Name

Corneal dystrophy, epithelial basement membrane Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, epithelial basement membrane from the curated CTD Gene-Disease Associations dataset.

corneal dystrophy, epithelial basement membrane Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, epithelial basement membrane phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophies, hereditary; hereditary corneal dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Corneal epithelial dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal epithelial dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Lisch Epithelial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Lisch Epithelial from the curated CTD Gene-Disease Associations dataset.

juvenile epithelial corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile epithelial corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corneal dystrophy, lisch epithelial Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lisch epithelial phenotype from the curated OMIM Gene-Disease Associations dataset.

basement membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

basement membrane collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

basement membrane collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

basement membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

anti-basement membrane glomerulonephritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anti-basement membrane glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

nephropathy, basement membrane Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephropathy, basement membrane in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anti-glomerular basement membrane disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anti-glomerular basement membrane disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basement membrane assembly Gene Set

From GO Biological Process Annotations

genes participating in the basement membrane assembly biological process from the curated GO Biological Process Annotations dataset.

glomerular basement membrane development Gene Set

From GO Biological Process Annotations

genes participating in the glomerular basement membrane development biological process from the curated GO Biological Process Annotations dataset.

basement membrane disassembly Gene Set

From GO Biological Process Annotations

genes participating in the basement membrane disassembly biological process from the curated GO Biological Process Annotations dataset.

basement membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the basement membrane organization biological process from the curated GO Biological Process Annotations dataset.

metanephric glomerular basement membrane development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric glomerular basement membrane development biological process from the curated GO Biological Process Annotations dataset.

basement membrane Gene Set

From GO Cellular Component Annotations

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

basement membrane collagen trimer Gene Set

From GO Cellular Component Annotations

proteins localized to the basement membrane collagen trimer cellular component from the curated GO Cellular Component Annotations dataset.

thickening of the glomerular basement membrane Gene Set

From HPO Gene-Disease Associations

genes associated with the thickening of the glomerular basement membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tubular basement membrane disintegration Gene Set

From HPO Gene-Disease Associations

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

thin glomerular basement membrane Gene Set

From HPO Gene-Disease Associations

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

diffuse glomerular basement membrane lamellation Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse glomerular basement membrane lamellation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Anti-Glomerular Basement Membrane Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anti-Glomerular Basement Membrane Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal renal glomerulus basement membrane thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired basement membrane formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired basement membrane formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear basement membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear basement membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal renal glomerulus basement membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal glomerulus basement membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basement membrane morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased renal glomerulus basement membrane thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased renal glomerulus basement membrane thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

corneal epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fleck corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thiel-Behnke corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Reis-Bucklers' corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, fuchs endothelial, 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy, fuchs endothelial, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, fuchs endothelial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy, fuchs endothelial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, fuchs endothelial, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy, fuchs endothelial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy Fuchs endothelial 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy Fuchs endothelial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schnyder crystalline corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy type 3A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal endothelial dystrophy type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal endothelial dystrophy type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Groenouw corneal dystrophy type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Stromal Corneal Dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype 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.

Corneal dystrophy Avellino type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 6 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 3 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Endothelial, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset.

Lattice corneal dystrophy type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Fuchs' endothelial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 2 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Crystalline, of Schnyder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Crystalline, of Schnyder from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Fuchs' endothelial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 1 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.

Corneal endothelial dystrophy type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal endothelial dystrophy type 2 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fleck Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fleck from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Posterior Polymorphous, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 7 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Posterior Polymorphous, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Posterior Polymorphous, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 from the curated CTD Gene-Disease Associations dataset.

CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Congenital Stromal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Thiel-Behnke type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset.

Groenouw type I corneal dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Lattice Type IIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 5 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 4 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy of Bowman layer, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, corneal type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset.

lattice corneal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal granular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macular corneal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

granular corneal dystrophy Gene Set

From GAD Gene-Disease Associations

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

gelatinous droplike corneal dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gelatinous droplike corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular corneal dystrophy. Gene Set

From GAD Gene-Disease Associations

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

lattice corneal dystrophy type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular corneal dystrophy Gene Set

From GAD Gene-Disease Associations

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

Fuchs's corneal dystrophy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

corneal dystrophy Gene Set

From GWASdb SNP-Disease Associations

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

polymorphous posterior corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

lattice corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the lattice corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

granular corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the granular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

map-dot-fingerprint corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the map-dot-fingerprint corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

speckled corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the speckled corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

crystalline corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the crystalline corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

marginal corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the marginal corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nodular corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the nodular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mosaic corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the mosaic corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

punctate corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the punctate corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

corneal dystrophy, schnyder type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract with late-onset corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, congenital stromal Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, congenital stromal phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lattice type iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, gelatinous drop-like Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, gelatinous drop-like phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, posterior polymorphous, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, posterior polymorphous, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy and perceptive deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy and perceptive deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy 1, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, reis-bucklers type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, thiel-behnke type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, thiel-behnke type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, endothelial, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy 2, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lattice type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type i phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, posterior polymorphous 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, groenouw type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.

