| Name |
|---|
<strong>G2strong> <strong>andstrong> S phase-expressed protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the <strong>G2strong> <strong>andstrong> S phase-expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phase 2 - plateau phase Gene Setproteins participating in the Phase 2 - plateau phase pathway from the Reactome Pathways 2024 dataset. |
Presynaptic phase of homologous DNA pairing <strong>andstrong> str<strong>andstrong> exchange Gene Setproteins participating in the Presynaptic phase of homologous DNA pairing <strong>andstrong> str<strong>andstrong> exchange pathway from the Reactome Pathways dataset. |
Metapathway biotransformation Phase I <strong>andstrong> II Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Metapathway biotransformation Phase I <strong>andstrong> II pathway from the WikiPathways Pathways 2024 dataset. |
Mitotic G1 phase <strong>andstrong> G1/S transition Gene Setproteins participating in the Mitotic G1 phase <strong>andstrong> G1/S transition pathway from the Reactome Pathways 2024 dataset. |
Presynaptic phase of homologous DNA pairing <strong>andstrong> str<strong>andstrong> exchange Gene Setproteins participating in the Presynaptic phase of homologous DNA pairing <strong>andstrong> str<strong>andstrong> exchange pathway from the Reactome Pathways 2024 dataset. |
S-phase kinase-associated protein 1-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the S-phase kinase-associated protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
M-phase-specific PLK1-interacting protein-like, vertebrate Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase-specific PLK1-interacting protein-like, vertebrate protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
S-phase kinase-associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the S-phase kinase-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
M-phase-specific PLK1-interacting protein-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase-specific PLK1-interacting protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal acute phase protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal acute phase protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal acute phase protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal acute phase protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Transport of glucose <strong>andstrong> other sugars, bile salts <strong>andstrong> organic acids, metal ions <strong>andstrong> amine compounds Gene Setproteins participating in the Transport of glucose <strong>andstrong> other sugars, bile salts <strong>andstrong> organic acids, metal ions <strong>andstrong> amine compounds pathway from the Reactome Pathways dataset. |
Myeloid <strong>andstrong> lymphoid neoplasms with eosinophilia <strong>andstrong> abnormalities of PDGFRA, PDGFRB, <strong>andstrong> FGFR1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid <strong>andstrong> lymphoid neoplasms with eosinophilia <strong>andstrong> abnormalities of PDGFRA, PDGFRB, <strong>andstrong> FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myeloid <strong>andstrong> lymphoid neoplasms with eosinophilia <strong>andstrong> abnormalities of PDGFRA, PDGFRB, <strong>andstrong> FGFR1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid <strong>andstrong> lymphoid neoplasms with eosinophilia <strong>andstrong> abnormalities of PDGFRA, PDGFRB, <strong>andstrong> FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
50S ribosomal protein L18Ae/60S ribosomal protein L20 <strong>andstrong> L18a Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 50S ribosomal protein L18Ae/60S ribosomal protein L20 <strong>andstrong> L18a protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cleft lip <strong>andstrong> palate transmembrane protein 1-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cleft lip <strong>andstrong> palate transmembrane protein 1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
V-set <strong>andstrong> transmembrane domain-containing protein 2-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the V-set <strong>andstrong> transmembrane domain-containing protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Advanced sleep phase syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Advanced sleep phase syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LINC complex, S-phase Gene Setproteins in the LINC complex, S-phase protein complex from the CORUM Protein Complexes dataset. |
S-phase-specific E2F-p107 complex Gene Setproteins in the S-phase-specific E2F-p107 complex protein complex from the CORUM Protein Complexes dataset. |
RC complex during S-phase of cell cycle Gene Setproteins in the RC complex during S-phase of cell cycle protein complex from the CORUM Protein Complexes dataset. |
RC complex during <strong>G2strong>/M-phase of cell cycle Gene Setproteins in the RC complex during <strong>G2strong>/M-phase of cell cycle protein complex from the CORUM Protein Complexes dataset. |
Acute-Phase Reaction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acute-Phase Reaction from the curated CTD Gene-Disease Associations dataset. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset. |
Leukemia, Myeloid, Chronic-Phase Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Leukemia, Myeloid, Chronic-Phase in GWAS <strong>andstrong> other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
advanced sleep phase syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease advanced sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
delayed sleep phase syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin response, first phase; insulitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin response, first phase; insulitis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; blast phase; leukemia, myeloid, acute Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; blast phase; leukemia, myeloid, acute in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delayed sleep phase syndrome. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome. in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction; tuberculosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; tuberculosis; tuberculosis, pulmonary in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, chronic-phase Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, chronic-phase in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase serum amyloid a Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase serum amyloid a in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; blast phase; myeloproliferative disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; blast phase; myeloproliferative disorders in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction; community-acquired infections; pneumonia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; community-acquired infections; pneumonia in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
phase Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term phase in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
positive regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell cycle <strong>g2strong>/m phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell cycle <strong>g2strong>/m phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair cycle phase Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair cycle phase biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cell cycle g1/s phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cell cycle g1/s phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell cycle g1/s phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell cycle g1/s phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell cycle <strong>g2strong>/m phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell cycle <strong>g2strong>/m phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
biological phase Gene SetFrom GO Biological Process Annotations 2015 genes participating in the biological phase biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
menstrual cycle phase Gene SetFrom GO Biological Process Annotations 2015 genes participating in the menstrual cycle phase biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cell cycle <strong>g2strong>/m phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cell cycle <strong>g2strong>/m phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cell cycle g1/s phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cell cycle g1/s phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cell cycle <strong>g2strong>/m phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cell cycle <strong>g2strong>/m phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell cycle g1/s phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell cycle g1/s phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
acute-phase response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the acute-phase response biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular component disassembly involved in execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular component disassembly involved in execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset. |
cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Molecular Function Annotations 2015 genes performing the cysteine-type endopeptidase activity involved in execution phase of apoptosis molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
prolonged <strong>g2strong> phase of cell cycle Gene SetFrom HPO Gene-Disease Associations genes associated with the prolonged <strong>g2strong> phase of cell cycle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Acute-Phase Reaction Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Acute-Phase Reaction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Leukemia, Myeloid, Chronic-Phase Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Leukemia, Myeloid, Chronic-Phase phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
M-phase inducer phosphatase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase inducer phosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
M-phase phosphoprotein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase phosphoprotein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
M-phase phosphoprotein 9 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase phosphoprotein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal hair cycle telogen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
advanced circadian phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the advanced circadian phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle anagen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle anagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
meiotic nondisjunction during m1 phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the meiotic nondisjunction during m1 phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed circadian phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed circadian phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle catagen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle catagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circadian phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circadian phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
advanced sleep phase syndrome, familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{delayed sleep phase syndrome, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {delayed sleep phase syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
advanced sleep-phase syndrome, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
s-phase Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term s-phase in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
<strong>g2strong>-phase Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term <strong>g2strong>-phase in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
g1-phase Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term g1-phase in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Late Phase of HIV Life Cycle Gene Setproteins participating in the Late Phase of HIV Life Cycle pathway from the Reactome Pathways dataset. |
G1 Phase Gene Setproteins participating in the G1 Phase pathway from the Reactome Pathways dataset. |
Cyclin A:Cdk2-associated events at S phase entry Gene Setproteins participating in the Cyclin A:Cdk2-associated events at S phase entry pathway from the Reactome Pathways dataset. |
Apoptotic execution phase Gene Setproteins participating in the Apoptotic execution phase pathway from the Reactome Pathways dataset. |
<strong>G2strong> Phase Gene Setproteins participating in the <strong>G2strong> Phase pathway from the Reactome Pathways dataset. |
Phase 1 - Functionalization of compounds Gene Setproteins participating in the Phase 1 - Functionalization of compounds pathway from the Reactome Pathways dataset. |
S Phase Gene Setproteins participating in the S Phase pathway from the Reactome Pathways dataset. |
M Phase Gene Setproteins participating in the M Phase pathway from the Reactome Pathways dataset. |
Early Phase of HIV Life Cycle Gene Setproteins participating in the Early Phase of HIV Life Cycle pathway from the Reactome Pathways dataset. |
Attenuation phase Gene Setproteins participating in the Attenuation phase pathway from the Reactome Pathways dataset. |
Phase II conjugation Gene Setproteins participating in the Phase II conjugation pathway from the Reactome Pathways dataset. |
growth phase culture Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue growth phase culture in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
stationary phase culture Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue stationary phase culture in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
logarithmic phase culture Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue logarithmic phase culture in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
lag phase culture Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue lag phase culture in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Phase I biontransformations, non P450(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Phase I biontransformations, non P450(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Phase I biotransformations, non P450(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Phase I biotransformations, non P450(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Blast Phase Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Blast Phase in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Sleep Phase Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep Phase Syndrome in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Delayed Sleep Phase Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase Syndrome in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Delayed Sleep Phase Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute-Phase Reaction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute-Phase Reaction in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Advanced Sleep Phase Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Advanced Sleep Phase in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Sleep Phase Disorder, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Sleep Phase Disorder, Susceptibility To in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prolonged <strong>G2strong> Phase Of Cell Cycle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged <strong>G2strong> Phase Of Cell Cycle in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
negative regulation of cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2023 dataset. |
acute-phase response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the acute-phase response biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitotic G1 phase Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitotic G1 phase biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cysteine-type endopeptidase activity involved in execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset. |
cysteine-type endopeptidase activity involved in execution phase of apoptosis Gene SetFrom GO Molecular Function Annotations 2023 genes performing the cysteine-type endopeptidase activity involved in execution phase of apoptosis molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal hair cycle catagen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle catagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed circadian behavior phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed circadian behavior phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circadian behavior phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circadian behavior phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cycle anagen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle anagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
advanced circadian behavior phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the advanced circadian behavior phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cycle telogen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
early exit from anagen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the early exit from anagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed exit from anagen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed exit from anagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
meiotic nondisjunction during M1 phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the meiotic nondisjunction during M1 phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Oogenesis phase fetal germ cell_Fetal gonad_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Oogenesis phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mitotic arrest phase fetal germ cell_Fetal gonad_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Mitotic arrest phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Migration phase fetal germ cell_Fetal gonad_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Migration phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Gonadal mitotic phase fetal germ cell_Fetal gonad_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Gonadal mitotic phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Phase I biotransformations non P450 Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Phase I biotransformations non P450 pathway from the WikiPathways Pathways 2024 dataset. |
Apoptotic execution phase Gene Setproteins participating in the Apoptotic execution phase pathway from the Reactome Pathways 2024 dataset. |
Attenuation phase Gene Setproteins participating in the Attenuation phase pathway from the Reactome Pathways 2024 dataset. |
Cyclin A:Cdk2-associated events at S phase entry Gene Setproteins participating in the Cyclin A:Cdk2-associated events at S phase entry pathway from the Reactome Pathways 2024 dataset. |
Early Phase of HIV Life Cycle Gene Setproteins participating in the Early Phase of HIV Life Cycle pathway from the Reactome Pathways 2024 dataset. |
G1 Phase Gene Setproteins participating in the G1 Phase pathway from the Reactome Pathways 2024 dataset. |
<strong>G2strong> Phase Gene Setproteins participating in the <strong>G2strong> Phase pathway from the Reactome Pathways 2024 dataset. |
Late Phase of HIV Life Cycle Gene Setproteins participating in the Late Phase of HIV Life Cycle pathway from the Reactome Pathways 2024 dataset. |
M Phase Gene Setproteins participating in the M Phase pathway from the Reactome Pathways 2024 dataset. |
Phase 0 - rapid depolarisation Gene Setproteins participating in the Phase 0 - rapid depolarisation pathway from the Reactome Pathways 2024 dataset. |
Phase 1 - inactivation of fast Na+ channels Gene Setproteins participating in the Phase 1 - inactivation of fast Na+ channels pathway from the Reactome Pathways 2024 dataset. |
Phase 3 - rapid repolarisation Gene Setproteins participating in the Phase 3 - rapid repolarisation pathway from the Reactome Pathways 2024 dataset. |
