Name

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

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.

dandy-walker malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the dandy-walker malformation phenotype by mapping known disease genes to disease phenotypes from the HPO 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.

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.

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.

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.

Dandy-Walker Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dandy-Walker Syndrome from the curated CTD Gene-Disease Associations dataset.

Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.

dandy-walker syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease dandy-walker syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

dandy-walker syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dandy-walker syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the dandy-walker syndrome phenotype from the curated OMIM 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.

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 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.

Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrioventricular septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrioventricular septal defect 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set

From CTD Gene-Disease Associations

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

Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set

From CTD Gene-Disease Associations

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

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.

atrioventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

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.

complete atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

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

From OMIM Gene-Disease Associations

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

atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

atrioventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

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

atrioventricular septal defect 4 Gene Set

From OMIM Gene-Disease Associations

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

atrioventricular septal defect 5 Gene Set

From OMIM Gene-Disease Associations

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

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.

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.

Capillary malformation without arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary malformation-arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation-arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary Malformation-Arteriovenous Malformation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Capillary Malformation-Arteriovenous Malformation from the curated CTD Gene-Disease Associations dataset.

capillary malformation-arteriovenous malformation Gene Set

From OMIM Gene-Disease Associations

genes associated with the capillary malformation-arteriovenous malformation phenotype from the curated OMIM Gene-Disease Associations dataset.

Marden Walker like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Marden Walker like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular Canal Defect Gene Set

From CTD Gene-Disease Associations

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

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.

atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

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

complete atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

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

Ventricular septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Ventricular septal defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial septal defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial septal defect 6 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Atrial septal defect 2 Gene Set

From CTD Gene-Disease Associations

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

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.

Atrial Septal Defect 4 Gene Set

From CTD Gene-Disease Associations

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

Atrial Septal Defect 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset.

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 Septal Defect 5 Gene Set

From CTD Gene-Disease Associations

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

Atrial Septal Defect 1 Gene Set

From CTD Gene-Disease Associations

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

atrial heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

atrial heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

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.

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.

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.

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.

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.

ventricular septal defect Gene Set

From HPO Gene-Disease Associations

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

secundum atrial septal defect Gene Set

From HPO Gene-Disease Associations

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

inlet ventricular septal defect Gene Set

From HPO Gene-Disease Associations

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

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

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

congenital septal defect Gene Set

From HPO Gene-Disease Associations

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

perimembranous ventricular septal defect Gene Set

From HPO Gene-Disease Associations

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

primum atrial septal defect Gene Set

From HPO Gene-Disease Associations

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

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.

atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

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

ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

perimembraneous ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

inlet ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

aorticopulmonary septal defect Gene Set

From MPO Gene-Phenotype Associations

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

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

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

ostium primum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

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

ostium secundum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

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

ventricular septal defect 2 Gene Set

From OMIM Gene-Disease Associations

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

ventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 6 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 5 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 4 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 3 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 2 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 1 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 9 Gene Set

From OMIM Gene-Disease Associations

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

atrial septal defect 8 Gene Set

From OMIM Gene-Disease Associations

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

ventricular septal defect 1 Gene Set

From OMIM Gene-Disease Associations

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

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.

Walker-Warburg congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Marden-Walker syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Marden-Walker syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Walker-Warburg Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Walker-Warburg Syndrome from the curated CTD Gene-Disease Associations dataset.

walker-warburg syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease walker-warburg syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

walker-warburg syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

walker Gene Set

From GeneRIF Biological Term Annotations

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

?marden-walker syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?marden-walker syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

walker carcinoma 256 cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue walker carcinoma 256 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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.

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.

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.

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.

Atrioventricular Block Gene Set

From CTD Gene-Disease Associations

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

atrioventricular block Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

atrioventricular block; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrioventricular block; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrioventricular block; death, sudden; syncope; torsades de pointes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrioventricular block; death, sudden; syncope; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrioventricular Gene Set

From GeneRIF Biological Term Annotations

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

atrioventricular node development Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular node development biological process from the curated GO Biological Process Annotations dataset.

atrioventricular bundle cell differentiation Gene Set

From GO Biological Process Annotations

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

atrioventricular valve morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular valve morphogenesis biological process from the curated GO Biological Process Annotations dataset.

atrioventricular node cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular node cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

atrioventricular valve formation Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular valve formation biological process from the curated GO Biological Process Annotations dataset.

atrioventricular node cell development Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular node cell development biological process from the curated GO Biological Process Annotations dataset.

atrioventricular canal development Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular canal development biological process from the curated GO Biological Process Annotations dataset.

atrioventricular valve development Gene Set

From GO Biological Process Annotations

genes participating in the atrioventricular valve development biological process from the curated GO Biological Process Annotations dataset.

Atrioventricular conduction Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

abnormal atrioventricular conduction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

third degree atrioventricular block Gene Set

From HPO Gene-Disease Associations

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

abnormal atrioventricular conduction Gene Set

From HPO Gene-Disease Associations

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

abnormality of the atrioventricular valves Gene Set

From HPO Gene-Disease Associations

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

abnormal atrioventricular connection Gene Set

From HPO Gene-Disease Associations

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

first degree atrioventricular block Gene Set

From HPO Gene-Disease Associations

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

atrioventricular block Gene Set

From HPO Gene-Disease Associations

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

Atrioventricular Block Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

increased atrioventricular cushion size Gene Set

From MPO Gene-Phenotype Associations

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

decreased atrioventricular cushion size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal atrioventricular node conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal atrioventricular node conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fetal atrioventricular canal septation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fetal atrioventricular canal septation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fetal atrioventricular canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

biventricular, discordant atrioventricular connection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the biventricular, discordant atrioventricular connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent atrioventricular cushions Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrioventricular bundle conduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal atrioventricular bundle conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

biventricular, ambiguous atrioventricular connection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the biventricular, ambiguous atrioventricular connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

unbalanced complete common atrioventricular canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the unbalanced complete common atrioventricular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

common atrioventricular valve Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrioventricular cushion morphology Gene Set

From MPO Gene-Phenotype Associations

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

thin atrioventricular cushion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrioventricular node morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrioventricular bundle morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrioventricular valve morphology Gene Set

From MPO Gene-Phenotype Associations

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

failure of atrioventricular cushion closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of atrioventricular cushion closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrioventricular valve regurgitation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrioventricular septum morphology Gene Set

From MPO Gene-Phenotype Associations

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

atrioventricular block Gene Set

From MPO Gene-Phenotype Associations

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

Malformation of the heart Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Malformation of the heart phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly-capillary malformation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly-capillary malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-Hand/Foot Malformation 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 6 from the curated CTD Gene-Disease Associations dataset.