meesmann corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal fleck dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal fleck dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

macular corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, avellino type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset.

basement Gene Set

From GeneRIF Biological Term Annotations

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

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Epithelial membrane protein EMP-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial membrane protein EMP-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epithelial membrane protein EMP-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial membrane protein EMP-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epithelial membrane protein EMP-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial membrane protein EMP-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

nuclear outer membrane-endoplasmic reticulum membrane network Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear outer membrane-endoplasmic reticulum membrane network cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear outer membrane-endoplasmic reticulum membrane network Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

plasma membrane-derived chromatophore membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fusion of virus membrane with host plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the fusion of virus membrane with host plasma membrane biological process from the curated GO Biological Process Annotations dataset.

tail-anchored membrane protein insertion into er membrane Gene Set

From GO Biological Process Annotations

genes participating in the tail-anchored membrane protein insertion into er membrane biological process from the curated GO Biological Process Annotations dataset.

membrane to membrane docking Gene Set

From GO Biological Process Annotations

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

nuclear outer membrane-endoplasmic reticulum membrane network Gene Set

From GO Cellular Component Annotations

proteins localized to the nuclear outer membrane-endoplasmic reticulum membrane network cellular component from the curated GO Cellular Component Annotations dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

Cutis laxa-corneal clouding-oligophrenia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa-corneal clouding-oligophrenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal Neovascularization Gene Set

From CTD Gene-Disease Associations

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

Corneal Diseases Gene Set

From CTD Gene-Disease Associations

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

Corneal Opacity Gene Set

From CTD Gene-Disease Associations

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

Corneal Dystrophies, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.

Corneal Ulcer Gene Set

From CTD Gene-Disease Associations

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

Corneal Topography Gene Set

From dbGAP Gene-Trait Associations

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

corneal disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

corneal disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

corneal disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal staphyloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

recurrent corneal erosion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal ectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal neovascularization Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal abscess Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

perforated corneal ulcer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

idiopathic corneal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal ulcer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal dystrophies, hereditary; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal dystrophies, hereditary; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal topography Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; corneal diseases; dry eye syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; corneal diseases; dry eye syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal dystrophies Gene Set

From GAD Gene-Disease Associations

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

blind vision; blindness; corneal diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; corneal diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal dystrophies, hereditary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal dystrophies, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal ulcer; eye infections, bacterial; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal ulcer; eye infections, bacterial; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal Gene Set

From GeneRIF Biological Term Annotations

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

compound eye corneal lens development Gene Set

From GO Biological Process Annotations

genes participating in the compound eye corneal lens development biological process from the curated GO Biological Process Annotations dataset.

Central corneal thickness Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Corneal curvature Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Corneal astigmatism Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Corneal structure Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

corneal disease Gene Set

From GWASdb SNP-Disease Associations

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

decreased corneal thickness Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the decreased corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased corneal curvature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased corneal curvature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal endothelium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of corneal thickness Gene Set

From GWASdb SNP-Phenotype Associations

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

herpetiform corneal ulceration Gene Set

From HPO Gene-Disease Associations

genes associated with the herpetiform corneal ulceration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corneal scarring Gene Set

From HPO Gene-Disease Associations

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

corneal crystals Gene Set

From HPO Gene-Disease Associations

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

decreased corneal reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased corneal reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

opacification of the corneal epithelium Gene Set

From HPO Gene-Disease Associations

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

corneal opacity Gene Set

From HPO Gene-Disease Associations

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

corneal ulceration Gene Set

From HPO Gene-Disease Associations

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

corneal erosion Gene Set

From HPO Gene-Disease Associations

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

corneal perforation Gene Set

From HPO Gene-Disease Associations

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

corneal guttata Gene Set

From HPO Gene-Disease Associations

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

decreased corneal thickness Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of corneal epithelium Gene Set

From HPO Gene-Disease Associations

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

increased corneal thickness Gene Set

From HPO Gene-Disease Associations

genes associated with the increased corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corneal arcus Gene Set

From HPO Gene-Disease Associations

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

recurrent corneal erosions Gene Set

From HPO Gene-Disease Associations

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

opacification of the corneal stroma Gene Set

From HPO Gene-Disease Associations

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

increased corneal curvature Gene Set

From HPO Gene-Disease Associations

genes associated with the increased corneal curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of corneal endothelium Gene Set

From HPO Gene-Disease Associations

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

reduced number of corneal endothelial cells Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced number of corneal endothelial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corneal neovascularization Gene Set

From HPO Gene-Disease Associations

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

abnormality of corneal stroma Gene Set

From HPO Gene-Disease Associations

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

corneal degeneration Gene Set

From HPO Gene-Disease Associations

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

abnormality of corneal thickness Gene Set

From HPO Gene-Disease Associations

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

abnormal migration of corneal endothelium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corneal stromal edema Gene Set

