BRISC and BRCA1-A complex member 1

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Results for "BRISC and BRCA1-A complex member 1": 1001 gene sets

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BRISC and BRCA1-A complex member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BRISC and BRCA1-A complex member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
brisc complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the brisc complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
brisc complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the brisc complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
brisc complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the brisc complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
FAM175 family, BRISC complex, Abro1 subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FAM175 family, BRISC complex, Abro1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BRISC complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the BRISC complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
BRISC complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the BRISC complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
BASC (Ab 80) complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC (Ab 80) complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
BASC (Ab C-20) complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC (Ab C-20) complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
BASC (Ab 81) complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC (Ab 81) complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
BASC complex (BRCA1-associated genome surveillance complex) Gene Set From CORUM Protein Complexes proteins in the BASC complex (BRCA1-associated genome surveillance complex) protein complex from the CORUM Protein Complexes dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
brca1-bard1 complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the brca1-bard1 complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
brca1-a complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the brca1-a complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
brca1-bard1 complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the brca1-bard1 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
brca1-b complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the brca1-b complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
brca1-c complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the brca1-c complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
brca1-a complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the brca1-a complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
BRCA1-BARD1-BACH1-DNA damage complex II Gene Set From CORUM Protein Complexes proteins in the BRCA1-BARD1-BACH1-DNA damage complex II protein complex from the CORUM Protein Complexes dataset.
BRCA1-BACH1 complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-BACH1 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1 A complex Gene Set From CORUM Protein Complexes proteins in the BRCA1 A complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-core RNA polymerase II complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-core RNA polymerase II complex protein complex from the CORUM Protein Complexes dataset.
LMO4-BRCA1-CTIP-LDB1 complex Gene Set From CORUM Protein Complexes proteins in the LMO4-BRCA1-CTIP-LDB1 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1 C complex Gene Set From CORUM Protein Complexes proteins in the BRCA1 C complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-BARD1-BRCA2-DNA damage complex III Gene Set From CORUM Protein Complexes proteins in the BRCA1-BARD1-BRCA2-DNA damage complex III protein complex from the CORUM Protein Complexes dataset.
BRCA1-CTIP-ZBRK1 repressor complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-CTIP-ZBRK1 repressor complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-VCP complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-VCP complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-RAD50-MRE11-NBS1 complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-RAD50-MRE11-NBS1 complex protein complex from the CORUM Protein Complexes dataset.
RAD50-BRCA1 complex Gene Set From CORUM Protein Complexes proteins in the RAD50-BRCA1 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-IRIS-pre-replication complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-IRIS-pre-replication complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-CtIP-CtBP complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-CtIP-CtBP complex protein complex from the CORUM Protein Complexes dataset.
BARD1-BRCA1-CSTF complex Gene Set From CORUM Protein Complexes proteins in the BARD1-BRCA1-CSTF complex protein complex from the CORUM Protein Complexes dataset.
BRCA1 B complex Gene Set From CORUM Protein Complexes proteins in the BRCA1 B complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-BARD1-BACH1-DNA damage complex I Gene Set From CORUM Protein Complexes proteins in the BRCA1-BARD1-BACH1-DNA damage complex I protein complex from the CORUM Protein Complexes dataset.
SWI-SNF chromatin remodeling-related-BRCA1 complex Gene Set From CORUM Protein Complexes proteins in the SWI-SNF chromatin remodeling-related-BRCA1 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-LMO4-CTIP complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-LMO4-CTIP complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-HDAC1-HDAC2 complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-HDAC1-HDAC2 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-RNA polymerase II complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-RNA polymerase II complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-BARD1-POLR2A complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-BARD1-POLR2A complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-SMAD3 complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-SMAD3 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-cABL complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-cABL complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-RAD51 complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-RAD51 complex protein complex from the CORUM Protein Complexes dataset.
BARD1-BRCA1-CSTF64 complex Gene Set From CORUM Protein Complexes proteins in the BARD1-BRCA1-CSTF64 complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-BARD1-UbcH5c complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-BARD1-UbcH5c complex protein complex from the CORUM Protein Complexes dataset.
BRCA1-BARD1-UbcH7c complex Gene Set From CORUM Protein Complexes proteins in the BRCA1-BARD1-UbcH7c complex protein complex from the CORUM Protein Complexes dataset.
brca1-bard1 complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the brca1-bard1 complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
brca1-a complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the brca1-a complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
FAM175 family, BRCA1-A complex, Abraxas subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FAM175 family, BRCA1-A complex, Abraxas subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BRCA1-BARD1 complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the BRCA1-BARD1 complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
BRCA1-BARD1 complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the BRCA1-BARD1 complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
BRCA1-A complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the BRCA1-A complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
BRCA1-BARD1 complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the BRCA1-BARD1 complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
BRCA1-C complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the BRCA1-C complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
BRCA1-B complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the BRCA1-B complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
BRCA1-A complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the BRCA1-A complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
BRCA1-BARD1 complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the BRCA1-BARD1 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
BRCA1-C complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the BRCA1-C complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
BRCA1-B complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the BRCA1-B complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
BRCA1-Rad51 complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the BRCA1-Rad51 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
brca1 dependent ub ligase activity Gene Set From Biocarta Pathways proteins participating in the brca1 dependent ub ligase activity pathway from the Biocarta Pathways dataset.
BRCA1 Gene Set From ENCODE Transcription Factor Targets target genes of the BRCA1 transcription factor in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
germline brca1 mutation Gene Set From GAD Gene-Disease Associations genes associated with the disease germline brca1 mutation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genotyping of frequent brca1/2 snps Gene Set From GAD Gene-Disease Associations genes associated with the disease genotyping of frequent brca1/2 snps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brca1 Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term brca1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Ovarian cancer in BRCA1 mutation carriers Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Ovarian cancer in BRCA1 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Breast Cancer in BRCA1 mutation carriers Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Breast Cancer in BRCA1 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
BRCA1 Gene Set From Hub Proteins Protein-Protein Interactions interacting proteins for hub protein BRCA1 from the curated Hub Proteins Protein-Protein Interactions dataset.
BRCA1-associated 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BRCA1-associated 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Breast cancer type 1 susceptibility protein (BRCA1) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Breast cancer type 1 susceptibility protein (BRCA1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BRCA1, serine-rich domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BRCA1, serine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cofactor of BRCA1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cofactor of BRCA1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BRCA1 Gene Set From JASPAR Predicted Transcription Factor Targets target genes of the BRCA1 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset.
BRCA1 Gene Set From MSigDB Cancer Gene Co-expression Modules co-expressed genes for BRCA1 from the MSigDB Cancer Gene Co-expression Modules dataset.
SC-6954 (BRCA1) Gene Set From NURSA Protein Complexes proteins in the SC-6954 (BRCA1) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.
AB80 (BRCA1) Gene Set From NURSA Protein Complexes proteins in the AB80 (BRCA1) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.
AB81 (BRCA1) Gene Set From NURSA Protein Complexes proteins in the AB81 (BRCA1) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.
BRCA1 Gene Set From NURSA Protein-Protein Interactions interacting proteins for BRCA1 from the NURSA Protein-Protein Interactions dataset.
BRCA1 Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for BRCA1 from the Pathway Commons Protein-Protein Interactions dataset.
brca1 Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term brca1 in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Brca1 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brca1 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Breast/Ovarian Cancer - Brca1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Breast/Ovarian Cancer - Brca1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
BRCA1 Gene Set From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the BRCA1 gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.
