene Set From GAD Gene-Disease Associations genes associated with the disease receptors, tumor necrosis factor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
receptors Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term receptors in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
somatic diversification of immune receptors via germline recombination within a single locus Gene Set From GO Biological Process Annotations 2015 genes participating in the somatic diversification of immune receptors via germline recombination within a single locus biological process from the curated GO Biological Process Annotations 2015 dataset.
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2015 genes participating in the adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset.
extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
somatic diversification of immune receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the somatic diversification of immune receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
somatic diversification of immune receptors via somatic mutation Gene Set From GO Biological Process Annotations 2015 genes participating in the somatic diversification of immune receptors via somatic mutation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
increased number of cd4-/cd8- t cells expressing alpha/beta t-cell receptors Gene Set From HPO Gene-Disease Associations genes associated with the increased number of cd4-/cd8- t cells expressing alpha/beta t-cell receptors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations 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.
Signalling lymphocyte activation molecule family receptors Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Signalling lymphocyte activation molecule family receptors protein domain from the InterPro Predicted Protein Domain Annotations dataset.
receptors Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term receptors in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
receptors-n-methyl-d-aspartate Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term receptors-n-methyl-d-aspartate in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Retinoic acid receptors-mediated signaling Gene Set From PID Pathways proteins participating in the Retinoic acid receptors-mediated signaling pathway from the PID Pathways dataset.
Class C/3 (Metabotropic glutamate/pheromone receptors) Gene Set From Reactome Pathways 2014 proteins participating in the Class C/3 (Metabotropic glutamate/pheromone receptors) pathway from the Reactome Pathways dataset.
Hydroxycarboxylic acid-binding receptors Gene Set From Reactome Pathways 2014 proteins participating in the Hydroxycarboxylic acid-binding receptors pathway from the Reactome Pathways dataset.
Nucleotide-like (purinergic) receptors Gene Set From Reactome Pathways 2014 proteins participating in the Nucleotide-like (purinergic) receptors pathway from the Reactome Pathways dataset.
Eicosanoid ligand-binding receptors Gene Set From Reactome Pathways 2014 proteins participating in the Eicosanoid ligand-binding receptors pathway from the Reactome Pathways dataset.
Activation of Na-permeable Kainate Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Activation of Na-permeable Kainate Receptors 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.
Scavenging by Class A Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Scavenging by Class A 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.
Calcitonin-like ligand receptors Gene Set From Reactome Pathways 2014 proteins participating in the Calcitonin-like ligand 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.
Histamine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Histamine receptors pathway from the Reactome Pathways dataset.
Toll-Like Receptors Cascades Gene Set From Reactome Pathways 2014 proteins participating in the Toll-Like Receptors Cascades pathway from the Reactome Pathways dataset.
Thrombin signalling through proteinase activated receptors (PARs) Gene Set From Reactome Pathways 2014 proteins participating in the Thrombin signalling through proteinase activated receptors (PARs) pathway from the Reactome Pathways dataset.
Amine ligand-binding receptors Gene Set From Reactome Pathways 2014 proteins participating in the Amine ligand-binding receptors pathway from the Reactome Pathways dataset.
Peptide ligand-binding receptors Gene Set From Reactome Pathways 2014 proteins participating in the Peptide ligand-binding receptors pathway from the Reactome Pathways dataset.
Vasopressin-like receptors Gene Set From Reactome Pathways 2014 proteins participating in the Vasopressin-like receptors pathway from the Reactome Pathways dataset.
Trafficking of GluR2-containing AMPA receptors Gene Set From Reactome Pathways 2014 proteins participating in the Trafficking of GluR2-containing AMPA receptors pathway from the Reactome Pathways dataset.
Activation of TRKA receptors Gene Set From Reactome Pathways 2014 proteins participating in the Activation of TRKA receptors pathway from the Reactome Pathways dataset.
Class A/1 (Rhodopsin-like receptors) Gene Set From Reactome Pathways 2014 proteins participating in the Class A/1 (Rhodopsin-like receptors) pathway from the Reactome Pathways dataset.
Relaxin receptors Gene Set From Reactome Pathways 2014 proteins participating in the Relaxin receptors pathway from the Reactome Pathways dataset.
Class B/2 (Secretin family receptors) Gene Set From Reactome Pathways 2014 proteins participating in the Class B/2 (Secretin family 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.
Serotonin receptors Gene Set From Reactome Pathways 2014 proteins participating in the Serotonin receptors pathway from the Reactome Pathways dataset.
Trafficking of AMPA receptors Gene Set From Reactome Pathways 2014 proteins participating in the Trafficking of AMPA receptors pathway from the Reactome Pathways dataset.
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters Gene Set From Reactome Pathways 2014 proteins participating in the Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters pathway from the Reactome Pathways dataset.
Activation of Kainate Receptors upon glutamate binding Gene Set From Reactome Pathways 2014 proteins participating in the Activation of Kainate Receptors upon glutamate binding 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.
Scavenging by Class H Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Scavenging by Class H Receptors pathway from the Reactome Pathways dataset.
Activation of AMPA receptors Gene Set From Reactome Pathways 2014 proteins participating in the Activation of AMPA receptors pathway from the Reactome Pathways dataset.
Prostanoid ligand receptors Gene Set From Reactome Pathways 2014 proteins participating in the Prostanoid ligand receptors pathway from the Reactome Pathways dataset.
Presynaptic function of Kainate receptors Gene Set From Reactome Pathways 2014 proteins participating in the Presynaptic function of Kainate receptors pathway from the Reactome Pathways dataset.
Tachykinin receptors bind tachykinins Gene Set From Reactome Pathways 2014 proteins participating in the Tachykinin receptors bind tachykinins pathway from the Reactome Pathways dataset.
Ionotropic activity of Kainate Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Ionotropic activity of Kainate Receptors pathway from the Reactome Pathways dataset.
Scavenging by Class B Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Scavenging by Class B Receptors pathway from the Reactome Pathways dataset.
Hormone ligand-binding receptors Gene Set From Reactome Pathways 2014 proteins participating in the Hormone ligand-binding receptors 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.
Chemokine receptors bind chemokines Gene Set From Reactome Pathways 2014 proteins participating in the Chemokine receptors bind chemokines pathway from the Reactome Pathways dataset.
Leukotriene receptors Gene Set From Reactome Pathways 2014 proteins participating in the Leukotriene receptors pathway from the Reactome Pathways dataset.
Adenosine P1 receptors Gene Set From Reactome Pathways 2014 proteins participating in the Adenosine P1 receptors pathway from the Reactome Pathways dataset.