From HPO Gene-Disease Associations

genes associated with the corneal stromal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of corneal size Gene Set

From HPO Gene-Disease Associations

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

Corneal Ulcer Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Corneal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Corneal Opacity Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Corneal Dystrophies, Hereditary Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Corneal Dystrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal corneal stroma development Gene Set

From MPO Gene-Phenotype Associations

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

decreased corneal stroma thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased corneal stroma thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

corneal scarring Gene Set

From MPO Gene-Phenotype Associations

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

corneal opacity Gene Set

From MPO Gene-Phenotype Associations

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

increased corneal stroma thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased corneal stroma thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal corneal epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased corneal light-scattering Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased corneal light-scattering phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal corneal endothelium morphology Gene Set

From MPO Gene-Phenotype Associations

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

corneal abrasion Gene Set

From MPO Gene-Phenotype Associations

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

corneal vascularization Gene Set

From MPO Gene-Phenotype Associations

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

corneal deposits Gene Set

From MPO Gene-Phenotype Associations

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

increased incidence of corneal inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased incidence of corneal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent corneal endothelium Gene Set

From MPO Gene-Phenotype Associations

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

corneal-lenticular stalk Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the corneal-lenticular stalk phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal corneal stroma morphology Gene Set

From MPO Gene-Phenotype Associations

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

?corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal opacification and other ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal opacification and other ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal clouding, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal clouding, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue corneal cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

corneal epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

corneal fibroblast cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue corneal fibroblast cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

corneal fibroblast cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

corneal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

corneal epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Ovarian epithelial cancer Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ovarian epithelial cancer from the curated CTD Gene-Disease Associations dataset.

Neoplasms, Glandular and Epithelial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Glandular and Epithelial from the curated CTD Gene-Disease Associations dataset.

Thymic epithelial tumor Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thymic epithelial tumor from the curated CTD Gene-Disease Associations dataset.

malignant epithelial mesothelioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ovary epithelial cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

focal epithelial hyperplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

epithelial-myoepithelial carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

punctate epithelial keratoconjunctivitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

malignant ovarian surface epithelial-stromal neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease malignant ovarian surface epithelial-stromal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

epithelial predominant wilms' tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease epithelial predominant wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

epithelial malignant thymoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

H3K79me2_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K79me2_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_retinal pigment epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_retinal pigment epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_retinal pigment epithelial cell_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_retinal pigment epithelial cell_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K9me3_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9me3_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_choroid plexus epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_choroid plexus epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_choroid plexus epithelial cell_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_choroid plexus epithelial cell_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_mammary epithelial cell_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_mammary epithelial cell_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_mammary epithelial cell_hg19_3 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_mammary epithelial cell_hg19_3 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H4K20me1_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H4K20me1_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K9ac_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9ac_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me1_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me1_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_kidney epithelial cell_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_kidney epithelial cell_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_kidney epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_kidney epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K27ac_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27ac_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_bronchial epithelial cell_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_bronchial epithelial cell_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_bronchial epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_bronchial epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me2_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me2_mammary epithelial cell_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H2AFZ_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H2AFZ_mammary epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_bronchial epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_bronchial epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K27me3_mammary epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K27me3_mammary epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K27me3_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K27me3_mammary epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K27me3_bronchial epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K27me3_bronchial epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K27me3_bronchial epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K27me3_bronchial epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K36me3_bronchial epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K36me3_bronchial epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K36me3_bronchial epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K36me3_bronchial epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K27me3_kidney epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K27me3_kidney epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K27me3_kidney epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K27me3_kidney epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K36me3_kidney epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K36me3_kidney epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_mammary epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_mammary epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_mammary epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_mammary epithelial cell_hg19_3 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_mammary epithelial cell_hg19_3 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_choroid plexus epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_choroid plexus epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_choroid plexus epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_choroid plexus epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_retinal pigment epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_retinal pigment epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_retinal pigment epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_retinal pigment epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

EZH2_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2_mammary epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K36me3_kidney epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K36me3_kidney epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

H3K36me3_mammary epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the H3K36me3_mammary epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_kidney epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_kidney epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_kidney epithelial cell_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_kidney epithelial cell_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_bronchial epithelial cell_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_bronchial epithelial cell_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

endometriosis; neoplasms, glandular and epithelial; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometriosis; neoplasms, glandular and epithelial; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epithelial ovarian cancer Gene Set

From GAD Gene-Disease Associations

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

lung neoplasms; neoplasms, glandular and epithelial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung neoplasms; neoplasms, glandular and epithelial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; neoplasms, glandular and epithelial; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; neoplasms, glandular and epithelial; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

focal epithelial hyperplasia Gene Set

From GAD Gene-Disease Associations

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

neoplasms, glandular and epithelial; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, glandular and epithelial; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epithelial Gene Set