Defective DNA double strand break response due to BRCA1 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective DNA double strand break response due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function Gene Set From Reactome Pathways 2024 proteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function pathway from the Reactome Pathways 2024 dataset.
Defective homologous recombination repair (HRR) due to BRCA1 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective homologous recombination repair (HRR) due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset.
UWB1.289+BRCA1 cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue UWB1.289+BRCA1 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
BRCA1-related cancer predisposition Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BRCA1-related cancer predisposition phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BRCA1 mutation in breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the BRCA1 mutation in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
BRCA1/2-negative high-risk breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the BRCA1/2-negative high-risk breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast Cancer in BRCA1 mutation carriers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast Cancer in BRCA1 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
BRCA1 Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the BRCA1 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
Acyl-CoA dehydrogenase family, member 9, deficiency of Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acyl-CoA dehydrogenase family, member 9, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of from the curated CTD Gene-Disease Associations dataset.
member Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term member in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
negative regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2015 dataset.
Cadherin-related family member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cadherin-related family member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cadherin-related family member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cadherin-related family member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily C member 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily C member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily C member 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily C member 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pleckstrin homology domain-containing family O member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pleckstrin homology domain-containing family O member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette sub-family A member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette sub-family A member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Potassium voltage-gated channel subfamily H member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium voltage-gated channel subfamily H member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Potassium voltage-gated channel subfamily H member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium voltage-gated channel subfamily H member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Potassium voltage-gated channel subfamily H member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium voltage-gated channel subfamily H member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily V member 5/6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily V member 5/6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Schlafen family member 12 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Schlafen family member 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Schlafen family member 13 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Schlafen family member 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Schlafen family member 11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Schlafen family member 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Schlafen family member 14 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Schlafen family member 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Taste receptor type 2 member 38 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Taste receptor type 2 member 38 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tumor necrosis factor ligand superfamily member 15 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor necrosis factor ligand superfamily member 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Potassium channel subfamily K member 15 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium channel subfamily K member 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Calcium-transporting ATPase type 2C member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium-transporting ATPase type 2C member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Calcium-transporting ATPase type 2C member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium-transporting ATPase type 2C member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Golgin subfamily A member 6-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Golgin subfamily A member 6-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 12 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Golgin subfamily B member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Golgin subfamily B member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ectonucleotide pyrophosphatase/phosphodiesterase family member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ectonucleotide pyrophosphatase/phosphodiesterase family member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ectonucleotide pyrophosphatase/phosphodiesterase family member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ectonucleotide pyrophosphatase/phosphodiesterase family member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ectonucleotide pyrophosphatase/phosphodiesterase family member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ectonucleotide pyrophosphatase/phosphodiesterase family member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily G member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily G member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DnaJ homologue subfamily C member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DnaJ homologue subfamily C member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dehydrogenase/reductase SDR member 4-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dehydrogenase/reductase SDR member 4-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 8 (testis anion transporter 1) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 8 (testis anion transporter 1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily B member 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily B member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily B member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily B member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 43 member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 43 member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dehydrogenase/reductase SDR member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dehydrogenase/reductase SDR member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Potassium channel subfamily K member 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium channel subfamily K member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Potassium channel subfamily K member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium channel subfamily K member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ABI gene family member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ABI gene family member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 35 member F3/F4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 35 member F3/F4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily B member 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily B member 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 12 member 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 12 member 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Golgin subfamily A member 7/ERF4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Golgin subfamily A member 7/ERF4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 12 member 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 12 member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 12 member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 12 member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
WAS/WASL-interacting protein family member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the WAS/WASL-interacting protein family member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
WAS/WASL-interacting protein family member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the WAS/WASL-interacting protein family member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Golgin subfamily A member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Golgin subfamily A member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 35 member SLC35F1/F2/F6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 35 member SLC35F1/F2/F6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 26 member 3 (DRA) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 26 member 3 (DRA) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interleukin-1 family member 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interleukin-1 family member 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Taste receptor type 2 member 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Taste receptor type 2 member 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Taste receptor type 2 member 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Taste receptor type 2 member 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily M member 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily M member 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 10 member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 10 member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 10 member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 10 member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 10 member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 10 member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DnaJ homologue subfamily C member 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DnaJ homologue subfamily C member 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tumor necrosis factor ligand superfamily member 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor necrosis factor ligand superfamily member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transient receptor potential cation channel subfamily V member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transient receptor potential cation channel subfamily V member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Schlafen family member 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Schlafen family member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily C member 11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily C member 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 10 member 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 10 member 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 10 member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 10 member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 10 member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 10 member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Secretoglobin family 1C member 1/2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Secretoglobin family 1C member 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ATP-binding cassette subfamily A member 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATP-binding cassette subfamily A member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 23 member 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 23 member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DnaJ homologue, subfamily C, member 28, conserved domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DnaJ homologue, subfamily C, member 28, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