P2Y receptors Gene Set From Reactome Pathways 2014 proteins participating in the P2Y receptors pathway from the Reactome Pathways dataset.
Dopamine receptors Gene Set From Reactome Pathways 2014 proteins participating in the Dopamine receptors pathway from the Reactome Pathways dataset.
Free fatty acid receptors Gene Set From Reactome Pathways 2014 proteins participating in the Free fatty acid receptors pathway from the Reactome Pathways dataset.
Activation of GABAB receptors Gene Set From Reactome Pathways 2014 proteins participating in the Activation of GABAB receptors pathway from the Reactome Pathways dataset.
Glucagon-type ligand receptors Gene Set From Reactome Pathways 2014 proteins participating in the Glucagon-type ligand receptors pathway from the Reactome Pathways dataset.
Scavenging by Class F Receptors Gene Set From Reactome Pathways 2014 proteins participating in the Scavenging by Class F Receptors pathway from the Reactome Pathways dataset.
Nuclear Receptors(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nuclear Receptors(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Nuclear Receptors(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Nuclear Receptors(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2023 genes participating in the adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset.
Nuclear receptors Gene Set From WikiPathways Pathways 2024 proteins participating in the Nuclear receptors pathway from the WikiPathways Pathways 2024 dataset.
Nuclear receptors meta pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Nuclear receptors meta pathway pathway from the WikiPathways Pathways 2024 dataset.
Selective expression of chemokine receptors during T cell polarization Gene Set From WikiPathways Pathways 2024 proteins participating in the Selective expression of chemokine receptors during T cell polarization pathway from the WikiPathways Pathways 2024 dataset.
Activation of AMPA receptors Gene Set From Reactome Pathways 2024 proteins participating in the Activation of AMPA receptors pathway from the Reactome Pathways 2024 dataset.
Activation of GABAB receptors Gene Set From Reactome Pathways 2024 proteins participating in the Activation of GABAB receptors pathway from the Reactome Pathways 2024 dataset.
Activation of Na-permeable kainate receptors Gene Set From Reactome Pathways 2024 proteins participating in the Activation of Na-permeable kainate receptors pathway from the Reactome Pathways 2024 dataset.
Activation of TRKA receptors Gene Set From Reactome Pathways 2024 proteins participating in the Activation of TRKA receptors pathway from the Reactome Pathways 2024 dataset.
Activation of kainate receptors upon glutamate binding Gene Set From Reactome Pathways 2024 proteins participating in the Activation of kainate receptors upon glutamate binding pathway from the Reactome Pathways 2024 dataset.
Adenosine P1 receptors Gene Set From Reactome Pathways 2024 proteins participating in the Adenosine P1 receptors pathway from the Reactome Pathways 2024 dataset.
Amine ligand-binding receptors Gene Set From Reactome Pathways 2024 proteins participating in the Amine ligand-binding receptors pathway from the Reactome Pathways 2024 dataset.
C-type lectin receptors (CLRs) Gene Set From Reactome Pathways 2024 proteins participating in the C-type lectin receptors (CLRs) pathway from the Reactome Pathways 2024 dataset.
Calcitonin-like ligand receptors Gene Set From Reactome Pathways 2024 proteins participating in the Calcitonin-like ligand receptors pathway from the Reactome Pathways 2024 dataset.
Caspase activation via Death Receptors in the presence of ligand Gene Set From Reactome Pathways 2024 proteins participating in the Caspase activation via Death Receptors in the presence of ligand pathway from the Reactome Pathways 2024 dataset.
Caspase activation via Dependence Receptors in the absence of ligand Gene Set From Reactome Pathways 2024 proteins participating in the Caspase activation via Dependence Receptors in the absence of ligand pathway from the Reactome Pathways 2024 dataset.
Chemokine receptors bind chemokines Gene Set From Reactome Pathways 2024 proteins participating in the Chemokine receptors bind chemokines pathway from the Reactome Pathways 2024 dataset.
Class A/1 (Rhodopsin-like receptors) Gene Set From Reactome Pathways 2024 proteins participating in the Class A/1 (Rhodopsin-like receptors) pathway from the Reactome Pathways 2024 dataset.
Class B/2 (Secretin family receptors) Gene Set From Reactome Pathways 2024 proteins participating in the Class B/2 (Secretin family receptors) pathway from the Reactome Pathways 2024 dataset.
Class C/3 (Metabotropic glutamate/pheromone receptors) Gene Set From Reactome Pathways 2024 proteins participating in the Class C/3 (Metabotropic glutamate/pheromone receptors) pathway from the Reactome Pathways 2024 dataset.
Dopamine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Dopamine receptors pathway from the Reactome Pathways 2024 dataset.
Eicosanoid ligand-binding receptors Gene Set From Reactome Pathways 2024 proteins participating in the Eicosanoid ligand-binding receptors pathway from the Reactome Pathways 2024 dataset.
Free fatty acid receptors Gene Set From Reactome Pathways 2024 proteins participating in the Free fatty acid receptors pathway from the Reactome Pathways 2024 dataset.
Glucagon-type ligand receptors Gene Set From Reactome Pathways 2024 proteins participating in the Glucagon-type ligand receptors pathway from the Reactome Pathways 2024 dataset.
HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand Gene Set From Reactome Pathways 2024 proteins participating in the HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand 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.
Histamine receptors Gene Set From Reactome Pathways 2024 proteins participating in the Histamine receptors pathway from the Reactome Pathways 2024 dataset.
Hormone ligand-binding receptors Gene Set From Reactome Pathways 2024 proteins participating in the Hormone ligand-binding receptors pathway from the Reactome Pathways 2024 dataset.
Hydroxycarboxylic acid-binding receptors Gene Set From Reactome Pathways 2024 proteins participating in the Hydroxycarboxylic acid-binding receptors pathway from the Reactome Pathways 2024 dataset.
Ionotropic activity of kainate receptors Gene Set From Reactome Pathways 2024 proteins participating in the Ionotropic activity of kainate receptors pathway from the Reactome Pathways 2024 dataset.
Leukotriene receptors Gene Set From Reactome Pathways 2024 proteins participating in the Leukotriene 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.
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters Gene Set From Reactome Pathways 2024 proteins participating in the Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters pathway from the Reactome Pathways 2024 dataset.
Nucleotide-like (purinergic) receptors Gene Set From Reactome Pathways 2024 proteins participating in the Nucleotide-like (purinergic) receptors pathway from the Reactome Pathways 2024 dataset.
P2Y receptors Gene Set From Reactome Pathways 2024 proteins participating in the P2Y receptors pathway from the Reactome Pathways 2024 dataset.
Peptide ligand-binding receptors Gene Set From Reactome Pathways 2024 proteins participating in the Peptide ligand-binding 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 function of Kainate receptors Gene Set From Reactome Pathways 2024 proteins participating in the Presynaptic function of Kainate 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.
Prostanoid ligand receptors Gene Set From Reactome Pathways 2024 proteins participating in the Prostanoid ligand receptors pathway from the Reactome Pathways 2024 dataset.
ROBO receptors bind AKAP5 Gene Set From Reactome Pathways 2024 proteins participating in the ROBO receptors bind AKAP5 pathway from the Reactome Pathways 2024 dataset.
Relaxin receptors Gene Set From Reactome Pathways 2024 proteins participating in the Relaxin receptors pathway from the Reactome Pathways 2024 dataset.
