Name

double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Transposition of Great Vessels Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Transposition of Great Vessels from the curated CTD Gene-Disease Associations dataset.

heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Double outlet right ventricle Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Double outlet right ventricle phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Double Outlet Right Ventricle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Double Outlet Right Ventricle from the curated CTD Gene-Disease Associations dataset.

double outlet right ventricle Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease double outlet right ventricle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

double outlet right ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the double outlet right ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

double outlet right ventricle Gene Set

From MPO Gene-Phenotype Associations

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

double outlet right ventricle, taussig bing type Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle, taussig bing type 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.

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.

double-outlet right ventricle Gene Set

From OMIM Gene-Disease Associations

genes associated with the double-outlet right ventricle phenotype from the curated OMIM Gene-Disease Associations dataset.

Persistent truncus arteriosus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Persistent truncus arteriosus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Truncus Arteriosus, Persistent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Truncus Arteriosus, Persistent from the curated CTD Gene-Disease Associations dataset.

persistent truncus arteriosus type i Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent truncus arteriosus type i phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistent truncus arteriosus type ii Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent truncus arteriosus type ii phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistent truncus arteriosus type iv Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent truncus arteriosus type iv phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistent truncus arteriosus Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent truncus arteriosus phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malformation of the heart and great vessels Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the malformation of the heart and great vessels phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

malformation of the heart and great vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the malformation of the heart and great vessels 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.

Transposition of great arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Transposition of great arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Transposition of the Great Arteries, Dextro-Looped 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Transposition of the Great Arteries, Dextro-Looped 1 from the curated CTD Gene-Disease Associations dataset.

transposition of the great arteries Gene Set

From HPO Gene-Disease Associations

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

d-loop transposition of the great arteries Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the d-loop transposition of the great arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

transposition of great arteries Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the transposition of great arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

transposition of the great arteries, dextro-looped 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the transposition of the great arteries, dextro-looped 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

transposition of the great arteries, dextro-looped 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the transposition of the great arteries, dextro-looped 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

transposition of great arteries, dextro-looped 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the transposition of great arteries, dextro-looped 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

truncus arteriosus Gene Set

From HPO Gene-Disease Associations

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

abnormal truncus arteriosus septation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal truncus arteriosus septation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ductus arteriosus, patent; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

persistent truncus arteriosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent truncus arteriosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Tetralogy of Fallot Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tetralogy of Fallot phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tetralogy of Fallot Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tetralogy of Fallot from the curated CTD Gene-Disease Associations dataset.

tetralogy of fallot Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cardiovascular abnormalities; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular abnormalities; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, inborn; syndrome; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, inborn; syndrome; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

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

dilatation, pathologic; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dilatation, pathologic; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Tetralogy of Fallot Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Tetralogy of Fallot phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

tetralogy of fallot Gene Set

From GWASdb SNP-Disease Associations

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

tetralogy of fallot Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the tetralogy of fallot phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

tetralogy of fallot Gene Set

From HPO Gene-Disease Associations

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

Tetralogy of Fallot Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Tetralogy of Fallot phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

tetralogy of fallot Gene Set

From OMIM Gene-Disease Associations

genes associated with the tetralogy of fallot phenotype from the curated OMIM Gene-Disease Associations dataset.

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; patent ductus arteriosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; patent ductus arteriosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; patent ductus arteriosus; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; patent ductus arteriosus; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double inlet heart left ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double inlet heart left ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal heart right ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart right ventricle outflow tract stenosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right ventricle pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart right ventricle degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart right ventricle hypertrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased heart right ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased heart right ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart right ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart right ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right ventricle outflow tract morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle outflow tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart right ventricle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart right ventricle aneurysm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent heart right ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent heart right ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased heart right ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart right ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

right ventricular outlet obstruction Gene Set

From HPO Gene-Disease Associations

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

heart septal defects, ventricular; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal heart and great artery attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart and great artery attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart and great vessel attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart and great vessel attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heart Defects, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.

congenital heart defects Gene Set

From GAD Gene-Disease Associations

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

heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dilatation, pathologic; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dilatation, pathologic; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathies; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathies; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Defects, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Defects, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital heart defects, and posterior embryotoxon Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

agenesis of pulmonary vessels Gene Set

From HPO Gene-Disease Associations

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

congenital malformation of the great arteries Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital malformation of the great arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent right dorsal aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent right dorsal aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital ductus arteriosus aneurysm Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital ductus arteriosus aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital malformation of the right heart Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital malformation of the right heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

heart anomalies, congenital; pulmonary hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary artery atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the pulmonary artery atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary valve atresia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cardiac right ventricle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac right ventricle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

cardiac right ventricle formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac right ventricle formation biological process from the curated GO Biological Process Annotations dataset.

abnormality of the right ventricle Gene Set

From HPO Gene-Disease Associations

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

increased right ventricle systolic pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased right ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased right ventricle peak pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased right ventricle peak pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

coronary-cameral fistula to right ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the coronary-cameral fistula to right ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased right ventricle systolic pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased right ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

right ventricle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

left-right laterality defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left-right laterality defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

truncus Gene Set

From GeneRIF Biological Term Annotations

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

congenital pyloric atresia Gene Set

From HPO Gene-Disease Associations

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

aural atresia, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the aural atresia, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary valve defects Gene Set