YIP1 family member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the YIP1 family member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 23 member 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 23 member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Solute carrier family 23 member 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Solute carrier family 23 member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-Coa Dehydrogenase Family, Member 9, Deficiency Of Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acyl-Coa Dehydrogenase Family, Member 9, Deficiency Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Solute Carrier Family 35 Member A2 Congenital Disorder Of Glycosylation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Solute Carrier Family 35 Member A2 Congenital Disorder Of Glycosylation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Caused By Mutation In The Tbc1 Domain Family, Member 24 Gene (Tbc1D24, 613577.0004) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Tbc1 Domain Family, Member 24 Gene (Tbc1D24, 613577.0004) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2023 dataset.
decreased tumor necrosis factor (ligand) superfamily member 11 level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased tumor necrosis factor (ligand) superfamily member 11 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased tumor necrosis factor receptor superfamily member 11b level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased tumor necrosis factor receptor superfamily member 11b level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased tumor necrosis factor (ligand) superfamily member 11 level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased tumor necrosis factor (ligand) superfamily member 11 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
positive regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set From CORUM Protein Complexes proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.
PBAF complex (Polybromo- and BAF containing complex) Gene Set From CORUM Protein Complexes proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.
electron transporter, transferring electrons from coqh2-cytochrome c reductase complex and cytochrome c oxidase complex activity Gene Set From GO Molecular Function Annotations 2015 genes performing the electron transporter, transferring electrons from coqh2-cytochrome c reductase complex and cytochrome c oxidase complex activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Formation of the ternary complex, and subsequently, the 43S complex Gene Set From Reactome Pathways 2014 proteins participating in the Formation of the ternary complex, and subsequently, the 43S complex pathway from the Reactome Pathways dataset.
Formation of the ternary complex, and subsequently, the 43S complex Gene Set From Reactome Pathways 2024 proteins participating in the Formation of the ternary complex, and subsequently, the 43S complex pathway from the Reactome Pathways 2024 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set From CORUM Protein Complexes proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.
6S methyltransferase and RG-containing Sm proteins complex Gene Set From CORUM Protein Complexes proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.
Remodeling and spacing factor (RSF) complex Gene Set From CORUM Protein Complexes proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Nucleic and chromatin Fanconi complex Gene Set From CORUM Protein Complexes proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set From CORUM Protein Complexes proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.
20S methylosome and RG-containing Sm protein complex Gene Set From CORUM Protein Complexes proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
positive regulation of immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2015 dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
mitochondrial sorting and assembly machinery complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Neoplasms, Complex and Mixed Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Complex and Mixed phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mediator complex, subunit Med25, PTOV activation and synapsin 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mediator complex, subunit Med25, PTOV activation and synapsin 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
CST complex subunit Ten1, animal and plant type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the CST complex subunit Ten1, animal and plant type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Conserved oligomeric Golgi complex subunit 8, Metazoal and Viridiplantae Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Conserved oligomeric Golgi complex subunit 8, Metazoal and Viridiplantae protein domain from the InterPro Predicted Protein Domain Annotations dataset.
disassembly of the destruction complex and recruitment of AXIN to the membrane Gene Set From Reactome Pathways 2014 proteins participating in the disassembly of the destruction complex and recruitment of AXIN to the membrane pathway from the Reactome Pathways dataset.
Regulation of cytoskeletal remodeling and cell spreading by IPP complex components Gene Set From Reactome Pathways 2014 proteins participating in the Regulation of cytoskeletal remodeling and cell spreading by IPP complex components pathway from the Reactome Pathways dataset.
TAK1 activates NFkB by phosphorylation and activation of IKKs complex Gene Set From Reactome Pathways 2014 proteins participating in the TAK1 activates NFkB by phosphorylation and activation of IKKs complex pathway from the Reactome Pathways dataset.
Fibular Hypoplasia And Complex Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibular Hypoplasia And Complex Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bladder Exstrophy And Epispadias Complex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bladder Exstrophy And Epispadias Complex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2023 genes participating in the immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2023 dataset.
mRNA cleavage and polyadenylation specificity factor complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the mRNA cleavage and polyadenylation specificity factor complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
TCA cycle and deficiency of pyruvate dehydrogenase complex PDHc Gene Set From WikiPathways Pathways 2024 proteins participating in the TCA cycle and deficiency of pyruvate dehydrogenase complex PDHc pathway from the WikiPathways Pathways 2024 dataset.
Disassembly of the destruction complex and recruitment of AXIN to the membrane Gene Set From Reactome Pathways 2024 proteins participating in the Disassembly of the destruction complex and recruitment of AXIN to the membrane pathway from the Reactome Pathways 2024 dataset.
Regulation of cytoskeletal remodeling and cell spreading by IPP complex components Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of cytoskeletal remodeling and cell spreading by IPP complex components pathway from the Reactome Pathways 2024 dataset.
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 Gene Set From Reactome Pathways 2024 proteins participating in the Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 pathway from the Reactome Pathways 2024 dataset.
immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2025 genes participating in the immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of immune complex clearance by monocytes and macrophages Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of immune complex clearance by monocytes and macrophages biological process from the curated GO Biological Process Annotations 2025 dataset.
mRNA cleavage and polyadenylation specificity factor complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the mRNA cleavage and polyadenylation specificity factor complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fibular hypoplasia and complex brachydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
mRNA cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the mRNA cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
mRNA cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the mRNA cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Nuclear pore complex and nucleocytoplasmic transport Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Nuclear pore complex and nucleocytoplasmic transport assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Protein folding and complex assembly regulation Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein folding and complex assembly regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
DNA repair and telomere maintenance complex Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising DNA repair and telomere maintenance complex assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Protein quality control and DNA repair complex Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control and DNA repair complex assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
mRNA cleavage and polyadenylation specificity factor complex Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising mRNA cleavage and polyadenylation specificity factor complex assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
THO complex and transcription export Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising THO complex and transcription export assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
proteasome core complex, alpha-subunit complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proteasome core complex, alpha-subunit complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
tho complex part of transcription export complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the tho complex part of transcription export complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
light-harvesting complex, core complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the light-harvesting complex, core complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
light-harvesting complex, peripheral complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
ORC 2-5 complex (origin recognition 2-5 complex) Gene Set From CORUM Protein Complexes proteins in the ORC 2-5 complex (origin recognition 2-5 complex) protein complex from the CORUM Protein Complexes dataset.
ORC 1-5 complex (origin recognition 1-5 complex) Gene Set From CORUM Protein Complexes proteins in the ORC 1-5 complex (origin recognition 1-5 complex) protein complex from the CORUM Protein Complexes dataset.
MRN complex (MRE11-RAD50-NBS1 complex) Gene Set From CORUM Protein Complexes proteins in the MRN complex (MRE11-RAD50-NBS1 complex) protein complex from the CORUM Protein Complexes dataset.
Exon junction complex (EIF4A3-MLN51-MAGOH-Y14), RNA-protein complex Gene Set From CORUM Protein Complexes proteins in the Exon junction complex (EIF4A3-MLN51-MAGOH-Y14), RNA-protein complex protein complex from the CORUM Protein Complexes dataset.
PHAX-CBC complex (cap binding complex) Gene Set From CORUM Protein Complexes proteins in the PHAX-CBC complex (cap binding complex) protein complex from the CORUM Protein Complexes dataset.
RFC complex (activator A 1 complex) Gene Set From CORUM Protein Complexes proteins in the RFC complex (activator A 1 complex) protein complex from the CORUM Protein Complexes dataset.
TFTC complex (TATA-binding protein-free TAF-II-containing complex) Gene Set From CORUM Protein Complexes proteins in the TFTC complex (TATA-binding protein-free TAF-II-containing complex) protein complex from the CORUM Protein Complexes dataset.
hs4 enhancer complex (slow migrating complex) Gene Set From CORUM Protein Complexes proteins in the hs4 enhancer complex (slow migrating complex) protein complex from the CORUM Protein Complexes dataset.
CF IIAm complex (Cleavage factor IIAm complex) Gene Set From CORUM Protein Complexes proteins in the CF IIAm complex (Cleavage factor IIAm complex) protein complex from the CORUM Protein Complexes dataset.
NELF complex (Negative elongation factor complex) Gene Set From CORUM Protein Complexes proteins in the NELF complex (Negative elongation factor complex) protein complex from the CORUM Protein Complexes dataset.