Arnold-Chiari Malformation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arnold-Chiari Malformation from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 4 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 5 from the curated CTD Gene-Disease Associations dataset.

SPLIT-HAND/FOOT MALFORMATION 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPLIT-HAND/FOOT MALFORMATION 2 from the curated CTD Gene-Disease Associations dataset.

Split-hand/foot malformation with long bone deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset.

arteriovenous malformation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chiari type i malformation and syringomyelia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chiari type i malformation and syringomyelia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriovenous malformations; congenital arteriovenous malformation; hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intracranial arteriovenous malformation; intracranial arteriovenous malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial arteriovenous malformation; intracranial arteriovenous malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

wilms' tumor and congenital male genitourinary malformation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; intracranial arteriovenous malformation; intracranial arteriovenous malformations; intracranial hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; intracranial arteriovenous malformation; intracranial arteriovenous malformations; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic nerve malformation Gene Set

From GAD Gene-Disease Associations

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

malformation Gene Set

From GeneRIF Biological Term Annotations

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

thyroid malformation Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease thyroid malformation in GWAS and other genetic association datasets from the GWASdb SNP-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.

external ear malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the external ear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gastrointestinal arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

hepatic arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

arnold-chiari malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the arnold-chiari malformation 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.

cochlear malformation Gene Set

From HPO Gene-Disease Associations

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

retinal vascular malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal vascular malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

arnold-chiari type i malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the arnold-chiari type i malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

retinal malformation Gene Set

From HPO Gene-Disease Associations

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

malformation of the hepatic ductal plate Gene Set

From HPO Gene-Disease Associations

genes associated with the malformation of the hepatic ductal plate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

venous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the venous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO 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.

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.

spinal arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

cerebellar malformation Gene Set

From HPO Gene-Disease Associations

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

Arnold-Chiari Malformation Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Arnold-Chiari Malformation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cerebral arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cerebral arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

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

arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

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

microcephaly-capillary malformation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly-capillary malformation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

split hand/foot malformation 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split hand/foot malformation 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split hand/foot malformation 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split hand/foot malformation 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 3, gene duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 3, gene duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

megalencephaly-capillary malformation-polymicrogyria syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephaly-capillary malformation-polymicrogyria syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

insulin-like growth factor-1; insulin-like growth factor-3 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-1; insulin-like growth factor-3 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

Transcription elongation factor A-like/Brain expressed X-linked-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription elongation factor A-like/Brain expressed X-linked-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EGF-like repeat and discoidin I-like domain-containing protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EGF-like repeat and discoidin I-like domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thrombomodulin-like, EGF-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thrombomodulin-like, EGF-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAUS augmin-like complex subunit 7-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAUS augmin-like complex subunit 7-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) Gene Set

From Reactome Pathways

proteins participating in the Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) pathway from the Reactome Pathways dataset.

septal nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in septal nuclei, left 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.

lateral septal nucleus, intermedio-ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermedio-ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermediate part, periventricular Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermediate part, periventricular relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus, caudal (caudodorsal) part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus, caudal (caudodorsal) part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

triangular septal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in triangular septal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medial septal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medial septal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lambdoid septal zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lambdoid septal zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal complex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal complex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medial septal complex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medial septal complex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermedio-dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermedio-dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermedio-intermediate part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermedio-intermediate part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus, rostral (rostroventral) part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus, rostral (rostroventral) part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

medial septal nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

VZ in septal region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in septal region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

septal organ Gene Set

From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles

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

septal periplasm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

septal myocardial infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pronounced septal hypertrophy Gene Set

From GAD Gene-Disease Associations

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

septal Gene Set

From GeneRIF Biological Term Annotations

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

absent nasal septal cartilage Gene Set

From HPO Gene-Disease Associations

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

left ventricular septal hypertrophy Gene Set

From HPO Gene-Disease Associations

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

asymmetric septal hypertrophy Gene Set

From HPO Gene-Disease Associations

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

atrial septal aneurysm Gene Set

From HPO Gene-Disease Associations

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

atrial septal aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

lateral septal area Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ventral septal area Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

septal area Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue septal area 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.

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.

Protan defect Gene Set

From ClinVar Gene-Phenotype Associations

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

Cardiac conduction defect, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Forebrain defects Gene Set

From ClinVar Gene-Phenotype Associations

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

Phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Neutral 1 amino acid transport defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Laron-type isolated somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

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

Iodotyrosine deiodination defect Gene Set

From ClinVar Gene-Phenotype Associations

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

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

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

Renal carnitine transport defect Gene Set

From ClinVar Gene-Phenotype Associations

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

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

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

Erythrocyte lactate transporter defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

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

Oocyte maturation defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Iodotyrosyl coupling defect Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

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.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Cardiac Conduction Defect Gene Set

From CTD Gene-Disease Associations

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

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.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

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

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

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

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

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

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.

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

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

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.

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

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

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.

NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

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

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.

Erythrocyte Lactate Transporter Defect Gene Set

From CTD Gene-Disease Associations

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

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.

Micronuclei, Chromosome-Defective Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Micronuclei, Chromosome-Defective 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.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

alcohol-related birth defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital bile acid synthesis defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

qualitative platelet defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

defective colour vision Gene Set

From GAD Gene-Disease Associations

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

micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD 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.