From HPO Gene-Disease Associations

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

increased heart ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased heart left ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased heart left ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased heart left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart ventricle outflow tract morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart ventricle outflow tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased heart left ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart ventricle pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart left ventricle outflow tract stenosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart left ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left ventricle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left ventricle outflow tract morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left ventricle outflow tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart left ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart left ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left ventricle pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart ventricle wall thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart ventricle wall thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart atrium and ventricle connection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart atrium and ventricle connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

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

heart left ventricle hypertrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart left ventricle hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart ventricle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

heart ventricle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Heart Septal Defects, Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Ventricular from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects, Atrial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Atrial from the curated CTD Gene-Disease Associations dataset.

atrial fibrillation; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects Gene Set

From GAD Gene-Disease Associations

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

Conotruncal heart defects Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Conotruncal heart defects phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Heart Septal Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Heart Septal Defects, Atrial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Atrial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

transposition Gene Set

From GeneRIF Biological Term Annotations

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

regulation of transposition Gene Set

From GO Biological Process Annotations

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

transposition, dna-mediated Gene Set

From GO Biological Process Annotations

genes participating in the transposition, dna-mediated biological process from the curated GO Biological Process Annotations dataset.

negative regulation of transposition Gene Set

From GO Biological Process Annotations

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

transposition Gene Set

From GO Biological Process Annotations

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

congenital hypertrophy of left ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital hypertrophy of left ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thoracic outlet syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gastric outlet obstruction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

outlet Gene Set

From GeneRIF Biological Term Annotations

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

gastric outlet obstruction Gene Set

From GWASdb SNP-Disease Associations

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

Gastric Outlet Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Gastric Outlet Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

great Gene Set

From GeneRIF Biological Term Annotations

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

great saphenous vein Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

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

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

paraventricular nuclei, right of thalamus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paraventricular nuclei, right of thalamus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

tetralogy Gene Set

From GeneRIF Biological Term Annotations

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

fallot Gene Set

From GeneRIF Biological Term Annotations

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

tetrology of fallot Gene Set

From OMIM Gene-Disease Associations

genes associated with the tetrology of fallot phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

right pulmonary isomerism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the right pulmonary isomerism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Blood Vessels Gene Set

From dbGAP Gene-Trait Associations

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

blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood vessels Gene Set

From GAD Gene-Disease Associations

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

vessels Gene Set

From GeneRIF Biological Term Annotations

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

apoptotic process involved in patterning of blood vessels Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic process involved in patterning of blood vessels biological process from the curated GO Biological Process Annotations dataset.

patterning of blood vessels Gene Set

From GO Biological Process Annotations

genes participating in the patterning of blood vessels biological process from the curated GO Biological Process Annotations dataset.

hypoplasia of lymphatic vessels Gene Set

From HPO Gene-Disease Associations

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

tortuosity of conjunctival vessels Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lymphatic vessels Gene Set

From HPO Gene-Disease Associations

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

arteriovenous fistulas of celiac and mesenteric vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the arteriovenous fistulas of celiac and mesenteric vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prominent superficial blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the prominent superficial blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal umbilical cord blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

calcification of the small brain vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the calcification of the small brain vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

venous varicosities of celiac and mesenteric vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the venous varicosities of celiac and mesenteric vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

attenuation of retinal blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the attenuation of retinal blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent intersomitic vessels Gene Set

From MPO Gene-Phenotype Associations

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

absent vitelline blood vessels Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vitelline blood vessels phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent lymphatic vessels Gene Set

From MPO Gene-Phenotype Associations

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

absent coronary vessels Gene Set

From MPO Gene-Phenotype Associations

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

Ductus Arteriosus, Patent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ductus Arteriosus, Patent from the curated CTD Gene-Disease Associations dataset.

patent ductus arteriosus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

patent ductus arteriosus Gene Set

From GAD Gene-Disease Associations

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

ductus arteriosus, patent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosus Gene Set

From GeneRIF Biological Term Annotations

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

ductus arteriosus closure Gene Set

From GO Biological Process Annotations

genes participating in the ductus arteriosus closure biological process from the curated GO Biological Process Annotations dataset.

patent ductus arteriosus Gene Set

From HPO Gene-Disease Associations

genes associated with the patent ductus arteriosus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Ductus Arteriosus, Patent Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ductus Arteriosus, Patent phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

patent ductus arteriosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the patent ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature closure of the ductus arteriosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature closure of the ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fetal ductus arteriosus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fetal ductus arteriosus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent fetal ductus arteriosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent fetal ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{patent ductus arteriosus, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {patent ductus arteriosus, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertension, pulmonary; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

postoperative complications; pulmonary embolism; pulmonary embolisms; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postoperative complications; pulmonary embolism; pulmonary embolisms; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary fibrosis; sarcoidosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary fibrosis; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyspnea; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyspnea; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leg injuries; pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leg injuries; pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney diseases; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney diseases; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sarcoidosis, pulmonary; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sarcoidosis, pulmonary; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

determination of heart left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of heart left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

enlarged heart right atrium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged heart right atrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right atrium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right atrium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart right atrium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart right atrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

chronic pulmonary heart disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

chronic pulmonary heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute pulmonary heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Pulmonary Heart Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Pulmonary Heart Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Persistent hyperinsulinemic hypoglycemia of infancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Persistent hyperinsulinemic hypoglycemia of infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Persistent hyperplastic primary vitreous, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Persistent hyperplastic primary vitreous, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Persistent Mullerian duct syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Persistent Mullerian duct syndrome from the curated CTD Gene-Disease Associations dataset.

STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.

Persistent Fetal Circulation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Persistent Fetal Circulation Syndrome from the curated CTD Gene-Disease Associations dataset.

Stuttering, Familial Persistent 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.

persistent fetal circulation syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

persistent vegetative state Gene Set

From GAD Gene-Disease Associations

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

persistent bronchial hyperresponsiveness Gene Set

From GAD Gene-Disease Associations

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

persistent hyperinsulinemia hypoglycemia of infancy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease persistent hyperinsulinemia hypoglycemia of infancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperinsulinism; hypoglycemia; persistent hyperinsulinemia hypoglycemia of infancy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperinsulinism; hypoglycemia; persistent hyperinsulinemia hypoglycemia of infancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

persistently Gene Set

From GeneRIF Biological Term Annotations

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

persistent Gene Set

From GeneRIF Biological Term Annotations

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

persistentrecurrent Gene Set

From GeneRIF Biological Term Annotations

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

persistent bleeding after trauma Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent bleeding after trauma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent left superior vena cava Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent left superior vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent pupillary membrane Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent pupillary membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent open anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent open anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent hyperplastic primary vitreous Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent hyperplastic primary vitreous phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Persistent Hyperinsulinemia Hypoglycemia of Infancy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Persistent Hyperinsulinemia Hypoglycemia of Infancy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Persistent Fetal Circulation Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Persistent Fetal Circulation Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Persistent Vegetative State Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Persistent Vegetative State phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

persistent hyaloid artery Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent hyaloid artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistent ductus caroticus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent ductus caroticus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistent hyperplastic primary vitreous Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the persistent hyperplastic primary vitreous phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

persistent cloaca Gene Set

From MPO Gene-Phenotype Associations

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

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent polyclonal b-cell lymphocytosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent polyclonal b-cell lymphocytosis phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent mullerian duct syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent mullerian duct syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent mullerian duct syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent mullerian duct syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent hyperplastic primary vitreous, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent hyperplastic primary vitreous, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart valve diseases; rheumatic heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart valve diseases; rheumatic heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen Storage Disease of Heart, Lethal Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.

congenital heart disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital heart block Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cardiomyopathy; heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy; heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune-associated congenital heart block. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune-associated congenital heart block. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart disease Gene Set

From GAD Gene-Disease Associations

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

heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Congenital heart malformation Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Congenital heart malformation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Congenital heart disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Congenital heart disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

congenital heart disease Gene Set

From GWASdb SNP-Disease Associations

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

congenital malformation of the left heart Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital malformation of the left heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

?testicular anomalies with or without congenital heart disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.

glycogen storage disease of heart, lethal congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the glycogen storage disease of heart, lethal congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

Epidermolysis bullosa simplex with pyloric atresia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa simplex with pyloric atresia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa with pyloric atresia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa with pyloric atresia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyloric Atresia Gene Set

From CTD Gene-Disease Associations

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

Epidermolysis bullosa with pyloric atresia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis bullosa with pyloric atresia from the curated CTD Gene-Disease Associations dataset.

Biliary Atresia Gene Set

From CTD Gene-Disease Associations

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

CHOANAL ATRESIA AND LYMPHEDEMA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset.

Epidermolysis Bullosa Simplex With Pyloric Atresia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa Simplex With Pyloric Atresia from the curated CTD Gene-Disease Associations dataset.

biliary atresia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

biliary atresia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

esophageal atresia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

choanal atresia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cholestasis; biliary atresia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis; biliary atresia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

biliary atresia Gene Set

From GAD Gene-Disease Associations

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

biliary atresia; choledochal cyst; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease biliary atresia; choledochal cyst; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal atresia Gene Set

From GAD Gene-Disease Associations

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

biliary atresia; liver diseases; primary graft dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

biliary atresia; Gene Set

From GAD Gene-Disease Associations

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

atresia Gene Set

From GeneRIF Biological Term Annotations

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

ovarian follicle atresia Gene Set

From GO Biological Process Annotations

genes participating in the ovarian follicle atresia biological process from the curated GO Biological Process Annotations dataset.

Biliary atresia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Biliary atresia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

biliary atresia Gene Set

From GWASdb SNP-Disease Associations

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

biliary atresia Gene Set

From GWASdb SNP-Phenotype Associations

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

laryngeal atresia Gene Set

From HPO Gene-Disease Associations

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

anal atresia Gene Set

From HPO Gene-Disease Associations

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

genital tract atresia Gene Set

From HPO Gene-Disease Associations

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

biliary atresia Gene Set

From HPO Gene-Disease Associations

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

jejunal atresia Gene Set

From HPO Gene-Disease Associations

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

aortic valve atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the aortic valve atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gastrointestinal atresia Gene Set

From HPO Gene-Disease Associations

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

vaginal atresia Gene Set

From HPO Gene-Disease Associations

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

distal ileal atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the distal ileal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior choanal atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior choanal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal atresia Gene Set