NUMAC complex (nucleosomal methylation activator complex) Gene Set From CORUM Protein Complexes proteins in the NUMAC complex (nucleosomal methylation activator complex) protein complex from the CORUM Protein Complexes dataset.
Exon junction complex, EIF4A3-MLN51-MAGOH-Y14 (RNA-protein complex) Gene Set From CORUM Protein Complexes proteins in the Exon junction complex, EIF4A3-MLN51-MAGOH-Y14 (RNA-protein complex) protein complex from the CORUM Protein Complexes dataset.
FA core complex (Fanconi anemia core complex) Gene Set From CORUM Protein Complexes proteins in the FA core complex (Fanconi anemia core complex) protein complex from the CORUM Protein Complexes dataset.
STAGA core complex (SPT3-TAF9-GCN5 acetyltransferase complex) Gene Set From CORUM Protein Complexes proteins in the STAGA core complex (SPT3-TAF9-GCN5 acetyltransferase complex) protein complex from the CORUM Protein Complexes dataset.
RNA polymerase II complex, incomplete (CDK8 complex), chromatin structure modifying Gene Set From CORUM Protein Complexes proteins in the RNA polymerase II complex, incomplete (CDK8 complex), chromatin structure modifying protein complex from the CORUM Protein Complexes dataset.
RC complex (Replication competent complex) Gene Set From CORUM Protein Complexes proteins in the RC complex (Replication competent complex) protein complex from the CORUM Protein Complexes dataset.
R/M complex (RAD50-MRE11 complex) Gene Set From CORUM Protein Complexes proteins in the R/M complex (RAD50-MRE11 complex) protein complex from the CORUM Protein Complexes dataset.
hs4 enhancer complex (faster migrating complex) Gene Set From CORUM Protein Complexes proteins in the hs4 enhancer complex (faster migrating complex) protein complex from the CORUM Protein Complexes dataset.
MRN complex (MRE11-RAD50-NBN complex) Gene Set From CORUM Protein Complexes proteins in the MRN complex (MRE11-RAD50-NBN complex) protein complex from the CORUM Protein Complexes dataset.
CRM1-RAN-PHAX-CBC complex (cap binding complex) Gene Set From CORUM Protein Complexes proteins in the CRM1-RAN-PHAX-CBC complex (cap binding complex) protein complex from the CORUM Protein Complexes dataset.
DJ-1-SNCA complex, high molecular weight complex Gene Set From CORUM Protein Complexes proteins in the DJ-1-SNCA complex, high molecular weight complex protein complex from the CORUM Protein Complexes dataset.
ORC complex (origin recognition complex) Gene Set From CORUM Protein Complexes proteins in the ORC complex (origin recognition complex) protein complex from the CORUM Protein Complexes dataset.
DNA ligase IV-XRCC4 complex (LX complex) Gene Set From CORUM Protein Complexes proteins in the DNA ligase IV-XRCC4 complex (LX complex) protein complex from the CORUM Protein Complexes dataset.
Cdk5/p35 complex (Cdk5-Cdk5r1 complex) Gene Set From CORUM Protein Complexes proteins in the Cdk5/p35 complex (Cdk5-Cdk5r1 complex) protein complex from the CORUM Protein Complexes dataset.
Nucleolar remodeling complex (NoRC complex) Gene Set From CORUM Protein Complexes proteins in the Nucleolar remodeling complex (NoRC complex) protein complex from the CORUM Protein Complexes dataset.
SAP complex (Sin3-associated protein complex) Gene Set From CORUM Protein Complexes proteins in the SAP complex (Sin3-associated protein complex) protein complex from the CORUM Protein Complexes dataset.
FA core complex 1 (Fanconi anemia core complex 1) Gene Set From CORUM Protein Complexes proteins in the FA core complex 1 (Fanconi anemia core complex 1) protein complex from the CORUM Protein Complexes dataset.
STAGA complex (SPT3-TAF9-GCN5 acetyltransferase complex) Gene Set From CORUM Protein Complexes proteins in the STAGA complex (SPT3-TAF9-GCN5 acetyltransferase complex) protein complex from the CORUM Protein Complexes dataset.
DSIF complex (DRB sensitivity-inducing factor complex) Gene Set From CORUM Protein Complexes proteins in the DSIF complex (DRB sensitivity-inducing factor complex) protein complex from the CORUM Protein Complexes dataset.
TLE1 corepressor complex (MASH1 promoter-corepressor complex) Gene Set From CORUM Protein Complexes proteins in the TLE1 corepressor complex (MASH1 promoter-corepressor complex) protein complex from the CORUM Protein Complexes dataset.
CCT complex (chaperonin containing TCP1 complex) Gene Set From CORUM Protein Complexes proteins in the CCT complex (chaperonin containing TCP1 complex) protein complex from the CORUM Protein Complexes dataset.
MRN-TRRAP complex (MRE11A-RAD50-NBN-TRRAP complex) Gene Set From CORUM Protein Complexes proteins in the MRN-TRRAP complex (MRE11A-RAD50-NBN-TRRAP complex) protein complex from the CORUM Protein Complexes dataset.
LARC complex (LCR-associated remodeling complex) Gene Set From CORUM Protein Complexes proteins in the LARC complex (LCR-associated remodeling complex) protein complex from the CORUM Protein Complexes dataset.
CERF complex (CECR2-containing remodeling factor complex) Gene Set From CORUM Protein Complexes proteins in the CERF complex (CECR2-containing remodeling factor complex) protein complex from the CORUM Protein Complexes dataset.
FA complex (Fanconi anemia complex), cytoplasmic Gene Set From CORUM Protein Complexes proteins in the FA complex (Fanconi anemia complex), cytoplasmic protein complex from the CORUM Protein Complexes dataset.
CCT complex (chaperonin containing TCP1 complex), testis specific Gene Set From CORUM Protein Complexes proteins in the CCT complex (chaperonin containing TCP1 complex), testis specific protein complex from the CORUM Protein Complexes dataset.
FA complex (Fanconi anemia complex) Gene Set From CORUM Protein Complexes proteins in the FA complex (Fanconi anemia complex) protein complex from the CORUM Protein Complexes dataset.
CAK complex (Cdk-activating kinase complex) Gene Set From CORUM Protein Complexes proteins in the CAK complex (Cdk-activating kinase complex) protein complex from the CORUM Protein Complexes dataset.
Chromatin assembly complex (CAF-1 complex) Gene Set From CORUM Protein Complexes proteins in the Chromatin assembly complex (CAF-1 complex) protein complex from the CORUM Protein Complexes dataset.
CAK core complex (Cdk-activating kinase core complex) Gene Set From CORUM Protein Complexes proteins in the CAK core complex (Cdk-activating kinase core complex) protein complex from the CORUM Protein Complexes dataset.
CBC complex (cap binding complex) Gene Set From CORUM Protein Complexes proteins in the CBC complex (cap binding complex) protein complex from the CORUM Protein Complexes dataset.
ORC 2-4 complex (origin recognition 2-4 complex) Gene Set From CORUM Protein Complexes proteins in the ORC 2-4 complex (origin recognition 2-4 complex) protein complex from the CORUM Protein Complexes dataset.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.
aids dementia complex; aids related dementia complex Gene Set From GAD Gene-Disease Associations genes associated with the disease aids dementia complex; aids related dementia complex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proteasome core complex, alpha-subunit complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the proteasome core complex, alpha-subunit complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
tho complex part of transcription export complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the tho complex part of transcription export complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
ATPase, F1 complex beta subunit/V1 complex, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ATPase, F1 complex beta subunit/V1 complex, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
mitochondrial respiratory chain complex II, succinate dehydrogenase complex (ubiquinone) Gene Set From GO Cellular Component Annotations 2023 proteins localized to the mitochondrial respiratory chain complex II, succinate dehydrogenase complex (ubiquinone) cellular component from the curated GO Cellular Component Annotations 2023 dataset.
THO complex part of transcription export complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the THO complex part of transcription export complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
core TFIIH complex portion of holo TFIIH complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the core TFIIH complex portion of holo TFIIH complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
TRAF6-mediated induction of TAK1 complex within TLR4 complex Gene Set From Reactome Pathways 2024 proteins participating in the TRAF6-mediated induction of TAK1 complex within TLR4 complex pathway from the Reactome Pathways 2024 dataset.
THO complex part of transcription export complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the THO complex part of transcription export complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
core TFIIH complex portion of holo TFIIH complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the core TFIIH complex portion of holo TFIIH complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
THO complex part of transcription export complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the THO complex part of transcription export complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Core TFIIH complex portion of holo TFIIH complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Core TFIIH complex portion of holo TFIIH complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Proteasome core complex, alpha-subunit complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proteasome core complex, alpha-subunit complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Proteasome core complex, beta-subunit complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proteasome core complex, beta-subunit complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Mitochondrial respiratory chain complex II, succinate dehydrogenase complex (ubiquinone) Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial respiratory chain complex II, succinate dehydrogenase complex (ubiquinone) cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
light-harvesting complex, peripheral complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
light-harvesting complex, core complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the light-harvesting complex, core complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Proteasome core complex, beta-subunit complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proteasome core complex, beta-subunit complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
THO complex part of transcription export complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the THO complex part of transcription export complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Proteasome core complex, alpha-subunit complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proteasome core complex, alpha-subunit complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multicentric osteolysis, nodulosis and arthropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy dilated with woolly hair and keratoderma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone fragility with contractures, arterial rupture, and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor v and factor viii, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary Paragangliomas and Pheochromocytomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Band-like calcification with simplified gyration and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Monocyte and dendritic cell deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined malonic and methylmalonic aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis Gyrata syndrome of Beare and Stevenson Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniosynostosis and dental anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebroretinal microangiopathy with calcifications and cysts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, normal intelligence and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Calcification of joints and arteries Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pineal hyperplasia AND diabetes mellitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Morbid obesity and spermatogenic failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of factor V and factor VIII, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Camptodactyly, tall stature, and hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth deficiency and mental retardation with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, cochlear, with myopia and intellectual impairment Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of sialidase AND beta galactosidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Cleavage and polyadenylation factor (CPSF) Gene Set From CORUM Protein Complexes proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.