From GeneRIF Biological Term Annotations

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

APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy_Thymic epithelial cell_GSE85 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy_Thymic epithelial cell_GSE85 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Type 1 diabetes mellitus_Thymic epithelial cell_GSE11 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Type 1 diabetes mellitus_Thymic epithelial cell_GSE11 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

not applicable_asthma_GSE43696_369_mouse_bronchial epithelial cell Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the not applicable_asthma_GSE43696_369_mouse_bronchial epithelial cell gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

MYC_OE_GDS4763_332_human_MCF10A - immortalized breast epithelial cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the MYC_OE_GDS4763_332_human_MCF10A - immortalized breast epithelial cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

BRCA1_DEPLETION_GDS2189_121_human_MCF10A mammary epithelial cells (MECs) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the BRCA1_DEPLETION_GDS2189_121_human_MCF10A mammary epithelial cells (MECs) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

AIRE_KO_GDS2015_33_mouse_thymic epithelial cells Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the AIRE_KO_GDS2015_33_mouse_thymic epithelial cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

HER2_OE_GDS4763_331_human_MCF10A - immortalized breast epithelial cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the HER2_OE_GDS4763_331_human_MCF10A - immortalized breast epithelial cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TRIM33_KD_GDS4071_449_human_HMEC-TR mammary epithelial cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TRIM33_KD_GDS4071_449_human_HMEC-TR mammary epithelial cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

CtIP_DEPLETION_GDS2189_122_human_MCF10A mammary epithelial cells (MECs) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the CtIP_DEPLETION_GDS2189_122_human_MCF10A mammary epithelial cells (MECs) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

glomerular visceral epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the glomerular visceral epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial to mesenchymal transition biological process from the curated GO Biological Process Annotations dataset.

glomerular visceral epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

epithelial cell maturation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell maturation biological process from the curated GO Biological Process Annotations dataset.

epithelial to mesenchymal transition involved in endocardial cushion formation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial to mesenchymal transition involved in endocardial cushion formation biological process from the curated GO Biological Process Annotations dataset.

polarized epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

regulation of epithelial cell differentiation involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

epithelial fluid transport Gene Set

From GO Biological Process Annotations

genes participating in the epithelial fluid transport biological process from the curated GO Biological Process Annotations dataset.

glandular epithelial cell maturation Gene Set

From GO Biological Process Annotations

genes participating in the glandular epithelial cell maturation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of metanephric glomerular visceral epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of metanephric glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

regulation of epithelial cell proliferation involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial cell migration biological process from the curated GO Biological Process Annotations dataset.

igg immunoglobulin transcytosis in epithelial cells mediated by fcrn immunoglobulin receptor Gene Set

From GO Biological Process Annotations

genes participating in the igg immunoglobulin transcytosis in epithelial cells mediated by fcrn immunoglobulin receptor biological process from the curated GO Biological Process Annotations dataset.

stromal-epithelial cell signaling involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the stromal-epithelial cell signaling involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

morphogenesis of an epithelial fold Gene Set

From GO Biological Process Annotations

genes participating in the morphogenesis of an epithelial fold biological process from the curated GO Biological Process Annotations dataset.

epithelial cell morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell morphogenesis biological process from the curated GO Biological Process Annotations dataset.

mesenchymal-epithelial cell signaling involved in lung development Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal-epithelial cell signaling involved in lung development biological process from the curated GO Biological Process Annotations dataset.

epithelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell migration biological process from the curated GO Biological Process Annotations dataset.

ureter epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

negative regulation of epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

positive regulation of epithelial cell proliferation involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

immunoglobulin transcytosis in epithelial cells Gene Set

From GO Biological Process Annotations

genes participating in the immunoglobulin transcytosis in epithelial cells biological process from the curated GO Biological Process Annotations dataset.

intestinal epithelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the intestinal epithelial cell migration biological process from the curated GO Biological Process Annotations dataset.

columnar/cuboidal epithelial cell maturation Gene Set

From GO Biological Process Annotations

genes participating in the columnar/cuboidal epithelial cell maturation biological process from the curated GO Biological Process Annotations dataset.

morphogenesis of an epithelial bud Gene Set

From GO Biological Process Annotations

genes participating in the morphogenesis of an epithelial bud biological process from the curated GO Biological Process Annotations dataset.

mesenchymal-epithelial cell signaling involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal-epithelial cell signaling involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations dataset.

mesenchymal to epithelial transition involved in renal vesicle formation Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal to epithelial transition involved in renal vesicle formation biological process from the curated GO Biological Process Annotations dataset.