From HPO Gene-Disease Associations

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

ureteral atresia Gene Set

From HPO Gene-Disease Associations

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

duodenal atresia Gene Set

From HPO Gene-Disease Associations

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

esophageal atresia Gene Set

From HPO Gene-Disease Associations

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

choanal atresia Gene Set

From HPO Gene-Disease Associations

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

mitral atresia Gene Set

From HPO Gene-Disease Associations

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

atresia of the external auditory canal Gene Set

From HPO Gene-Disease Associations

genes associated with the atresia of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lacrimal duct atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the lacrimal duct atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

urethral atresia Gene Set

From HPO Gene-Disease Associations

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

ileal atresia Gene Set

From HPO Gene-Disease Associations

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

Choanal Atresia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Biliary Atresia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tricuspid Atresia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Esophageal Atresia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Intestinal Atresia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

aortic valve atresia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anal atresia Gene Set

From MPO Gene-Phenotype Associations

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

oral atresia Gene Set

From MPO Gene-Phenotype Associations

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

urethra atresia Gene Set

From MPO Gene-Phenotype Associations

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

rectal atresia Gene Set

From MPO Gene-Phenotype Associations

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

cecal atresia Gene Set

From MPO Gene-Phenotype Associations

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

mitral valve atresia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the mitral valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

esophageal atresia Gene Set

From MPO Gene-Phenotype Associations

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

choanal atresia Gene Set

From MPO Gene-Phenotype Associations

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

ureteropelvic junction atresia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureteropelvic junction atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

uterus atresia Gene Set

From MPO Gene-Phenotype Associations

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

vagina atresia Gene Set

From MPO Gene-Phenotype Associations

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

tricuspid valve atresia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the tricuspid valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal atresia, multiple Gene Set

From OMIM Gene-Disease Associations

genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset.

epidermolysis bullosa, junctional, with pyloric atresia Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa, junctional, with pyloric atresia phenotype from the curated OMIM Gene-Disease Associations dataset.

epidermolysis bullosa simplex with pyloric atresia Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa simplex with pyloric atresia phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

choanal atresia and lymphedema Gene Set

From OMIM Gene-Disease Associations

genes associated with the choanal atresia and lymphedema phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double stranded rna induced gene expression Gene Set

From Biocarta Pathways

proteins participating in the double stranded rna induced gene expression pathway from the Biocarta Pathways dataset.

site of double-strand break Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the site of double-strand break cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

site of double-strand break Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the site of double-strand break cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

DNA double-strand break end-joining complex Gene Set

From CORUM Protein Complexes

proteins in the DNA double-strand break end-joining complex protein complex from the CORUM Protein Complexes dataset.

Double Oxidized Cysteine Gene Set

From DrugBank Drug Targets

interacting proteins for the Double Oxidized Cysteine drug from the curated DrugBank Drug Targets dataset.

double homozygosity for receptor polymorphisms of platelet gpia and gpiiia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double homozygosity for receptor polymorphisms of platelet gpia and gpiiia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of double-strand break repair via homologous recombination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of double-strand break repair via homologous recombination biological process from the curated GO Biological Process Annotations dataset.

dna double-strand break processing involved in repair via single-strand annealing Gene Set

From GO Biological Process Annotations

genes participating in the dna double-strand break processing involved in repair via single-strand annealing biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair via nonhomologous end joining Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair via nonhomologous end joining biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair via homologous recombination Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair via homologous recombination biological process from the curated GO Biological Process Annotations dataset.

dna double-strand break processing Gene Set

From GO Biological Process Annotations

genes participating in the dna double-strand break processing biological process from the curated GO Biological Process Annotations dataset.

regulation of single stranded viral rna replication via double stranded dna intermediate Gene Set

From GO Biological Process Annotations

genes participating in the regulation of single stranded viral rna replication via double stranded dna intermediate biological process from the curated GO Biological Process Annotations dataset.

negative regulation of double-strand break repair via nonhomologous end joining Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of double-strand break repair via nonhomologous end joining biological process from the curated GO Biological Process Annotations dataset.

regulation of double-strand break repair via nonhomologous end joining Gene Set

From GO Biological Process Annotations

genes participating in the regulation of double-strand break repair via nonhomologous end joining biological process from the curated GO Biological Process Annotations dataset.

negative regulation of double-strand break repair Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of double-strand break repair biological process from the curated GO Biological Process Annotations dataset.

single stranded viral rna replication via double stranded dna intermediate Gene Set

From GO Biological Process Annotations

genes participating in the single stranded viral rna replication via double stranded dna intermediate biological process from the curated GO Biological Process Annotations dataset.

protein localization to site of double-strand break Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to site of double-strand break biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair via alternative nonhomologous end joining Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair via alternative nonhomologous end joining biological process from the curated GO Biological Process Annotations dataset.

regulation of double-strand break repair Gene Set

From GO Biological Process Annotations

genes participating in the regulation of double-strand break repair biological process from the curated GO Biological Process Annotations dataset.

positive regulation of single stranded viral rna replication via double stranded dna intermediate Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of single stranded viral rna replication via double stranded dna intermediate biological process from the curated GO Biological Process Annotations dataset.

positive regulation of double-strand break repair Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of double-strand break repair biological process from the curated GO Biological Process Annotations dataset.

positive regulation of double-strand break repair via nonhomologous end joining Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of double-strand break repair via nonhomologous end joining biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair via classical nonhomologous end joining Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair via classical nonhomologous end joining biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair biological process from the curated GO Biological Process Annotations dataset.

regulation of double-strand break repair via homologous recombination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of double-strand break repair via homologous recombination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of single stranded viral rna replication via double stranded dna intermediate Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of single stranded viral rna replication via double stranded dna intermediate biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair via break-induced replication Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair via break-induced replication biological process from the curated GO Biological Process Annotations dataset.