SUMOylation of intracellular receptors Gene Set From Reactome Pathways 2024 proteins participating in the SUMOylation of intracellular receptors pathway from the Reactome Pathways 2024 dataset.
Scavenging by Class A Receptors Gene Set From Reactome Pathways 2024 proteins participating in the Scavenging by Class A Receptors pathway from the Reactome Pathways 2024 dataset.
Scavenging by Class B Receptors Gene Set From Reactome Pathways 2024 proteins participating in the Scavenging by Class B Receptors pathway from the Reactome Pathways 2024 dataset.
Scavenging by Class F Receptors Gene Set From Reactome Pathways 2024 proteins participating in the Scavenging by Class F Receptors pathway from the Reactome Pathways 2024 dataset.
Scavenging by Class H Receptors Gene Set From Reactome Pathways 2024 proteins participating in the Scavenging by Class H Receptors pathway from the Reactome Pathways 2024 dataset.
Serotonin receptors Gene Set From Reactome Pathways 2024 proteins participating in the Serotonin receptors pathway from the Reactome Pathways 2024 dataset.
Signaling by Nuclear Receptors Gene Set From Reactome Pathways 2024 proteins participating in the Signaling by Nuclear Receptors pathway from the Reactome Pathways 2024 dataset.
Signaling by ROBO receptors Gene Set From Reactome Pathways 2024 proteins participating in the Signaling by ROBO receptors pathway from the Reactome Pathways 2024 dataset.
TNFs bind their physiological receptors Gene Set From Reactome Pathways 2024 proteins participating in the TNFs bind their physiological receptors pathway from the Reactome Pathways 2024 dataset.
Tachykinin receptors bind tachykinins Gene Set From Reactome Pathways 2024 proteins participating in the Tachykinin receptors bind tachykinins pathway from the Reactome Pathways 2024 dataset.
Thrombin signalling through proteinase activated receptors (PARs) Gene Set From Reactome Pathways 2024 proteins participating in the Thrombin signalling through proteinase activated receptors (PARs) pathway from the Reactome Pathways 2024 dataset.
Trafficking of AMPA receptors Gene Set From Reactome Pathways 2024 proteins participating in the Trafficking of AMPA receptors pathway from the Reactome Pathways 2024 dataset.
Trafficking of GluR2-containing AMPA receptors Gene Set From Reactome Pathways 2024 proteins participating in the Trafficking of GluR2-containing AMPA receptors pathway from the Reactome Pathways 2024 dataset.
Vasopressin-like receptors Gene Set From Reactome Pathways 2024 proteins participating in the Vasopressin-like receptors pathway from the Reactome Pathways 2024 dataset.
extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2025 genes participating in the adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset.
role of erk5 in neuronal survival pathway Gene Set From Biocarta Pathways proteins participating in the role of erk5 in neuronal survival pathway pathway from the Biocarta Pathways dataset.
Ceroid lipofuscinosis, neuronal, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis, neuronal, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 4B autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 4B autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis, neuronal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis, neuronal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ceroid lipofuscinosis neuronal 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ceroid lipofuscinosis neuronal 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
neuronal cell body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal cell body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
neuronal cell body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
neuronal ribonucleoprotein granule Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal ribonucleoprotein granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
neuronal cell body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the neuronal cell body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
neuronal ribonucleoprotein granule Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the neuronal ribonucleoprotein granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Ceroid lipofuscinosis, neuronal 1, infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 1, infantile from the curated CTD Gene-Disease Associations dataset.
Ceroid Lipofuscinosis, Neuronal, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 10 from the curated CTD Gene-Disease Associations dataset.
Ceroid lipofuscinosis, neuronal 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 8 from the curated CTD Gene-Disease Associations dataset.
Ceroid lipofuscinosis, neuronal 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 5 from the curated CTD Gene-Disease Associations dataset.
Ceroid Lipofuscinosis, Neuronal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 2 from the curated CTD Gene-Disease Associations dataset.
Ceroid Lipofuscinosis, Neuronal, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 1 from the curated CTD Gene-Disease Associations dataset.
Ceroid Lipofuscinosis, Neuronal, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 6 from the curated CTD Gene-Disease Associations dataset.
Ceroid Lipofuscinosis, Neuronal, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 7 from the curated CTD Gene-Disease Associations dataset.
Ceroid lipofuscinosis, neuronal 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 9 from the curated CTD Gene-Disease Associations dataset.
Neuronal Ceroid-Lipofuscinoses Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronal Ceroid-Lipofuscinoses from the curated CTD Gene-Disease Associations dataset.
neuronal ceroid lipofuscinosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neuronal ceroid lipofuscinosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
neuronal ceroid lipofuscinosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuronal ceroid lipofuscinosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neuronal ceroid-lipofuscinoses Gene Set From GAD Gene-Disease Associations genes associated with the disease neuronal ceroid-lipofuscinoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intestinal neuronal dysplasia type b (ind b) Gene Set From GAD Gene-Disease Associations genes associated with the disease intestinal neuronal dysplasia type b (ind b) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuronal hyperexcitability Gene Set From GAD Gene-Disease Associations genes associated with the disease neuronal hyperexcitability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variant late infantile neuronal ceroid lipofuscinosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuronal no synthase (nos1) gene polymorphism Gene Set From GAD Gene-Disease Associations genes associated with the disease neuronal no synthase (nos1) gene polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ischemic neuronal cell death Gene Set From GAD Gene-Disease Associations genes associated with the disease ischemic neuronal cell death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuronal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term neuronal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
regulation of short-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
gonadotrophin-releasing hormone neuronal migration to the hypothalamus Gene Set From GO Biological Process Annotations 2015 genes participating in the gonadotrophin-releasing hormone neuronal migration to the hypothalamus biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of neuronal action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of neuronal action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal ion channel clustering Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal ion channel clustering biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal signal transduction Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