Amino Acids, Peptides, and Proteins Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.
Bile Acids and Salts Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.
Prime and Bond NT Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.
drospirenone and ethinyl estradiol combination Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.
Hypophosphatemic Rickets And Hyperparathyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.
Synovitis granulomatous with uveitis and cranial neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.
Combined Cellular And Humoral Immune Defects With Granulomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.
Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.
Craniosynostosis, anal anomalies, and porokeratosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.
Classical Lissencephalies and Subcortical Band Heterotopias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Russe type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.
Hypotrichosis And Recurrent Skin Vesicles Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.
Signs and Symptoms, Digestive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset.
Head and Neck Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Cataract, Juvenile, With Microcornea And Glucosuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous and Mucosal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.
Postoperative Nausea and Vomiting Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and 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 Set From 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, And Dysequilibrium Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.
Hypopituitarism and septooptic 'dysplasia' Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set From 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, And Muscle Cramps Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset.
Aplasia of Lacrimal and Salivary Glands Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set From 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, And Sperm Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set From 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 and Isosthenuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.
Calcification of Joints and Arteries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset.
CHOANAL ATRESIA AND LYMPHEDEMA Gene Set From 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, and Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.
Asthma, Nasal Polyps, And Aspirin Intolerance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset.
Neoplasms, Germ Cell and Embryonal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.
Cutis Gyrata Syndrome of Beare And Stevenson Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From 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 Set From 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 Set From 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 and Injuries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wounds and Injuries from the curated CTD Gene-Disease Associations dataset.
Schizophrenia and Disorders with Psychotic Features Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblF Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset.
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Cataract and cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene Set From 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 Set From 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 and sensory, Okinawa type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.
Hereditary Breast and Ovarian Cancer Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset.
Keratosis palmoplantaris with periodontopathia and onychogryposis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia and onychogryposis from the curated CTD Gene-Disease Associations dataset.
Intracranial Embolism and Thrombosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset.
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set From 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, And Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene Set From 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 And Eye Coloboma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset.
Nevi and Melanomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nevi and Melanomas from the curated CTD Gene-Disease Associations dataset.
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Attention Deficit and Disruptive Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit and Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy dilated with Woolly hair and keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset.
Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From 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, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset.
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set From 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 and Hyperandrogenism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Esophageal and Gastric Varices Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal and Gastric Varices from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set From 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 and Isolated growth hormone deficiency, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.
Carcinoma, squamous cell of head and neck Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, squamous cell of head and neck from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.
Extravasation of Diagnostic and Therapeutic Materials Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Extravasation of Diagnostic and Therapeutic Materials from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Knuckle pads, leuconychia and sensorineural deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Knuckle pads, leuconychia and sensorineural deafness from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset.
Hyperekplexia and Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.
Iris hypoplasia and glaucoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset.
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set From 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 and Fraumeni Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma family syndrome of Li and Fraumeni from the curated CTD Gene-Disease Associations dataset.
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set From 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 and Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy with Pretibial Epidermolysis Bullosa and Deafness from the curated CTD Gene-Disease Associations dataset.
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.
Lipoid Proteinosis of Urbach and Wiethe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid Proteinosis of Urbach and Wiethe from the curated CTD Gene-Disease Associations dataset.
Hypertelorism with esophageal abnormality and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset.
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset.
Jervell And Lange-Nielsen Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jervell And Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Neoplasms, Glandular and Epithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Glandular and Epithelial from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.
Pyogenic arthritis, pyoderma gangrenosum, and acne Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyogenic arthritis, pyoderma gangrenosum, and acne from the curated CTD Gene-Disease Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
Cleft Palate, Isolated, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Absent radii and thrombocytopenia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Absent radii and thrombocytopenia from the curated CTD Gene-Disease Associations dataset.
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene Set From 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 and Digital Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset.
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.
STAPES ANKYLOSIS WITH BROAD THUMB AND TOES Gene Set From 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, And Urinary Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities from the curated CTD Gene-Disease Associations dataset.
Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and 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, and Autoimmunity Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity from the curated CTD Gene-Disease Associations dataset.
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Signs and Symptoms, Respiratory Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Respiratory from the curated CTD Gene-Disease Associations dataset.
Renal cysts and diabetes syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, LOM type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, LOM type from the curated CTD Gene-Disease Associations dataset.
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor from the curated CTD Gene-Disease Associations dataset.
Hereditary Angioedema Types I and II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Types I and II from the curated CTD Gene-Disease Associations dataset.
Drug-Related Side Effects and Adverse Reactions Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Drug-Related Side Effects and Adverse Reactions from the curated CTD Gene-Disease Associations dataset.
Insect Bites and Stings Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insect Bites and Stings from the curated CTD Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.
Foveal Hypoplasia and Anterior Segment Dysgenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.
Cubitus Valgus with Mental Retardation and Unusual Facies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cubitus Valgus with Mental Retardation and Unusual Facies from the curated CTD Gene-Disease Associations dataset.
Ophthalmoplegia, External, and Myopia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, External, and Myopia from the curated CTD Gene-Disease Associations dataset.
Deafness, Sensorineural, And Male Infertility Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Sensorineural, And Male Infertility from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Autonomic Neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Autonomic Neuropathies from the curated CTD Gene-Disease Associations dataset.
Histiocytosis with joint contractures and sensorineural deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytosis with joint contractures and sensorineural deafness from the curated CTD Gene-Disease Associations dataset.
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.
Leiomyomatosis, esophageal and vulval, with nephropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leiomyomatosis, esophageal and vulval, with nephropathy from the curated CTD Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations dataset.
Embolism and Thrombosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset.
Religion and Psychology Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Religion and Psychology in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Attention Deficit and Disruptive Behavior Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Attention Deficit and Disruptive Behavior Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Body Weights and Measures Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Body Weights and Measures in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Nevi and Melanomas Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Nevi and Melanomas in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Head and Neck Neoplasms Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Head and Neck Neoplasms in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