meiotic dna double-strand break formation Gene Set

From GO Biological Process Annotations

genes participating in the meiotic dna double-strand break formation biological process from the curated GO Biological Process Annotations dataset.

site of double-strand break Gene Set

From GO Cellular Component Annotations

proteins localized to the site of double-strand break cellular component from the curated GO Cellular Component Annotations dataset.

double-stranded rna-specific ribonuclease activity Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded rna-specific ribonuclease activity molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded dna exodeoxyribonuclease activity Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded dna exodeoxyribonuclease activity molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded rna binding Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded rna binding molecular function from the curated GO Molecular Function Annotations dataset.

double-strand/single-strand dna junction binding Gene Set

From GO Molecular Function Annotations

genes performing the double-strand/single-strand dna junction binding molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded telomeric dna binding Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded telomeric dna binding molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded rna adenosine deaminase activity Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded rna adenosine deaminase activity molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded dna-dependent atpase activity Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded dna-dependent atpase activity molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded methylated dna binding Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded methylated dna binding molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded dna 5'-3' exodeoxyribonuclease activity Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded dna 5'-3' exodeoxyribonuclease activity molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded dna binding Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded dna binding molecular function from the curated GO Molecular Function Annotations dataset.

double-stranded dna 3'-5' exodeoxyribonuclease activity Gene Set

From GO Molecular Function Annotations

genes performing the double-stranded dna 3'-5' exodeoxyribonuclease activity molecular function from the curated GO Molecular Function Annotations dataset.

double tooth Gene Set

From HPO Gene-Disease Associations

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

DNA double-strand break repair and VJ recombination XRCC4, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA double-strand break repair and VJ recombination XRCC4, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Zinc finger, double-stranded RNA binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Zinc finger, double-stranded RNA binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Double zinc ribbon Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Double zinc ribbon protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Double-stranded RNA-specific adenosine deaminase (DRADA) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Double-stranded RNA-specific adenosine deaminase (DRADA) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Double C2 protein, alpha/beta/gamma Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Double C2 protein, alpha/beta/gamma protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Double-stranded RNA-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Double-stranded RNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Double-strand recombination repair protein, Mei5-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Double-strand recombination repair protein, Mei5-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

double kidney pelvis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double kidney pelvis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal double-strand dna break repair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal double-strand dna break repair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased double-negative t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased double-negative t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased anti-double stranded dna antibody level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased anti-double stranded dna antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal double-negative t cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal double-negative t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double aortic arch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double ureter Gene Set

From MPO Gene-Phenotype Associations

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

decreased double-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased double-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal double-positive t cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal double-positive t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased double-negative t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased double-negative t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased anti-double stranded dna antibody level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased anti-double stranded dna antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased double-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased double-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dna-breaks-double-stranded Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term dna-breaks-double-stranded in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Assembly of the RAD50-MRE11-NBS1 complex at DNA double-strand breaks Gene Set

From Reactome Pathways

proteins participating in the Assembly of the RAD50-MRE11-NBS1 complex at DNA double-strand breaks pathway from the Reactome Pathways dataset.

Processing of DNA double-strand break ends Gene Set

From Reactome Pathways

proteins participating in the Processing of DNA double-strand break ends pathway from the Reactome Pathways dataset.

Double-Strand Break Repair Gene Set

From Reactome Pathways

proteins participating in the Double-Strand Break Repair pathway from the Reactome Pathways dataset.

Recruitment of repair and signaling proteins to double-strand breaks Gene Set

From Reactome Pathways

proteins participating in the Recruitment of repair and signaling proteins to double-strand breaks pathway from the Reactome Pathways dataset.

ATM mediated response to DNA double-strand break Gene Set

From Reactome Pathways

proteins participating in the ATM mediated response to DNA double-strand break pathway from the Reactome Pathways dataset.

Homologous recombination repair of replication-independent double-strand breaks Gene Set

From Reactome Pathways

proteins participating in the Homologous recombination repair of replication-independent double-strand breaks pathway from the Reactome Pathways dataset.

choroid plexus of the lateral ventricle Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in choroid plexus of the lateral ventricle relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

choroid plexus of the fourth ventricle Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in choroid plexus of the fourth ventricle relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

cerebral ventricle cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ventricle Gene Set

From GeneRIF Biological Term Annotations

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

cardiac ventricle formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac ventricle formation biological process from the curated GO Biological Process Annotations dataset.

lateral ventricle development Gene Set

From GO Biological Process Annotations

genes participating in the lateral ventricle development biological process from the curated GO Biological Process Annotations dataset.

cardiac ventricle development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac ventricle development biological process from the curated GO Biological Process Annotations dataset.

third ventricle development Gene Set

From GO Biological Process Annotations

genes participating in the third ventricle development biological process from the curated GO Biological Process Annotations dataset.

fourth ventricle development Gene Set

From GO Biological Process Annotations

genes participating in the fourth ventricle development biological process from the curated GO Biological Process Annotations dataset.

cardiac left ventricle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac left ventricle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

cardiac left ventricle formation Gene Set

From GO Biological Process Annotations

genes participating in the cardiac left ventricle formation biological process from the curated GO Biological Process Annotations dataset.