Phase 4 - resting membrane potential Gene Setproteins participating in the Phase 4 - resting membrane potential pathway from the Reactome Pathways 2024 dataset. |
Phase I - Functionalization of compounds Gene Setproteins participating in the Phase I - Functionalization of compounds pathway from the Reactome Pathways 2024 dataset. |
Phase II - Conjugation of compounds Gene Setproteins participating in the Phase II - Conjugation of compounds pathway from the Reactome Pathways 2024 dataset. |
S Phase Gene Setproteins participating in the S Phase pathway from the Reactome Pathways 2024 dataset. |
negative regulation of cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2025 dataset. |
acute-phase response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the acute-phase response biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cell cycle <strong>G2strong>/M phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cell cycle <strong>G2strong>/M phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cell cycle G1/S phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of execution phase of apoptosis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of execution phase of apoptosis biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of meiotic cell cycle phase transition Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset. |
Delayed sleep phase syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Delayed sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Advanced sleep phase syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Advanced sleep phase syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Advanced sleep phase syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
M/G1 phase-specific MADS box-forkhead transcription factor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the M/G1 phase-specific MADS box-forkhead transcription factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Advanced sleep phase syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Advanced sleep phase syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proinsulin levels (late-phase conversion) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proinsulin levels (late-phase conversion) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Proinsulin levels (early-phase conversion) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proinsulin levels (early-phase conversion) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
basic mechanism of action of ppara pparb(d) <strong>andstrong> pparg <strong>andstrong> effects on gene expression Gene SetFrom Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) <strong>andstrong> pparg <strong>andstrong> effects on gene expression pathway from the Biocarta Pathways dataset. |
BRCA1 <strong>andstrong> BRCA2 Hereditary Breast <strong>andstrong> Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 <strong>andstrong> BRCA2 Hereditary Breast <strong>andstrong> Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Centromeric instability of chromosomes 1,9 <strong>andstrong> 16 <strong>andstrong> immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 <strong>andstrong> 16 <strong>andstrong> immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coloboma, uveal, with cleft lip <strong>andstrong> palate <strong>andstrong> mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip <strong>andstrong> palate <strong>andstrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination with brainstem <strong>andstrong> spinal cord involvement <strong>andstrong> leg spasticity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem <strong>andstrong> spinal cord involvement <strong>andstrong> leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukoencephalopathy with Brainstem <strong>andstrong> Spinal Cord Involvement <strong>andstrong> Lactate Elevation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem <strong>andstrong> Spinal Cord Involvement <strong>andstrong> Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth <strong>andstrong> mental retardation, m<strong>andstrong>ibulofacial dysostosis, microcephaly, <strong>andstrong> cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth <strong>andstrong> mental retardation, m<strong>andstrong>ibulofacial dysostosis, microcephaly, <strong>andstrong> cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures <strong>andstrong> cerebral <strong>andstrong> cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures <strong>andstrong> cerebral <strong>andstrong> cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation <strong>andstrong> microcephaly with pontine <strong>andstrong> cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation <strong>andstrong> microcephaly with pontine <strong>andstrong> cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Leukoencephalopathy with Brainstem <strong>andstrong> Spinal Cord Involvement <strong>andstrong> Lactate Elevation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem <strong>andstrong> Spinal Cord Involvement <strong>andstrong> Lactate Elevation from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, <strong>andstrong> Neonatal Diseases <strong>andstrong> Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, <strong>andstrong> Neonatal Diseases <strong>andstrong> Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation <strong>Andstrong> Microcephaly With Pontine <strong>Andstrong> Cerebellar Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation <strong>Andstrong> Microcephaly With Pontine <strong>Andstrong> Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory <strong>Andstrong> Autonomic, Type I, With Cough <strong>Andstrong> Gastroesophageal Reflux Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory <strong>Andstrong> Autonomic, Type I, With Cough <strong>Andstrong> Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, <strong>andstrong> Anogenital <strong>andstrong> Renal Malformations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, <strong>andstrong> Anogenital <strong>andstrong> Renal Malformations from the curated CTD Gene-Disease Associations dataset. |
postheparin plasma lipase activities body fat <strong>andstrong> plasma lipid <strong>andstrong> lipoprotein concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat <strong>andstrong> plasma lipid <strong>andstrong> lipoprotein concentrations in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety <strong>andstrong> hostility <strong>andstrong> depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety <strong>andstrong> hostility <strong>andstrong> depression in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor <strong>andstrong> sensory neuropathies; hereditary sensory <strong>andstrong> motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor <strong>andstrong> sensory neuropathies; hereditary sensory <strong>andstrong> motor neuropathy in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
frontotemporal dementia <strong>andstrong> pick-like 3r <strong>andstrong> 4r tauopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia <strong>andstrong> pick-like 3r <strong>andstrong> 4r tauopathy in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipose tissue lipoprotein lipase activity <strong>andstrong> lipoprotein lipid <strong>andstrong> glucose concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity <strong>andstrong> lipoprotein lipid <strong>andstrong> glucose concentrations in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
squamous cell carcinomas of the head <strong>andstrong> neck (scchn) <strong>andstrong> breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head <strong>andstrong> neck (scchn) <strong>andstrong> breast cancer in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vitamins <strong>andstrong> metabolites in pregnant women <strong>andstrong> neonates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vitamins <strong>andstrong> metabolites in pregnant women <strong>andstrong> neonates in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
racemase <strong>andstrong> epimerase activity, acting on amino acids <strong>andstrong> derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase <strong>andstrong> epimerase activity, acting on amino acids <strong>andstrong> derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
racemase <strong>andstrong> epimerase activity, acting on carbohydrates <strong>andstrong> derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase <strong>andstrong> epimerase activity, acting on carbohydrates <strong>andstrong> derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leukoencephalopathy with brain stem <strong>andstrong> spinal cord involvement <strong>andstrong> lactate elevation Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem <strong>andstrong> spinal cord involvement <strong>andstrong> lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset. |
microspherophakia <strong>andstrong>/or megalocornea, with ectopia lentis <strong>andstrong> with or without secondary glaucoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microspherophakia <strong>andstrong>/or megalocornea, with ectopia lentis <strong>andstrong> with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypomyelination with brainstem <strong>andstrong> spinal cord involvement <strong>andstrong> leg spasticity Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem <strong>andstrong> spinal cord involvement <strong>andstrong> leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, mental retardation, <strong>andstrong> distinctive facies, with cardiac <strong>andstrong> genitourinary malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, <strong>andstrong> distinctive facies, with cardiac <strong>andstrong> genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
mental retardation <strong>andstrong> microcephaly with pontine <strong>andstrong> cerebellar hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation <strong>andstrong> microcephaly with pontine <strong>andstrong> cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, <strong>andstrong> cerebral <strong>andstrong> cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, <strong>andstrong> cerebral <strong>andstrong> cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
craniosynostosis with radiohumeral fusions <strong>andstrong> other skeletal <strong>andstrong> craniofacial anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions <strong>andstrong> other skeletal <strong>andstrong> craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
Activation of the mRNA upon binding of the cap-binding complex <strong>andstrong> eIFs, <strong>andstrong> subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex <strong>andstrong> eIFs, <strong>andstrong> subsequent binding to 43S pathway from the Reactome Pathways dataset. |
Cooperation of Prefoldin <strong>andstrong> TriC/CCT in actin <strong>andstrong> tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin <strong>andstrong> TriC/CCT in actin <strong>andstrong> tubulin folding pathway from the Reactome Pathways dataset. |
PI <strong>andstrong> PC transport between ER <strong>andstrong> Golgi membranes Gene Setproteins participating in the PI <strong>andstrong> PC transport between ER <strong>andstrong> Golgi membranes pathway from the Reactome Pathways dataset. |
Orexin <strong>andstrong> neuropeptides FF <strong>andstrong> QRFP bind to their respective receptors Gene Setproteins participating in the Orexin <strong>andstrong> neuropeptides FF <strong>andstrong> QRFP bind to their respective receptors pathway from the Reactome Pathways dataset. |
FGFR1c <strong>andstrong> Klotho lig<strong>andstrong> binding <strong>andstrong> activation Gene Setproteins participating in the FGFR1c <strong>andstrong> Klotho lig<strong>andstrong> binding <strong>andstrong> activation pathway from the Reactome Pathways dataset. |
Transport of nucleosides <strong>andstrong> free purine <strong>andstrong> pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides <strong>andstrong> free purine <strong>andstrong> pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset. |
Synthesis <strong>andstrong> processing of ENV <strong>andstrong> VPU Gene Setproteins participating in the Synthesis <strong>andstrong> processing of ENV <strong>andstrong> VPU pathway from the Reactome Pathways dataset. |
Synthesis <strong>andstrong> interconversion of nucleotide di- <strong>andstrong> triphosphates Gene Setproteins participating in the Synthesis <strong>andstrong> interconversion of nucleotide di- <strong>andstrong> triphosphates pathway from the Reactome Pathways dataset. |
SREBF <strong>andstrong> miR33 in cholesterol <strong>andstrong> lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF <strong>andstrong> miR33 in cholesterol <strong>andstrong> lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF <strong>andstrong> miR33 in cholesterol <strong>andstrong> lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF <strong>andstrong> miR33 in cholesterol <strong>andstrong> lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
SRF <strong>andstrong> miRs in Smooth Muscle Differentiation <strong>andstrong> Proliferation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SRF <strong>andstrong> miRs in Smooth Muscle Differentiation <strong>andstrong> Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
High-Grade B-Cell Lymphoma, With Myc <strong>Andstrong> Bcl2 <strong>Andstrong>/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc <strong>Andstrong> Bcl2 <strong>Andstrong>/Or Bcl6 Rearrangements in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, <strong>Andstrong> Anogenital <strong>Andstrong> Renal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, <strong>Andstrong> Anogenital <strong>Andstrong> Renal Malformations in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypomyelination With Brain Stem <strong>Andstrong> Spinal Cord Involvement <strong>Andstrong> Leg Spasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem <strong>Andstrong> Spinal Cord Involvement <strong>Andstrong> Leg Spasticity in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth <strong>Andstrong> Mental Retardation, M<strong>andstrong>ibulofacial Dysostosis, Microcephaly, <strong>Andstrong> Cleft Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth <strong>Andstrong> Mental Retardation, M<strong>andstrong>ibulofacial Dysostosis, Microcephaly, <strong>Andstrong> Cleft Palate in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Contractures Of The Limbs <strong>Andstrong> Face, Hypotonia, <strong>Andstrong> Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs <strong>Andstrong> Face, Hypotonia, <strong>Andstrong> Developmental Delay in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microspherophakia <strong>Andstrong>/Or Megalocornea, With Ectopia Lentis <strong>Andstrong> With Or Without Secondary Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia <strong>Andstrong>/Or Megalocornea, With Ectopia Lentis <strong>Andstrong> With Or Without Secondary Glaucoma in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Intraepithelial Neoplasia I <strong>Andstrong> Ii (Ain I <strong>Andstrong> Ii) (Histologically Confirmed) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I <strong>Andstrong> Ii (Ain I <strong>Andstrong> Ii) (Histologically Confirmed) in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pierre Robin Sequence With Pectus Excavatum <strong>Andstrong> Rib <strong>Andstrong> Scapular Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum <strong>Andstrong> Rib <strong>Andstrong> Scapular Anomalies in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
racemase <strong>andstrong> epimerase activity, acting on carbohydrates <strong>andstrong> derivatives Gene SetFrom GO Molecular Function Annotations 2023 genes performing the racemase <strong>andstrong> epimerase activity, acting on carbohydrates <strong>andstrong> derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SRF <strong>andstrong> miRs in smooth muscle differentiation <strong>andstrong> proliferation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SRF <strong>andstrong> miRs in smooth muscle differentiation <strong>andstrong> proliferation pathway from the WikiPathways Pathways 2024 dataset. |
SREBF <strong>andstrong> miR33 in cholesterol <strong>andstrong> lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF <strong>andstrong> miR33 in cholesterol <strong>andstrong> lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
RIOK1 <strong>andstrong> RIOK2 in EGFR <strong>andstrong> PI3K mediated tumorigenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the RIOK1 <strong>andstrong> RIOK2 in EGFR <strong>andstrong> PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset. |
ApoE <strong>andstrong> miR 146 in inflammation <strong>andstrong> atherosclerosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ApoE <strong>andstrong> miR 146 in inflammation <strong>andstrong> atherosclerosis pathway from the WikiPathways Pathways 2024 dataset. |
Biosynthesis <strong>andstrong> regeneration of tetrahydrobiopterin <strong>andstrong> catabolism of phenylalanine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Biosynthesis <strong>andstrong> regeneration of tetrahydrobiopterin <strong>andstrong> catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset. |
Somatroph axis GH <strong>andstrong> its relationship to dietary restriction <strong>andstrong> aging Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH <strong>andstrong> its relationship to dietary restriction <strong>andstrong> aging pathway from the WikiPathways Pathways 2024 dataset. |
Mechanoregulation <strong>andstrong> pathology of YAP TAZ via Hippo <strong>andstrong> non Hippo mechanisms Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mechanoregulation <strong>andstrong> pathology of YAP TAZ via Hippo <strong>andstrong> non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine <strong>andstrong> pancreas <strong>andstrong> role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine <strong>andstrong> pancreas <strong>andstrong> role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Activation of the mRNA upon binding of the cap-binding complex <strong>andstrong> eIFs, <strong>andstrong> subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex <strong>andstrong> eIFs, <strong>andstrong> subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of protectin <strong>andstrong> resolvin conjugates in tissue regeneration (PCTR <strong>andstrong> RCTR) Gene Setproteins participating in the Biosynthesis of protectin <strong>andstrong> resolvin conjugates in tissue regeneration (PCTR <strong>andstrong> RCTR) pathway from the Reactome Pathways 2024 dataset. |
Cooperation of Prefoldin <strong>andstrong> TriC/CCT in actin <strong>andstrong> tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin <strong>andstrong> TriC/CCT in actin <strong>andstrong> tubulin folding pathway from the Reactome Pathways 2024 dataset. |
FGFR1c <strong>andstrong> Klotho lig<strong>andstrong> binding <strong>andstrong> activation Gene Setproteins participating in the FGFR1c <strong>andstrong> Klotho lig<strong>andstrong> binding <strong>andstrong> activation pathway from the Reactome Pathways 2024 dataset. |
MLL4 <strong>andstrong> MLL3 complexes regulate expression of PPARG target genes in adipogenesis <strong>andstrong> hepatic steatosis Gene Setproteins participating in the MLL4 <strong>andstrong> MLL3 complexes regulate expression of PPARG target genes in adipogenesis <strong>andstrong> hepatic steatosis pathway from the Reactome Pathways 2024 dataset. |
Orexin <strong>andstrong> neuropeptides FF <strong>andstrong> QRFP bind to their respective receptors Gene Setproteins participating in the Orexin <strong>andstrong> neuropeptides FF <strong>andstrong> QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset. |
PI <strong>andstrong> PC transport between ER <strong>andstrong> Golgi membranes Gene Setproteins participating in the PI <strong>andstrong> PC transport between ER <strong>andstrong> Golgi membranes pathway from the Reactome Pathways 2024 dataset. |