blepharophimosis, ptosis, and epicanthus inversus syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease blepharophimosis, ptosis, and epicanthus inversus syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
degeneration of macula and posterior pole Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
eye and adnexa disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye and adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
combined t cell and b cell immunodeficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease combined t cell and b cell immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
eye and adnexa disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye and adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
inflammatory and toxic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inflammatory and toxic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mucinous tubular and spindle renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mucinous tubular and spindle renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pustulosis of palm and sole Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pustulosis of palm and sole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hand, foot and mouth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth and nail syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth and nail syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extrapyramidal and movement disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrapyramidal and movement disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mononeuritis of upper limb and mononeuritis multiplex Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung mixed small cell and squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autoimmune disease of skin and connective tissue Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
histiocytic and dendritic cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease histiocytic and dendritic cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
methylmalonic aciduria and homocystinuria type cblc Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease methylmalonic aciduria and homocystinuria type cblc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
blepharophimosis, ptosis, and epicanthus inversus syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease blepharophimosis, ptosis, and epicanthus inversus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
germ cell and embryonal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease germ cell and embryonal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed endometrial stromal and smooth muscle tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal canal and spinal cord meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal canal and spinal cord meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian germ cell monodermal and highly specialized teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian germ cell monodermal and highly specialized teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
degeneration of macula and posterior pole Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
combined t cell and b cell immunodeficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease combined t cell and b cell immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mature t-cell and nk-cell lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mature t-cell and nk-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eye and adnexa disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye and adnexa disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
breast and lung cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease breast and lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased chromosome aberrations and higher lung cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease increased chromosome aberrations and higher lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyper-ige syndrome and severe eczema. atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease hyper-ige syndrome and severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
factor viii and factor ix genes Gene Set From GAD Gene-Disease Associations genes associated with the disease factor viii and factor ix genes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
flecainide and paroxetine Gene Set From GAD Gene-Disease Associations genes associated with the disease flecainide and paroxetine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pre-term delivery infant mortality and malaria morbidity Gene Set From GAD Gene-Disease Associations genes associated with the disease pre-term delivery infant mortality and malaria morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alopecia and lumbar herniated disk Gene Set From GAD Gene-Disease Associations genes associated with the disease alopecia and lumbar herniated disk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
baroreflex and blood pressure regulation Gene Set From GAD Gene-Disease Associations genes associated with the disease baroreflex and blood pressure regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, hereditary motor and sensory Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, hereditary motor and sensory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psoriasis, psoriatic arthritis, and sapho syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease psoriasis, psoriatic arthritis, and sapho syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
platelet reactivity and clopidogrel resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease platelet reactivity and clopidogrel resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients Gene Set From GAD Gene-Disease Associations genes associated with the disease low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jervell and lange-nielsen syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease jervell and lange-nielsen syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anovulation and fecundity Gene Set From GAD Gene-Disease Associations genes associated with the disease anovulation and fecundity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proteinuria and cardiovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease proteinuria and cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thyroid and neurological abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease thyroid and neurological abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
homocysteine, folate and vitamin b12 levels Gene Set From GAD Gene-Disease Associations genes associated with the disease homocysteine, folate and vitamin b12 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension and obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension and obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
child hyperactivity-impulsivity and oppositional behaviors Gene Set From GAD Gene-Disease Associations genes associated with the disease child hyperactivity-impulsivity and oppositional behaviors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma and atopy Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma and atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv-rna and cellular hiv-dna levels Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv-rna and cellular hiv-dna levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin release and insulin sensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin release and insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip bone loss and fracture Gene Set From GAD Gene-Disease Associations genes associated with the disease hip bone loss and fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
risperidone and perospirone Gene Set From GAD Gene-Disease Associations genes associated with the disease risperidone and perospirone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infectious risk and outcome in surgical intensive care patients Gene Set From GAD Gene-Disease Associations genes associated with the disease infectious risk and outcome in surgical intensive care patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip and palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip and palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
reduced muscle mrna levels and insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease reduced muscle mrna levels and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemostatic factors and hematological phenotypes Gene Set From GAD Gene-Disease Associations genes associated with the disease hemostatic factors and hematological phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
reduced gene expression and lower plasma levels of beta2-glycoprotein i Gene Set From GAD Gene-Disease Associations genes associated with the disease reduced gene expression and lower plasma levels of beta2-glycoprotein i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarche and menopause (age at onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease menarche and menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; shock, septic; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; head and neck neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; head and neck neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adiposity and abdominal obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease adiposity and abdominal obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast and carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease breast and carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tropical pancreatitis and type ii diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease tropical pancreatitis and type ii diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polymyositis and dermatomyositis. Gene Set From GAD Gene-Disease Associations genes associated with the disease polymyositis and dermatomyositis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; neoplasms, squamous cell Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasms, squamous cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; atopy; dermatitis and eczema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; atopy; dermatitis and eczema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-syndromic cleft lip and palate Gene Set From GAD Gene-Disease Associations genes associated with the disease non-syndromic cleft lip and palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
postoperative nausea and vomiting Gene Set From GAD Gene-Disease Associations genes associated with the disease postoperative nausea and vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
calcium homeostasis and peripheral bone density Gene Set From GAD Gene-Disease Associations genes associated with the disease calcium homeostasis and peripheral bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal adenomatous polyps and adenocarcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal adenomatous polyps and adenocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin and homa levels Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin and homa levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
financial and psychological risk attitudes Gene Set From GAD Gene-Disease Associations genes associated with the disease financial and psychological risk attitudes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mother and child behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease mother and child behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rna expression of carboxylesterases 1 and 2. Gene Set From GAD Gene-Disease Associations genes associated with the disease rna expression of carboxylesterases 1 and 2. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cigarette smoking behavior and reward Gene Set From GAD Gene-Disease Associations genes associated with the disease cigarette smoking behavior and reward in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
serum estrogen and progesterone concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease serum estrogen and progesterone concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