commitment of neuronal cell to specific neuron type in forebrain Gene Set From GO Biological Process Annotations 2015 genes participating in the commitment of neuronal cell to specific neuron type in forebrain biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal action potential propagation Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal action potential propagation biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal stem cell maintenance Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal stem cell maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of neuronal signal transduction Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of neuronal signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal stem cell division Gene Set From GO Biological Process Annotations 2015 genes participating in the neuronal stem cell division biological process from the curated GO Biological Process Annotations 2015 dataset.
cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset.
neuronal cell body Gene Set From GO Cellular Component Annotations 2015 proteins localized to the neuronal cell body cellular component from the curated GO Cellular Component Annotations 2015 dataset.
neuronal cell body membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the neuronal cell body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
neuronal postsynaptic density Gene Set From GO Cellular Component Annotations 2015 proteins localized to the neuronal postsynaptic density cellular component from the curated GO Cellular Component Annotations 2015 dataset.
neuronal ribonucleoprotein granule Gene Set From GO Cellular Component Annotations 2015 proteins localized to the neuronal ribonucleoprotein granule cellular component from the curated GO Cellular Component Annotations 2015 dataset.
white matter neuronal heterotopia Gene Set From HPO Gene-Disease Associations genes associated with the white matter neuronal heterotopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of neuronal migration Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of neuronal migration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased neuronal autofluorescent lipopigment Gene Set From HPO Gene-Disease Associations genes associated with the increased neuronal autofluorescent lipopigment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neuronal loss in the cerebral cortex Gene Set From HPO Gene-Disease Associations genes associated with the neuronal loss in the cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neuronal loss in basal ganglia Gene Set From HPO Gene-Disease Associations genes associated with the neuronal loss in basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neuronal loss in central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the neuronal loss in central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neuronal Ceroid-Lipofuscinoses Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neuronal Ceroid-Lipofuscinoses phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Neuronal migration protein doublecortin, chordata Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuronal migration protein doublecortin, chordata protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dopamine/cAMP-regulated neuronal phosphoprotein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dopamine/cAMP-regulated neuronal phosphoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ceroid-lipofuscinosis neuronal protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ceroid-lipofuscinosis neuronal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ceroid-lipofuscinosis neuronal protein 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ceroid-lipofuscinosis neuronal protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Neuronal protein 3.1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuronal protein 3.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cell cycle exit/neuronal differentiation protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell cycle exit/neuronal differentiation protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1/2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
premature neuronal precursor differentiation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the premature neuronal precursor differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neuronal intranuclear inclusions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neuronal intranuclear inclusions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuronal stem cell self-renewal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to neuronal excitotoxicity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal stem cell self-renewal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal stem cell physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal stem cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal neuronal layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal neuronal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased neuronal stem cell self-renewal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal stem cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal stem cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to neuronal excitotoxicity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neuronal cytoplasmic inclusions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neuronal cytoplasmic inclusions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuronal precursor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent neuronal precursor cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent neuronal precursor cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal precursor proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal precursor proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal precursor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased neuronal precursor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
?ceroid lipofuscinosis, neuronal, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the ?ceroid lipofuscinosis, neuronal, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, kufs type, adult onset Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, kufs type, adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 4, parry type Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 4, parry type phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
ceroid lipofuscinosis, neuronal, 13, kufs type Gene Set From OMIM Gene-Disease Associations genes associated with the ceroid lipofuscinosis, neuronal, 13, kufs type phenotype from the curated OMIM Gene-Disease Associations dataset.
intestinal pseudoobstruction, neuronal Gene Set From OMIM Gene-Disease Associations genes associated with the intestinal pseudoobstruction, neuronal phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronal Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term neuronal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Neuronal System Gene Set From Reactome Pathways 2014 proteins participating in the Neuronal System pathway from the Reactome Pathways dataset.
H3K4me3_H1 Derived Neuronal Progenitor Cultured Cells Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_H1 Derived Neuronal Progenitor Cultured Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
H3K27ac_H1 Derived Neuronal Progenitor Cultured Cells Gene Set From Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_H1 Derived Neuronal Progenitor Cultured Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.
neuronal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue neuronal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