PTK6 Regulates RTKs <strong>andstrong> Their Effectors AKT1 <strong>andstrong> DOK1 Gene Setproteins participating in the PTK6 Regulates RTKs <strong>andstrong> Their Effectors AKT1 <strong>andstrong> DOK1 pathway from the Reactome Pathways 2024 dataset. |
Recruitment <strong>andstrong> ATM-mediated phosphorylation of repair <strong>andstrong> signaling proteins at DNA double str<strong>andstrong> breaks Gene Setproteins participating in the Recruitment <strong>andstrong> ATM-mediated phosphorylation of repair <strong>andstrong> signaling proteins at DNA double str<strong>andstrong> breaks pathway from the Reactome Pathways 2024 dataset. |
Synthesis <strong>andstrong> processing of ENV <strong>andstrong> VPU Gene Setproteins participating in the Synthesis <strong>andstrong> processing of ENV <strong>andstrong> VPU pathway from the Reactome Pathways 2024 dataset. |
Transcriptional <strong>andstrong> post-translational regulation of MITF-M expression <strong>andstrong> activity Gene Setproteins participating in the Transcriptional <strong>andstrong> post-translational regulation of MITF-M expression <strong>andstrong> activity pathway from the Reactome Pathways 2024 dataset. |
Transport of bile salts <strong>andstrong> organic acids, metal ions <strong>andstrong> amine compounds Gene Setproteins participating in the Transport of bile salts <strong>andstrong> organic acids, metal ions <strong>andstrong> amine compounds pathway from the Reactome Pathways 2024 dataset. |
Transport of nucleosides <strong>andstrong> free purine <strong>andstrong> pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides <strong>andstrong> free purine <strong>andstrong> pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset. |
racemase <strong>andstrong> epimerase activity, acting on carbohydrates <strong>andstrong> derivatives Gene SetFrom GO Molecular Function Annotations 2025 genes performing the racemase <strong>andstrong> epimerase activity, acting on carbohydrates <strong>andstrong> derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Vertebral anomalies <strong>andstrong> variable endocrine <strong>andstrong> T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies <strong>andstrong> variable endocrine <strong>andstrong> T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies <strong>andstrong> variable endocrine <strong>andstrong> T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies <strong>andstrong> variable endocrine <strong>andstrong> T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Regulation of gene expression <strong>andstrong> signal transduction in immune <strong>andstrong> stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression <strong>andstrong> signal transduction in immune <strong>andstrong> stress responses assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Gastroesophageal reflux disease, peptic ulcer disease <strong>andstrong>/or corresponding medications <strong>andstrong> treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease <strong>andstrong>/or corresponding medications <strong>andstrong> treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
estrogen responsive protein efp controls cell cycle <strong>andstrong> breast tumors growth Gene SetFrom Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle <strong>andstrong> breast tumors growth pathway from the Biocarta Pathways dataset. |
Trifunctional protein deficiency with myopathy <strong>andstrong> neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy <strong>andstrong> neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
calcium- <strong>andstrong> calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- <strong>andstrong> calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
calcium- <strong>andstrong> calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- <strong>andstrong> calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Apoptosis- <strong>andstrong> splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Setproteins in the Apoptosis- <strong>andstrong> splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- <strong>andstrong> splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Setproteins in the Apoptosis- <strong>andstrong> splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset. |
20S methylosome <strong>andstrong> RG-containing Sm protein complex Gene Setproteins in the 20S methylosome <strong>andstrong> RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset. |
Trifunctional Protein Deficiency With Myopathy <strong>Andstrong> Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy <strong>Andstrong> Neuropathy from the curated CTD Gene-Disease Associations dataset. |
circulating protein c levels <strong>andstrong> thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease circulating protein c levels <strong>andstrong> thrombotic risk in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma protein c levels <strong>andstrong> thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma protein c levels <strong>andstrong> thrombotic risk in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma triglyceride <strong>andstrong> c-reactive protein, fasting glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma triglyceride <strong>andstrong> c-reactive protein, fasting glucose in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis <strong>andstrong> resistance to activated protein c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis <strong>andstrong> resistance to activated protein c in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antigen processing <strong>andstrong> presentation of exogenous protein antigen via mhc class ib, tap-dependent Gene SetFrom GO Biological Process Annotations 2015 genes participating in the antigen processing <strong>andstrong> presentation of exogenous protein antigen via mhc class ib, tap-dependent biological process from the curated GO Biological Process Annotations 2015 dataset. |
calcium- <strong>andstrong> calmodulin-dependent protein kinase complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the calcium- <strong>andstrong> calmodulin-dependent protein kinase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, <strong>andstrong> incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, <strong>andstrong> incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
C-reactive protein <strong>andstrong> white blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the C-reactive protein <strong>andstrong> white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
decreased beta-glucocerebrosidase protein <strong>andstrong> activity Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased beta-glucocerebrosidase protein <strong>andstrong> activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Transmembrane <strong>andstrong> coiled-coil domain-containing protein 2/5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transmembrane <strong>andstrong> coiled-coil domain-containing protein 2/5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fasciculation <strong>andstrong> elongation protein zeta, FEZ Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fasciculation <strong>andstrong> elongation protein zeta, FEZ protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM <strong>andstrong> senescent cell antigen-like-containing domain protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM <strong>andstrong> senescent cell antigen-like-containing domain protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane-associated guanylate kinase, WW <strong>andstrong> PDZ domain-containing protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW <strong>andstrong> PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Septin <strong>andstrong> tuftelin interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin <strong>andstrong> tuftelin interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
V-set <strong>andstrong> immunoglobulin domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the V-set <strong>andstrong> immunoglobulin domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination <strong>andstrong> repair protein RecA-like, ATP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination <strong>andstrong> repair protein RecA-like, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Growth arrest <strong>andstrong> DNA damage-inducible protein GADD45 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth arrest <strong>andstrong> DNA damage-inducible protein GADD45 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Neuropilin <strong>andstrong> tolloid-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuropilin <strong>andstrong> tolloid-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM domain <strong>andstrong> actin-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM domain <strong>andstrong> actin-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Neuropilin <strong>andstrong> tolloid-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuropilin <strong>andstrong> tolloid-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FERM <strong>andstrong> PDZ domain-containing protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FERM <strong>andstrong> PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Centrosome <strong>andstrong> spindle pole associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Centrosome <strong>andstrong> spindle pole associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Methylmalonic aciduria <strong>andstrong> homocystinuria type D protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Methylmalonic aciduria <strong>andstrong> homocystinuria type D protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aurora kinase A <strong>andstrong> ninein interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aurora kinase A <strong>andstrong> ninein interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cattle cerebrum <strong>andstrong> skeletal muscle-specific protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cattle cerebrum <strong>andstrong> skeletal muscle-specific protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cell cycle <strong>andstrong> apoptosis regulator protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell cycle <strong>andstrong> apoptosis regulator protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin <strong>andstrong> lymphocyte (MAL) protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin <strong>andstrong> lymphocyte (MAL) protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat <strong>andstrong> fibronectin type-III domain-containing protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat <strong>andstrong> fibronectin type-III domain-containing protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine <strong>andstrong> tyrosine-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine <strong>andstrong> tyrosine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PDZ <strong>andstrong> LIM domain protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PDZ <strong>andstrong> LIM domain protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EGF-like repeat <strong>andstrong> discoidin I-like domain-containing protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EGF-like repeat <strong>andstrong> discoidin I-like domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane-associated guanylate kinase, WW <strong>andstrong> PDZ domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW <strong>andstrong> PDZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane-associated guanylate kinase, WW <strong>andstrong> PDZ domain-containing protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW <strong>andstrong> PDZ domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WD repeat-containing <strong>andstrong> planar cell polarity effector protein Fritz Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WD repeat-containing <strong>andstrong> planar cell polarity effector protein Fritz protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Janus kinase <strong>andstrong> microtubule-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Janus kinase <strong>andstrong> microtubule-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CUB <strong>andstrong> zona pellucida-like domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CUB <strong>andstrong> zona pellucida-like domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger <strong>andstrong> BTB domain-containing protein 22 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger <strong>andstrong> BTB domain-containing protein 22 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Disintegrin <strong>andstrong> metalloproteinase domain-containing protein 10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Disintegrin <strong>andstrong> metalloproteinase domain-containing protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TRIO <strong>andstrong> F-actin-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRIO <strong>andstrong> F-actin-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spindle <strong>andstrong> kinetochore-associated protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle <strong>andstrong> kinetochore-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fasciculation <strong>andstrong> elongation protein zeta 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fasciculation <strong>andstrong> elongation protein zeta 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger <strong>andstrong> BTB domain-containing protein 40 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger <strong>andstrong> BTB domain-containing protein 40 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SLP adapter <strong>andstrong> CSK-interacting membrane protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SLP adapter <strong>andstrong> CSK-interacting membrane protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calcium-binding <strong>andstrong> spermatid-specific protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium-binding <strong>andstrong> spermatid-specific protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination <strong>andstrong> repair protein, RecA-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination <strong>andstrong> repair protein, RecA-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination <strong>andstrong> repair protein Rad51, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination <strong>andstrong> repair protein Rad51, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination <strong>andstrong> repair protein RecA, monomer-monomer interface Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination <strong>andstrong> repair protein RecA, monomer-monomer interface protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM <strong>andstrong> calponin homology domains-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM <strong>andstrong> calponin homology domains-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuole morphology <strong>andstrong> inheritance protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuole morphology <strong>andstrong> inheritance protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
von Willebr<strong>andstrong> factor C <strong>andstrong> EGF domain-containing protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebr<strong>andstrong> factor C <strong>andstrong> EGF domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kelch repeat <strong>andstrong> BTB domain-containing protein 8 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kelch repeat <strong>andstrong> BTB domain-containing protein 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nucleolar <strong>andstrong> spindle-associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleolar <strong>andstrong> spindle-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Testis <strong>andstrong> ovary-specific PAZ domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Testis <strong>andstrong> ovary-specific PAZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WASP homologue-associated protein with actin, membranes <strong>andstrong> microtubules Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WASP homologue-associated protein with actin, membranes <strong>andstrong> microtubules protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Centriole, cilia <strong>andstrong> spindle-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Centriole, cilia <strong>andstrong> spindle-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cell cycle <strong>andstrong> apoptosis regulator protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell cycle <strong>andstrong> apoptosis regulator protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fasciculation <strong>andstrong> elongation protein zeta 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fasciculation <strong>andstrong> elongation protein zeta 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heterotrimeric G-protein signaling pathway-Gi alpha <strong>andstrong> Gs alpha mediated pathway Gene SetFrom PANTHER Pathways proteins participating in the Heterotrimeric G-protein signaling pathway-Gi alpha <strong>andstrong> Gs alpha mediated pathway pathway from the PANTHER Pathways dataset. |
Heterotrimeric G-protein signaling pathway-Gq alpha <strong>andstrong> Go alpha mediated pathway Gene SetFrom PANTHER Pathways proteins participating in the Heterotrimeric G-protein signaling pathway-Gq alpha <strong>andstrong> Go alpha mediated pathway pathway from the PANTHER Pathways dataset. |
protein-interaction-domains-<strong>andstrong>-motifs Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term protein-interaction-domains-<strong>andstrong>-motifs in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Activation <strong>andstrong> oligomerization of BAK protein Gene Setproteins participating in the Activation <strong>andstrong> oligomerization of BAK protein pathway from the Reactome Pathways dataset. |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) <strong>andstrong> transfer to a nascent protein Gene Setproteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) <strong>andstrong> transfer to a nascent protein pathway from the Reactome Pathways dataset. |
Trifunctional Protein Deficiency With Myopathy <strong>Andstrong> Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy <strong>Andstrong> Neuropathy in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complement Hyperactivation, Angiopathic Thrombosis, <strong>Andstrong> Protein-Losing Enteropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complement Hyperactivation, Angiopathic Thrombosis, <strong>Andstrong> Protein-Losing Enteropathy in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Caused By Mutation In The Zinc Finger- <strong>Andstrong> Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Zinc Finger- <strong>Andstrong> Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) in GWAS <strong>andstrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, <strong>andstrong> incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, <strong>andstrong> incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Bone morphogenic protein signaling <strong>andstrong> regulation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Bone morphogenic protein signaling <strong>andstrong> regulation pathway from the WikiPathways Pathways 2024 dataset. |
mRNA protein <strong>andstrong> metabolite inducation pathway by cyclosporin A Gene SetFrom WikiPathways Pathways 2024 proteins participating in the mRNA protein <strong>andstrong> metabolite inducation pathway by cyclosporin A pathway from the WikiPathways Pathways 2024 dataset. |
Transcription co factors SKI <strong>andstrong> SKIL protein partners Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Transcription co factors SKI <strong>andstrong> SKIL protein partners pathway from the WikiPathways Pathways 2024 dataset. |
Activation <strong>andstrong> oligomerization of BAK protein Gene Setproteins participating in the Activation <strong>andstrong> oligomerization of BAK protein pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) <strong>andstrong> transfer to a nascent protein Gene Setproteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) <strong>andstrong> transfer to a nascent protein pathway from the Reactome Pathways 2024 dataset. |