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.

familial defective apolipoprotein b100. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b100. 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.

defective dr beta 4 chain expression to the hla-drb1 gene Gene Set

From GAD Gene-Disease Associations

genes associated with the disease defective dr beta 4 chain expression to the hla-drb1 gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial defective apolipoprotein b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; micronuclei, chromosome-defective 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.

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.

down syndrome; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

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

dna damage; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; micronuclei, chromosome-defective 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.

dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung 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.

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.

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.

familial defective apolipoprotein b-100 in a chinese man Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b-100 in a chinese man 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.

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.

human spermatogenic defect Gene Set

From GAD Gene-Disease Associations

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

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.

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.

defective heparin binding associated Gene Set

From GAD Gene-Disease Associations

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

flushing; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease flushing; micronuclei, chromosome-defective 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.

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.

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.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective 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.

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.

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.

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.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

congenital goiter and defective tg synthesis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital goiter and defective tg synthesis. 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 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.

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.

defectiveness Gene Set

From GeneRIF Biological Term Annotations

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

defectsaffected Gene Set

From GeneRIF Biological Term Annotations

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

defective Gene Set

From GeneRIF Biological Term Annotations

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

defect Gene Set

From GeneRIF Biological Term Annotations

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

Conotruncal 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.

conotruncal defect Gene Set

From GWASdb SNP-Phenotype Associations

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

thyroid hormone receptor defect Gene Set

From HPO Gene-Disease Associations

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

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.

midline defect of mandible Gene Set

From HPO Gene-Disease Associations

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

vertebral segmentation defect Gene Set

From HPO Gene-Disease Associations

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

electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set

From HPO Gene-Disease Associations

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

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.

dynein arm defect of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

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

thyroid defect in oxidation and organification of iodide Gene Set

From HPO Gene-Disease Associations

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

adrenocorticotropin (acth) receptor (acthr) defect Gene Set

From HPO Gene-Disease Associations

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

sacral segmentation defect Gene Set

From HPO Gene-Disease Associations

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

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.

abdominal wall defect Gene Set

From HPO Gene-Disease Associations

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

visual field defect Gene Set

From HPO Gene-Disease Associations

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

defective dna repair after ultraviolet radiation damage Gene Set

From HPO Gene-Disease Associations

genes associated with the defective dna repair after ultraviolet radiation damage 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.

defective lymphocyte apoptosis Gene Set

From HPO Gene-Disease Associations

genes associated with the defective lymphocyte apoptosis 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.

defective b cell activation Gene Set

From HPO Gene-Disease Associations

genes associated with the defective b cell activation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defect in the atrial septum Gene Set

From HPO Gene-Disease Associations

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

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.

respiratory insufficiency due to defective ciliary clearance Gene Set

From HPO Gene-Disease Associations

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

skull defect Gene Set

From HPO Gene-Disease Associations

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

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.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

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

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.

cervical segmentation defect Gene Set

From HPO Gene-Disease Associations

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

midline defect of the nose Gene Set

From HPO Gene-Disease Associations

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

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.

defective dehydrogenation of isovaleryl coa and butyryl coa Gene Set

From HPO Gene-Disease Associations

genes associated with the defective dehydrogenation of isovaleryl coa and butyryl coa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defective b cell differentiation Gene Set

From HPO Gene-Disease Associations

genes associated with the defective b cell differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large central visual field defect Gene Set

From HPO Gene-Disease Associations

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

conotruncal defect Gene Set

From HPO Gene-Disease Associations

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

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.

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.

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.

Micronuclei, Chromosome-Defective Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Micronuclei, Chromosome-Defective 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.

Mannose-P-dolichol utilization defect 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

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

Defective-in-cullin neddylation protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Defective-in-cullin neddylation protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

defective assembly of class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective assembly of class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective assembly of class ii molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective assembly of class ii molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iodide oxidation defect Gene Set

From MPO Gene-Phenotype Associations

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

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.

defective intracellular transport of class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective intracellular transport of class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

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

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.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

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

schizophrenia, neurophysiologic defect in Gene Set

From OMIM Gene-Disease Associations

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

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

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.

hypercholesterolemia, due to ligand-defective apo b Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, due to ligand-defective apo b 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.

erythrocyte lactate transporter defect Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

forebrain defects Gene Set

From OMIM Gene-Disease Associations

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

selective t-cell defect Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

{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.

?male pseudohermaphroditism due to defective lh Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male pseudohermaphroditism due to defective lh 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.

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.

bile acid synthesis defect, congenital, 1 Gene Set

From OMIM Gene-Disease Associations

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

bile acid synthesis defect, congenital, 3 Gene Set

From OMIM Gene-Disease Associations

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

bile acid synthesis defect, congenital, 2 Gene Set

From OMIM Gene-Disease Associations

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

bile acid synthesis defect, congenital, 4 Gene Set

From OMIM Gene-Disease Associations

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

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.

cardiac conduction defect, nonspecific Gene Set

From OMIM Gene-Disease Associations

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

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.

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

From OMIM Gene-Disease Associations

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

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.

oocyte maturation defect Gene Set

From OMIM Gene-Disease Associations

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

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

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

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.

{cardiac conduction defect, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

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.

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

From OMIM Gene-Disease Associations

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

Defective PAPSS2 causes SEMD-PA Gene Set

From Reactome Pathways

proteins participating in the Defective PAPSS2 causes SEMD-PA pathway from the Reactome Pathways dataset.

Defective FMO3 causes Trimethylaminuria (TMAU) Gene Set

From Reactome Pathways

proteins participating in the Defective FMO3 causes Trimethylaminuria (TMAU) pathway from the Reactome Pathways dataset.

Defective MAOA causes Brunner syndrome (BRUNS) Gene Set

From Reactome Pathways

proteins participating in the Defective MAOA causes Brunner syndrome (BRUNS) pathway from the Reactome Pathways dataset.

Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3) pathway from the Reactome Pathways dataset.