non-neuronal cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue non-neuronal cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Late-Infantile Neuronal Ceroid Lipfuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Infantile Neuronal Ceroid Lipfuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Intestinal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Intestinal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Neuronal Ceroid Lipofuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Neuronal Ceroid Lipofuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Ceroid Lipofuscinosies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Ceroid Lipofuscinosies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Choristoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Choristoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Heterotopia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Heterotopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Neuronal Ceroid Lipofuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Neuronal Ceroid Lipofuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuronal Ceroid Lipofuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuronal Ceroid Lipofuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Intranuclear Inclusion Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Intranuclear Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Intestinal Pseudoobstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Intestinal Pseudoobstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Loss In Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neuronal Loss In The Cerebral Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In The Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Neuronal Autofluorescent Lipopigment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Neuronal Autofluorescent Lipopigment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neuronal Loss In Basal Ganglia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of short-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal dense core vesicle exocytosis Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal dense core vesicle exocytosis biological process from the curated GO Biological Process Annotations 2023 dataset.
gonadotrophin-releasing hormone neuronal migration to the hypothalamus Gene Set From GO Biological Process Annotations 2023 genes participating in the gonadotrophin-releasing hormone neuronal migration to the hypothalamus biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset.
anterograde neuronal dense core vesicle transport Gene Set From GO Biological Process Annotations 2023 genes participating in the anterograde neuronal dense core vesicle transport biological process from the curated GO Biological Process Annotations 2023 dataset.
retrograde neuronal dense core vesicle transport Gene Set From GO Biological Process Annotations 2023 genes participating in the retrograde neuronal dense core vesicle transport biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of neuronal action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of neuronal action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of neuronal signal transduction Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of neuronal signal transduction biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal-glial interaction involved in hindbrain glial-mediated radial cell migration Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal-glial interaction involved in hindbrain glial-mediated radial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of neuronal action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of neuronal action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal action potential propagation Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal action potential propagation biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal stem cell division Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal stem cell division biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal ion channel clustering Gene Set From GO Biological Process Annotations 2023 genes participating in the neuronal ion channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.
commitment of neuronal cell to specific neuron type in forebrain Gene Set From GO Biological Process Annotations 2023 genes participating in the commitment of neuronal cell to specific neuron type in forebrain biological process from the curated GO Biological Process Annotations 2023 dataset.
neuronal dense core vesicle Gene Set From GO Cellular Component Annotations 2023 proteins localized to the neuronal dense core vesicle cellular component from the curated GO Cellular Component Annotations 2023 dataset.
neuronal ribonucleoprotein granule Gene Set From GO Cellular Component Annotations 2023 proteins localized to the neuronal ribonucleoprotein granule cellular component from the curated GO Cellular Component Annotations 2023 dataset.
extrinsic component of neuronal dense core vesicle membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the extrinsic component of neuronal dense core vesicle membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
neuronal dense core vesicle lumen Gene Set From GO Cellular Component Annotations 2023 proteins localized to the neuronal dense core vesicle lumen cellular component from the curated GO Cellular Component Annotations 2023 dataset.
neuronal dense core vesicle membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the neuronal dense core vesicle membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal retina neuronal layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina neuronal layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neuronal migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased neuronal precursor cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased neuronal precursor cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptibility to neuronal excitotoxicity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neuronal precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased neuronal precursor cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased neuronal precursor cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neuronal intranuclear inclusions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neuronal intranuclear inclusions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to neuronal excitotoxicity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent neuronal precursor cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent neuronal precursor cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased neuronal precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased neuronal precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature neuronal precursor differentiation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature neuronal precursor differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neuronal precursor cell migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal precursor cell migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neuronal precursor cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal precursor cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neuronal stem cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal stem cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased neuronal stem cell self-renewal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased neuronal stem cell self-renewal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neuronal cytoplasmic inclusions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neuronal cytoplasmic inclusions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased neuronal stem cell self-renewal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased neuronal stem cell self-renewal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neuronal stem cell physiology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal stem cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased neuronal precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased neuronal precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - Motor Cortex - Class - Non-neuronal cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Class - Non-neuronal cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Mouse - Motor Cortex - Class - Non-neuronal cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Class - Non-neuronal cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Heart - L1 - Neuronal Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Heart - L1 - Neuronal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Heart - L2 - Neuronal Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Heart - L2 - Neuronal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
neuronal dense core vesicle lumen Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term neuronal dense core vesicle lumen from the SynGO Synaptic Gene Annotations dataset.