Cooperation of PDCL (PhLP1) <strong>andstrong> TRiC/CCT in G-protein beta folding Gene Setproteins participating in the Cooperation of PDCL (PhLP1) <strong>andstrong> TRiC/CCT in G-protein beta folding pathway from the Reactome Pathways 2024 dataset. |
Gene <strong>andstrong> protein expression by JAK-STAT signaling after Interleukin-12 stimulation Gene Setproteins participating in the Gene <strong>andstrong> protein expression by JAK-STAT signaling after Interleukin-12 stimulation pathway from the Reactome Pathways 2024 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, <strong>andstrong> incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, <strong>andstrong> incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
calcium- <strong>andstrong> calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the calcium- <strong>andstrong> calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
calcium- <strong>andstrong> calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the calcium- <strong>andstrong> calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Myopathy due to calsequestrin <strong>andstrong> SERCA1 protein overload Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy due to calsequestrin <strong>andstrong> SERCA1 protein overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intracellular protein transport <strong>andstrong> DNA repair Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Intracellular protein transport <strong>andstrong> DNA repair assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein quality control <strong>andstrong> ubiquitin-proteasome system regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control <strong>andstrong> ubiquitin-proteasome system regulation assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein folding <strong>andstrong> complex assembly regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein folding <strong>andstrong> complex assembly regulation assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein quality control <strong>andstrong> DNA repair Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control <strong>andstrong> DNA repair assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Mitochondrial biogenesis <strong>andstrong> protein quality control Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial biogenesis <strong>andstrong> protein quality control assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein folding <strong>andstrong> stress response regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein folding <strong>andstrong> stress response regulation assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of gene expression <strong>andstrong> protein quality control Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression <strong>andstrong> protein quality control assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of gene expression <strong>andstrong> protein modification Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression <strong>andstrong> protein modification assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein processing <strong>andstrong> intracellular signaling Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein processing <strong>andstrong> intracellular signaling assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein quality control <strong>andstrong> DNA repair complex Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control <strong>andstrong> DNA repair complex assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of mRNA processing <strong>andstrong> protein ubiquitination Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of mRNA processing <strong>andstrong> protein ubiquitination assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
G-protein signaling <strong>andstrong> cell cycle regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising G-protein signaling <strong>andstrong> cell cycle regulation assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Mitochondrial metabolism <strong>andstrong> protein regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial metabolism <strong>andstrong> protein regulation assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of Gene Expression <strong>andstrong> Protein Ubiquitination Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of Gene Expression <strong>andstrong> Protein Ubiquitination assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein Stability <strong>andstrong> Turnover Regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein Stability <strong>andstrong> Turnover Regulation assembly using integrated AP-MS <strong>andstrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
C-reactive protein <strong>andstrong> white blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the C-reactive protein <strong>andstrong> white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis <strong>andstrong> C-reactive protein levels (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis <strong>andstrong> C-reactive protein levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Viral protein interaction with cytokine <strong>andstrong> cytokine receptor Gene SetFrom KEGG Pathways 2026 proteins participating in the Viral protein interaction with cytokine <strong>andstrong> cytokine receptor pathway from the KEGG Pathways 2026 dataset. |
Protein digestion <strong>andstrong> absorption Gene SetFrom KEGG Pathways 2026 proteins participating in the Protein digestion <strong>andstrong> absorption pathway from the KEGG Pathways 2026 dataset. |
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein maturation by protein folding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein maturation by protein folding biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of signaling protein activity involved in unfolded protein response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of signaling protein activity involved in unfolded protein response biological process from the curated GO Biological Process Annotations 2015 dataset. |
desensitization of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein kinase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein kinase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
desensitization of g-protein coupled receptor protein signaling pathway by arrestin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway by arrestin biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein binding involved in protein folding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the protein binding involved in protein folding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Vacuolar protein sorting-associated protein 54 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 54 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumour protein p53-inducible nuclear protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour protein p53-inducible nuclear protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ADP-ribosylation factor-like protein 6-interacting protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the ADP-ribosylation factor-like protein 6-interacting protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dyslexia-associated protein KIAA0319-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dyslexia-associated protein KIAA0319-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein/late cornified envelope protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase A anchor protein, RI-RII subunit-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, RI-RII subunit-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Guanine nucleotide binding protein (G-protein), alpha subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Guanine nucleotide binding protein (G-protein), alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein transport protein SecG/Sec61-beta/Sbh Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein transport protein SecG/Sec61-beta/Sbh protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3669, zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3669, zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Actin-related protein 2/3 complex subunit 5-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 2/3 complex subunit 5-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EH domain-binding protein 1-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EH domain-binding protein 1-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SWR1-complex protein 5/Craniofacial development protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 5/Craniofacial development protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 36, GLUE domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 36, GLUE domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
UV radiation resistance protein/autophagy-related protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the UV radiation resistance protein/autophagy-related protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Four-jointed box protein 1/four-jointed protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Four-jointed box protein 1/four-jointed protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G protein-coupled receptor kinase-interacting protein 1 C term Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G protein-coupled receptor kinase-interacting protein 1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coiled-coil domain-containing protein 18/Cytoskeletal protein Sojo Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coiled-coil domain-containing protein 18/Cytoskeletal protein Sojo protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13A N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13A N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 26 related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 26 related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 41 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 41 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bone morphogenetic protein 1/tolloid-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bone morphogenetic protein 1/tolloid-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Synaptonemal complex protein 2/protein 2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex protein 2/protein 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sterol regulatory element-binding protein cleavage-activating protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sterol regulatory element-binding protein cleavage-activating protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Polyadenylate-binding protein/Hyperplastic disc protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Polyadenylate-binding protein/Hyperplastic disc protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised protein family WW domain-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised protein family WW domain-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor-transporting protein/CXXC-type zinc finger protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor-transporting protein/CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor tyrosine-protein phosphatase C-associated protein CD45-AP Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor tyrosine-protein phosphatase C-associated protein CD45-AP protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 8, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 8, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Growth arrest/ DNA-damage-inducible protein-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth arrest/ DNA-damage-inducible protein-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 16 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane protein-associated protein B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane protein-associated protein A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein LIN-9/Protein ALWAYS EARLY Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Steroid receptor RNA activator-protein/coat protein complex II, Sec31 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Steroid receptor RNA activator-protein/coat protein complex II, Sec31 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 35, Vps35 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 35, Vps35 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3697, ubiquitin-associated protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3697, ubiquitin-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Retinoic acid-induced protein 2/sine oculis-binding protein homologue Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinoic acid-induced protein 2/sine oculis-binding protein homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tetracycline resistance protein, TetA/multidrug resistance protein MdtG Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tetracycline resistance protein, TetA/multidrug resistance protein MdtG protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TYRO protein tyrosine kinase-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TYRO protein tyrosine kinase-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Usher syndrome type-1C protein-binding protein 1, PDZ domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Usher syndrome type-1C protein-binding protein 1, PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L1/ribosomal biogenesis protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L1/ribosomal biogenesis protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Actin-related protein 8/Plant actin-related protein 9 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 8/Plant actin-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Regulator of G-protein signalling 9-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of G-protein signalling 9-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane-protein-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane-protein-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 11, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 11, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 33 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 33 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase A anchor protein, nuclear localisation signal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, nuclear localisation signal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spermatogenesis-associated protein 2-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
A-kinase anchor protein 6/Centrosomal protein of 68kDa Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the A-kinase anchor protein 6/Centrosomal protein of 68kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PodNet: protein-protein interactions in the podocyte(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the PodNet: protein-protein interactions in the podocyte(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
XPodNet - protein-protein interactions in the podocyte exp<strong>andstrong>ed by STRING(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the XPodNet - protein-protein interactions in the podocyte exp<strong>andstrong>ed by STRING(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein kinase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein kinase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein initiator methionine removal involved in protein maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein initiator methionine removal involved in protein maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
Protein-protein interactions at synapses Gene Setproteins participating in the Protein-protein interactions at synapses pathway from the Reactome Pathways 2024 dataset. |
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
Basic cell groups <strong>andstrong> regions Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups <strong>andstrong> regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
head <strong>andstrong> face region of M1 Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head <strong>andstrong> 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 <strong>andstrong> immortality Gene SetFrom Biocarta Pathways proteins participating in the telomeres telomerase cellular aging <strong>andstrong> immortality pathway from the Biocarta Pathways dataset. |
mcalpain <strong>andstrong> friends in cell motility Gene SetFrom Biocarta Pathways proteins participating in the mcalpain <strong>andstrong> friends in cell motility pathway from the Biocarta Pathways dataset. |
role of ppar-gamma coactivators in obesity <strong>andstrong> thermogenesis Gene SetFrom Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity <strong>andstrong> thermogenesis pathway from the Biocarta Pathways dataset. |
il12 <strong>andstrong> stat4 dependent signaling pathway in th1 development Gene SetFrom Biocarta Pathways proteins participating in the il12 <strong>andstrong> stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset. |
hypoxia <strong>andstrong> p53 in the cardiovascular system Gene SetFrom Biocarta Pathways proteins participating in the hypoxia <strong>andstrong> p53 in the cardiovascular system pathway from the Biocarta Pathways dataset. |
lissencephaly gene (lis1) in neuronal migration <strong>andstrong> development Gene SetFrom Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration <strong>andstrong> development pathway from the Biocarta Pathways dataset. |
role of erbb2 in signal transduction <strong>andstrong> oncology Gene SetFrom Biocarta Pathways proteins participating in the role of erbb2 in signal transduction <strong>andstrong> oncology pathway from the Biocarta Pathways dataset. |
corticosteroids <strong>andstrong> cardioprotection Gene SetFrom Biocarta Pathways proteins participating in the corticosteroids <strong>andstrong> cardioprotection pathway from the Biocarta Pathways dataset. |
cyclins <strong>andstrong> cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the cyclins <strong>andstrong> cell cycle regulation pathway from the Biocarta Pathways dataset. |
mechanism of acetaminophen activity <strong>andstrong> toxicity Gene SetFrom Biocarta Pathways proteins participating in the mechanism of acetaminophen activity <strong>andstrong> toxicity pathway from the Biocarta Pathways dataset. |
nfat <strong>andstrong> hypertrophy of the heart Gene SetFrom Biocarta Pathways proteins participating in the nfat <strong>andstrong> hypertrophy of the heart pathway from the Biocarta Pathways dataset. |
acetylation <strong>andstrong> deacetylation of rela in nucleus Gene SetFrom Biocarta Pathways proteins participating in the acetylation <strong>andstrong> deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset. |
thrombin signaling <strong>andstrong> protease-activated receptors Gene SetFrom Biocarta Pathways proteins participating in the thrombin signaling <strong>andstrong> protease-activated receptors pathway from the Biocarta Pathways dataset. |
antigen processing <strong>andstrong> presentation Gene SetFrom Biocarta Pathways proteins participating in the antigen processing <strong>andstrong> presentation pathway from the Biocarta Pathways dataset. |
stathmin <strong>andstrong> breast cancer resistance to antimicrotubule agents Gene SetFrom Biocarta Pathways proteins participating in the stathmin <strong>andstrong> breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset. |
role of ß-arrestins in the activation <strong>andstrong> targeting of map kinases Gene SetFrom Biocarta Pathways proteins participating in the role of ß-arrestins in the activation <strong>andstrong> targeting of map kinases pathway from the Biocarta Pathways dataset. |
cystic fibrosis transmembrane conductance regulator (cftr) <strong>andstrong> beta 2 adrenergic receptor (b2ar) pathway Gene SetFrom Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) <strong>andstrong> beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset. |