regulation of epithelial cell migration Gene Set

From GO Biological Process Annotations

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

canonical wnt signaling pathway involved in positive regulation of epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in positive regulation of epithelial to mesenchymal transition biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

secretion by lung epithelial cell involved in lung growth Gene Set

From GO Biological Process Annotations

genes participating in the secretion by lung epithelial cell involved in lung growth biological process from the curated GO Biological Process Annotations dataset.

secretory columnal luminar epithelial cell differentiation involved in prostate glandular acinus development Gene Set

From GO Biological Process Annotations

genes participating in the secretory columnal luminar epithelial cell differentiation involved in prostate glandular acinus development biological process from the curated GO Biological Process Annotations dataset.

squamous basal epithelial stem cell differentiation involved in prostate gland acinus development Gene Set

From GO Biological Process Annotations

genes participating in the squamous basal epithelial stem cell differentiation involved in prostate gland acinus development biological process from the curated GO Biological Process Annotations dataset.

glomerular epithelial cell development Gene Set

From GO Biological Process Annotations

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

negative regulation of epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of epithelial to mesenchymal transition biological process from the curated GO Biological Process Annotations dataset.

epithelial cell maturation involved in salivary gland development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell maturation involved in salivary gland development biological process from the curated GO Biological Process Annotations dataset.

epithelial-mesenchymal signaling involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial-mesenchymal signaling involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

regulation of epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis biological process from the curated GO Biological Process Annotations dataset.

glomerular epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

branching morphogenesis of an epithelial tube Gene Set

From GO Biological Process Annotations

genes participating in the branching morphogenesis of an epithelial tube biological process from the curated GO Biological Process Annotations dataset.

epithelial structure maintenance Gene Set

From GO Biological Process Annotations

genes participating in the epithelial structure maintenance biological process from the curated GO Biological Process Annotations dataset.

regulation of polarized epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

epithelial cell proliferation involved in liver morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in liver morphogenesis biological process from the curated GO Biological Process Annotations dataset.

establishment or maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations

genes participating in the establishment or maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations dataset.

epithelial cell differentiation involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

regulation of branching involved in salivary gland morphogenesis by extracellular matrix-epithelial cell signaling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of branching involved in salivary gland morphogenesis by extracellular matrix-epithelial cell signaling biological process from the curated GO Biological Process Annotations dataset.

cardiac epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the cardiac epithelial to mesenchymal transition biological process from the curated GO Biological Process Annotations dataset.

lung epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

columnar/cuboidal epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the columnar/cuboidal epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of nephron tubule epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

multi-ciliated epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

regulation of epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the regulation of epithelial to mesenchymal transition biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mammary gland epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

dichotomous subdivision of an epithelial terminal unit Gene Set

From GO Biological Process Annotations

genes participating in the dichotomous subdivision of an epithelial terminal unit biological process from the curated GO Biological Process Annotations dataset.

positive regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations dataset.

epithelial tube formation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial tube formation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

epithelial cell proliferation involved in mammary gland duct elongation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in mammary gland duct elongation biological process from the curated GO Biological Process Annotations dataset.

mammary gland epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

epithelial cilium movement Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cilium movement biological process from the curated GO Biological Process Annotations dataset.

glandular epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

negative regulation of epithelial cell proliferation involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

epithelial cilium movement involved in determination of left/right asymmetry Gene Set

From GO Biological Process Annotations

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

intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations

genes participating in the intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lens epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lens epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

intestinal epithelial cell maturation Gene Set

From GO Biological Process Annotations

genes participating in the intestinal epithelial cell maturation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell proliferation involved in salivary gland morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in salivary gland morphogenesis biological process from the curated GO Biological Process Annotations dataset.

mammary gland epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the mammary gland epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

establishment of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations

genes participating in the establishment of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations dataset.

epithelial to mesenchymal transition Gene Set

From GO Biological Process Annotations

genes participating in the epithelial to mesenchymal transition biological process from the curated GO Biological Process Annotations dataset.

negative regulation of epithelial cell proliferation Gene Set

From GO Biological Process Annotations

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

immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor Gene Set

From GO Biological Process Annotations

genes participating in the immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor biological process from the curated GO Biological Process Annotations dataset.

negative regulation of epithelial cell differentiation involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

regulation of branching involved in salivary gland morphogenesis by epithelial-mesenchymal signaling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of branching involved in salivary gland morphogenesis by epithelial-mesenchymal signaling biological process from the curated GO Biological Process Annotations dataset.

epithelial cell fate commitment Gene Set

From GO Biological Process Annotations

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

regulation of epithelial cell proliferation involved in lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

epithelial cell proliferation involved in lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial cell differentiation involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

glomerular visceral epithelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the glomerular visceral epithelial cell migration biological process from the curated GO Biological Process Annotations dataset.

regulation of metanephric glomerular visceral epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of metanephric glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mammary gland epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

intestinal epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

negative regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis biological process from the curated GO Biological Process Annotations dataset.