Defective ALG8 causes ALG8-CDG (CDG-1h) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG8 causes ALG8-CDG (CDG-1h) pathway from the Reactome Pathways dataset.

Defective MGAT2 causes MGAT2-CDG (CDG-2a) Gene Set

From Reactome Pathways

proteins participating in the Defective MGAT2 causes MGAT2-CDG (CDG-2a) pathway from the Reactome Pathways dataset.

Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) pathway from the Reactome Pathways dataset.

Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Gene Set

From Reactome Pathways

proteins participating in the Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC pathway from the Reactome Pathways dataset.

Defective MMAB causes methylmalonic aciduria type cblB Gene Set

From Reactome Pathways

proteins participating in the Defective MMAB causes methylmalonic aciduria type cblB pathway from the Reactome Pathways dataset.

Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) pathway from the Reactome Pathways dataset.

Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Gene Set

From Reactome Pathways

proteins participating in the Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) pathway from the Reactome Pathways dataset.

Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP19A1 causes Aromatase excess syndrome (AEXS) pathway from the Reactome Pathways dataset.

Defective ACY1 causes encephalopathy Gene Set

From Reactome Pathways

proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways 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.

Defective CYP1B1 causes Glaucoma Gene Set

From Reactome Pathways

proteins participating in the Defective CYP1B1 causes Glaucoma pathway from the Reactome Pathways dataset.

Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) pathway from the Reactome Pathways dataset.

Defective AMN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective AMN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defective RFT1 causes RFT1-CDG (CDG-1n) Gene Set

From Reactome Pathways

proteins participating in the Defective RFT1 causes RFT1-CDG (CDG-1n) pathway from the Reactome Pathways dataset.

Defective ALG6 causes ALG6-CDG (CDG-1c) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG6 causes ALG6-CDG (CDG-1c) pathway from the Reactome Pathways dataset.

Defective MMAA causes methylmalonic aciduria type cblA Gene Set

From Reactome Pathways

proteins participating in the Defective MMAA causes methylmalonic aciduria type cblA pathway from the Reactome Pathways dataset.

Defective CHSY1 causes TPBS Gene Set

From Reactome Pathways

proteins participating in the Defective CHSY1 causes TPBS pathway from the Reactome Pathways dataset.

Defective EXT2 causes exostoses 2 Gene Set

From Reactome Pathways

proteins participating in the Defective EXT2 causes exostoses 2 pathway from the Reactome Pathways dataset.

Defective B3GAT3 causes JDSSDHD Gene Set

From Reactome Pathways

proteins participating in the Defective B3GAT3 causes JDSSDHD pathway from the Reactome Pathways dataset.

Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Gene Set

From Reactome Pathways

proteins participating in the Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF pathway from the Reactome Pathways dataset.

Defective ALG9 causes ALG9-CDG (CDG-1l) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG9 causes ALG9-CDG (CDG-1l) pathway from the Reactome Pathways dataset.

Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) pathway from the Reactome Pathways dataset.

Defective MTR causes methylmalonic aciduria and homocystinuria type cblG Gene Set

From Reactome Pathways

proteins participating in the Defective MTR causes methylmalonic aciduria and homocystinuria type cblG pathway from the Reactome Pathways dataset.

Defective GGT1 causes Glutathionuria (GLUTH) Gene Set

From Reactome Pathways

proteins participating in the Defective GGT1 causes Glutathionuria (GLUTH) pathway from the Reactome Pathways dataset.

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

From Reactome Pathways

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

Defective ALG1 causes ALG1-CDG (CDG-1k) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG1 causes ALG1-CDG (CDG-1k) pathway from the Reactome Pathways dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.

Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Gene Set

From Reactome Pathways

proteins participating in the Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD pathway from the Reactome Pathways dataset.

Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD) Gene Set

From Reactome Pathways

proteins participating in the Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD) pathway from the Reactome Pathways dataset.

Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) pathway from the Reactome Pathways dataset.

Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) Gene Set

From Reactome Pathways

proteins participating in the Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) pathway from the Reactome Pathways dataset.

Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) pathway from the Reactome Pathways dataset.

Defective EXT1 causes exostoses 1, TRPS2 and CHDS Gene Set

From Reactome Pathways

proteins participating in the Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway from the Reactome Pathways dataset.

Defective MPDU1 causes MPDU1-CDG (CDG-1f) Gene Set

From Reactome Pathways

proteins participating in the Defective MPDU1 causes MPDU1-CDG (CDG-1f) pathway from the Reactome Pathways dataset.

Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) pathway from the Reactome Pathways dataset.

Defective CUBN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective CUBN causes hereditary megaloblastic anemia 1 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.

Defective GIF causes intrinsic factor deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective GIF causes intrinsic factor deficiency pathway from the Reactome Pathways dataset.

Defective UGT1A4 causes hyperbilirubinemia Gene Set

From Reactome Pathways

proteins participating in the Defective UGT1A4 causes hyperbilirubinemia pathway from the Reactome Pathways dataset.

Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Gene Set

From Reactome Pathways

proteins participating in the Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway from the Reactome Pathways dataset.

Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) pathway from the Reactome Pathways dataset.

Defective ALG11 causes ALG11-CDG (CDG-1p) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG11 causes ALG11-CDG (CDG-1p) pathway from the Reactome Pathways dataset.

Defective SLC26A2 causes chondrodysplasias Gene Set

From Reactome Pathways

proteins participating in the Defective SLC26A2 causes chondrodysplasias pathway from the Reactome Pathways dataset.

Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Gene Set

From Reactome Pathways

proteins participating in the Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE pathway from the Reactome Pathways dataset.

Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) pathway from the Reactome Pathways dataset.

Defective TCN2 causes hereditary megaloblastic anemia Gene Set

From Reactome Pathways

proteins participating in the Defective TCN2 causes hereditary megaloblastic anemia pathway from the Reactome Pathways dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective MUT causes methylmalonic aciduria mut type Gene Set

From Reactome Pathways

proteins participating in the Defective MUT causes methylmalonic aciduria mut type pathway from the Reactome Pathways dataset.