role of pi3k subunit p85 in regulation of actin organization <strong>andstrong> cell migration Gene SetFrom Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization <strong>andstrong> cell migration pathway from the Biocarta Pathways dataset. |
btg family proteins <strong>andstrong> cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the btg family proteins <strong>andstrong> cell cycle regulation pathway from the Biocarta Pathways dataset. |
control of skeletal myogenesis by hdac <strong>andstrong> calcium/calmodulin-dependent kinase (camk) Gene SetFrom Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac <strong>andstrong> calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset. |
endocytotic role of ndk phosphins <strong>andstrong> dynamin Gene SetFrom Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins <strong>andstrong> dynamin pathway from the Biocarta Pathways dataset. |
regulation of eif-4e <strong>andstrong> p70s6 kinase Gene SetFrom Biocarta Pathways proteins participating in the regulation of eif-4e <strong>andstrong> p70s6 kinase pathway from the Biocarta Pathways dataset. |
vegf hypoxia <strong>andstrong> angiogenesis Gene SetFrom Biocarta Pathways proteins participating in the vegf hypoxia <strong>andstrong> angiogenesis pathway from the Biocarta Pathways dataset. |
yaci <strong>andstrong> bcma stimulation of b cell immune responses Gene SetFrom Biocarta Pathways proteins participating in the yaci <strong>andstrong> bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset. |
lck <strong>andstrong> fyn tyrosine kinases in initiation of tcr activation Gene SetFrom Biocarta Pathways proteins participating in the lck <strong>andstrong> fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset. |
hiv-1 nef: negative effector of fas <strong>andstrong> tnf Gene SetFrom Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas <strong>andstrong> tnf pathway from the Biocarta Pathways dataset. |
nuclear receptors coordinate the activities of chromatin remodeling complexes <strong>andstrong> coactivators to facilitate initiation of transcription in carcinoma cells Gene SetFrom Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes <strong>andstrong> coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset. |
ucalpain <strong>andstrong> friends in cell spread Gene SetFrom Biocarta Pathways proteins participating in the ucalpain <strong>andstrong> friends in cell spread pathway from the Biocarta Pathways dataset. |
ionomycin <strong>andstrong> phorbal ester signaling pathway Gene SetFrom Biocarta Pathways proteins participating in the ionomycin <strong>andstrong> phorbal ester signaling pathway pathway from the Biocarta Pathways dataset. |
carm1 <strong>andstrong> regulation of the estrogen receptor Gene SetFrom Biocarta Pathways proteins participating in the carm1 <strong>andstrong> regulation of the estrogen receptor pathway from the Biocarta Pathways dataset. |
phosphoinositides <strong>andstrong> their downstream targets Gene SetFrom Biocarta Pathways proteins participating in the phosphoinositides <strong>andstrong> their downstream targets pathway from the Biocarta Pathways dataset. |
melanocyte development <strong>andstrong> pigmentation pathway Gene SetFrom Biocarta Pathways proteins participating in the melanocyte development <strong>andstrong> pigmentation pathway pathway from the Biocarta Pathways dataset. |
akap95 role in mitosis <strong>andstrong> chromosome dynamics Gene SetFrom Biocarta Pathways proteins participating in the akap95 role in mitosis <strong>andstrong> chromosome dynamics pathway from the Biocarta Pathways dataset. |
transcription factor creb <strong>andstrong> its extracellular signals Gene SetFrom Biocarta Pathways proteins participating in the transcription factor creb <strong>andstrong> its extracellular signals pathway from the Biocarta Pathways dataset. |
visceral fat deposits <strong>andstrong> the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits <strong>andstrong> the metabolic syndrome pathway from the Biocarta Pathways dataset. |
the igf-1 receptor <strong>andstrong> longevity Gene SetFrom Biocarta Pathways proteins participating in the the igf-1 receptor <strong>andstrong> longevity pathway from the Biocarta Pathways dataset. |
cdc25 <strong>andstrong> chk1 regulatory pathway in response to dna damage Gene SetFrom Biocarta Pathways proteins participating in the cdc25 <strong>andstrong> chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset. |
human cytomegalovirus <strong>andstrong> map kinase pathways Gene SetFrom Biocarta Pathways proteins participating in the human cytomegalovirus <strong>andstrong> map kinase pathways pathway from the Biocarta Pathways dataset. |
influence of ras <strong>andstrong> rho proteins on g1 to s transition Gene SetFrom Biocarta Pathways proteins participating in the influence of ras <strong>andstrong> rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset. |
proteolysis <strong>andstrong> signaling pathway of notch Gene SetFrom Biocarta Pathways proteins participating in the proteolysis <strong>andstrong> signaling pathway of notch pathway from the Biocarta Pathways dataset. |
apoptotic dna-fragmentation <strong>andstrong> tissue homeostasis Gene SetFrom Biocarta Pathways proteins participating in the apoptotic dna-fragmentation <strong>andstrong> tissue homeostasis pathway from the Biocarta Pathways dataset. |
ion channels <strong>andstrong> their functional role in vascular endothelium Gene SetFrom Biocarta Pathways proteins participating in the ion channels <strong>andstrong> their functional role in vascular endothelium pathway from the Biocarta Pathways dataset. |
alpha-synuclein <strong>andstrong> parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein <strong>andstrong> parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
fosb gene expression <strong>andstrong> drug abuse Gene SetFrom Biocarta Pathways proteins participating in the fosb gene expression <strong>andstrong> drug abuse pathway from the Biocarta Pathways dataset. |
links between pyk2 <strong>andstrong> map kinases Gene SetFrom Biocarta Pathways proteins participating in the links between pyk2 <strong>andstrong> map kinases pathway from the Biocarta Pathways dataset. |
opposing roles of aif in apoptosis <strong>andstrong> cell survival Gene SetFrom Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis <strong>andstrong> cell survival pathway from the Biocarta Pathways dataset. |
degradation of the rar <strong>andstrong> rxr by the proteasome Gene SetFrom Biocarta Pathways proteins participating in the degradation of the rar <strong>andstrong> rxr by the proteasome pathway from the Biocarta Pathways dataset. |
cadmium induces dna synthesis <strong>andstrong> proliferation in macrophages Gene SetFrom Biocarta Pathways proteins participating in the cadmium induces dna synthesis <strong>andstrong> proliferation in macrophages pathway from the Biocarta Pathways dataset. |
erk <strong>andstrong> pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom Biocarta Pathways proteins participating in the erk <strong>andstrong> pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset. |
role of brca1 brca2 <strong>andstrong> atr in cancer susceptibility Gene SetFrom Biocarta Pathways proteins participating in the role of brca1 brca2 <strong>andstrong> atr in cancer susceptibility pathway from the Biocarta Pathways dataset. |
chrebp regulation by carbohydrates <strong>andstrong> camp Gene SetFrom Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates <strong>andstrong> camp pathway from the Biocarta Pathways dataset. |
pten dependent cell cycle arrest <strong>andstrong> apoptosis Gene SetFrom Biocarta Pathways proteins participating in the pten dependent cell cycle arrest <strong>andstrong> apoptosis pathway from the Biocarta Pathways dataset. |
induction of apoptosis through dr3 <strong>andstrong> dr4/5 death receptors Gene SetFrom Biocarta Pathways proteins participating in the induction of apoptosis through dr3 <strong>andstrong> dr4/5 death receptors pathway from the Biocarta Pathways dataset. |
CIITA-18437201-Raji B cells <strong>andstrong> iDC-human Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells <strong>andstrong> iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
VDR-23401126-LCL-AND-THP1-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Hypothyroidism, central, <strong>andstrong> testicular enlargement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, <strong>andstrong> testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, <strong>andstrong> short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, <strong>andstrong> short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holoprosencephaly, ectrodactyly, <strong>andstrong> bilateral cleft lip/palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, <strong>andstrong> bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia <strong>andstrong> presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia <strong>andstrong> presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, mental retardation, <strong>andstrong> seizures Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, <strong>andstrong> seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vater association with macrocephaly <strong>andstrong> ventriculomegaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly <strong>andstrong> ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal hamartomas nephroblastomatosis <strong>andstrong> fetal gigantism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis <strong>andstrong> fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, <strong>andstrong> genital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, <strong>andstrong> genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Exocrine pancreatic insufficiency, dyserythropoietic anemia, <strong>andstrong> calvarial hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, <strong>andstrong> calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, <strong>andstrong> sideroblastic anemia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, <strong>andstrong> sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microtia, hearing impairment, <strong>andstrong> cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, <strong>andstrong> cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, <strong>andstrong> hyper-ige Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, <strong>andstrong> hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, spastic quadriplegia, <strong>andstrong> mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, <strong>andstrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermanganesemia with dystonia, polycythemia <strong>andstrong> cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia <strong>andstrong> cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined cellular <strong>andstrong> humoral immune defects with granulomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined cellular <strong>andstrong> humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, <strong>andstrong> congenital heart defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, <strong>andstrong> congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined d-2- <strong>andstrong> l-2-hydroxyglutaric aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- <strong>andstrong> l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sinoatrial node dysfunction <strong>andstrong> deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction <strong>andstrong> deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, <strong>andstrong> lymphedema Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, <strong>andstrong> lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, recurrent infections, <strong>andstrong> autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, <strong>andstrong> autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, <strong>andstrong> palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, <strong>andstrong> palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation with language impairment <strong>andstrong> autistic features Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment <strong>andstrong> autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warts, hypogammaglobulinemia, infections, <strong>andstrong> myelokathexis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, <strong>andstrong> myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia <strong>andstrong> complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia <strong>andstrong> complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoinflammation, antibody deficiency, <strong>andstrong> immune dysregulation, plc<strong>g2strong>-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, <strong>andstrong> immune dysregulation, plc<strong>g2strong>-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, anterior maxillary protrusion, <strong>andstrong> strabismus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, <strong>andstrong> strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile convulsions <strong>andstrong> paroxysmal choreoathetosis, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions <strong>andstrong> paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, <strong>andstrong> pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, <strong>andstrong> pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis <strong>andstrong> apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis <strong>andstrong> apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proliferative vasculopathy <strong>andstrong> hydranencephaly-hydrocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy <strong>andstrong> hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, <strong>andstrong> bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, <strong>andstrong> bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with pre- <strong>andstrong> postsynaptic defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- <strong>andstrong> postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sensory ataxic neuropathy, dysarthria, <strong>andstrong> ophthalmoparesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, <strong>andstrong> ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial anomalies <strong>andstrong> anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies <strong>andstrong> anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness with labyrinthine aplasia microtia <strong>andstrong> microdontia (LAMM) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia <strong>andstrong> microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Cutaneous <strong>andstrong> Mucosal Venous Malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous <strong>andstrong> Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy hereditary sensory <strong>andstrong> autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory <strong>andstrong> autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly with mental retardation <strong>andstrong> digital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation <strong>andstrong> digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, <strong>andstrong> pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, <strong>andstrong> pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, <strong>andstrong> hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, <strong>andstrong> hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, <strong>andstrong> neoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, <strong>andstrong> neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth retardation, developmental delay, coarse facies, <strong>andstrong> early death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, <strong>andstrong> early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin <strong>andstrong> bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin <strong>andstrong> bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylglutaconic aciduria with deafness, encephalopathy, <strong>andstrong> Leigh-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, <strong>andstrong> Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anemia sideroblastic <strong>andstrong> spinocerebellar ataxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic <strong>andstrong> spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial dysmorphism, immunodeficiency, livedo, <strong>andstrong> short stature Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, <strong>andstrong> short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, congenital heart defects, <strong>andstrong> posterior embryotoxon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, <strong>andstrong> posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy <strong>andstrong> sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy <strong>andstrong> sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infertility associated with multi-tailed spermatozoa <strong>andstrong> excessive DNA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa <strong>andstrong> excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iris coloboma with ptosis, hypertelorism, <strong>andstrong> mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, <strong>andstrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal recessive arteriopathy with subcortical infarcts <strong>andstrong> leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts <strong>andstrong> leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rigidity <strong>andstrong> multifocal seizure syndrome, lethal neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rigidity <strong>andstrong> multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alopecia, neurologic defects, <strong>andstrong> endocrinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, <strong>andstrong> endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mullerian aplasia <strong>andstrong> hyper<strong>andstrong>rogenism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia <strong>andstrong> hyper<strong>andstrong>rogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Knuckle pads, deafness AND leukonychia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, <strong>andstrong> cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, <strong>andstrong> cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