cardiac ventricle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac ventricle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

abnormality of cardiac ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the left ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

lateral ventricle Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in lateral ventricle relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

abnormality of cardiac ventricle Gene Set

From HPO Gene-Disease Associations

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

abnormality of lateral ventricle Gene Set

From HPO Gene-Disease Associations

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

single ventricle Gene Set

From HPO Gene-Disease Associations

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

dilated fourth ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the dilated fourth ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fourth ventricle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the left ventricle Gene Set

From HPO Gene-Disease Associations

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

Cerebral Ventricle Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

increased left ventricle developed pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased left ventricle developed pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal third ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

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

enlarged third ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged third ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased left ventricle systolic pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased left ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged fourth ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged fourth ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricle myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricle myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ventricle myocardium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased left ventricle developed pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased left ventricle developed pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased left ventricle diastolic pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased left ventricle diastolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lateral ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased left ventricle systolic pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased left ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased left ventricle diastolic pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased left ventricle diastolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated third ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated third ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin ventricle myocardium compact layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin ventricle myocardium compact layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ventricle papillary muscle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ventricle papillary muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased ventricle muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased ventricle muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased left ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated fourth ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated fourth ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fourth ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

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

common ventricle Gene Set

From MPO Gene-Phenotype Associations

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

increased ventricle muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased ventricle muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent fourth ventricle Gene Set

From MPO Gene-Phenotype Associations

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

brain ventricle stenosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the brain ventricle stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain ventricle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

left ventricle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

lateral ventricle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

lateral ventricle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

brain ventricle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

lateral ventricle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

brain ventricle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

fourth ventricle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

left ventricle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Forebrain defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Forebrain defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

Neural Tube Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural Tube Defects from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Laterality Defects, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laterality Defects, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Color Vision Defects 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.

cleft palate and calvaria defects. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft palate and calvaria defects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; dihydropyrimidine dehydrogenase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; dihydropyrimidine dehydrogenase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac defects Gene Set

From GAD Gene-Disease Associations

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

birth defects Gene Set

From GAD Gene-Disease Associations

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

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

axial skeletal defects Gene Set

From GAD Gene-Disease Associations

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

neural tube defects and preeclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects and preeclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects Gene Set

From GAD Gene-Disease Associations

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

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

visual field defects Gene Set

From GAD Gene-Disease Associations

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

neural tube defects; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defects Gene Set

From GeneRIF Biological Term Annotations

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

progressive visual field defects Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lung segmentation defects Gene Set

From HPO Gene-Disease Associations

genes associated with the lung segmentation defects 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.

symmetrical, oval parietal bone defects Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical, oval parietal bone defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

forearm reduction defects Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Endocardial Cushion Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Endocardial Cushion Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Color Vision Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neural Tube Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neural Tube Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

forebrain defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the forebrain defects phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

combined cellular and humoral immune defects with granulomas Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined cellular and humoral immune defects with granulomas phenotype from the curated OMIM Gene-Disease Associations dataset.

neural tube defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome 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.

Defects in cobalamin (B12) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in cobalamin (B12) metabolism pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Defects in biotin (Btn) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in biotin (Btn) metabolism pathway from the Reactome Pathways dataset.

precentral gyrus, right, inferior lateral aspect of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in precentral gyrus, right, inferior lateral aspect of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cuneus, right, peristriate Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cuneus, right, peristriate relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

amygdalohippocampal transition zone, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in amygdalohippocampal transition zone, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

facial motor nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in facial motor nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

temporal pole, right, inferior aspect Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in temporal pole, right, inferior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Crus II, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in Crus II, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

spinal trigeminal nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

trochlear nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in trochlear nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

arcuate nucleus of medulla, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in arcuate nucleus of medulla, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, retrosplenial part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, retrosplenial part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

subiculum, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in subiculum, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

frontal pole, right, medial aspect Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in frontal pole, right, medial aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior occipital gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior occipital gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

gracile nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gracile nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

precentral gyrus, right, bank of the central sulcus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in precentral gyrus, right, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lingual gyrus, right, striate Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lingual gyrus, right, striate relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior parietal lobule, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior parietal lobule, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

subthalamic nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in subthalamic nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior temporal gyrus, right, bank of mts Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior temporal gyrus, right, bank of mts relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial habenular nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial habenular nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

interstitial nucleus of Cajal, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in interstitial nucleus of Cajal, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paraventricular nucleus of the hypothalamus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paraventricular nucleus of the hypothalamus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior temporal gyrus, right, bank of the its Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior temporal gyrus, right, bank of the its relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VIIB, right, lateral hemisphere Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VIIB, right, lateral hemisphere relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

pontine reticular formation, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pontine reticular formation, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior rostral gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior rostral gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

arcuate nucleus of the hypothalamus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in arcuate nucleus of the hypothalamus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

CA2 field, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in CA2 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior frontal gyrus, right, lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior frontal gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior orbital gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

nucleus accumbens, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in nucleus accumbens, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cuneiform nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cuneiform nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

precentral gyrus, right, superior lateral aspect of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in precentral gyrus, right, superior lateral aspect of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

red nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in red nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, internal segment, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, internal segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

caudal group of intralaminar nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in caudal group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

rostral group of intralaminar nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

III, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in III, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior frontal gyrus, triangular part, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior frontal gyrus, triangular part, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

dentate nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in dentate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paraterminal gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paraterminal gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, parietal part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, parietal part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

V, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in V, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

middle frontal gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in middle frontal gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

fusiform gyrus, right, bank of cos Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in fusiform gyrus, right, bank of cos relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

gigantocellular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gigantocellular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, mammillary region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, mammillary region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, right, ventral division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, right, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

transverse gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in transverse gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

head of caudate nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head of caudate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

substantia nigra, pars compacta, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in substantia nigra, pars compacta, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

zona incerta, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in zona incerta, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

IV, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in IV, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

long insular gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in long insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VI, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VI, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VIIIA, right, lateral hemisphere Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VIIIA, right, lateral hemisphere relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

CA1 field, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in CA1 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

short insular gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in short insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

angular gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in angular gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VI, right, lateral hemisphere Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VI, right, lateral hemisphere relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

precentral gyrus, right, bank of the precentral sulcus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in precentral gyrus, right, bank of the precentral sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior olivary complex, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior olivary complex, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

nucleus subceruleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in nucleus subceruleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

postcentral gyrus, right, superior lateral aspect of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in postcentral gyrus, right, superior lateral aspect of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior occipital gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior occipital gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior occipital gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior occipital gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, external segment, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, external segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

fastigial nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in fastigial nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

precuneus, right, superior lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in precuneus, right, superior lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

pontine nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pontine nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior colliculus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior colliculus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral medullary reticular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

middle temporal gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in middle temporal gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globose nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globose nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

planum temporale, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in planum temporale, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

parahippocampal gyrus, right, lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in parahippocampal gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

middle temporal gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in middle temporal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cortico-medial group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cortico-medial group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

CA3 field, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in CA3 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

mammillary body, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in mammillary body, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cuneus, right, striate Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cuneus, right, striate relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

angular gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in angular gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

postcentral gyrus, right, inferior lateral aspect of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in postcentral gyrus, right, inferior lateral aspect of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior frontal gyrus, right, medial bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior frontal gyrus, right, medial bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, retrosplenial part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, retrosplenial part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

tail of caudate nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in tail of caudate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

claustrum, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in claustrum, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central gray substance of midbrain, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central gray substance of midbrain, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

body of caudate nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in body of caudate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

putamen, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in putamen, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulum bundle, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulum bundle, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

motor nucleus of trigeminal nerve, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in motor nucleus of trigeminal nerve, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

ventral tegmental area, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in ventral tegmental area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior olivary complex, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior olivary complex, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

CA4 field, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in CA4 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

locus ceruleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in locus ceruleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

frontal pole, right, inferior aspect Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in frontal pole, right, inferior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior temporal gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior temporal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

dorsal lateral geniculate nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsal lateral geniculate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior temporal gyrus, right, lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior temporal gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central gray of the pons, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central gray of the pons, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

septal nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in septal nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial orbital gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VIIIB, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VIIIB, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

occipito-temporal gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in occipito-temporal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior hypothalamic area, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

emboliform nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in emboliform nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, parietal part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, parietal part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

hypoglossal nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in hypoglossal nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior parietal lobule, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior parietal lobule, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

fusiform gyrus, right, bank of the its Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in fusiform gyrus, right, bank of the its relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Crus II, right, lateral hemisphere Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in Crus II, right, lateral hemisphere relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

middle frontal gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in middle frontal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial geniculate complex, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial geniculate complex, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

dorsal motor nucleus of the vagus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsal motor nucleus of the vagus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

occipito-temporal gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in occipito-temporal gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

frontal operculum, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in frontal operculum, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

supramarginal gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in supramarginal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, frontal part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, frontal part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, posterior part, right, bank of cingulate sulcus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, posterior part, right, bank of cingulate sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Heschl's gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in Heschl's gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

preoptic region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in preoptic region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral parabrachial nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral parabrachial nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

substantia nigra, pars reticulata, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in substantia nigra, pars reticulata, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

dentate gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in dentate gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral habenular nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral habenular nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior temporal gyrus, right, lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior temporal gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

supramarginal gyrus, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in supramarginal gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

IX, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in IX, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cochlear nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cochlear nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior frontal gyrus, orbital part, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior frontal gyrus, orbital part, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral orbital gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior hypothalamic area, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, frontal part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, frontal part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior rostral gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior rostral gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

vestibular nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in vestibular nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Edinger-Westphal nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in Edinger-Westphal nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

frontal pole, right, superior aspect Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in frontal pole, right, superior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

parahippocampal gyrus, right, bank of the cos Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in parahippocampal gyrus, right, bank of the cos relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

midbrain reticular formation, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in midbrain reticular formation, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lingual gyrus, right, peristriate Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lingual gyrus, right, peristriate relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

temporal pole, right, medial aspect Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in temporal pole, right, medial aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, right, dorsal division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, right, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior occipital gyrus, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior occipital gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

basomedial nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basomedial nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

gyrus rectus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gyrus rectus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

oculomotor nuclear complex, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in oculomotor nuclear complex, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

subcallosal cingulate gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in subcallosal cingulate gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Crus I, right, lateral hemisphere Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in Crus I, right, lateral hemisphere relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

supraoptic nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in supraoptic nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central medullary reticular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, posterior part, right, lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, posterior part, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

substantia innominata, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in substantia innominata, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VIIIA, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VIIIA, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

basolateral nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basolateral nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

postcentral gyrus, right, bank of the central sulcus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in postcentral gyrus, right, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

temporal pole, right, superior aspect Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in temporal pole, right, superior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

postcentral gyrus, right, bank of the posterior central sulcus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in postcentral gyrus, right, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior orbital gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

subcuneiform nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in subcuneiform nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial parabrachial nucleus,right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial parabrachial nucleus,right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

inferior frontal gyrus, opercular part, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inferior frontal gyrus, opercular part, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Crus I, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in Crus I, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

abducens nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in abducens nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