prostate epithelial cord arborization involved in prostate glandular acinus morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the prostate epithelial cord arborization involved in prostate glandular acinus morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of epithelial cell migration Gene Set

From GO Biological Process Annotations

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

mesenchymal to epithelial transition involved in metanephric renal vesicle formation Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal to epithelial transition involved in metanephric renal vesicle formation biological process from the curated GO Biological Process Annotations dataset.

nephron tubule epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell differentiation involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell differentiation involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

morphogenesis of an epithelial sheet Gene Set

From GO Biological Process Annotations

genes participating in the morphogenesis of an epithelial sheet biological process from the curated GO Biological Process Annotations dataset.

mesenchymal to epithelial transition involved in metanephros morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal to epithelial transition involved in metanephros morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of polarized epithelial cell differentiation Gene Set

From GO Biological Process Annotations

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

metanephric glomerular epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric glomerular epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

glomerular parietal epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the glomerular parietal epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial cell proliferation involved in wound healing Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial cell proliferation involved in wound healing biological process from the curated GO Biological Process Annotations dataset.

regulation of mammary gland epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell-cell adhesion Gene Set

From GO Biological Process Annotations

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

negative regulation of epithelial cell proliferation involved in lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

mesenchymal-epithelial cell signaling Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal-epithelial cell signaling biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell proliferation involved in renal tubule morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in renal tubule morphogenesis biological process from the curated GO Biological Process Annotations dataset.

glandular epithelial cell development Gene Set

From GO Biological Process Annotations

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

intestinal epithelial cell development Gene Set

From GO Biological Process Annotations

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

epithelial tube branching involved in lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial tube branching involved in lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of nephron tubule epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

epithelial-mesenchymal cell signaling Gene Set

From GO Biological Process Annotations

genes participating in the epithelial-mesenchymal cell signaling biological process from the curated GO Biological Process Annotations dataset.

regulation of metanephric nephron tubule epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of metanephric nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell proliferation involved in prostatic bud elongation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in prostatic bud elongation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell proliferation involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations dataset.

prostate epithelial cord elongation Gene Set

From GO Biological Process Annotations

genes participating in the prostate epithelial cord elongation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of nephron tubule epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell apoptotic process involved in palatal shelf morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell apoptotic process involved in palatal shelf morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of lens epithelial cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lens epithelial cell proliferation biological process from the curated GO Biological Process Annotations dataset.

colon epithelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the colon epithelial cell migration biological process from the curated GO Biological Process Annotations dataset.

regulation of epithelial cell proliferation Gene Set

From GO Biological Process Annotations

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

columnar/cuboidal epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the columnar/cuboidal epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of epithelial cell proliferation involved in lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

epithelial tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of metanephric nephron tubule epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of metanephric nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

mesenchymal to epithelial transition Gene Set

From GO Biological Process Annotations

genes participating in the mesenchymal to epithelial transition biological process from the curated GO Biological Process Annotations dataset.

epithelial cell development Gene Set

From GO Biological Process Annotations

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

metanephric glomerular visceral epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

regulation of branching involved in salivary gland morphogenesis by mesenchymal-epithelial signaling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of branching involved in salivary gland morphogenesis by mesenchymal-epithelial signaling biological process from the curated GO Biological Process Annotations dataset.

epithelial cell differentiation involved in mammary gland alveolus development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell differentiation involved in mammary gland alveolus development biological process from the curated GO Biological Process Annotations dataset.

embryonic epithelial tube formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic epithelial tube formation biological process from the curated GO Biological Process Annotations dataset.

epithelial cell maturation involved in prostate gland development Gene Set

From GO Biological Process Annotations

genes participating in the epithelial cell maturation involved in prostate gland development biological process from the curated GO Biological Process Annotations dataset.

glomerular parietal epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the glomerular parietal epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

establishment of epithelial cell polarity Gene Set

From GO Biological Process Annotations

genes participating in the establishment of epithelial cell polarity biological process from the curated GO Biological Process Annotations dataset.

retinal pigment epithelial atrophy Gene Set

From HPO Gene-Disease Associations

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

macular retinal pigment epithelial mottling Gene Set

From HPO Gene-Disease Associations

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

Neoplasms, Glandular and Epithelial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Glandular and Epithelial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Focal Epithelial Hyperplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Focal Epithelial Hyperplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Epithelial-stromal interaction protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial-stromal interaction protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epithelial sodium channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial sodium channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lens epithelial cell protein LEP503 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lens epithelial cell protein LEP503 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epithelial discoidin domain-containing receptor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial discoidin domain-containing receptor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

epithelial cell signaling in helicobacter pylori infection Gene Set

From KEGG Pathways

proteins participating in the epithelial cell signaling in helicobacter pylori infection pathway from the KEGG Pathways dataset.