M<strong>andstrong>ibular hypoplasia, deafness, progeroid features, <strong>andstrong> lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the M<strong>andstrong>ibular hypoplasia, deafness, progeroid features, <strong>andstrong> lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, <strong>andstrong> muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, <strong>andstrong> muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease <strong>andstrong> frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease <strong>andstrong> frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multicentric osteolysis, nodulosis <strong>andstrong> arthropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis <strong>andstrong> arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stapes ankylosis with broad thumb <strong>andstrong> toes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb <strong>andstrong> toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy <strong>andstrong> perceptive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy <strong>andstrong> perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, <strong>andstrong> developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, <strong>andstrong> developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma <strong>andstrong> woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma <strong>andstrong> woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus <strong>andstrong> sensorineural deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus <strong>andstrong> sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proteinuria, low molecular weight, with hypercalciuria <strong>andstrong> nephrocalcinosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria <strong>andstrong> nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome <strong>andstrong> Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome <strong>andstrong> Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, <strong>andstrong> sideroblastic anemia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, <strong>andstrong> sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor <strong>andstrong> sensory, Okinawa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor <strong>andstrong> sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, onychodysplasia, facial dysmorphism, <strong>andstrong> hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, <strong>andstrong> hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, short stature, <strong>andstrong> impaired glucose metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, <strong>andstrong> impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemorrhagic destruction of the brain, subependymal calcification, <strong>andstrong> cataracts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, <strong>andstrong> cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell <strong>andstrong> Lange-Nielsen syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell <strong>andstrong> Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly, alopecia, cutis laxa, <strong>andstrong> scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, <strong>andstrong> scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination <strong>andstrong> Congenital Cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination <strong>andstrong> Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial dysmorphism, skeletal anomalies, <strong>andstrong> mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, <strong>andstrong> mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, <strong>andstrong> autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, <strong>andstrong> autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair <strong>andstrong> keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair <strong>andstrong> keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, <strong>andstrong> cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, <strong>andstrong> cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract <strong>andstrong> cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract <strong>andstrong> cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin <strong>andstrong> bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin <strong>andstrong> bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia <strong>andstrong> distinctive facial appearance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia <strong>andstrong> distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, microphthalmia <strong>andstrong> nystagmus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia <strong>andstrong> nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia <strong>andstrong> anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia <strong>andstrong> anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperuricemia, pulmonary hypertension, renal failure, <strong>andstrong> alkalosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, <strong>andstrong> alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, <strong>andstrong> deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, <strong>andstrong> deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectrodactyly, ectodermal dysplasia, <strong>andstrong> cleft lip/palate syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, <strong>andstrong> cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy with inner retinal dysfunction <strong>andstrong> ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction <strong>andstrong> ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid <strong>andstrong> retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid <strong>andstrong> retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna <strong>andstrong> fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna <strong>andstrong> fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, <strong>andstrong> natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, <strong>andstrong> natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v <strong>andstrong> factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v <strong>andstrong> factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, <strong>andstrong> dysphagia, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, <strong>andstrong> 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, <strong>andstrong> autoimmunity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, <strong>andstrong> autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas <strong>andstrong> Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas <strong>andstrong> Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked rol<strong>andstrong>ic epilepsy with mental retardation <strong>andstrong> speech dyspraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked rol<strong>andstrong>ic epilepsy with mental retardation <strong>andstrong> speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
B<strong>andstrong>-like calcification with simplified gyration <strong>andstrong> polymicrogyria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the B<strong>andstrong>-like calcification with simplified gyration <strong>andstrong> polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia <strong>andstrong> vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia <strong>andstrong> vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, epilepsy, <strong>andstrong> diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, <strong>andstrong> diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia <strong>andstrong> hypogonadotropic hypogonadism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia <strong>andstrong> hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain <strong>andstrong> eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epilepsy, X-linked, with variable learning disabilities <strong>andstrong> behavior disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities <strong>andstrong> behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy <strong>andstrong> cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy <strong>andstrong> cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, juvenile, with microcornea <strong>andstrong> glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea <strong>andstrong> glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, <strong>andstrong> Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, <strong>andstrong> Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with microcephaly, growth retardation, <strong>andstrong> sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, <strong>andstrong> sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, deafness, <strong>andstrong> narcolepsy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, <strong>andstrong> narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, <strong>andstrong> urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, <strong>andstrong> urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal dominant arteriopathy with subcortical infarcts <strong>andstrong> leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts <strong>andstrong> leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile macular degeneration <strong>andstrong> hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration <strong>andstrong> hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor <strong>andstrong> sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor <strong>andstrong> sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis <strong>andstrong> renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis <strong>andstrong> renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte <strong>andstrong> dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte <strong>andstrong> dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, <strong>andstrong> epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, <strong>andstrong> epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, hiatal hernia <strong>andstrong> nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia <strong>andstrong> nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, congenital alopecia <strong>andstrong> nail dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia <strong>andstrong> nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis <strong>andstrong> congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis <strong>andstrong> congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, <strong>andstrong> pallidal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, <strong>andstrong> pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, rod-cone dystrophy, cataract, <strong>andstrong> posterior staphyloma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, <strong>andstrong> posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell <strong>andstrong> Lange-Nielsen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell <strong>andstrong> Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined malonic <strong>andstrong> methylmalonic aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined malonic <strong>andstrong> methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, <strong>andstrong> telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, <strong>andstrong> telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, stereotypic movements, epilepsy, <strong>andstrong>/or cerebral malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, <strong>andstrong>/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia <strong>andstrong> isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia <strong>andstrong> isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, <strong>andstrong> imbalanced globin synthesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, <strong>andstrong> imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis Gyrata syndrome of Beare <strong>andstrong> Stevenson Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare <strong>andstrong> Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly <strong>andstrong> chorioretinopathy, autosomal recessive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly <strong>andstrong> chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal intraepithelial dyskeratosis <strong>andstrong> ectodermal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis <strong>andstrong> ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aniridia, cerebellar ataxia, <strong>andstrong> mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, <strong>andstrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor <strong>andstrong> sensory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor <strong>andstrong> sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, proximal, with ocular abnormalities <strong>andstrong> mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities <strong>andstrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniosynostosis <strong>andstrong> dental anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis <strong>andstrong> dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mycobacterial <strong>andstrong> viral infections, susceptibility to, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial <strong>andstrong> viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, hyperphagia, <strong>andstrong> developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, <strong>andstrong> developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebroretinal microangiopathy with calcifications <strong>andstrong> cysts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications <strong>andstrong> cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Generalized epilepsy <strong>andstrong> paroxysmal dyskinesia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy <strong>andstrong> paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alacrima, achalasia, <strong>andstrong> mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, <strong>andstrong> mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, normal intelligence <strong>andstrong> immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence <strong>andstrong> immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Calcification of joints <strong>andstrong> arteries Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints <strong>andstrong> arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis <strong>andstrong> recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis <strong>andstrong> recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epidermolysa bullosa simplex <strong>andstrong> limb girdle muscular dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex <strong>andstrong> limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, <strong>andstrong> dysequilibrium syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, <strong>andstrong> dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, <strong>andstrong> dysequilibrium syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, <strong>andstrong> dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, <strong>andstrong> dysequilibrium syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, <strong>andstrong> dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antley-Bixler syndrome with genital anomalies <strong>andstrong> disordered steroidogenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies <strong>andstrong> disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Psychomotor retardation, epilepsy, <strong>andstrong> craniofacial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, <strong>andstrong> craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, with myopia <strong>andstrong> conductive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia <strong>andstrong> conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frontotemporal dementia <strong>andstrong>/or amyotrophic lateral sclerosis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia <strong>andstrong>/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia <strong>andstrong> cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia <strong>andstrong> cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pineal hyperplasia AND diabetes mellitus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Morbid obesity <strong>andstrong> spermatogenic failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity <strong>andstrong> spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, <strong>andstrong> mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, <strong>andstrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, <strong>andstrong> developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, <strong>andstrong> developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Striatal necrosis, bilateral, <strong>andstrong> progressive polyneuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, <strong>andstrong> progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sensory <strong>andstrong> autonomic neuropathy type IIA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory <strong>andstrong> autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopia, high, with cataract <strong>andstrong> vitreoretinal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract <strong>andstrong> vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V <strong>andstrong> factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V <strong>andstrong> factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Camptodactyly, tall stature, <strong>andstrong> hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, <strong>andstrong> hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum <strong>andstrong> acne Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum <strong>andstrong> acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, <strong>andstrong> dysphagia, early-onset, mild variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, <strong>andstrong> dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth deficiency <strong>andstrong> mental retardation with facial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency <strong>andstrong> mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, <strong>andstrong> Neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, <strong>andstrong> Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, cochlear, with myopia <strong>andstrong> intellectual impairment Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia <strong>andstrong> intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of sialidase AND beta galactosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism <strong>andstrong> abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism <strong>andstrong> abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures <strong>andstrong> brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures <strong>andstrong> brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy, dilated, with woolly hair, keratoderma, <strong>andstrong> tooth agenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, <strong>andstrong> tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, iris coloboma, <strong>andstrong> comedogenic acne syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, <strong>andstrong> comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia <strong>andstrong> skeletal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia <strong>andstrong> skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, <strong>andstrong> other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, <strong>andstrong> other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, follicular atrophoderma, hypotrichosis, <strong>andstrong> hypohidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, <strong>andstrong> hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mrna cleavage <strong>andstrong> polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage <strong>andstrong> polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial sorting <strong>andstrong> assembly machinery complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting <strong>andstrong> assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical layer of collagen <strong>andstrong> cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen <strong>andstrong> cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen <strong>andstrong> cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen <strong>andstrong> cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mrna cleavage <strong>andstrong> polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage <strong>andstrong> polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen <strong>andstrong> cuticulin-based cuticle extracellular matrix part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen <strong>andstrong> 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 <strong>andstrong> assembly machinery complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting <strong>andstrong> 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 <strong>andstrong> subunits of the 60S ribosomal particle) Gene Setproteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 <strong>andstrong> subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset. |
NRD complex (Nucleosome remodeling <strong>andstrong> deacetylation complex) Gene Setproteins in the NRD complex (Nucleosome remodeling <strong>andstrong> deacetylation complex) protein complex from the CORUM Protein Complexes dataset. |
6S methyltransferase <strong>andstrong> RG-containing Sm proteins complex Gene Setproteins in the 6S methyltransferase <strong>andstrong> RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset. |
Remodeling <strong>andstrong> spacing factor (RSF) complex Gene Setproteins in the Remodeling <strong>andstrong> spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset. |
