Name

dynein arm defect of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal central microtubular pair morphology of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal axonemal organization of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent respiratory motile cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent respiratory motile cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased respiratory motile cilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased respiratory motile cilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

outer dynein arm Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the outer dynein arm cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

inner dynein arm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the inner dynein arm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

outer dynein arm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the outer dynein arm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

outer dynein arm assembly Gene Set

From GO Biological Process Annotations

genes participating in the outer dynein arm assembly biological process from the curated GO Biological Process Annotations dataset.

inner dynein arm assembly Gene Set

From GO Biological Process Annotations

genes participating in the inner dynein arm assembly biological process from the curated GO Biological Process Annotations dataset.

outer dynein arm Gene Set

From GO Cellular Component Annotations

proteins localized to the outer dynein arm cellular component from the curated GO Cellular Component Annotations dataset.

absent brain ependyma motile cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent brain ependyma motile cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal respiratory motile cilium morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory motile cilium physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory motile cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory motile cilium number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory motile cilium number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ciliary dyskinesias; ciliary motility disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ciliary dyskinesias; ciliary motility disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory insufficiency due to defective ciliary clearance Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

immotile respiratory cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the immotile respiratory cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

arm Gene Set

From GeneRIF Biological Term Annotations

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

abnormality of the upper arm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

mesomelic arm shortening Gene Set

From HPO Gene-Disease Associations

genes associated with the mesomelic arm shortening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of the arm Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of the arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tRNA-binding arm Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the tRNA-binding arm protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ku70/Ku80 C-terminal arm Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ku70/Ku80 C-terminal arm protein domain from the InterPro Predicted Protein Domain Annotations dataset.

arm Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue arm in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

asthma; recurrence; respiratory sounds; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; recurrence; respiratory sounds; respiratory syncytial virus infections 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.

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.

respiratory syncytial virus infections; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, adult; respiratory insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, adult; respiratory insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; respiratory hypersensitivity; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; respiratory hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

motile primary cilium Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the motile primary cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

motile cilium Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the motile cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

motile primary cilium Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the motile primary cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

motile cilium Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the motile cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

motile Gene Set

From GeneRIF Biological Term Annotations

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

motile cilium assembly Gene Set

From GO Biological Process Annotations

genes participating in the motile cilium assembly biological process from the curated GO Biological Process Annotations dataset.

motile primary cilium Gene Set

From GO Cellular Component Annotations

proteins localized to the motile primary cilium cellular component from the curated GO Cellular Component Annotations dataset.

motile cilium Gene Set

From GO Cellular Component Annotations

proteins localized to the motile cilium cellular component from the curated GO Cellular Component Annotations dataset.

abnormal motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal motile primary cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal motile primary cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal motile primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ependyma motile cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ependyma motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ependyma motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent oviduct epithelium motile cilium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent oviduct epithelium motile cilium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal motile cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ependyma motile cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal oviduct epithelium motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal oviduct epithelium motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ependyma motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ependyma motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dynein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the dynein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

axonemal dynein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the axonemal dynein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cytoplasmic dynein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic dynein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

dynein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the dynein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

axonemal dynein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the axonemal dynein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cytoplasmic dynein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cytoplasmic dynein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

dynein Gene Set

From GeneRIF Biological Term Annotations

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

axonemal dynein complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the axonemal dynein complex assembly biological process from the curated GO Biological Process Annotations dataset.

dynein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the dynein complex cellular component from the curated GO Cellular Component Annotations dataset.

axonemal dynein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the axonemal dynein complex cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic dynein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic dynein complex cellular component from the curated GO Cellular Component Annotations dataset.

dynein binding Gene Set

From GO Molecular Function Annotations

genes performing the dynein binding molecular function from the curated GO Molecular Function Annotations dataset.

dynein intermediate chain binding Gene Set

From GO Molecular Function Annotations

genes performing the dynein intermediate chain binding molecular function from the curated GO Molecular Function Annotations dataset.