neuronal dense core vesicle Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term neuronal dense core vesicle from the SynGO Synaptic Gene Annotations dataset.
extrinsic component of neuronal dense core vesicle membrane Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term extrinsic component of neuronal dense core vesicle membrane from the SynGO Synaptic Gene Annotations dataset.
integral component of neuronal dense core vesicle membrane Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term integral component of neuronal dense core vesicle membrane from the SynGO Synaptic Gene Annotations dataset.
Neuronal-like cell_Spinal cord_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal-like cell_Spinal cord_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal progenitor cell_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal progenitor cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Pan-neuronal cell_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Pan-neuronal cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal progenitor cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal progenitor cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal stem cell_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal stem cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Pan-neuronal cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Pan-neuronal cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Adult neuronal stem cell_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Adult neuronal stem cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Adult neuronal stem cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Adult neuronal stem cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal intermediate progenitor cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal intermediate progenitor cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Pan-neuronal cell_Prefrontal cortex_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Pan-neuronal cell_Prefrontal cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Late neuronal progenitor cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Late neuronal progenitor cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Suprachiasmatic neuronal cell_Eye_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Suprachiasmatic neuronal cell_Eye_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal glial cell_Heart_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal glial cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Pan-neuronal cell_Enteric neural crest_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Pan-neuronal cell_Enteric neural crest_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal Cell (Axon Only)_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal Cell (Axon Only)_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Neuronal progenitor cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neuronal progenitor cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Phosphodiesterases in neuronal function Gene Set From WikiPathways Pathways 2024 proteins participating in the Phosphodiesterases in neuronal function pathway from the WikiPathways Pathways 2024 dataset.
Cell lineage map for neuronal differentiation Gene Set From WikiPathways Pathways 2024 proteins participating in the Cell lineage map for neuronal differentiation pathway from the WikiPathways Pathways 2024 dataset.
Diseases of the neuronal system Gene Set From Reactome Pathways 2024 proteins participating in the Diseases of the neuronal system pathway from the Reactome Pathways 2024 dataset.
Negative regulation of NMDA receptor-mediated neuronal transmission Gene Set From Reactome Pathways 2024 proteins participating in the Negative regulation of NMDA receptor-mediated neuronal transmission pathway from the Reactome Pathways 2024 dataset.
Neuronal System Gene Set From Reactome Pathways 2024 proteins participating in the Neuronal System pathway from the Reactome Pathways 2024 dataset.
regulation of short-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal dense core vesicle exocytosis Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal dense core vesicle exocytosis biological process from the curated GO Biological Process Annotations 2025 dataset.
gonadotrophin-releasing hormone neuronal migration to the hypothalamus Gene Set From GO Biological Process Annotations 2025 genes participating in the gonadotrophin-releasing hormone neuronal migration to the hypothalamus biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
anterograde neuronal dense core vesicle transport Gene Set From GO Biological Process Annotations 2025 genes participating in the anterograde neuronal dense core vesicle transport biological process from the curated GO Biological Process Annotations 2025 dataset.
retrograde neuronal dense core vesicle transport Gene Set From GO Biological Process Annotations 2025 genes participating in the retrograde neuronal dense core vesicle transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of neuronal action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of neuronal action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of neuronal signal transduction Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of neuronal signal transduction biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal-glial interaction involved in hindbrain glial-mediated radial cell migration Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal-glial interaction involved in hindbrain glial-mediated radial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of neuronal action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of neuronal action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal action potential propagation Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal action potential propagation biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal stem cell division Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal stem cell division biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal ion channel clustering Gene Set From GO Biological Process Annotations 2025 genes participating in the neuronal ion channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.
commitment of neuronal cell to specific neuron type in forebrain Gene Set From GO Biological Process Annotations 2025 genes participating in the commitment of neuronal cell to specific neuron type in forebrain biological process from the curated GO Biological Process Annotations 2025 dataset.
commitment of multipotent stem cells to neuronal lineage in forebrain Gene Set From GO Biological Process Annotations 2025 genes participating in the commitment of multipotent stem cells to neuronal lineage in forebrain biological process from the curated GO Biological Process Annotations 2025 dataset.
neuronal dense core vesicle Gene Set From GO Cellular Component Annotations 2025 proteins localized to the neuronal dense core vesicle cellular component from the curated GO Cellular Component Annotations 2025 dataset.
neuronal ribonucleoprotein granule Gene Set From GO Cellular Component Annotations 2025 proteins localized to the neuronal ribonucleoprotein granule cellular component from the curated GO Cellular Component Annotations 2025 dataset.