quantitative variation in lipid and lipoprotein traits Gene Set From GAD Gene-Disease Associations genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chiari type i malformation and syringomyelia Gene Set From GAD Gene-Disease Associations genes associated with the disease chiari type i malformation and syringomyelia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hunger and satiety Gene Set From GAD Gene-Disease Associations genes associated with the disease hunger and satiety in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate and calvaria defects. Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate and calvaria defects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung cancer susceptibility and prognosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer susceptibility and prognosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophic cardiomyopathy and cytochrome c oxidase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophic cardiomyopathy and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endometriosis; neoplasms, glandular and epithelial; ovarian neoplasm; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease endometriosis; neoplasms, glandular and epithelial; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung cancer; colorectal cancer; esophageal cancer; head and neck cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; head and neck cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proximal chromosome 9p to q and distal chromosome 9q Gene Set From GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
loperamide disposition and central nervous system effects. Gene Set From GAD Gene-Disease Associations genes associated with the disease loperamide disposition and central nervous system effects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cutaneous and uterine leiomyomata Gene Set From GAD Gene-Disease Associations genes associated with the disease cutaneous and uterine leiomyomata in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyper-igm syndrome can form oligomers and trigger cd40-mediated signals Gene Set From GAD Gene-Disease Associations genes associated with the disease hyper-igm syndrome can form oligomers and trigger cd40-mediated signals in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major and bipolar depressives Gene Set From GAD Gene-Disease Associations genes associated with the disease major and bipolar depressives in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma glucose, basal hepatic glucose and increased insulin release Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leigh syndrome and cytochrome c oxidase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease leigh syndrome and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrence and early onset of venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrence and early onset of venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
normal and arrhythmia Gene Set From GAD Gene-Disease Associations genes associated with the disease normal and arrhythmia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fasting total cholesterol and ldl-cholesterol concentrations only Gene Set From GAD Gene-Disease Associations genes associated with the disease fasting total cholesterol and ldl-cholesterol concentrations only in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetically deficient metabolism of debrisoquine and other drugs Gene Set From GAD Gene-Disease Associations genes associated with the disease genetically deficient metabolism of debrisoquine and other drugs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nevi and melanomas Gene Set From GAD Gene-Disease Associations genes associated with the disease nevi and melanomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aberrant promoter methylation of p16(ink4a) and o(6)-methylguanine-dna methyltransferase Gene Set From GAD Gene-Disease Associations genes associated with the disease aberrant promoter methylation of p16(ink4a) and o(6)-methylguanine-dna methyltransferase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms, germ cell and embryonal; seminoma Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms, germ cell and embryonal; seminoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile lipid composition and cholesterol gallstone Gene Set From GAD Gene-Disease Associations genes associated with the disease bile lipid composition and cholesterol gallstone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ptx3 production and fertility Gene Set From GAD Gene-Disease Associations genes associated with the disease ptx3 production and fertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
low insulin and cholesterol levels Gene Set From GAD Gene-Disease Associations genes associated with the disease low insulin and cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amygdalar and hippocampal volumes Gene Set From GAD Gene-Disease Associations genes associated with the disease amygdalar and hippocampal volumes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
medical history histopathology and environmental exposures Gene Set From GAD Gene-Disease Associations genes associated with the disease medical history histopathology and environmental exposures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age and adiposity Gene Set From GAD Gene-Disease Associations genes associated with the disease age and adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depression, psychosis and antipsychotic response Gene Set From GAD Gene-Disease Associations genes associated with the disease depression, psychosis and antipsychotic response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute and chronic kidney transplant outcome Gene Set From GAD Gene-Disease Associations genes associated with the disease acute and chronic kidney transplant outcome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma high density lipoprotein cholesterol and apolipoprotein ai Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma high density lipoprotein cholesterol and apolipoprotein ai in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; carcinoma, papillary; carcinoma, papillary, follicular; papillary and follicular adenocarcinoma; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; carcinoma, papillary; carcinoma, papillary, follicular; papillary and follicular adenocarcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
type ii diabetes and hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease type ii diabetes and hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
verbal and figural creative achievement Gene Set From GAD Gene-Disease Associations genes associated with the disease verbal and figural creative achievement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; pneumonia, ventilator-associated; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; pneumonia, ventilator-associated; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar and unipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar and unipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weights and measures Gene Set From GAD Gene-Disease Associations genes associated with the disease body weights and measures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreases transcriptional activity and responsiveness to interleukin-6 Gene Set From GAD Gene-Disease Associations genes associated with the disease decreases transcriptional activity and responsiveness to interleukin-6 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction and stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction and stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
estrogen and estrogen/testosterone ratio Gene Set From GAD Gene-Disease Associations genes associated with the disease estrogen and estrogen/testosterone ratio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lead and mercury metabolism Gene Set From GAD Gene-Disease Associations genes associated with the disease lead and mercury metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tumour kinetics and chromosomal instability Gene Set From GAD Gene-Disease Associations genes associated with the disease tumour kinetics and chromosomal instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasma total homocysteine and folate concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease plasma total homocysteine and folate concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
growth hormone secretion and height Gene Set From GAD Gene-Disease Associations genes associated with the disease growth hormone secretion and height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
free thyroxine and triiodothyronine Gene Set From GAD Gene-Disease Associations genes associated with the disease free thyroxine and triiodothyronine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit and disruptive behavior disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit and disruptive behavior disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary and sporadic prostate cancer risk. Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary and sporadic prostate cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; neoplasm metastasis; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasm metastasis; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased serum iron transferrin saturation and hemoglobin Gene Set From GAD Gene-Disease Associations genes associated with the disease increased serum iron transferrin saturation and hemoglobin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
serum lipoprotein lipid and apolipoprotein levels Gene Set From GAD Gene-Disease Associations genes associated with the disease serum lipoprotein lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder and conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder and conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal neoplasms; esophageal neoplasms; head and neck neoplasms; lung neoplasms; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; esophageal neoplasms; head and neck neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acid lipase deficiency and cholesterol ester storage disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acid lipase deficiency and cholesterol ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete androgen insensitivity syndrome and sertoli cell adenoma Gene Set From GAD Gene-Disease Associations genes associated with the disease complete androgen insensitivity syndrome and sertoli cell adenoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; infection of amniotic sac and membranes Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
two major non-ribosomal nucleolar proteins and its implication Gene Set From GAD Gene-Disease Associations genes associated with the disease two major non-ribosomal nucleolar proteins and its implication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cores and rods is associated Gene Set From GAD Gene-Disease Associations genes associated with the disease cores and rods is associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease and ibd Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease and ibd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
circulating protein c levels and thrombotic risk Gene Set From GAD Gene-Disease Associations genes associated with the disease circulating protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
reduced serum c-peptide and insulin responses to an oral glucose challenge Gene Set From GAD Gene-Disease Associations genes associated with the disease reduced serum c-peptide and insulin responses to an oral glucose challenge in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
critical illness; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar medulloblastomas and cutaneous basal cell carcinomas. Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar medulloblastomas and cutaneous basal cell carcinomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic intoxication; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic intoxication; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck squamous cell cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck squamous cell cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatic iron and fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatic iron and fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Harmonizome 3.0

