Name

red color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

red vs non-red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red vs non-red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Red vs non-red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

red-green color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

black vs red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease black vs red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Black vs. red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blue color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

red, far-red light phototransduction Gene Set

From GO Biological Process Annotations

genes participating in the red, far-red light phototransduction biological process from the curated GO Biological Process Annotations dataset.

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

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

Eye Color Gene Set

From dbGAP Gene-Trait Associations

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

Hair Color Gene Set

From dbGAP Gene-Trait Associations

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

eye color Gene Set

From GAD Gene-Disease Associations

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

hair color Gene Set

From GAD Gene-Disease Associations

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

skin color Gene Set

From GAD Gene-Disease Associations

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

iris color Gene Set

From GAD Gene-Disease Associations

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

black vs blond hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease black vs blond hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

blond vs brown hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blond vs brown hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cutaneous melanoma which is largely independent of skin type and hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

color Gene Set

From GeneRIF Biological Term Annotations

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

Eye color traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Eye color traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Iris color Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Eye color Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Blond vs. brown hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blond vs. brown hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Black vs. blond hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Black vs. blond hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of dental color Gene Set

From HPO Gene-Disease Associations

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

abnormality of color vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of nail color Gene Set

From HPO Gene-Disease Associations

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

Color Vision Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Color Perception Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal incisor color Gene Set

From MPO Gene-Phenotype Associations

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

darkened coat color Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the darkened coat color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

variegated coat color Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the variegated coat color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

mosaic coat color Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the mosaic coat color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tooth color Gene Set

From MPO Gene-Phenotype Associations

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

abnormal urine color Gene Set

From MPO Gene-Phenotype Associations

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

diluted coat color Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the diluted coat color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

yellow coat color Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the yellow coat color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bile color Gene Set

From MPO Gene-Phenotype Associations

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

red nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

red nucleus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

red nucleus, parvicellular part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Red nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

red nucleus, magnocellular part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

red nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

Renal tubular acidosis, distal, with normal red cell morphology Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ruthenium Red Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Ruthenium Red from the curated CTD Gene-Chemical Interactions dataset.

Alizarin Red S Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Alizarin Red S from the curated CTD Gene-Chemical Interactions dataset.

Allura Red AC Dye Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Allura Red AC Dye from the curated CTD Gene-Chemical Interactions dataset.

Scarlet Red Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Scarlet Red from the curated CTD Gene-Chemical Interactions dataset.

Congo Red Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Congo Red from the curated CTD Gene-Chemical Interactions dataset.

Red-Cell Aplasia, Pure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Red-Cell Aplasia, Pure from the curated CTD Gene-Disease Associations dataset.

Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.

Pyruvate Kinase Deficiency of Red Cells Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Kinase Deficiency of Red Cells from the curated CTD Gene-Disease Associations dataset.

pure red-cell aplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

red cell folate concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red cell folate concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; kidney diseases; red-cell aplasia, pure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

red-cell aplasia, pure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid in plasma and red blood cell folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid in plasma and red blood cell folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

red Gene Set

From GeneRIF Biological Term Annotations

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

ruthenium red Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ruthenium red ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Red blood cell traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red blood cell traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Red blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

red hair Gene Set

From GWASdb SNP-Phenotype Associations

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

anemia due to reduced life span of red cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased red cell sickling tendency Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased red cell sickling tendency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

cherry red spot of the macula Gene Set

From HPO Gene-Disease Associations

genes associated with the cherry red spot of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

red hair Gene Set

From HPO Gene-Disease Associations

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

anemia due to reduced life span of red cells Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red cell osmotic fragility Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red cell osmotic fragility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ragged-red muscle fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the ragged-red muscle fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red cell sickling tendency Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red cell sickling tendency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red cell osmotic resistance Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red cell osmotic resistance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red cell hemolysis by shear stress Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red cell hemolysis by shear stress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

red-green dyschromatopsia Gene Set

From HPO Gene-Disease Associations

genes associated with the red-green dyschromatopsia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red blood cell mass Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red blood cell mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

RED-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

Protein RED, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

Opsin red/green sensitive Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Opsin red/green sensitive protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sensitivity To Red Light Reduced-like, SRR1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sensitivity To Red Light Reduced-like, SRR1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased spleen red pulp amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spleen red pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spleen red pulp morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spleen red pulp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intermingled spleen red and white pulp Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spleen red pulp amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spleen red pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent red nucleus Gene Set

From MPO Gene-Phenotype Associations

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

decreased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red blood cell deformability Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal red blood cell deformability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red nucleus morphology Gene Set

From MPO Gene-Phenotype Associations

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

[skin/hair/eye pigmentation 2, red hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

pseudohyperkalemia, familial, 2, due to red cell leak Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

red bone marrow Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Congenital stationary night blindness, autosomal dominant 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, autosomal dominant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Blindness, Cortical Gene Set

From CTD Gene-Disease Associations

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

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.

Night Blindness Gene Set

From CTD Gene-Disease Associations

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

Blindness Gene Set

From CTD Gene-Disease Associations

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

Night blindness, congenital stationary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night blindness, congenital stationary from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A from the curated CTD Gene-Disease Associations dataset.

congenital stationary night blindness Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

night blindness Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cortical blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

night blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary night blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital stationary night blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blind vision; blindness; retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

blindness; trachoma Gene Set

From GAD Gene-Disease Associations

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

blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

blindness; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

night blindness; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease night blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness 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.

blind vision; blindness; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

blindness; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

blindness Gene Set

From GeneRIF Biological Term Annotations

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

night blindness Gene Set

From HPO Gene-Disease Associations

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

congenital blindness Gene Set

From HPO Gene-Disease Associations

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

blindness Gene Set

From HPO Gene-Disease Associations

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

congenital stationary night blindness Gene Set

From HPO Gene-Disease Associations

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

adult-onset night blindness Gene Set

From HPO Gene-Disease Associations

genes associated with the adult-onset night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive night blindness Gene Set

From HPO Gene-Disease Associations

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

Night Blindness Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Blindness Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

blindness Gene Set

From MPO Gene-Phenotype Associations

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

night blindness, congenital stationary, autosomal dominant 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary, autosomal dominant 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1f, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1f, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1b, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1b, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1c, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1c, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary, autosomal dominant 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2b, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2b, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1e, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1e, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1d, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1d, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.