neuronal dense core vesicle lumen Gene Set From GO Cellular Component Annotations 2025 proteins localized to the neuronal dense core vesicle lumen cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Neuronal ceroid lipofuscinosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 6A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 6A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 7 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 7 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 11 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 11 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 10 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 10 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 8 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 8 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuronal ceroid lipofuscinosis 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 8 northern epilepsy variant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal intranuclear inclusion disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal intranuclear inclusion disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 6A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 6A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 6B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 6B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal intestinal dysplasia type B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal intestinal dysplasia type B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuronal ceroid lipofuscinosis 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-neuronal cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue non-neuronal cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Neuronal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Neuronal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Neuronal cell body Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuronal cell body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Neuronal ribonucleoprotein granule Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuronal ribonucleoprotein granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Neuronal cell body membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuronal cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Neuronal dense core vesicle Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuronal dense core vesicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Neuronal dense core vesicle lumen Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuronal dense core vesicle lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Neuronal cell body Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Neuronal cell body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Neuronal ribonucleoprotein granule Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Neuronal ribonucleoprotein granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Neuronal dense core vesicle Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Neuronal dense core vesicle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Neuronal cell body membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Neuronal cell body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-infantile neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-infantile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuronal ceroid lipofuscinosis 8 northern epilepsy variant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuronal Ceroid-Lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuronal Ceroid-Lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormality of neuronal migration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of neuronal migration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CAMSAP1-related neuronal migration disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CAMSAP1-related neuronal migration disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene 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.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene 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.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene 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.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multicentric osteolysis, nodulosis and arthropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy dilated with woolly hair and keratoderma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone fragility with contractures, arterial rupture, and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor v and factor viii, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary Paragangliomas and Pheochromocytomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Band-like calcification with simplified gyration and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Monocyte and dendritic cell deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene 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.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined malonic and methylmalonic aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis Gyrata syndrome of Beare and Stevenson Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniosynostosis and dental anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebroretinal microangiopathy with calcifications and cysts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, normal intelligence and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Calcification of joints and arteries Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pineal hyperplasia AND diabetes mellitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Morbid obesity and spermatogenic failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of factor V and factor VIII, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Camptodactyly, tall stature, and hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth deficiency and mental retardation with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, cochlear, with myopia and intellectual impairment Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of sialidase AND beta galactosidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set From CORUM Protein Complexes proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set From CORUM Protein Complexes proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.
6S methyltransferase and RG-containing Sm proteins complex Gene Set From CORUM Protein Complexes proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.
Remodeling and spacing factor (RSF) complex Gene Set From CORUM Protein Complexes proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.
PBAF complex (Polybromo- and BAF containing complex) Gene Set From CORUM Protein Complexes proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.
Cleavage and polyadenylation factor (CPSF) Gene Set From CORUM Protein Complexes proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene 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.
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Nucleic and chromatin Fanconi complex Gene Set From CORUM Protein Complexes proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene 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.
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set From CORUM Protein Complexes proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.
20S methylosome and RG-containing Sm protein complex Gene Set From CORUM Protein Complexes proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.
Amino Acids, Peptides, and Proteins Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.
Bile Acids and Salts Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.
Prime and Bond NT Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.
drospirenone and ethinyl estradiol combination Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.
Hypophosphatemic Rickets And Hyperparathyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
Synovitis granulomatous with uveitis and cranial neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.
Combined Cellular And Humoral Immune Defects With Granulomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.
Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.
Craniosynostosis, anal anomalies, and porokeratosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.
Classical Lissencephalies and Subcortical Band Heterotopias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Russe type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.
Hypotrichosis And Recurrent Skin Vesicles Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.
Signs and Symptoms, Digestive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset.
Head and Neck Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Cataract, Juvenile, With Microcornea And Glucosuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous and Mucosal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.
Postoperative Nausea and Vomiting Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