VIIB, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VIIB, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

reticular nucleus of thalamus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in reticular nucleus of thalamus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

precuneus, right, inferior lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in precuneus, right, inferior lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

planum polare, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in planum polare, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cuneate nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cuneate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

ventromedial hypothalamic nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in ventromedial hypothalamic nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

parolfactory gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in parolfactory gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

fusiform gyrus, right, lateral bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in fusiform gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

principal sensory nucleus of trigeminal nerve, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in principal sensory nucleus of trigeminal nerve, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Left-right axis malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left-right axis malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertrophy, Right Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrophy, Right Ventricular from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Ventricular Dysfunction, Right Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

right bundle branch block Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease right bundle branch block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

arrhythmogenic right ventricular dysplasia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; cardiomyopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left-right axis malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left-right axis malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

right Gene Set

From GeneRIF Biological Term Annotations

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

Arrhythmogenic Right Ventricular Cardiomyopathy_Myocardial tissue_GSE4120 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Arrhythmogenic Right Ventricular Cardiomyopathy_Myocardial tissue_GSE4120 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

determination of left/right symmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of left/right symmetry biological process from the curated GO Biological Process Annotations dataset.

positive regulation of nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

determination of intestine left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of intestine left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

right lung development Gene Set

From GO Biological Process Annotations

genes participating in the right lung development biological process from the curated GO Biological Process Annotations dataset.

right ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the right ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the regulation of nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

epithelial cilium movement involved in determination of left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cilium movement involved in determination of left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

planar cell polarity pathway involved in cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

nodal signaling pathway involved in determination of left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the nodal signaling pathway involved in determination of left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

determination of pancreatic left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of pancreatic left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

determination of left/right asymmetry in lateral mesoderm Gene Set

From GO Biological Process Annotations

genes participating in the determination of left/right asymmetry in lateral mesoderm biological process from the curated GO Biological Process Annotations dataset.

determination of stomach left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of stomach left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

determination of left/right asymmetry in nervous system Gene Set

From GO Biological Process Annotations

genes participating in the determination of left/right asymmetry in nervous system biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in determination of left/right symmetry Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in determination of left/right symmetry biological process from the curated GO Biological Process Annotations dataset.

right lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the right lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

determination of liver left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of liver left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

determination of digestive tract left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of digestive tract left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

left/right axis specification Gene Set

From GO Biological Process Annotations

genes participating in the left/right axis specification biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in cardiac right atrium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of nodal signaling pathway involved in determination of left/right asymmetry Gene Set

From GO Biological Process Annotations

genes participating in the regulation of nodal signaling pathway involved in determination of left/right asymmetry biological process from the curated GO Biological Process Annotations dataset.

right aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the right aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right-to-left shunt Gene Set

From HPO Gene-Disease Associations

genes associated with the right-to-left shunt phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular hypertrophy Gene Set

From HPO Gene-Disease Associations

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

right ventricular failure Gene Set

From HPO Gene-Disease Associations

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

right ventricular cardiomyopathy Gene Set

From HPO Gene-Disease Associations

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

elevated right atrial pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated right atrial pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular dilatation Gene Set

From HPO Gene-Disease Associations

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

right bundle branch block Gene Set

From HPO Gene-Disease Associations

genes associated with the right bundle branch block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right aortic arch with mirror image branching Gene Set

From HPO Gene-Disease Associations

genes associated with the right aortic arch with mirror image branching phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right atrial isomerism Gene Set

From HPO Gene-Disease Associations

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

Hypertrophy, Right Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hypertrophy, Right Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Dysfunction, Right Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Arrhythmogenic Right Ventricular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Left- Right determination factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Left- Right determination factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

absent right lung accessory lobe Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent right lung accessory lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal right lung morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal right lung middle lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal right lung middle lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

right aortic arch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the right aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aberrant origin of the right subclavian artery Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aberrant origin of the right subclavian artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal left-right axis symmetry of the somites Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal left-right axis symmetry of the somites phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal right lung caudal lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal right lung caudal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal left-right axis patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal left-right axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal right renal artery morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal right renal artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused right lung lobes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused right lung lobes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent right subclavian artery Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent right subclavian artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

right-sided isomerism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the right-sided isomerism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal right subclavian artery morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal right subclavian artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

right-sided stomach Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the right-sided stomach phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retroesophageal right subclavian artery Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retroesophageal right subclavian artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal right bundle morphology Gene Set

From MPO Gene-Phenotype Associations

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

right atrial isomerism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal right lung accessory lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal right lung accessory lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

arrhythmogenic right ventricular dysplasia 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

right atrial isomerism Gene Set

From OMIM Gene-Disease Associations

genes associated with the right atrial isomerism phenotype from the curated OMIM Gene-Disease Associations dataset.

right middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

right colon Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

right colon mucosa Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

right atrium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pulmonary hypertension, primary, fenfluramine-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pulmonary hypertension, primary, fenfluramine-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 4