Defective MAN1B1 causes MRT15 Gene Set

From Reactome Pathways

proteins participating in the Defective MAN1B1 causes MRT15 pathway from the Reactome Pathways dataset.

Defective CHST6 causes MCDC1 Gene Set

From Reactome Pathways

proteins participating in the Defective CHST6 causes MCDC1 pathway from the Reactome Pathways dataset.

Defective ALG2 causes ALG2-CDG (CDG-1i) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG2 causes ALG2-CDG (CDG-1i) pathway from the Reactome Pathways dataset.

Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective CHST14 causes EDS, musculocontractural type Gene Set

From Reactome Pathways

proteins participating in the Defective CHST14 causes EDS, musculocontractural type pathway from the Reactome Pathways dataset.

Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) Gene Set

From Reactome Pathways

proteins participating in the Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) pathway from the Reactome Pathways dataset.

Defective CD320 causes methylmalonic aciduria Gene Set

From Reactome Pathways

proteins participating in the Defective CD320 causes methylmalonic aciduria 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.

Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) Gene Set

From Reactome Pathways

proteins participating in the Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) pathway from the Reactome Pathways dataset.

Defective ALG12 causes ALG12-CDG (CDG-1g) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG12 causes ALG12-CDG (CDG-1g) pathway from the Reactome Pathways dataset.

Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.

Defective UGT1A1 causes hyperbilirubinemia Gene Set

From Reactome Pathways

proteins participating in the Defective UGT1A1 causes hyperbilirubinemia pathway from the Reactome Pathways dataset.

Defective ALG3 causes ALG3-CDG (CDG-1d) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG3 causes ALG3-CDG (CDG-1d) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.

Defective CHST3 causes SEDCJD Gene Set

From Reactome Pathways

proteins participating in the Defective CHST3 causes SEDCJD pathway from the Reactome Pathways dataset.

Defective BTD causes biotidinase deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective BTD causes biotidinase deficiency pathway from the Reactome Pathways dataset.

Defective B4GALT7 causes EDS, progeroid type Gene Set

From Reactome Pathways

proteins participating in the Defective B4GALT7 causes EDS, progeroid type pathway from the Reactome Pathways dataset.

Defective MOGS causes MOGS-CDG (CDG-2b) Gene Set

From Reactome Pathways

proteins participating in the Defective MOGS causes MOGS-CDG (CDG-2b) pathway from the Reactome Pathways dataset.

Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) Gene Set

From Reactome Pathways

proteins participating in the Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) pathway from the Reactome Pathways dataset.

Defective HLCS causes multiple carboxylase deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset.

Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 Gene Set

From Reactome Pathways

proteins participating in the Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 pathway from the Reactome Pathways dataset.

Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) pathway from the Reactome Pathways dataset.

Processing-defective Hh variants abrogate ligand secretion Gene Set

From Reactome Pathways

proteins participating in the Processing-defective Hh variants abrogate ligand secretion pathway from the Reactome Pathways dataset.

Striatum-like amygdalar nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Striatum-like amygdalar nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

toll-like receptor pathway Gene Set

From Biocarta Pathways

proteins participating in the toll-like receptor pathway pathway from the Biocarta Pathways dataset.

Ataxia-telangiectasia-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

C-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the C-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Weill-Marchesani-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Weill-Marchesani-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nijmegen breakage syndrome-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-like growth factor 1 resistance to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-like growth factor 1 resistance to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pitt-Hopkins-like syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pitt-Hopkins-like syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pitt-Hopkins-like syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pitt-Hopkins-like syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Townes-Brocks-branchiootorenal-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Townes-Brocks-branchiootorenal-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Band-like calcification with simplified gyration and polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephronophthisis-like nephropathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephronophthisis-like nephropathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-like growth factor I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-like growth factor I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylocheirodysplasia, Ehlers-Danlos syndrome-like Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylocheirodysplasia, Ehlers-Danlos syndrome-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prader-Willi-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prader-Willi-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wolfram-like syndrome, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wolfram-like syndrome, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

insulin-like growth factor binding protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the insulin-like growth factor binding protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

insulin-like growth factor ternary complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

elg1 rfc-like complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the elg1 rfc-like complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ctf18 rfc-like complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ctf18 rfc-like complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

insulin-like growth factor binding protein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the insulin-like growth factor binding protein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

insulin-like growth factor binary complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

rad17 rfc-like complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the rad17 rfc-like complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

lewy body-like hyaline inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

skein-like inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

slik (saga-like) complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

digoxin-like factors Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical digoxin-like factors from the curated CTD Gene-Chemical Interactions dataset.

hirulog-like peptide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical hirulog-like peptide from the curated CTD Gene-Chemical Interactions dataset.

Vaccines, Virus-Like Particle Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Vaccines, Virus-Like Particle from the curated CTD Gene-Chemical Interactions dataset.

Huntington Disease-Like 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, gelatinous drop-like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

Larsen-Like Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Larsen-Like Syndrome from the curated CTD Gene-Disease Associations dataset.

BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.

Seborrhea-Like Dermatitis with Psoriasiform Elements Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Seborrhea-Like Dermatitis with Psoriasiform Elements from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 3 from the curated CTD Gene-Disease Associations dataset.

Insulin-Like Growth Factor I, Resistance To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insulin-Like Growth Factor I, Resistance To from the curated CTD Gene-Disease Associations dataset.

Cowden-Like Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cowden-Like Syndrome from the curated CTD Gene-Disease Associations dataset.

Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like from the curated CTD Gene-Disease Associations dataset.

ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.

Nijmegen Breakage Syndrome-Like Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nijmegen Breakage Syndrome-Like Disorder from the curated CTD Gene-Disease Associations dataset.

Weill-Marchesani-Like Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Weill-Marchesani-Like Syndrome from the curated CTD Gene-Disease Associations dataset.

Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.

NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 from the curated CTD Gene-Disease Associations dataset.

Insulin-Like Growth Factor I Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insulin-Like Growth Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.

Cataract, Coppock-Like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Coppock-Like from the curated CTD Gene-Disease Associations dataset.