MECP2 regulates neuronal receptors and channels Gene Set

MECP2 regulates transcription of neuronal ligands Gene Set

MECP2 regulates transcription factors Gene Set

MECP2 regulates transcription of genes involved in GABA signaling Gene Set

TFAP2 (AP-2) family regulates transcription of growth factors and their receptors Gene Set

TP53 Regulates Transcription of Death Receptors and Ligands Gene Set

PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set

MECP2 and associated Rett syndrome Gene Set

Regulation of MECP2 expression and activity Gene Set

ion channels and their functional role in vascular endothelium Gene Set

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set

PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases Gene Set

RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function Gene Set

RUNX3 Regulates Immune Response and Cell Migration Gene Set

TP53 Regulates Transcription of Caspase Activators and Caspases Gene Set

PU.1-Sin3A-Hdac-MeCP2 complex Gene Set

MeCP2-SIN3A-HDAC complex Gene Set

Smarcb1/Ini1-Smarca2-Mecp2 complex Gene Set

Hdac1-Mecp2-Rcor1-Sin3a complex Gene Set

SWI/SNF chromatin-remodeling complex (Mecp2, Smarc) Gene Set

SMARCA2/BRM-BAF57-MECP2 complex Gene Set

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

mecp2 Gene Set

Methyl-CpG binding protein MeCP2 Gene Set

MECP2 Gene Set

MECP2 Gene Set

Loss of MECP2 binding ability to 5hmC-DNA Gene Set

Loss of MECP2 binding ability to 5mC-DNA Gene Set

Loss of MECP2 binding ability to the NCoR/SMRT complex Gene Set

Loss of function of MECP2 in Rett syndrome Gene Set

Loss of phosphorylation of MECP2 at T308 Gene Set

Transcriptional Regulation by MECP2 Gene Set

Severe congenital encephalopathy due to MECP2 mutation Gene Set

Severe congenital encephalopathy due to MECP2 mutation Gene Set

PMC6815046-13073_2019_678_MOESM3_ESM.xlsx-MECP2-Unnamed_0_MECP2 Gene Set

PMC6815046-13073_2019_678_MOESM2_ESM.xlsx-MECP2-Unnamed_0_MECP2 Gene Set

PMC6815046-13073_2019_678_MOESM4_ESM.xlsx-MECP2-Unnamed_0_MECP2 Gene Set

PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Non-metastasis_MECP2 Gene Set

PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Unnamed_1_MECP2 Gene Set

PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Metastasis_MECP2 Gene Set

PMC6292939-41598_2018_36168_MOESM8_ESM.xlsx-MECP2-Unnamed_5_MECP2 Gene Set

PMC11811132-41598_2025_89334_MOESM5_ESM.xlsx-MECP2-fromNode_MECP2 Gene Set

PMC11811132-41598_2025_89334_MOESM5_ESM.xlsx-MECP2-toNode_MECP2 Gene Set

MECP2 Gene Set

channels Gene Set

clustering of voltage-gated sodium channels Gene Set

clustering of voltage-gated potassium channels Gene Set

Shal-type voltage-gated potassium channels Gene Set

channels Gene Set

Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits Gene Set

Classical Kir channels Gene Set

Ca2+ activated K+ channels Gene Set

HCN channels Gene Set

Potassium Channels Gene Set

Activation of G protein gated Potassium channels Gene Set

Inwardly rectifying K+ channels Gene Set

Tandem pore domain potassium channels Gene Set

Tandem of pore domain in a weak inwardly rectifying K+ channels (TWIK) Gene Set

Depolarization of the Presynaptic Terminal Triggers the Opening of Calcium Channels Gene Set

TRP channels Gene Set

Stimuli-sensing channels Gene Set

Voltage gated Potassium channels Gene Set

ATP sensitive Potassium channels Gene Set

Potassium transport channels Gene Set

G protein gated Potassium channels Gene Set

clustering of voltage-gated sodium channels Gene Set

clustering of voltage-gated potassium channels Gene Set

ATP sensitive Potassium channels Gene Set

Activation of G protein gated Potassium channels Gene Set

Ca2+ activated K+ channels Gene Set

Classical Kir channels Gene Set

G protein gated Potassium channels Gene Set

HCN channels Gene Set

Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits Gene Set

Inwardly rectifying K+ channels Gene Set

Phase 1 - inactivation of fast Na+ channels Gene Set

Potassium Channels Gene Set