PBAF complex (Polybromo- <strong>andstrong> BAF containing complex) Gene Setproteins in the PBAF complex (Polybromo- <strong>andstrong> BAF containing complex) protein complex from the CORUM Protein Complexes dataset. |
Cleavage <strong>andstrong> polyadenylation factor (CPSF) Gene Setproteins in the Cleavage <strong>andstrong> polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate I/200kD <strong>andstrong> III/250kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate I/200kD <strong>andstrong> III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Nucleic <strong>andstrong> chromatin Fanconi complex Gene Setproteins in the Nucleic <strong>andstrong> chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate V/380kD <strong>andstrong> VI/480kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate V/380kD <strong>andstrong> VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
ATP-utilizing chromatin assembly <strong>andstrong> remodeling factor (hACF) complex Gene Setproteins in the ATP-utilizing chromatin assembly <strong>andstrong> remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset. |
Amino Acids, Peptides, <strong>andstrong> Proteins Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, <strong>andstrong> Proteins from the curated CTD Gene-Chemical Interactions dataset. |
Bile Acids <strong>andstrong> Salts Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids <strong>andstrong> Salts from the curated CTD Gene-Chemical Interactions dataset. |
Prime <strong>andstrong> Bond NT Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime <strong>andstrong> Bond NT from the curated CTD Gene-Chemical Interactions dataset. |
drospirenone <strong>andstrong> ethinyl estradiol combination Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone <strong>andstrong> ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset. |
Hypophosphatemic Rickets <strong>Andstrong> Hyperparathyroidism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets <strong>Andstrong> Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, <strong>andstrong> Sensitivity to Ionizing Radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, <strong>andstrong> Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset. |
Fibular hypoplasia <strong>andstrong> complex brachydactyly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia <strong>andstrong> complex brachydactyly from the curated CTD Gene-Disease Associations dataset. |
Synovitis granulomatous with uveitis <strong>andstrong> cranial neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis <strong>andstrong> cranial neuropathies from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene SetFrom 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 <strong>andstrong> Motor Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory <strong>andstrong> Motor Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Preaxial deficiency, postaxial polydactyly <strong>andstrong> hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly <strong>andstrong> hypospadias from the curated CTD Gene-Disease Associations dataset. |
Combined Cellular <strong>Andstrong> Humoral Immune Defects With Granulomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular <strong>Andstrong> Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset. |
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene SetFrom 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, <strong>andstrong> Micrognathia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, <strong>andstrong> Micrognathia from the curated CTD Gene-Disease Associations dataset. |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, <strong>andstrong> Microdontia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, <strong>andstrong> Microdontia from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, rol<strong>andstrong>ic with paroxysmal exercise-induced dystonia <strong>andstrong> writer's cramp Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rol<strong>andstrong>ic with paroxysmal exercise-induced dystonia <strong>andstrong> writer's cramp from the curated CTD Gene-Disease Associations dataset. |
Low Molecular Weight Proteinuria with Hypercalciuria <strong>andstrong> Nephrocalcinosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria <strong>andstrong> Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset. |
Keratosis Linearis with Ichthyosis Congenita <strong>andstrong> Sclerosing Keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita <strong>andstrong> Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset. |
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, <strong>andstrong> Lymphedema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, <strong>andstrong> Lymphedema from the curated CTD Gene-Disease Associations dataset. |
Microtia, Hearing Impairment, <strong>Andstrong> Cleft Palate Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, <strong>Andstrong> Cleft Palate from the curated CTD Gene-Disease Associations dataset. |
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene SetFrom 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 <strong>Andstrong> Autonomic, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory <strong>Andstrong> Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Acromegaloid features, overgrowth, cleft palate, <strong>andstrong> hernia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, <strong>andstrong> hernia from the curated CTD Gene-Disease Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, <strong>andstrong> palmoplantar keratoderma syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, <strong>andstrong> palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset. |
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene SetFrom 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, <strong>andstrong> Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, <strong>andstrong> Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Choreoathetosis, Hypothyroidism, <strong>Andstrong> Neonatal Respiratory Distress Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, <strong>Andstrong> Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset. |
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, <strong>andstrong> Calvarial Hyperostosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, <strong>andstrong> Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset. |
Craniosynostosis, anal anomalies, <strong>andstrong> porokeratosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, <strong>andstrong> porokeratosis from the curated CTD Gene-Disease Associations dataset. |
Sacral defect <strong>andstrong> anterior sacral meningocele Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect <strong>andstrong> anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset. |
Classical Lissencephalies <strong>andstrong> Subcortical B<strong>andstrong> Heterotopias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies <strong>andstrong> Subcortical B<strong>andstrong> Heterotopias from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, with Myopia <strong>andstrong> Conductive Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia <strong>andstrong> Conductive Deafness from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 <strong>andstrong> deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 <strong>andstrong> deafness from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor <strong>andstrong> sensory, Russe type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor <strong>andstrong> sensory, Russe type from the curated CTD Gene-Disease Associations dataset. |
Blepharophimosis, Ptosis, <strong>andstrong> Epicanthus Inversus Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, <strong>andstrong> Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset. |
Hypotrichosis <strong>Andstrong> Recurrent Skin Vesicles Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis <strong>Andstrong> Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset. |
Signs <strong>andstrong> Symptoms, Digestive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Signs <strong>andstrong> Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease <strong>Andstrong> Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease <strong>Andstrong> Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria <strong>andstrong> Homocystinuria, CblD Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria <strong>andstrong> Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset. |
Head <strong>andstrong> Neck Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Head <strong>andstrong> Neck Neoplasms from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene SetFrom 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 <strong>andstrong> Limb Defects Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma <strong>andstrong> Limb Defects from the curated CTD Gene-Disease Associations dataset. |
Cataract, Juvenile, With Microcornea <strong>Andstrong> Glucosuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea <strong>Andstrong> Glucosuria from the curated CTD Gene-Disease Associations dataset. |
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene SetFrom 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 <strong>andstrong> Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous <strong>andstrong> Mucosal from the curated CTD Gene-Disease Associations dataset. |
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene SetFrom 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 <strong>andstrong> Vomiting Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea <strong>andstrong> Vomiting from the curated CTD Gene-Disease Associations dataset. |
Myopathy with lactic acidosis <strong>andstrong> sideroblastic anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis <strong>andstrong> sideroblastic anemia from the curated CTD Gene-Disease Associations dataset. |
Albinism with hemorrhagic diathesis <strong>andstrong> pigmented reticuloendothelial cells Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis <strong>andstrong> pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom 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, <strong>andstrong> Deafness (KID) Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, <strong>andstrong> Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset. |
Bifid Nose With Or Without Anorectal <strong>Andstrong> Renal Anomalies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal <strong>Andstrong> Renal Anomalies from the curated CTD Gene-Disease Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, <strong>Andstrong> Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, <strong>Andstrong> Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy <strong>andstrong> perceptive deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy <strong>andstrong> perceptive deafness from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, <strong>Andstrong> Dysequilibrium Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, <strong>Andstrong> Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Skeletal Dysplasia, <strong>andstrong> Abducens Palsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, <strong>andstrong> Abducens Palsy from the curated CTD Gene-Disease Associations dataset. |
Hypopituitarism <strong>andstrong> septooptic 'dysplasia' Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism <strong>andstrong> septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset. |
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, <strong>Andstrong> Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, <strong>Andstrong> Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Aplasia of Lacrimal <strong>andstrong> Salivary Gl<strong>andstrong>s Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal <strong>andstrong> Salivary Gl<strong>andstrong>s from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Deafness, Cataract, Retinitis Pigmentosa, <strong>Andstrong> Sperm Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, <strong>Andstrong> Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset. |
Glomerulocystic Kidney Disease with Hyperuricemia <strong>andstrong> Isosthenuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia <strong>andstrong> Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Calcification of Joints <strong>andstrong> Arteries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints <strong>andstrong> Arteries from the curated CTD Gene-Disease Associations dataset. |
CHOANAL ATRESIA AND LYMPHEDEMA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly, Alopecia, Cutis Laxa, <strong>andstrong> Scoliosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, <strong>andstrong> Scoliosis from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor <strong>Andstrong> Sensory Neuropathy, Type IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor <strong>Andstrong> Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset. |
Asthma, Nasal Polyps, <strong>Andstrong> Aspirin Intolerance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, <strong>Andstrong> Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Germ Cell <strong>andstrong> Embryonal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell <strong>andstrong> Embryonal from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor <strong>Andstrong> Sensory Neuropathy VI Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor <strong>Andstrong> Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset. |
Cutis Gyrata Syndrome of Beare <strong>Andstrong> Stevenson Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare <strong>Andstrong> Stevenson from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Wounds <strong>andstrong> Injuries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wounds <strong>andstrong> Injuries from the curated CTD Gene-Disease Associations dataset. |
Schizophrenia <strong>andstrong> Disorders with Psychotic Features Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia <strong>andstrong> Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset. |
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, <strong>Andstrong> Pallidal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, <strong>Andstrong> Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Sleep Initiation <strong>andstrong> Maintenance Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation <strong>andstrong> Maintenance Disorders from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria <strong>andstrong> Homocystinuria, CblF Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria <strong>andstrong> Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset. |
Scaphocephaly, Maxillary Retrusion, <strong>Andstrong> Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, <strong>Andstrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Cataract <strong>andstrong> cardiomyopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract <strong>andstrong> cardiomyopathy from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, <strong>Andstrong> Cleft Lip/Palate Syndrome 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, <strong>Andstrong> Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor <strong>andstrong> sensory, Okinawa type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor <strong>andstrong> sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, <strong>andstrong> Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, <strong>andstrong> Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Generalized Epilepsy <strong>andstrong> Paroxysmal Dyskinesia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy <strong>andstrong> Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset. |
Hereditary Breast <strong>andstrong> Ovarian Cancer Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast <strong>andstrong> Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset. |
Keratosis palmoplantaris with periodontopathia <strong>andstrong> onychogryposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia <strong>andstrong> onychogryposis from the curated CTD Gene-Disease Associations dataset. |
Intracranial Embolism <strong>andstrong> Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism <strong>andstrong> Thrombosis from the curated CTD Gene-Disease Associations dataset. |
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, <strong>Andstrong> Cataract Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, <strong>Andstrong> Cataract from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset. |
Microtia With Nasolacrimal Duct Imperforation <strong>Andstrong> Eye Coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation <strong>Andstrong> Eye Coloboma from the curated CTD Gene-Disease Associations dataset. |
Nevi <strong>andstrong> Melanomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nevi <strong>andstrong> Melanomas from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, X-Linked, with Variable Learning Disabilities <strong>andstrong> Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities <strong>andstrong> Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Attention Deficit <strong>andstrong> Disruptive Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit <strong>andstrong> Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy dilated with Woolly hair <strong>andstrong> keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair <strong>andstrong> keratoderma from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, microphthalmia, ectrodactyly of lower limbs, <strong>andstrong> prognathism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, <strong>andstrong> prognathism from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy <strong>andstrong> cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy <strong>andstrong> cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Skeletal Defects, Genital Hypoplasia, <strong>Andstrong> Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, <strong>Andstrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Hypermanganesemia with Dystonia Polycythemia <strong>andstrong> Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia <strong>andstrong> Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Juvenile macular degeneration <strong>andstrong> hypotrichosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration <strong>andstrong> hypotrichosis from the curated CTD Gene-Disease Associations dataset. |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset. |
Mullerian Aplasia <strong>andstrong> Hyper<strong>andstrong>rogenism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia <strong>andstrong> Hyper<strong>andstrong>rogenism from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, <strong>Andstrong> Developmental Delay Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, <strong>Andstrong> Developmental Delay from the curated CTD Gene-Disease Associations dataset. |
Esophageal <strong>andstrong> Gastric Varices Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal <strong>andstrong> Gastric Varices from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset. |
Hypogammaglobulinemia <strong>andstrong> Isolated growth hormone deficiency, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia <strong>andstrong> Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, squamous cell of head <strong>andstrong> neck Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, squamous cell of head <strong>andstrong> neck from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial <strong>andstrong> congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial <strong>andstrong> congenital from the curated CTD Gene-Disease Associations dataset. |
Extravasation of Diagnostic <strong>andstrong> Therapeutic Materials Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Extravasation of Diagnostic <strong>andstrong> Therapeutic Materials from the curated CTD Gene-Disease Associations dataset. |
Ichthyosis, Leukocyte Vacuoles, Alopecia, <strong>Andstrong> Sclerosing Cholangitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, <strong>Andstrong> Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, <strong>Andstrong> Dysequilibrium Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, <strong>Andstrong> Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Knuckle pads, leuconychia <strong>andstrong> sensorineural deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Knuckle pads, leuconychia <strong>andstrong> sensorineural deafness from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities <strong>Andstrong> Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities <strong>Andstrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Immunodysregulation, Polyendocrinopathy, <strong>andstrong> Enteropathy, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, <strong>andstrong> Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Hyperekplexia <strong>andstrong> Epilepsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia <strong>andstrong> Epilepsy from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis <strong>andstrong> Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis <strong>andstrong> Apraxia from the curated CTD Gene-Disease Associations dataset. |
Epidermolysis Bullosa With Congenital Localized Absence Of Skin <strong>Andstrong> Deformity Of Nails Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin <strong>Andstrong> Deformity Of Nails from the curated CTD Gene-Disease Associations dataset. |
Iris hypoplasia <strong>andstrong> glaucoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia <strong>andstrong> glaucoma from the curated CTD Gene-Disease Associations dataset. |
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Sarcoma family syndrome of Li <strong>andstrong> Fraumeni Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma family syndrome of Li <strong>andstrong> Fraumeni from the curated CTD Gene-Disease Associations dataset. |
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset. |
Nephropathy with Pretibial Epidermolysis Bullosa <strong>andstrong> Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy with Pretibial Epidermolysis Bullosa <strong>andstrong> Deafness from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, <strong>andstrong> Obesity Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, <strong>andstrong> Obesity Syndrome from the curated CTD Gene-Disease Associations dataset. |
Lipoid Proteinosis of Urbach <strong>andstrong> Wiethe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid Proteinosis of Urbach <strong>andstrong> Wiethe from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality <strong>andstrong> hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality <strong>andstrong> hypospadias from the curated CTD Gene-Disease Associations dataset. |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, <strong>andstrong> Elliptocytosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, <strong>andstrong> Elliptocytosis from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, <strong>andstrong> Cleft Lip/Palate Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, <strong>andstrong> Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Bone Fragility with Contractures, Arterial Rupture, <strong>andstrong> Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, <strong>andstrong> Deafness from the curated CTD Gene-Disease Associations dataset. |
Thrombocytopenia, Platelet Dysfunction, Hemolysis, <strong>andstrong> Imbalanced Globin Synthesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, <strong>andstrong> Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset. |
Jervell <strong>Andstrong> Lange-Nielsen Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jervell <strong>Andstrong> Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Gl<strong>andstrong>ular <strong>andstrong> Epithelial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Gl<strong>andstrong>ular <strong>andstrong> Epithelial from the curated CTD Gene-Disease Associations dataset. |
Ectodermal dysplasia, ectrodactyly, <strong>andstrong> macular dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, <strong>andstrong> macular dystrophy from the curated CTD Gene-Disease Associations dataset. |
Alopecia, Neurologic Defects, <strong>andstrong> Endocrinopathy Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Neurologic Defects, <strong>andstrong> Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset. |
Retinitis Pigmentosa, X-Linked, <strong>Andstrong> Sinorespiratory Infections, With Or Without Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, <strong>Andstrong> Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset. |
Early-onset ataxia with oculomotor apraxia <strong>andstrong> hypoalbuminemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia <strong>andstrong> hypoalbuminemia from the curated CTD Gene-Disease Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum, <strong>andstrong> acne Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyogenic arthritis, pyoderma gangrenosum, <strong>andstrong> acne from the curated CTD Gene-Disease Associations dataset. |
Epidermolysa bullosa simplex <strong>andstrong> limb girdle muscular dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex <strong>andstrong> limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset. |
Cleft Palate, Isolated, <strong>Andstrong> Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Palate, Isolated, <strong>Andstrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Absent radii <strong>andstrong> thrombocytopenia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Absent radii <strong>andstrong> thrombocytopenia from the curated CTD Gene-Disease Associations dataset. |
Hypercarotenemia <strong>Andstrong> Vitamin A Deficiency, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypercarotenemia <strong>Andstrong> Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset. |
Microcephaly with Mental Retardation <strong>andstrong> Digital Anomalies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly with Mental Retardation <strong>andstrong> Digital Anomalies from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly with Multiple Epiphyseal Dysplasia <strong>andstrong> Distinctive Facies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia <strong>andstrong> Distinctive Facies from the curated CTD Gene-Disease Associations dataset. |
STAPES ANKYLOSIS WITH BROAD THUMB AND TOES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease STAPES ANKYLOSIS WITH BROAD THUMB AND TOES from the curated CTD Gene-Disease Associations dataset. |
Cutis Laxa With Severe Pulmonary, Gastrointestinal, <strong>Andstrong> Urinary Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Laxa With Severe Pulmonary, Gastrointestinal, <strong>Andstrong> Urinary Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Polyhydramnios, Megalencephaly, <strong>Andstrong> Symptomatic Epilepsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyhydramnios, Megalencephaly, <strong>Andstrong> Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset. |
Mental retardation, X-linked, with cerebellar hypoplasia <strong>andstrong> distinctive facial appearance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia <strong>andstrong> distinctive facial appearance from the curated CTD Gene-Disease Associations dataset. |
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, <strong>andstrong> Autoimmunity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, <strong>andstrong> Autoimmunity from the curated CTD Gene-Disease Associations dataset. |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, <strong>andstrong> Perinatal Edema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, <strong>andstrong> Perinatal Edema from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Severe, With Spasticity <strong>Andstrong> Pigmentary Tapetoretinal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity <strong>Andstrong> Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Signs <strong>andstrong> Symptoms, Respiratory Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Signs <strong>andstrong> Symptoms, Respiratory from the curated CTD Gene-Disease Associations dataset. |
Renal cysts <strong>andstrong> diabetes syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal cysts <strong>andstrong> diabetes syndrome from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor <strong>andstrong> sensory, LOM type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor <strong>andstrong> sensory, LOM type from the curated CTD Gene-Disease Associations dataset. |
Nephroblastomatosis, fetal ascites, macrosomia <strong>andstrong> Wilms tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephroblastomatosis, fetal ascites, macrosomia <strong>andstrong> Wilms tumor from the curated CTD Gene-Disease Associations dataset. |
Hereditary Angioedema Types I <strong>andstrong> II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Types I <strong>andstrong> II from the curated CTD Gene-Disease Associations dataset. |
Drug-Related Side Effects <strong>andstrong> Adverse Reactions Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Drug-Related Side Effects <strong>andstrong> Adverse Reactions from the curated CTD Gene-Disease Associations dataset. |
Insect Bites <strong>andstrong> Stings Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Insect Bites <strong>andstrong> Stings from the curated CTD Gene-Disease Associations dataset. |
T-cell immunodeficiency, congenital alopecia <strong>andstrong> nail dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia <strong>andstrong> nail dystrophy from the curated CTD Gene-Disease Associations dataset. |
Foveal Hypoplasia <strong>andstrong> Anterior Segment Dysgenesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia <strong>andstrong> Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset. |
Cubitus Valgus with Mental Retardation <strong>andstrong> Unusual Facies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cubitus Valgus with Mental Retardation <strong>andstrong> Unusual Facies from the curated CTD Gene-Disease Associations dataset. |
Ophthalmoplegia, External, <strong>andstrong> Myopia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, External, <strong>andstrong> Myopia from the curated CTD Gene-Disease Associations dataset. |
Deafness, Sensorineural, <strong>Andstrong> Male Infertility Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Sensorineural, <strong>Andstrong> Male Infertility from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory <strong>andstrong> Autonomic Neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory <strong>andstrong> Autonomic Neuropathies from the curated CTD Gene-Disease Associations dataset. |
Histiocytosis with joint contractures <strong>andstrong> sensorineural deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytosis with joint contractures <strong>andstrong> sensorineural deafness from the curated CTD Gene-Disease Associations dataset. |
Rol<strong>andstrong>ic Epilepsy, Mental Retardation, <strong>andstrong> Speech Dyspraxia, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rol<strong>andstrong>ic Epilepsy, Mental Retardation, <strong>andstrong> Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Leiomyomatosis, esophageal <strong>andstrong> vulval, with nephropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leiomyomatosis, esophageal <strong>andstrong> vulval, with nephropathy from the curated CTD Gene-Disease Associations dataset. |
Growth Retardation, Developmental Delay, Coarse Facies, <strong>Andstrong> Early Death Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, <strong>Andstrong> Early Death from the curated CTD Gene-Disease Associations dataset. |
Sensory ataxic neuropathy, dysarthria, <strong>andstrong> ophthalmoparesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, <strong>andstrong> ophthalmoparesis from the curated CTD Gene-Disease Associations dataset. |
Embolism <strong>andstrong> Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Embolism <strong>andstrong> Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Religion <strong>andstrong> Psychology Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Religion <strong>andstrong> Psychology in GWAS <strong>andstrong> other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Attention Deficit <strong>andstrong> Disruptive Behavior Disorders Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Attention Deficit <strong>andstrong> Disruptive Behavior Disorders in GWAS <strong>andstrong> other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Weights <strong>andstrong> Measures Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Weights <strong>andstrong> Measures in GWAS <strong>andstrong> other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Nevi <strong>andstrong> Melanomas Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Nevi <strong>andstrong> Melanomas in GWAS <strong>andstrong> other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Head <strong>andstrong> Neck Neoplasms Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Head <strong>andstrong> Neck Neoplasms in GWAS <strong>andstrong> other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
blepharophimosis, ptosis, <strong>andstrong> epicanthus inversus syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease blepharophimosis, ptosis, <strong>andstrong> epicanthus inversus syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
degeneration of macula <strong>andstrong> posterior pole Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease degeneration of macula <strong>andstrong> posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye <strong>andstrong> adnexa disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye <strong>andstrong> adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
combined t cell <strong>andstrong> b cell immunodeficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease combined t cell <strong>andstrong> b cell immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye <strong>andstrong> adnexa disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye <strong>andstrong> adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
inflammatory <strong>andstrong> toxic neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inflammatory <strong>andstrong> toxic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mucinous tubular <strong>andstrong> spindle renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mucinous tubular <strong>andstrong> spindle renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pustulosis of palm <strong>andstrong> sole Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pustulosis of palm <strong>andstrong> sole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
h<strong>andstrong>, foot <strong>andstrong> mouth disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease h<strong>andstrong>, foot <strong>andstrong> mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tooth <strong>andstrong> nail syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth <strong>andstrong> nail syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
extrapyramidal <strong>andstrong> movement disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrapyramidal <strong>andstrong> movement disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mononeuritis of upper limb <strong>andstrong> mononeuritis multiplex Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mononeuritis of upper limb <strong>andstrong> mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung mixed small cell <strong>andstrong> squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell <strong>andstrong> squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of skin <strong>andstrong> connective tissue Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of skin <strong>andstrong> connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
histiocytic <strong>andstrong> dendritic cell cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease histiocytic <strong>andstrong> dendritic cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
methylmalonic aciduria <strong>andstrong> homocystinuria type cblc Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease methylmalonic aciduria <strong>andstrong> homocystinuria type cblc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
blepharophimosis, ptosis, <strong>andstrong> epicanthus inversus syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease blepharophimosis, ptosis, <strong>andstrong> epicanthus inversus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
germ cell <strong>andstrong> embryonal cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease germ cell <strong>andstrong> embryonal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mixed endometrial stromal <strong>andstrong> smooth muscle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed endometrial stromal <strong>andstrong> smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spinal canal <strong>andstrong> spinal cord meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal canal <strong>andstrong> spinal cord meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian germ cell monodermal <strong>andstrong> highly specialized teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian germ cell monodermal <strong>andstrong> highly specialized teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
degeneration of macula <strong>andstrong> posterior pole Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease degeneration of macula <strong>andstrong> posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
combined t cell <strong>andstrong> b cell immunodeficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease combined t cell <strong>andstrong> b cell immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mature t-cell <strong>andstrong> nk-cell lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mature t-cell <strong>andstrong> nk-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye <strong>andstrong> adnexa disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye <strong>andstrong> adnexa disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast <strong>andstrong> lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast <strong>andstrong> lung cancer in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased chromosome aberrations <strong>andstrong> higher lung cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased chromosome aberrations <strong>andstrong> higher lung cancer risk in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyper-ige syndrome <strong>andstrong> severe eczema. atopy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyper-ige syndrome <strong>andstrong> severe eczema. atopy in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor viii <strong>andstrong> factor ix genes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor viii <strong>andstrong> factor ix genes in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
flecainide <strong>andstrong> paroxetine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease flecainide <strong>andstrong> paroxetine in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pre-term delivery infant mortality <strong>andstrong> malaria morbidity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pre-term delivery infant mortality <strong>andstrong> malaria morbidity in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alopecia <strong>andstrong> lumbar herniated disk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alopecia <strong>andstrong> lumbar herniated disk in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
baroreflex <strong>andstrong> blood pressure regulation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease baroreflex <strong>andstrong> blood pressure regulation in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuropathy, hereditary motor <strong>andstrong> sensory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuropathy, hereditary motor <strong>andstrong> sensory in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |
psoriasis, psoriatic arthritis, <strong>andstrong> sapho syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease psoriasis, psoriatic arthritis, <strong>andstrong> sapho syndrome in GWAS <strong>andstrong> other genetic association datasets from the GAD Gene-Disease Associations dataset. |