Insulin-Like Growth Factor Binding Protein 5 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Insulin-Like Growth Factor Binding Protein 5 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Insulin-Like Growth Factor Binding Protein 4 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Insulin-Like Growth Factor Binding Protein 4 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Insulin-Like Growth Factor I Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Insulin-Like Growth Factor I in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

lymphoepithelioma-like thymic carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease lymphoepithelioma-like thymic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lymphoepithelioma-like carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

insulin-like growth factor-1; estrogen metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-1; estrogen metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor binding protein 4 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor binding protein 4 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor-3; retinol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-3; retinol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder-like phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder-like phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autosomal dominant coral-like cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autosomal dominant coral-like cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast cancer; insulin-like growth factor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast cancer; insulin-like growth factor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pituitary anomalies and holoprosencephaly-like features. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pituitary anomalies and holoprosencephaly-like features. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile endogenous attack-like psychoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile endogenous attack-like psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor binding protein 5 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor binding protein 5 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

like Gene Set

From GeneRIF Biological Term Annotations

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

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 5 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 5 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of myd88-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of myd88-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 8 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 8 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor tlr1:tlr2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor tlr1:tlr2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of myd88-independent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of myd88-independent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor tlr6:tlr2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor tlr6:tlr2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 5 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 5 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 7 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 7 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tirap-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tirap-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

myd88-independent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the myd88-independent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tram-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tram-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 10 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 10 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 5 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 5 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 7 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 7 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 1 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 1 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

myd88-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the myd88-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tram-dependent toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tram-dependent toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 7 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 7 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tirap-dependent toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tirap-dependent toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

response to insulin-like growth factor stimulus Gene Set

From GO Biological Process Annotations

genes participating in the response to insulin-like growth factor stimulus biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

cellular response to insulin-like growth factor stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to insulin-like growth factor stimulus biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

trif-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the trif-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 6 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 6 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of myd88-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of myd88-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

insulin-like growth factor binding protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the insulin-like growth factor binding protein complex cellular component from the curated GO Cellular Component Annotations dataset.

ctf18 rfc-like complex Gene Set

From GO Cellular Component Annotations

proteins localized to the ctf18 rfc-like complex cellular component from the curated GO Cellular Component Annotations dataset.

x11-like protein binding Gene Set

From GO Molecular Function Annotations

genes performing the x11-like protein binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

toll-like receptor 2 binding Gene Set

From GO Molecular Function Annotations

genes performing the toll-like receptor 2 binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor-activated receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor-activated receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein conjugating enzyme activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein-specific isopeptidase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein-specific isopeptidase activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein transferase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein transferase activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein binding Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein binding molecular function from the curated GO Molecular Function Annotations dataset.

receptor tyrosine kinase-like orphan receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the receptor tyrosine kinase-like orphan receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein ligase binding Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein ligase binding molecular function from the curated GO Molecular Function Annotations dataset.

natural killer cell lectin-like receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the natural killer cell lectin-like receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor ii binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor ii binding molecular function from the curated GO Molecular Function Annotations dataset.

ring-like zinc finger domain binding Gene Set

From GO Molecular Function Annotations

genes performing the ring-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein conjugating enzyme binding Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein-specific protease activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein-specific protease activity molecular function from the curated GO Molecular Function Annotations dataset.

toll-like receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the toll-like receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

toll-like receptor 4 binding Gene Set

From GO Molecular Function Annotations

genes performing the toll-like receptor 4 binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor i binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor i binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

Social autistic-like traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Social autistic-like traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Insulin-like growth factors Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Insulin-like growth factors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

madelung-like forearm deformities Gene Set

From HPO Gene-Disease Associations

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

conjunctival whitish salt-like deposits Gene Set

From HPO Gene-Disease Associations

genes associated with the conjunctival whitish salt-like deposits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bird-like facies Gene Set

From HPO Gene-Disease Associations

genes associated with the bird-like facies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

doll-like facies Gene Set

From HPO Gene-Disease Associations

genes associated with the doll-like facies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

confetti-like hypopigmented macules Gene Set

From HPO Gene-Disease Associations

genes associated with the confetti-like hypopigmented macules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mask-like facies Gene Set

From HPO Gene-Disease Associations

genes associated with the mask-like facies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reye syndrome-like episodes Gene Set

From HPO Gene-Disease Associations

genes associated with the reye syndrome-like episodes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular, rachitic-like metaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular, rachitic-like metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

swan neck-like deformities of the fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the swan neck-like deformities of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

stroke-like episodes Gene Set

From HPO Gene-Disease Associations

genes associated with the stroke-like episodes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disc-like vertebral bodies Gene Set

From HPO Gene-Disease Associations

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

slit-like opening of the exterior auditory meatus Gene Set

From HPO Gene-Disease Associations

genes associated with the slit-like opening of the exterior auditory meatus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scheuermann-like vertebral changes Gene Set

From HPO Gene-Disease Associations

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

PHF5-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PHF5-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Class I glutamine amidotransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Class I glutamine amidotransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Putative Bcl-2 like protein of testis Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Putative Bcl-2 like protein of testis protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Riboflavin synthase-like beta-barrel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Riboflavin synthase-like beta-barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ferritin- like diiron domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ferritin- like diiron domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vesicle tethering protein p115-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vesicle tethering protein p115-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Restriction endonuclease type II-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Restriction endonuclease type II-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoporin, Nup133/Nup155-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoporin, Nup133/Nup155-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kringle-like fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kringle-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Microcephalin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Microcephalin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thiolase-like, subgroup Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thiolase-like, subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase, mitochondrial-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase, mitochondrial-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ssl1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ssl1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cystatin-9 like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cystatin-9 like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kelch-like protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kelch-like protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Signal-induced proliferation-associated 1-like protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Signal-induced proliferation-associated 1-like protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Galactose mutarotase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Galactose mutarotase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-like domain of Spt6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

SPOC like C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the SPOC like C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Acid sphingomyelinase-like phosphodiesterase, predicted Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acid sphingomyelinase-like phosphodiesterase, predicted protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transferrin receptor-like, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transferrin receptor-like, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RuvA domain 2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RuvA domain 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Genetic suppressor element-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Genetic suppressor element-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosducin, thioredoxin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosducin, thioredoxin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoporin, Nup153-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoporin, Nup153-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Steroidogenic acute regulatory protein-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Steroidogenic acute regulatory protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fringe-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fringe-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ASX-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ASX-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ASX-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ASX-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thrombospondin, type 3-like repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thrombospondin, type 3-like repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Threonine synthase-like 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Threonine synthase-like 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional regulator TACO1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional regulator TACO1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HbrB-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HbrB-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myelin protein zero-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin protein zero-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myelin protein zero-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin protein zero-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myelin protein zero-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin protein zero-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Rossmann-like alpha/beta/alpha sandwich fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rossmann-like alpha/beta/alpha sandwich fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Enolase N-terminal domain-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Enolase N-terminal domain-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ORM1-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ORM1-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tudor-like, plant Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tudor-like, plant protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Maf-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Maf-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transmembrane protein Tvp38/TMEM64-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transmembrane protein Tvp38/TMEM64-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nitroreductase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nitroreductase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kinesin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kinesin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Heterogeneous nuclear ribonucleoprotein U-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heterogeneous nuclear ribonucleoprotein U-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin-like 1 activating enzyme, catalytic cysteine domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin-like 1 activating enzyme, catalytic cysteine domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Carbohydrate-binding-like fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbohydrate-binding-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CDC48 domain 2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CDC48 domain 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Katanin p60 subunit A-like 1, chordates Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Katanin p60 subunit A-like 1, chordates protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-phase kinase-associated protein 1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-phase kinase-associated protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myo-inositol-1-phosphate synthase, GAPDH-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myo-inositol-1-phosphate synthase, GAPDH-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FRG1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FRG1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Translation initiation factor, beta propellor-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Translation initiation factor, beta propellor-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoredoxin-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoredoxin-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoredoxin-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoredoxin-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NHR2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NHR2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome c-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Enhancer of polycomb-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Enhancer of polycomb-like, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GyrI-like small molecule binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GyrI-like small molecule binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GPCR, family 2, secretin-like, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GPCR, family 2, secretin-like, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

LIM and senescent cell antigen-like-containing domain protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the LIM and senescent cell antigen-like-containing domain protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TRM13/UPF0224 family, U11-48K-like CHHC zinc finger domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TRM13/UPF0224 family, U11-48K-like CHHC zinc finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ADP-ribosylation factor-like protein 6-interacting protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ADP-ribosylation factor-like protein 6-interacting protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MiaB-like tRNA modifying enzyme, archaeal-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MiaB-like tRNA modifying enzyme, archaeal-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Serum albumin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Serum albumin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Globin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Globin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dyslexia-associated protein KIAA0319-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dyslexia-associated protein KIAA0319-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Activator of Hsp90 ATPase homologue 1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Activator of Hsp90 ATPase homologue 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NEDD4-binding protein 2-like 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NEDD4-binding protein 2-like 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ClpP/crotonase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ClpP/crotonase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase-like, PTPLA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase-like, PTPLA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

AmpG-like permease/Acetyl-coenzyme A transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the AmpG-like permease/Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myb/SANT-like DNA-binding domain-containing protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myb/SANT-like DNA-binding domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RNA polymerase Rpc34-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RNA polymerase Rpc34-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myosin, N-terminal, SH3-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myosin, N-terminal, SH3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAST kinase-like protein, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAST kinase-like protein, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Translation Initiation factor eIF- 4e-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Translation Initiation factor eIF- 4e-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

D-Tyr tRNAtyr deacylase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the D-Tyr tRNAtyr deacylase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

N2227-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the N2227-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Formyl transferase, C-terminal-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Formyl transferase, C-terminal-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GAS2-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GAS2-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GAS2-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GAS2-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Metalloenzyme, LuxS/M16 peptidase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Metalloenzyme, LuxS/M16 peptidase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fumarate reductase/succinate dehydrogenase flavoprotein-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fumarate reductase/succinate dehydrogenase flavoprotein-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

50S ribosomal protein L30e-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 50S ribosomal protein L30e-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chitobiase/beta-hexosaminidase domain 2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chitobiase/beta-hexosaminidase domain 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chordin-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chordin-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chordin-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chordin-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-repair protein, UmuC-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-repair protein, UmuC-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Membrane metallo-endopeptidase-like 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane metallo-endopeptidase-like 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lebercilin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lebercilin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-like protein 7B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-like protein 7B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-like protein 7A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-like protein 7A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sds3-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sds3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Distal-less-like homeobox protein, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epidermal growth factor-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epidermal growth factor-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphoribosyltransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphoribosyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

WD40-like Beta Propeller Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the WD40-like Beta Propeller protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Integrin beta-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Integrin beta-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Abscisic acid G-protein coupled receptor-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Abscisic acid G-protein coupled receptor-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Constitutive coactivator of PPAR-gamma-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Constitutive coactivator of PPAR-gamma-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Constitutive coactivator of PPAR-gamma-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Constitutive coactivator of PPAR-gamma-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