BRISC and BRCA1-A complex member 1 Gene Set

brisc complex Gene Set

brisc complex Gene Set

brisc complex Gene Set

FAM175 family, BRISC complex, Abro1 subunit Gene Set

BRISC complex Gene Set

BRISC complex Gene Set

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

BASC (Ab 80) complex (BRCA1-associated genome surveillance complex) Gene Set

BASC (Ab C-20) complex (BRCA1-associated genome surveillance complex) Gene Set

BASC (Ab 81) complex (BRCA1-associated genome surveillance complex) Gene Set

BASC complex (BRCA1-associated genome surveillance complex) Gene Set

role of brca1 brca2 and atr in cancer susceptibility Gene Set

brca1-bard1 complex Gene Set

brca1-a complex Gene Set

brca1-bard1 complex Gene Set

brca1-b complex Gene Set

brca1-c complex Gene Set

brca1-a complex Gene Set

BRCA1-BARD1-BACH1-DNA damage complex II Gene Set

BRCA1-BACH1 complex Gene Set

BRCA1 A complex Gene Set

BRCA1-core RNA polymerase II complex Gene Set

LMO4-BRCA1-CTIP-LDB1 complex Gene Set

BRCA1 C complex Gene Set

BRCA1-BARD1-BRCA2-DNA damage complex III Gene Set

BRCA1-CTIP-ZBRK1 repressor complex Gene Set

BRCA1-VCP complex Gene Set

BRCA1-RAD50-MRE11-NBS1 complex Gene Set

RAD50-BRCA1 complex Gene Set

BRCA1-IRIS-pre-replication complex Gene Set

BRCA1-CtIP-CtBP complex Gene Set

BARD1-BRCA1-CSTF complex Gene Set

BRCA1 B complex Gene Set

BRCA1-BARD1-BACH1-DNA damage complex I Gene Set

SWI-SNF chromatin remodeling-related-BRCA1 complex Gene Set

BRCA1-LMO4-CTIP complex Gene Set

BRCA1-HDAC1-HDAC2 complex Gene Set

BRCA1-RNA polymerase II complex Gene Set

BRCA1-BARD1-POLR2A complex Gene Set

BRCA1-SMAD3 complex Gene Set

BRCA1-cABL complex Gene Set

BRCA1-RAD51 complex Gene Set

BARD1-BRCA1-CSTF64 complex Gene Set

BRCA1-BARD1-UbcH5c complex Gene Set

BRCA1-BARD1-UbcH7c complex Gene Set

brca1-bard1 complex Gene Set

brca1-a complex Gene Set

FAM175 family, BRCA1-A complex, Abraxas subunit Gene Set

BRCA1-BARD1 complex Gene Set

BRCA1-BARD1 complex Gene Set

BRCA1-A complex Gene Set

BRCA1-BARD1 complex Gene Set

BRCA1-C complex Gene Set

BRCA1-B complex Gene Set

BRCA1-A complex Gene Set

BRCA1-BARD1 complex Gene Set

BRCA1-C complex Gene Set

BRCA1-B complex Gene Set

BRCA1-Rad51 complex Gene Set

brca1 dependent ub ligase activity Gene Set

BRCA1 Gene Set

germline brca1 mutation Gene Set

genotyping of frequent brca1/2 snps Gene Set

brca1 Gene Set

Ovarian cancer in BRCA1 mutation carriers Gene Set

Breast Cancer in BRCA1 mutation carriers Gene Set

BRCA1 Gene Set

BRCA1-associated 2 Gene Set

Breast cancer type 1 susceptibility protein (BRCA1) Gene Set

BRCA1, serine-rich domain Gene Set

Cofactor of BRCA1 Gene Set

BRCA1 Gene Set

BRCA1 Gene Set

SC-6954 (BRCA1) Gene Set

AB80 (BRCA1) Gene Set

AB81 (BRCA1) Gene Set

BRCA1 Gene Set

BRCA1 Gene Set