abnormal kidney epithelial cell primary cilium physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal renal tubule epithelial cell primary cilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

salivary gland epithelial hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the salivary gland epithelial hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac epithelial to mesenchymal transition Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac epithelial to mesenchymal transition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

stomach epithelial hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the stomach epithelial hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

bronchiolar epithelial hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the bronchiolar epithelial hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pulmonary alveolus epithelial cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pulmonary alveolus epithelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

prostate gland epithelial hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the prostate gland epithelial hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney epithelial cell primary cilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

bronchial epithelial hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the bronchial epithelial hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary epithelial necrosis Gene Set

From MPO Gene-Phenotype Associations

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

epithelial Gene Set

From Phosphosite Textmining Biological Term Annotations

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

TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) Gene Set

From Reactome Pathways

proteins participating in the TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) pathway from the Reactome Pathways dataset.

epithelial cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue epithelial cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

thyroid epithelial cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue thyroid epithelial cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

epithelial cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

liver epithelial cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue liver epithelial cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

bronchial epithelial cell Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue bronchial epithelial cell in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

buccal epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ovarian surface epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

mammary epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

human lens epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

colonic epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

tracheobronchial epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

amnion epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

epithelial stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thymic medullary epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

barrett's epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

mammary epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

lens epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

alveolar epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cervical epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

lung epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thyroid epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thymic cortical epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

tracheobronchial epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

gastric epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

liver epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

biliary epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

bronchial epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

breast epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

bronchial epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

amnion epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ovarian surface epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

oviduct epithelial cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ovarian epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

human amniotic epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

epithelial ovarian cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

oral epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ovarian epithelial carcinoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease ovarian epithelial carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Duchenne muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Patterned dystrophy of retinal pigment epithelium Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular dystrophy, vitelliform, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular dystrophy, vitelliform, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Merosin deficient congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Occult macular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Occult macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2S Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bietti crystalline corneoretinal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bietti crystalline corneoretinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Becker muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone dystrophy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitelliform dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitelliform dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Facioscapulohumeral muscular dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal cone dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONE DYSTROPHY 5, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONE DYSTROPHY 5, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ullrich congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Infantile neuroaxonal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular dystrophy, vitelliform, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular dystrophy, vitelliform, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal cone dystrophy 3B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, early-onset severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy amelogenesis imperfecta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Miyoshi Muscular Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Miyoshi Muscular Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.

Facioscapulohumeral muscular dystrophy 1a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 3A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, retinal, 1, North Carolina type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 8 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 7 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 5 from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, atypical vitelliform Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, atypical vitelliform from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, concentric annular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, concentric annular from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 13 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.

Macular Dystrophy, Retinal, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy congenital, merosin negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.

Bullous Dystrophy, Hereditary Macular Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset.

Reflex Sympathetic Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Reflex Sympathetic Dystrophy from the curated CTD Gene-Disease Associations dataset.

Scleroatonic muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scleroatonic muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

Cone Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

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

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.

Patterned dystrophy of retinal pigment epithelium Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Emery-Dreifuss Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.

MACULAR DYSTROPHY, RETINAL, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Bothnia Retinal Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy, X-Linked, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 3 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Cone Dystrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.

CONE-ROD DYSTROPHY 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY 9 from the curated CTD Gene-Disease Associations dataset.

CONE-ROD DYSTROPHY 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY 2 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.

Doyne honeycomb retinal dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.

Bietti Crystalline Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bietti Crystalline Dystrophy from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.

OCCULT MACULAR DYSTROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OCCULT MACULAR DYSTROPHY from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

Choroidal Dystrophy, Central Areolar 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset.

Asphyxiating Thoracic Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Oculopharyngeal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Merosin-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.

Toenail Dystrophy, Isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.

Retinal cone dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.

Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby from the curated CTD Gene-Disease Associations dataset.

Myotonic Dystrophy Gene Set

From CTD Gene-Disease Associations

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

Facioscapulohumeral Muscular Dystrophy 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy, limb-girdle, type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.

Vitelliform Macular Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vitelliform Macular Dystrophy from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Choroidal dystrophy central areolar Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 12 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 11 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 10 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

CONE-ROD DYSTROPHY, X-LINKED, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY, X-LINKED, 1 from the curated CTD Gene-Disease Associations dataset.

Newfoundland Rod-Cone Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Newfoundland Rod-Cone Dystrophy from the curated CTD Gene-Disease Associations dataset.

CONE-ROD DYSTROPHY 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY 15 from the curated CTD Gene-Disease Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Duchenne Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Lmna-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.

Limb-Girdle Muscular Dystrophy, Type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.