YqgF/RNase H-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the YqgF/RNase H-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Isochorismatase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Isochorismatase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fungal lipase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fungal lipase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein ASX-like, PHD domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein ASX-like, PHD domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nuclear pore localisation protein Npl4, ubiquitin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear pore localisation protein Npl4, ubiquitin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Polycomb protein ASX/ASX-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Polycomb protein ASX/ASX-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-like peptide 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-like peptide 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PKD/REJ-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PKD/REJ-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA mismatch repair protein MutS-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA mismatch repair protein MutS-like, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Raptor N-terminal CASPase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Raptor N-terminal CASPase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Choline transporter-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Choline transporter-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Exostosin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Exostosin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NmrA-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NmrA-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-like growth factor 2 mRNA-binding protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-like growth factor 2 mRNA-binding protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Rad21/Rec8-like protein, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rad21/Rec8-like protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoporin, Nup133/Nup155-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoporin, Nup133/Nup155-like, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin/SUMO-activating enzyme ubiquitin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin/SUMO-activating enzyme ubiquitin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Saposin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Saposin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Enamine/imine deaminase YjgF-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Enamine/imine deaminase YjgF-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal RNA large subunit methyltransferase F-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal RNA large subunit methyltransferase F-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Butirosin biosynthesis, BtrG-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Butirosin biosynthesis, BtrG-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional regulator TACO1-like, domain 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional regulator TACO1-like, domain 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Histone deacetylase complex subunit SAP30/SAP30-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Histone deacetylase complex subunit SAP30/SAP30-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TsaA-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TsaA-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Smac/DIABLO-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Smac/DIABLO-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Xylose isomerase-like, TIM barrel domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Xylose isomerase-like, TIM barrel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Endonuclease III-like, conserved site-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Endonuclease III-like, conserved site-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kinesin-like protein KIF20B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kinesin-like protein KIF20B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kinesin-like protein KIF20A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kinesin-like protein KIF20A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAUS augmin-like complex subunit 2, metazoa Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAUS augmin-like complex subunit 2, metazoa protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IA, REG-2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IA, REG-2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribonuclease H-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonuclease H-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coatomer, gamma subunit, appendage, Ig-like subdomain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coatomer, gamma subunit, appendage, Ig-like subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EGF-like domain, extracellular Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EGF-like domain, extracellular protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Rad60/SUMO-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rad60/SUMO-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cyclin PHO80-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cyclin PHO80-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Domain of unknown function SprT-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Domain of unknown function SprT-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cobalamin (vitamin B12) biosynthesis CobW-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cobalamin (vitamin B12) biosynthesis CobW-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA helicase, DnaB-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA helicase, DnaB-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Antistasin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Antistasin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA recombination and repair protein RecA-like, ATP-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA recombination and repair protein RecA-like, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RDM domain, Ret finger protein-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RDM domain, Ret finger protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Staphylococcal nuclease (SNase-like), OB-fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Staphylococcal nuclease (SNase-like), OB-fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

N1221-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the N1221-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

M-phase-specific PLK1-interacting protein-like, vertebrate Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the M-phase-specific PLK1-interacting protein-like, vertebrate protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Prion-like protein Doppel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Prion-like protein Doppel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional regulator TACO1-like, domain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional regulator TACO1-like, domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cleft lip and palate transmembrane protein 1-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cleft lip and palate transmembrane protein 1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tex-like protein, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tex-like protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Exportin-1/Importin-beta-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Exportin-1/Importin-beta-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Beta-catenin-like protein 1, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Beta-catenin-like protein 1, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EGF-like calcium-binding, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EGF-like calcium-binding, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L30, ferredoxin-like fold domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L30, ferredoxin-like fold domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UvrD-like Helicase, ATP-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UvrD-like Helicase, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Beta-casein-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Beta-casein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

V-ATPase proteolipid subunit C-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the V-ATPase proteolipid subunit C-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Citrate transporter-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Citrate transporter-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo-like helical Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo-like helical protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uroplakin-3b-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uroplakin-3b-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cholecystokinin like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cholecystokinin like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxypyruvate isomerase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxypyruvate isomerase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-ketoglutarate-dependent dioxygenase AlkB-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-ketoglutarate-dependent dioxygenase AlkB-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myb-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myb-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ezrin/radixin/moesin like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ezrin/radixin/moesin like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FERM, C-terminal PH-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FERM, C-terminal PH-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Stomatin-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Stomatin-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2D-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2D-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

V-set and transmembrane domain-containing protein 2-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the V-set and transmembrane domain-containing protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Probable inactive ribonuclease-like protein 12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Probable inactive ribonuclease-like protein 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RED-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RED-like, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neuropilin and tolloid-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuropilin and tolloid-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-like growth factor-binding protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-like growth factor-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/RNA-binding protein Alba-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/RNA-binding protein Alba-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-like growth factor-binding protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-like growth factor-binding protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-like growth factor-binding protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-like growth factor-binding protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PLC-like phosphodiesterase, TIM beta/alpha-barrel domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PLC-like phosphodiesterase, TIM beta/alpha-barrel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucosidase II beta subunit-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucosidase II beta subunit-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Numb/numb-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Numb/numb-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Misato Segment II tubulin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Misato Segment II tubulin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TRAM1-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TRAM1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcyphosin-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcyphosin-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

N-lysine methyltransferase See1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the N-lysine methyltransferase See1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ASX-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ASX-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2/20, immunoglobulin-like beta-sandwich domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2/20, immunoglobulin-like beta-sandwich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vesicle transport protein, SFT2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vesicle transport protein, SFT2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Actin-related protein 2/3 complex subunit 5-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Actin-related protein 2/3 complex subunit 5-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alkaline-phosphatase-like, core domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alkaline-phosphatase-like, core domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lethal giant larvae (Lgl)-like, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal giant larvae (Lgl)-like, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter Tap-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter Tap-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CYTH-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CYTH-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

60S ribosomal protein L22-like 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 60S ribosomal protein L22-like 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DBH-like monooxygenase protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DBH-like monooxygenase protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Quinonprotein alcohol dehydrogenase-like superfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Quinonprotein alcohol dehydrogenase-like superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TGS-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TGS-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Immunity-related GTPases-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Immunity-related GTPases-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nerve growth factor-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nerve growth factor-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Four-helical cytokine-like, core Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Four-helical cytokine-like, core protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transposase, Tc1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transposase, Tc1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Rhodanese-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rhodanese-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP synthase subunit s-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP synthase subunit s-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coiled-coil transcriptional coactivator-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coiled-coil transcriptional coactivator-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.