dynein heavy chain binding Gene Set

From GO Molecular Function Annotations

genes performing the dynein heavy chain binding molecular function from the curated GO Molecular Function Annotations dataset.

dynein complex binding Gene Set

From GO Molecular Function Annotations

genes performing the dynein complex binding molecular function from the curated GO Molecular Function Annotations dataset.

dynein light intermediate chain binding Gene Set

From GO Molecular Function Annotations

genes performing the dynein light intermediate chain binding molecular function from the curated GO Molecular Function Annotations dataset.

dynein light chain binding Gene Set

From GO Molecular Function Annotations

genes performing the dynein light chain binding molecular function from the curated GO Molecular Function Annotations dataset.

absent outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent/shortened outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shortened outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent/shortened dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/shortened dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent inner and outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner and outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent inner dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Dynein heavy chain, P-loop containing D4 domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain, P-loop containing D4 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytoplasmic dynein 2 heavy chain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytoplasmic dynein 2 heavy chain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytoplasmic dynein 1 intermediate chain 1/2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytoplasmic dynein 1 intermediate chain 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, dynein-related, AAA domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, dynein-related, AAA domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein regulator LIS1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein regulator LIS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein associated protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein assembly factor 1, axonemal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein assembly factor 1, axonemal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein light chain, type 1/2, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein light chain, type 1/2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Axonemal dynein light chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Axonemal dynein light chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain, domain-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain, domain-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain, domain-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain, domain-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein light chain, roadblock-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein light chain, roadblock-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain 1, axonemal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain 1, axonemal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein light chain, type 1/2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein light chain, type 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain 6, axonemal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain 6, axonemal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain 7, axonemal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain 7, axonemal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain, coiled coil stalk Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain, coiled coil stalk protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein family light intermediate chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein family light intermediate chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein light chain-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein light chain-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein 1 light intermediate chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein 1 light intermediate chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein heavy chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein heavy chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein assembly factor 3, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein assembly factor 3, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynein regulatory complex protein 1, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynein regulatory complex protein 1, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Protan defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac conduction defect, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac conduction defect, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects 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.

Phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neutral 1 amino acid transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular septal defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Laron-type isolated somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iodotyrosine deiodination defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal carnitine transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocyte lactate transporter defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocyte lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oocyte maturation defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iodotyrosyl coupling defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect 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.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

Cardiac Conduction Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Conduction Defect from the curated CTD Gene-Disease Associations dataset.

Atrial septal defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset.

ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.

Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset.

Atrioventricular Canal Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrioventricular Canal Defect from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 6 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.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease Associations dataset.

Erythrocyte Lactate Transporter Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrocyte Lactate Transporter Defect from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

atrial heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

alcohol-related birth defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrioventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital bile acid synthesis defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrial heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

qualitative platelet defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

human spermatogenic defect Gene Set

From GAD Gene-Disease Associations

genes associated with the disease human spermatogenic defect in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defect Gene Set

From GeneRIF Biological Term Annotations

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

conotruncal defect Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

thyroid hormone receptor defect Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid hormone receptor defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline defect of mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set

From HPO Gene-Disease Associations

genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

secundum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inlet ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thyroid defect in oxidation and organification of iodide Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid defect in oxidation and organification of iodide phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenocorticotropin (acth) receptor (acthr) defect Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sacral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the sacral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abdominal wall defect Gene Set

From HPO Gene-Disease Associations

genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

visual field defect Gene Set

From HPO Gene-Disease Associations

genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defect in the atrial septum Gene Set

From HPO Gene-Disease Associations

genes associated with the defect in the atrial septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skull defect Gene Set

From HPO Gene-Disease Associations

genes associated with the skull defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cervical segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

perimembranous ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline defect of the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

complete atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large central visual field defect Gene Set

From HPO Gene-Disease Associations

genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

conotruncal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the conotruncal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

primum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mannose-P-dolichol utilization defect 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mannose-P-dolichol utilization defect 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

perimembraneous ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

partial atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inlet ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle with atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iodide oxidation defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorticopulmonary septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle, ventricular defect committed to aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium primum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

complete atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium secundum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

schizophrenia, neurophysiologic defect in Gene Set

From OMIM Gene-Disease Associations

genes associated with the schizophrenia, neurophysiologic defect in phenotype from the curated OMIM Gene-Disease Associations dataset.

{atrioventricular septal defect, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocyte lactate transporter defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocyte lactate transporter defect phenotype from the curated OMIM Gene-Disease Associations dataset.

natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

selective t-cell defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the selective t-cell defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac conduction defect, nonspecific Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac conduction defect, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.

rickets due to defect in vitamin d 25-hydroxylation Gene Set

From OMIM Gene-Disease Associations

genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.

{atrioventricular septal defect, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

oocyte maturation defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the oocyte maturation defect phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, familial, due to ttf-1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{cardiac conduction defect, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {cardiac conduction defect, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.

CiliaryGanglion Gene Set

From BioGPS Human Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in CiliaryGanglion relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.

Ciliary dyskinesia, primary, 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary ciliary dyskinesia 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary ciliary dyskinesia 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary ciliary dyskinesia 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary ciliary dyskinesia 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 29 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 22 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ciliary dyskinesia, primary, 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ciliary dyskinesia, primary, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ciliary transition zone Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary transition zone cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary cytoplasm Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary cytoplasm cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary rootlet Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary rootlet cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary basal body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary basal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary neurotrophic factor receptor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary neurotrophic factor receptor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary transition zone Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary transition zone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary cytoplasm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary cytoplasm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary rootlet Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary rootlet cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary basal body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary pocket membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary pocket membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary neurotrophic factor receptor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary neurotrophic factor receptor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary pocket Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary pocket cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ciliary membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Ciliary Dyskinesia, Primary, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 6 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 13 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 11 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 10 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 9 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 7 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 8 from the curated CTD Gene-Disease Associations dataset.

Ciliary Motility Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Motility Disorders from the curated CTD Gene-Disease Associations dataset.

Primary ciliary dyskinesia, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Primary ciliary dyskinesia, 4 from the curated CTD Gene-Disease Associations dataset.

Ciliary Dyskinesia, Primary, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 12 from the curated CTD Gene-Disease Associations dataset.

Primary ciliary dyskinesia, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Primary ciliary dyskinesia, 3 from the curated CTD Gene-Disease Associations dataset.

primary ciliary dyskinesia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease primary ciliary dyskinesia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

primary ciliary dyskinesia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease primary ciliary dyskinesia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ciliary body cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ciliary body cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ciliary body disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ciliary body disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

malignant ciliary body melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease malignant ciliary body melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

immotile cilia syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease immotile cilia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ciliated Gene Set

From GeneRIF Biological Term Annotations

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

cilia Gene Set

From GeneRIF Biological Term Annotations

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

ciliarylocalized Gene Set

From GeneRIF Biological Term Annotations

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

cilial Gene Set

From GeneRIF Biological Term Annotations

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

ciliary Gene Set

From GeneRIF Biological Term Annotations

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

ciliadependent Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of protein localization to ciliary membrane Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of protein localization to ciliary membrane biological process from the curated GO Biological Process Annotations dataset.

negative regulation of lung ciliated cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of lung ciliated cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations dataset.

ciliary receptor clustering involved in smoothened signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the ciliary receptor clustering involved in smoothened signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of protein localization to ciliary membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein localization to ciliary membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of cilium beat frequency involved in ciliary motility Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cilium beat frequency involved in ciliary motility biological process from the curated GO Biological Process Annotations dataset.

multi-ciliated epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the multi-ciliated epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

protein localization to ciliary membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to ciliary membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lung ciliated cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations dataset.

ciliary body morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ciliary body morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ciliary neurotrophic factor-mediated signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the ciliary neurotrophic factor-mediated signaling pathway biological process from the curated GO Biological Process Annotations dataset.

ciliary basal body organization Gene Set

From GO Biological Process Annotations

genes participating in the ciliary basal body organization biological process from the curated GO Biological Process Annotations dataset.

lung ciliated cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations dataset.

ciliary transition zone Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary transition zone cellular component from the curated GO Cellular Component Annotations dataset.

ciliary inversin compartment Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary inversin compartment cellular component from the curated GO Cellular Component Annotations dataset.

ciliary neurotrophic factor receptor complex Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary neurotrophic factor receptor complex cellular component from the curated GO Cellular Component Annotations dataset.

ciliary rootlet Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary rootlet cellular component from the curated GO Cellular Component Annotations dataset.

ciliary transition fiber Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary transition fiber cellular component from the curated GO Cellular Component Annotations dataset.

ciliary base Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary base cellular component from the curated GO Cellular Component Annotations dataset.

ciliary basal body Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary basal body cellular component from the curated GO Cellular Component Annotations dataset.

ciliary part Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary part cellular component from the curated GO Cellular Component Annotations dataset.

ciliary tip Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary tip cellular component from the curated GO Cellular Component Annotations dataset.

ciliary membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the ciliary membrane cellular component from the curated GO Cellular Component Annotations dataset.

ciliary neurotrophic factor receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the ciliary neurotrophic factor receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

ciliary neurotrophic factor receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the ciliary neurotrophic factor receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

ciliary neurotrophic factor binding Gene Set

From GO Molecular Function Annotations

genes performing the ciliary neurotrophic factor binding molecular function from the curated GO Molecular Function Annotations dataset.

Ciliatine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Ciliatine metabolite from the curated HMDB Metabolites of Enzymes dataset.

ciliary dyskinesia Gene Set

From HPO Gene-Disease Associations

genes associated with the ciliary dyskinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

immotile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the immotile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ciliary body Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ciliary motility Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ciliary body Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Ciliary Motility Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ciliary Motility Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ciliary BBSome complex subunit 2, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ciliary BBSome complex subunit 2, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ciliary BBSome complex subunit 2, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ciliary BBSome complex subunit 2, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ciliary BBSome complex subunit 2, middle region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ciliary BBSome complex subunit 2, middle region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cilia/flagella-associated protein 20/WDR90/C3orf67 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cilia/flagella-associated protein 20/WDR90/C3orf67 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Centriole, cilia and spindle-associated protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Centriole, cilia and spindle-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cilia BBSome complex subunit 10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cilia BBSome complex subunit 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Primary ciliary dyskinesia protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Primary ciliary dyskinesia protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ciliary neurotrophic factor, CNTF Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ciliary neurotrophic factor, CNTF protein domain from the InterPro Predicted Protein Domain Annotations dataset.

absent embryonic cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent embryonic cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ciliary ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ciliary ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of eyelid cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of eyelid cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ciliary body pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ciliary body pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tracheal ciliated epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tracheal ciliated epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ciliary body morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ciliary body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ciliary dyskinesia, primary, 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 9, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 7, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 1, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 3, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary diskinesia, primary, 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary diskinesia, primary, 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

ARL13B-mediated ciliary trafficking of INPP5E Gene Set

From Reactome Pathways

proteins participating in the ARL13B-mediated ciliary trafficking of INPP5E pathway from the Reactome Pathways dataset.

ciliary body Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue ciliary body from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

ciliary epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue ciliary epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

ciliary muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ciliary muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

ciliary body Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ciliary body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

ciliary epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ciliary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

rostral ventral respiratory cell group Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral ventral respiratory cell group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles 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.

Hereditary myopathy with early respiratory failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary myopathy with early respiratory failure 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.

mitochondrial respiratory chain complex ii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex ii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iv Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iv cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex i Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex i cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

respiratory chain complex iv Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the respiratory chain complex iv cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

respiratory chain complex ii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the respiratory chain complex ii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

respiratory chain complex i Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the respiratory chain complex i cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

respiratory chain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the respiratory chain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

respiratory chain complex iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the respiratory chain complex iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iv Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iv cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

respiratory chain complex ii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the respiratory chain complex ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane respiratory chain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane respiratory chain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

respiratory chain complex iv Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the respiratory chain complex iv cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain supercomplex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain supercomplex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

respiratory chain complex i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the respiratory chain complex i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

respiratory chain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the respiratory chain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

respiratory chain complex iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the respiratory chain complex iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex ii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Respiratory chain complex I, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate VII/650kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate VII/650kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (lambda subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (lambda subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (gamma subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (gamma subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (beta subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (beta subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate IV/310kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate IV/310kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete intermediate), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete intermediate), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete intermediate ND1, ND2, ND3, CIA30 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete intermediate ND1, ND2, ND3, CIA30 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (holoenzyme), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (holoenzyme), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate II/230kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate II/230kD), mitochondrial 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.

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.

Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory Sounds Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Sounds 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.

Respiratory Tract Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Tract Infections from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy with respiratory distress 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.

Respiratory Tract Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Tract Diseases from the curated CTD Gene-Disease Associations dataset.

Severe Acute Respiratory Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Acute Respiratory Syndrome from the curated CTD Gene-Disease Associations dataset.

Respiratory Distress Syndrome, Newborn Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Distress Syndrome, Newborn from the curated CTD Gene-Disease Associations dataset.

Hereditary Myopathy with Early Respiratory Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.

Respiratory System Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory System Abnormalities from the curated CTD Gene-Disease Associations dataset.

Granuloma, Respiratory Tract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granuloma, Respiratory Tract from the curated CTD Gene-Disease Associations dataset.

Respiratory Syncytial Virus Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Syncytial Virus Infections from the curated CTD Gene-Disease Associations dataset.

Respiratory Insufficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Insufficiency from the curated CTD Gene-Disease Associations dataset.

Respiratory Paralysis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Paralysis from the curated CTD Gene-Disease Associations dataset.

Acidosis, Respiratory Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acidosis, Respiratory from the curated CTD Gene-Disease Associations dataset.

Respiratory Distress Syndrome, Adult Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Distress Syndrome, Adult 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.

Respiratory Hypersensitivity Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Hypersensitivity from the curated CTD Gene-Disease Associations dataset.

Respiratory Function Tests Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Respiratory Function Tests in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

respiratory system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease respiratory system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

lower respiratory tract disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease lower respiratory tract disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

respiratory system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease respiratory system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

respiratory system cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease respiratory system cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

lower respiratory tract disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease lower respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

upper respiratory tract disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

lower respiratory tract disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease lower respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

upper respiratory tract disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

respiratory failure Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

respiratory system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease respiratory system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

severe acute respiratory syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease severe acute respiratory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult respiratory distress syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult respiratory distress syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

newborn respiratory distress syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease newborn respiratory distress syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

respiratory bronchiolitis-associated interstitial lung disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease respiratory bronchiolitis-associated interstitial lung disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

respiratory system benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease respiratory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

neonatal respiratory failure Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

respiratory system cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease respiratory system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

respiratory syncytial virus infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory papillomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory papillomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory function tests Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory function tests in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; prenatal exposure delayed effects; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; prenatal exposure delayed effects; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory hypersensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pneumonia; respiratory distress syndrome, newborn; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pneumonia; respiratory distress syndrome, newborn; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory papillomatosis, juvenile-onset; recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiolitis, viral; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiolitis, viral; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases; hypersensitivity; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; eczema; food hypersensitivity; hypersensitivity, immediate; respiratory sounds; rhinitis, allergic, seasonal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; eczema; food hypersensitivity; hypersensitivity, immediate; respiratory sounds; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sars (severe acute respiratory syndrome) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sars (severe acute respiratory syndrome) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; hypersensitivity; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; hypersensitivity; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; respiratory distress syndrome, adult; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prenatal exposure delayed effects; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prenatal exposure delayed effects; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus (rsv) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus (rsv) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute respiratory distress syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute respiratory distress syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, neonatal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; ischemia; recurrence; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; ischemia; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; prenatal exposure delayed effects; recurrence; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; prenatal exposure delayed effects; recurrence; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypersensitivity; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

occupational diseases; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease occupational diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; recurrence; respiratory tract infections; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; recurrence; respiratory tract infections; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome (rds) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome (rds) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

communicable diseases; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxemia; anoxia; pneumonia, viral; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxemia; anoxia; pneumonia, viral; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory activity following radiotherapy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory activity following radiotherapy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory-distress syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory-distress syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchial hyperreactivity; hypersensitivity; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchial hyperreactivity; hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

critical illness; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease critical illness; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mycobacterium avium-intracellulare infection; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mycobacterium avium-intracellulare infection; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

otitis media; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease otitis media; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; eczema; hay fever; hypersensitivity; respiratory sounds; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; eczema; hay fever; hypersensitivity; respiratory sounds; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; dermatitis, atopic; eczema; hypersensitivity, immediate; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; dermatitis, atopic; eczema; hypersensitivity, immediate; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiectasis; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiectasis; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; respiratory syncytial virus; juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; respiratory syncytial virus; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mouth neoplasms; respiratory tract neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mouth neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sepsis; pneumonia; acute respiratory distress syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sepsis; pneumonia; acute respiratory distress syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

community-acquired infections; pneumonia; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease community-acquired infections; pneumonia; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lung injury; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lung injury; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

berylliosis; respiratory hypersensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease berylliosis; respiratory hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone necrosis; osteonecrosis; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; osteonecrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent respiratory infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrent respiratory infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

common variable immunodeficiency; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease common variable immunodeficiency; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent respiratory papillomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrent respiratory papillomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic rate; respiratory quotient Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic rate; respiratory quotient in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypersensitivity; inflammation; respiratory hypersensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypersensitivity; inflammation; respiratory hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiolitis; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiolitis; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pain, postoperative; postoperative nausea and vomiting; pruritus; pruritus nos; respiratory insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pain, postoperative; postoperative nausea and vomiting; pruritus; pruritus nos; respiratory insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypercapnic respiratory failure; hypoventilation; sleep apnea, central Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypercapnic respiratory failure; hypoventilation; sleep apnea, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; recurrence; respiratory sounds Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; recurrence; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiolitis; disease susceptibility; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiolitis; disease susceptibility; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; bronchiolitis, viral; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; bronchiolitis, viral; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; infant, premature, diseases; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; infant, premature, diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory airway resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory airway resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus bronchiolitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus bronchiolitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory Gene Set

From GeneRIF Biological Term Annotations

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

Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

mitochondrial respiratory chain complex ii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex ii biogenesis biological process from the curated GO Biological Process Annotations dataset.

respiratory tube development Gene Set

From GO Biological Process Annotations

genes participating in the respiratory tube development biological process from the curated GO Biological Process Annotations dataset.

respiratory burst Gene Set

From GO Biological Process Annotations

genes participating in the respiratory burst biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iv biogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of respiratory gaseous exchange by neurological system process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of respiratory gaseous exchange by neurological system process biological process from the curated GO Biological Process Annotations dataset.

respiratory system process Gene Set

From GO Biological Process Annotations

genes participating in the respiratory system process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex i assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex i assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iv assembly biological process from the curated GO Biological Process Annotations dataset.

respiratory system development Gene Set

From GO Biological Process Annotations

genes participating in the respiratory system development biological process from the curated GO Biological Process Annotations dataset.

regulation of respiratory system process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of respiratory system process biological process from the curated GO Biological Process Annotations dataset.

regulation of respiratory burst Gene Set

From GO Biological Process Annotations

genes participating in the regulation of respiratory burst biological process from the curated GO Biological Process Annotations dataset.

respiratory gaseous exchange Gene Set

From GO Biological Process Annotations

genes participating in the respiratory gaseous exchange biological process from the curated GO Biological Process Annotations dataset.

respiratory chain complex ii assembly Gene Set

From GO Biological Process Annotations

genes participating in the respiratory chain complex ii assembly biological process from the curated GO Biological Process Annotations dataset.

regulation of respiratory burst involved in inflammatory response Gene Set

From GO Biological Process Annotations

genes participating in the regulation of respiratory burst involved in inflammatory response biological process from the curated GO Biological Process Annotations dataset.

respiratory burst involved in defense response Gene Set

From GO Biological Process Annotations

genes participating in the respiratory burst involved in defense response biological process from the curated GO Biological Process Annotations dataset.

respiratory chain complex iv assembly Gene Set

From GO Biological Process Annotations

genes participating in the respiratory chain complex iv assembly biological process from the curated GO Biological Process Annotations dataset.

respiratory burst after phagocytosis Gene Set

From GO Biological Process Annotations

genes participating in the respiratory burst after phagocytosis biological process from the curated GO Biological Process Annotations dataset.

regulation of respiratory gaseous exchange Gene Set

From GO Biological Process Annotations

genes participating in the regulation of respiratory gaseous exchange biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex ii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex ii assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii assembly biological process from the curated GO Biological Process Annotations dataset.

positive regulation of respiratory burst Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of respiratory burst biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii biogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of respiratory burst involved in inflammatory response Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of respiratory burst involved in inflammatory response biological process from the curated GO Biological Process Annotations dataset.

positive regulation of respiratory burst involved in inflammatory response Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of respiratory burst involved in inflammatory response biological process from the curated GO Biological Process Annotations dataset.

negative regulation of respiratory burst Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of respiratory burst biological process from the curated GO Biological Process Annotations dataset.

respiratory chain complex iii assembly Gene Set

From GO Biological Process Annotations

genes participating in the respiratory chain complex iii assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex i biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex i biogenesis biological process from the curated GO Biological Process Annotations dataset.

respiratory electron transport chain Gene Set

From GO Biological Process Annotations

genes participating in the respiratory electron transport chain biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iv cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex i Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex i cellular component from the curated GO Cellular Component Annotations dataset.

respiratory chain complex ii Gene Set

From GO Cellular Component Annotations

proteins localized to the respiratory chain complex ii cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex ii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex ii cellular component from the curated GO Cellular Component Annotations dataset.

respiratory chain complex iv Gene Set

From GO Cellular Component Annotations

proteins localized to the respiratory chain complex iv cellular component from the curated GO Cellular Component Annotations dataset.

plasma membrane respiratory chain complex i Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane respiratory chain complex i cellular component from the curated GO Cellular Component Annotations dataset.

respiratory chain complex i Gene Set

From GO Cellular Component Annotations

proteins localized to the respiratory chain complex i cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain cellular component from the curated GO Cellular Component Annotations dataset.

respiratory chain Gene Set

From GO Cellular Component Annotations

proteins localized to the respiratory chain cellular component from the curated GO Cellular Component Annotations dataset.

respiratory chain complex iii Gene Set

From GO Cellular Component Annotations

proteins localized to the respiratory chain complex iii cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex iii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the curated GO Cellular Component Annotations dataset.

respiratory system disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease respiratory system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

respiratory system cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease respiratory system cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

lower respiratory tract disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease lower respiratory tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

upper respiratory tract disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease upper respiratory tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

neoplasm of the respiratory system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the neoplasm of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the respiratory system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional respiratory abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal respiratory system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

respiratory acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory distress Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory distress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory alkalosis Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory alkalosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the respiratory system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mixed respiratory and metabolic acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the mixed respiratory and metabolic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent lower respiratory tract infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory tract infection Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory tract infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory failure Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absence of bactericidal oxidative 'respiratory burst' in phagocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the absence of bactericidal oxidative 'respiratory burst' in phagocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent upper and lower respiratory tract infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

functional respiratory abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the functional respiratory abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive respiratory insufficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive respiratory insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent respiratory infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent respiratory infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the respiratory system Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper respiratory tract Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the upper respiratory tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory failure requiring assisted ventilation Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory failure requiring assisted ventilation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acute respiratory tract infection Gene Set

From HPO Gene-Disease Associations

genes associated with the acute respiratory tract infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal respiratory distress Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal respiratory distress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent upper respiratory tract infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory difficulties Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory difficulties phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory paralysis Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory paralysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory epithelium morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory arrest Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory arrest phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intermittent episodes of respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Respiratory Sounds Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Sounds phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Tract Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Tract Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Tract Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Tract Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Severe Acute Respiratory Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Severe Acute Respiratory Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Tract Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Tract Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Distress Syndrome, Newborn Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Distress Syndrome, Newborn phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Syncytial Virus Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Syncytial Virus Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Insufficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Paralysis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Paralysis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Distress Syndrome, Adult Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Distress Syndrome, Adult phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Hypersensitivity Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Hypersensitivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Nuclear respiratory factor-1, activation binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear respiratory factor-1, activation binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nuclear respiratory factor 1, NLS/DNA-binding, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear respiratory factor 1, NLS/DNA-binding, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased respiratory quotient Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased respiratory quotient phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pulmonary respiratory rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased respiratory mucosa goblet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory quotient Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory quotient phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

respiratory distress Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the respiratory distress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pulmonary respiratory rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory electron transport chain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory electron transport chain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased respiratory system tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased respiratory system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory bronchiole morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory bronchiole morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

respiratory system phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the respiratory system phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

respiratory failure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the respiratory failure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory sounds Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory sounds phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased respiratory quotient Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased respiratory quotient phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent respiratory mucosa goblet cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent respiratory mucosa goblet cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased respiratory mucosa goblet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated respiratory conducting tubes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated respiratory conducting tubes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory system development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

respiratory epithelium hypertrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the respiratory epithelium hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory mechanics Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory mechanics phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired branching involved in respiratory bronchiole morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in respiratory bronchiole morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory system morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pulmonary respiratory rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory mucosa goblet cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory mucosa goblet cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory transport Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory conducting tube morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory conducting tube morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal branching involved in respiratory bronchiole morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal branching involved in respiratory bronchiole morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

respiratory system inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the respiratory system inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory system physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal respiratory mucosa morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

complex i, mitochondrial respiratory chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the complex i, mitochondrial respiratory chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial respiratory chain complex ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial respiratory chain complex ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, proximal, with early respiratory muscle involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

choreoathetosis, hypothyroidism, and neonatal respiratory distress Gene Set

From OMIM Gene-Disease Associations

genes associated with the choreoathetosis, hypothyroidism, and neonatal respiratory distress phenotype from the curated OMIM Gene-Disease Associations dataset.

[respiratory rhythmicity in sleep] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [respiratory rhythmicity in sleep] phenotype from the curated OMIM Gene-Disease Associations dataset.

The citric acid (TCA) cycle and respiratory electron transport Gene Set

From Reactome Pathways

proteins participating in the The citric acid (TCA) cycle and respiratory electron transport pathway from the Reactome Pathways dataset.

Respiratory electron transport Gene Set

From Reactome Pathways

proteins participating in the Respiratory electron transport pathway from the Reactome Pathways dataset.

Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. Gene Set

From Reactome Pathways

proteins participating in the Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. pathway from the Reactome Pathways dataset.

respiratory epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue respiratory epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

respiratory mucosa Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue respiratory mucosa from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

respiratory system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue respiratory system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

respiratory system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue respiratory system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

respiratory epithelium Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue respiratory epithelium in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

respiratory mucosa Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory epithelium cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory smooth muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory smooth muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory mucus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory mucus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory bronchiole Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory bronchiole in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory epithelium cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory epithelium cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

respiratory epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue respiratory epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.