Fuchs Endothelial Dystrophy Gene Set

From dbGAP Gene-Trait Associations

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

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

limb-girdle muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ullrich congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cone-rod dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

asphyxiating thoracic dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

vitelliform macular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

myotonic dystrophy type 1 Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial central choroid dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

distal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vitelliform macular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary retinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

limb-girdle muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

reflex sympathetic dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ullrich congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vulvar dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

occult macular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fuchs' endothelial dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease fuchs' endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

becker muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cone-rod dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease emery-dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

asphyxiating thoracic dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bietti crystalline corneoretinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bietti crystalline corneoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neuroaxonal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fundus dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vitreoretinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

duchenne muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myotonic dystrophy type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy-dystroglycanopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myotonic dystrophy type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cone dystrophy Gene Set

From GAD Gene-Disease Associations

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

cone-rod dystrophy Gene Set

From GAD Gene-Disease Associations

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

machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fuchs endothelial dystrophy Gene Set

From GAD Gene-Disease Associations

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

myotonic dystrophy type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myotonic dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy, oculopharyngeal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinitis pigmentosa; macular dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinitis pigmentosa; macular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

ullrich congenital muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

chromosome disorders; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fuchs' endothelial dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fuchs' endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

cone-rod dystrophy; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cone-rod dystrophy; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibromyalgia; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

recessive cone-rod dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recessive cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystrophy Gene Set

From GeneRIF Biological Term Annotations

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

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

nail dystrophy Gene Set

From HPO Gene-Disease Associations

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

retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

limb-girdle muscular dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-rod dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-rod dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

macroreticular retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

choroidal dystrophy Gene Set

From HPO Gene-Disease Associations

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

chorioretinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

nonprogressive congenital retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

macular dystrophy Gene Set

From HPO Gene-Disease Associations

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

reticular retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

congenital muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

Reflex Sympathetic Dystrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Reflex Sympathetic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophy, Emery-Dreifuss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Vitelliform Macular Dystrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Vitelliform Macular Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Facioscapulohumeral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Myotonic Dystrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Dystrophy, Duchenne Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Duchenne phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Myotonic dystrophy protein kinase, coiled coil Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myotonic dystrophy protein kinase, coiled coil protein domain from the InterPro Predicted Protein Domain Annotations dataset.

nail dystrophy Gene Set

From MPO Gene-Phenotype Associations

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

axonal dystrophy Gene Set

From MPO Gene-Phenotype Associations

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

fascioscapulohumeral muscular dystrophy 2, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

newfoundland rod-cone dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the newfoundland rod-cone dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bothnia retinal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, megaconial type Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.

t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the t-cell immunodeficiency, congenital alopecia, and nail dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

occult macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.

microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy, x-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod retinal dystrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod retinal dystrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, retinal, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, retinal, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 6, 60177 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 6, 60177 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy, limb-girdle, type 2r Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

toenail dystrophy, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, rigid spine, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, merosin-positive Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2q Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2s Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2g Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2l Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2j Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.

hypotrichosis, congenital, with juvenile macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypotrichosis, congenital, with juvenile macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

ullrich congenital muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, north carolina type Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, north carolina type phenotype from the curated OMIM Gene-Disease Associations dataset.

tibial muscular dystrophy, tardive Gene Set

From OMIM Gene-Disease Associations

genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinol dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinol dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, patterned, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, patterned, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy with central cone involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy, progressive x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

choriodal dystrophy, central areolar 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myotonic dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myotonic dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myotonic dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myotonic dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

duchenne muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

infantile neuroaxonal dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 3, ar Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital Gene Set

From OMIM Gene-Disease Associations

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

limb-girdle muscular dystrophy, type 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

sorsby fundus dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the sorsby fundus dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with rimmed vacuoles Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

bietti crystalline corneoretinal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset, and pituitary dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 6, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with epidermolysis bullosa simplex Gene Set

From OMIM Gene-Disease Associations

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

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

vitelliform macular dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the vitelliform macular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

becker muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

?cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 7, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital merosin-deficient Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal cone dystrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, vitelliform, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, vitelliform, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, vitelliform, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, vitelliform, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, vitelliform, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, vitelliform, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Emery-Dreifuss muscular dystrophy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

myotonic dystrophy type1 Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease myotonic dystrophy type1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

golgi membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

plasma membrane part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

junctional sarcoplasmic reticulum membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

growth cone membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

outer acrosomal membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

er membrane insertion complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

basal plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

postsynaptic membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

membrane-bounded vesicle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

integral component of mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

trans-golgi network membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the trans-golgi network membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of cell outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of cell outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

synaptic vesicle membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of peroxisomal membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

anchored component of plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

anchored component of membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

rough endoplasmic reticulum membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

cytoplasmic membrane-bounded vesicle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic membrane-bounded vesicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

presynaptic membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

bounding membrane of organelle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

smooth endoplasmic reticulum membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

nuclear membrane part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

extracellular membrane-bounded organelle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extracellular membrane-bounded organelle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

transport vesicle membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

dendrite membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

intrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

host cell membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

intrinsic component of the cytoplasmic side of the plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of the cytoplasmic side of the plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic co