Name

neural retina Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

neural retina Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

regulation of neural retina development Gene Set

From GO Biological Process Annotations

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

neural retina development Gene Set

From GO Biological Process Annotations

genes participating in the neural retina development biological process from the curated GO Biological Process Annotations dataset.

Neural retina-specific leucine zipper protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural retina-specific leucine zipper protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural retinal development(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Neural retinal development(Mus musculus) pathway from the Wikipathways Pathways 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.

activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal artery occlusion; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD 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.

neural plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations

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

Neural Tube Defects Gene Set

From CTD Gene-Disease Associations

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

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

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

neural tube defects; dihydropyrimidine dehydrogenase Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

neural tube defects and preeclampsia Gene Set

From GAD Gene-Disease Associations

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

neural tube defects Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

neural tube defects; pregnancy complications Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

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

neural Gene Set

From GeneRIF Biological Term Annotations

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

planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural crest cell fate commitment Gene Set

From GO Biological Process Annotations

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

ventral trunk neural crest cell migration Gene Set

From GO Biological Process Annotations

genes participating in the ventral trunk neural crest cell migration biological process from the curated GO Biological Process Annotations dataset.

dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

neural plate morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the neural plate morphogenesis biological process from the curated GO Biological Process Annotations dataset.

neural tube development Gene Set

From GO Biological Process Annotations

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

regulation of neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

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

negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of planar polarity involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of planar polarity involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

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

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

rostrocaudal neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the rostrocaudal neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

neural crest formation Gene Set

From GO Biological Process Annotations

genes participating in the neural crest formation biological process from the curated GO Biological Process Annotations dataset.

neural nucleus development Gene Set

From GO Biological Process Annotations

genes participating in the neural nucleus development biological process from the curated GO Biological Process Annotations dataset.

neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

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

regulation of planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural fold formation Gene Set

From GO Biological Process Annotations

genes participating in the neural fold formation biological process from the curated GO Biological Process Annotations dataset.

neural plate mediolateral regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate mediolateral regionalization biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

establishment of planar polarity involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the establishment of planar polarity involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural crest cell differentiation Gene Set

From GO Biological Process Annotations

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

neural tube formation Gene Set

From GO Biological Process Annotations

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

neural plate pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the neural plate pattern specification biological process from the curated GO Biological Process Annotations dataset.

neural plate formation Gene Set

From GO Biological Process Annotations

genes participating in the neural plate formation biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell migration involved in outflow tract morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations dataset.

trunk neural crest cell migration Gene Set

From GO Biological Process Annotations

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

negative regulation of neural crest formation Gene Set

From GO Biological Process Annotations

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

canonical wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development biological process from the curated GO Biological Process Annotations dataset.

neural plate axis specification Gene Set

From GO Biological Process Annotations

genes participating in the neural plate axis specification biological process from the curated GO Biological Process Annotations dataset.

initiation of neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the initiation of neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural crest cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell fate specification biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell development involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell development involved in heart development biological process from the curated GO Biological Process Annotations dataset.

regulation of neural crest formation Gene Set

From GO Biological Process Annotations

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

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

neural crest cell migration involved in autonomic nervous system development Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell migration involved in autonomic nervous system development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

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

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural plate anterior/posterior regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations dataset.

neural crest cell migration Gene Set

From GO Biological Process Annotations

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

neural fold bending Gene Set

From GO Biological Process Annotations

genes participating in the neural fold bending biological process from the curated GO Biological Process Annotations dataset.

neural crest cell development Gene Set

From GO Biological Process Annotations

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

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell development involved in outflow tract morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell development involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations dataset.

convergent extension involved in neural plate elongation Gene Set

From GO Biological Process Annotations

genes participating in the convergent extension involved in neural plate elongation biological process from the curated GO Biological Process Annotations dataset.

regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural plate development Gene Set

From GO Biological Process Annotations

genes participating in the neural plate development biological process from the curated GO Biological Process Annotations dataset.

neural plate regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate regionalization biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural crest cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural crest cell differentiation biological process from the curated GO Biological Process Annotations dataset.

neural crest cell migration involved in sympathetic nervous system development Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell migration involved in sympathetic nervous system development biological process from the curated GO Biological Process Annotations dataset.

neural fold elevation formation Gene Set

From GO Biological Process Annotations

genes participating in the neural fold elevation formation biological process from the curated GO Biological Process Annotations dataset.

abnormality of neural tube closure Gene Set

From HPO Gene-Disease Associations

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

Neural Tube Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Neural cell adhesion Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural cell adhesion protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural proliferation differentiation control-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural proliferation differentiation control-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural Wiskott-Aldrich syndrome protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural Wiskott-Aldrich syndrome protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural chondroitin sulphate proteoglycan cytoplasmic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural chondroitin sulphate proteoglycan cytoplasmic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal neural fold elevation formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

neural tube degeneration Gene Set

From MPO Gene-Phenotype Associations

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

decreased enteric neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased enteric neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube mantle layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural plate morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cranial neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cranial neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

open neural tube Gene Set

From MPO Gene-Phenotype Associations

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

absent vagal neural crest cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vagal neural crest cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell delamination Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell delamination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent neural folds Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural tube morphology/development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trunk neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trunk neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cephalic neural fold morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cephalic neural fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal enteric neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enteric neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube marginal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube marginal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cranial neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cranial neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cranial neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cranial neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vagal neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vagal neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kinked neural tube Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cardiac neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased enteric neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased enteric neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cardiac neural crest cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cardiac neural crest cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased vagal neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased vagal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enteric neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enteric neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired cardiac neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cardiac neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural fold formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural fold formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cranial neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cranial neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube ventricular layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube ventricular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent enteric neural crest cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent enteric neural crest cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cranial neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cranial neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed neural tube closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased neural tube apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased neural tube apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural fold morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased cardiac neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cardiac neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cranial neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cranial neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enteric neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enteric neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

wavy neural tube Gene Set

From MPO Gene-Phenotype Associations

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

melanoma and neural system tumor syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the melanoma and neural system tumor syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

neural tube defects Gene Set

From OMIM Gene-Disease Associations

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

neural Gene Set

From Phosphosite Textmining Biological Term Annotations

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

neural plate Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

neural crest Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

neural arch Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

neural stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural tube Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural arch Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

embryonic neural stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural crest cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural crest-derived stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural crest Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural plate Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural cord Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural stem cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Neural Crest Differentiation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Neural Crest Differentiation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

retina Gene Set

From BioGPS Human Cell Type and Tissue Gene Expression Profiles

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

retina Gene Set

From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles

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

CCND1-20090754-RETINA-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CCND1-20090754-RETINA-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles 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.

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.

Rhegmatogenous retinal detachment, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fleck retina, familial benign Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fleck retina, familial benign 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.

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.

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.

N-(2-hydroxyethyl)retinamide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical N-(2-hydroxyethyl)retinamide from the curated CTD Gene-Chemical Interactions dataset.

retinal dimer Gene Set

From CTD Gene-Chemical Interactions

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

Retinaldehyde Gene Set

From CTD Gene-Chemical Interactions

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

9-cis-retinal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 9-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.

13-cis-retinal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 13-cis-retinal from the curated CTD Gene-Chemical Interactions 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.

Retinal Detachment Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Detachment 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.

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.

Retinal Artery Occlusion Gene Set

From CTD Gene-Disease Associations

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

Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy 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.

Retinal Dystrophies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Dystrophies 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.

Retinal Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Diseases 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.

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.

Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

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

Retinal Vein Occlusion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Vein Occlusion 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.

RETINAL DYSPLASIA, PRIMARY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY 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.

Retinal Telangiectasis Gene Set

From CTD Gene-Disease Associations

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

Retinal Nonattachment, Nonsyndromic Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.

Retinal Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Hemorrhage 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.

Late-Onset Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Retinal Vein Gene Set

From dbGAP Gene-Trait Associations

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

retinal cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal cell cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal vascular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vein occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal microaneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peripheral retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vasculitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macular retinal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease macular retinal edema 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.

retinal drusen Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retina lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vascular occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

abnormal retinal correspondence Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute retinal necrosis syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal ischemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vascular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

branch retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal cell cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal hemangioblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central retinal vein occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal detachment Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

N-Ethyl Retinamide Gene Set

From DrugBank Drug Targets

interacting proteins for the N-Ethyl Retinamide drug from the curated DrugBank Drug Targets dataset.

diabetes complications; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

branch retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease branch retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal function Gene Set

From GAD Gene-Disease Associations

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

adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein Gene Set

From GAD Gene-Disease Associations

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

geographic atrophy; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

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

retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness; retinal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; retinal disease 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.

hyperhomocysteinemia; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; retinal vein occlusion; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal vein occlusion; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

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

obesity; retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal detachment; vitreoretinopathy, proliferative Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal detachment; vitreoretinopathy, proliferative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal detachment Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal degeneration; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal degeneration; retinitis pigmentosa 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.

hypertension; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

behcet syndrome; retinal vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; retinal vasculitis 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.

retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein thrombosis Gene Set

From GAD Gene-Disease Associations

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

behcet's disease; retinal vasculitis; uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet's disease; retinal vasculitis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal diseases Gene Set

From GAD Gene-Disease Associations

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

retinal neoplasms; retinoblastoma Gene Set

From GAD Gene-Disease Associations

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

retinal vascular occlusive disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vascular occlusive disease 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.

diseases in twins; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

neovascularization, pathologic; retinal vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neovascularization, pathologic; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

hypertension; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; inflammation; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; inflammation; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set

From GAD Gene-Disease Associations

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

adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal dystrophies; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal dystrophies; retinitis pigmentosa 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.

retinae Gene Set

From GeneRIF Biological Term Annotations

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

retinal Gene Set

From GeneRIF Biological Term Annotations

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

retinas Gene Set

From GeneRIF Biological Term Annotations

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

retina Gene Set

From GeneRIF Biological Term Annotations

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

retinaldehyde Gene Set

From GeneRIF Biological Term Annotations

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

retinaspecific Gene Set

From GeneRIF Biological Term Annotations

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

NRL_Deficiency_GDS1693_238_mouse_Photoreceptors cells of retinas at P10 Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the NRL_Deficiency_GDS1693_238_mouse_Photoreceptors cells of retinas at P10 gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

NRL_Deficiency_GDS1693_235_mouse_Photoreceptors cells of retinas at E16 Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the NRL_Deficiency_GDS1693_235_mouse_Photoreceptors cells of retinas at E16 gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

NRL_Deficiency_GDS1693_236_mouse_Photoreceptors cells of retinas at P2 Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the NRL_Deficiency_GDS1693_236_mouse_Photoreceptors cells of retinas at P2 gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SYNCRIP_OE_GDS3186_84_mouse_wild type 129 mouse retina Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SYNCRIP_OE_GDS3186_84_mouse_wild type 129 mouse retina gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

NRL_Deficiency_GDS1693_239_mouse_Photoreceptors cells of retinas at 4 weeks Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the NRL_Deficiency_GDS1693_239_mouse_Photoreceptors cells of retinas at 4 weeks gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

NRL_Deficiency_GDS1693_237_mouse_Photoreceptors cells of retinas at P6 Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the NRL_Deficiency_GDS1693_237_mouse_Photoreceptors cells of retinas at P6 gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

retina development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

retinal bipolar neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

retina layer formation Gene Set

From GO Biological Process Annotations

genes participating in the retina layer formation biological process from the curated GO Biological Process Annotations dataset.

retinal pigment epithelium development Gene Set

From GO Biological Process Annotations

genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations dataset.

retinal blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

post-embryonic retina morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the post-embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell development Gene Set

From GO Biological Process Annotations

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

retinal metabolic process Gene Set

From GO Biological Process Annotations

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

embryonic retina morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

retinal cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations dataset.

regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retina vasculature development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

retina morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

retinal cone cell development Gene Set

From GO Biological Process Annotations

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

retina homeostasis Gene Set

From GO Biological Process Annotations

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

retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

regulation of retina development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retina development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

retina vasculature morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina vasculature morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell differentiation Gene Set

From GO Biological Process Annotations

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

retinal dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

retinal isomerase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations dataset.

all-trans retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

11-cis retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

retinal binding Gene Set

From GO Molecular Function Annotations

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

all-trans-retinal Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the all-trans-retinal ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Retinal vascular caliber Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Retinal vascular caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Rhegmatogenous retinal detachment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

retinal degeneration Gene Set

From GWASdb SNP-Disease Associations

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

retinal disease Gene Set

From GWASdb SNP-Disease Associations

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

retinal detachment Gene Set

From GWASdb SNP-Disease Associations

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

retinal vascular disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

retinal coloboma Gene Set

From GWASdb SNP-Phenotype Associations

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

rhegmatogenous retinal detachment Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

retinal detachment Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retina Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

4-OH-Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-OH-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

11-cis-Retinaldehyde Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 11-cis-Retinaldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.

Retinal Gene Set

From HMDB Metabolites of Enzymes

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

9-cis-Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 9-cis-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

adult retina Gene Set

From HPM Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in adult retina relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset.

retinal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal hypoplasia 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.

retinal dysplasia Gene Set

From HPO Gene-Disease Associations

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

retinal striation Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal atrophy Gene Set

From HPO Gene-Disease Associations

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

lacunar retinal depigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

focal retinal infarction Gene Set

From HPO Gene-Disease Associations

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

exudative retinal detachment Gene Set

From HPO Gene-Disease Associations

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

tractional retinal detachment Gene Set

From HPO Gene-Disease Associations

genes associated with the tractional retinal detachment 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.

aplasia/hypoplasia affecting the retina Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

rarefaction of retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

lipemia retinalis Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal folds Gene Set

From HPO Gene-Disease Associations

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

large hyperpigmented retinal spots Gene Set

From HPO Gene-Disease Associations

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

retinal telangiectasia Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal pigmentation abnormalities Gene Set

From HPO Gene-Disease Associations

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

absent retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

depigmented lesions of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the depigmented lesions of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

achromatic retinal patches Gene Set

From HPO Gene-Disease Associations

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

retinal calcification Gene Set

From HPO Gene-Disease Associations

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

retinal vascular malformation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retina Gene Set

From HPO Gene-Disease Associations

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

retinal neoplasm Gene Set

From HPO Gene-Disease Associations

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

retinal vascular tortuosity Gene Set

From HPO Gene-Disease Associations

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

retinal detachment Gene Set

From HPO Gene-Disease Associations

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

retinal flecks Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar constriction Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal avascularization Gene Set

From HPO Gene-Disease Associations

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

retinal nonattachment Gene Set

From HPO Gene-Disease Associations

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

decreased retinal pigmentation with dispersion Gene Set

From HPO Gene-Disease Associations

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

retinal malformation Gene Set

From HPO Gene-Disease Associations

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

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.

falciform retinal fold Gene Set

From HPO Gene-Disease Associations

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

congenital hypertrophy of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

retinal hemorrhage Gene Set

From HPO Gene-Disease Associations

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

pigmentary retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

loss of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

pigmentary retinal deposits Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the retinal vasculature 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.

retinal arteriolar tortuosity Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar occlusion Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal arteriolar occlusion 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.

abnormality of retinal arteries Gene Set

From HPO Gene-Disease Associations

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

rhegmatogenous retinal detachment Gene Set

From HPO Gene-Disease Associations

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

honeycomb retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

hypermyelinated retinal fibers Gene Set

From HPO Gene-Disease Associations

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

retinal coloboma Gene Set

From HPO Gene-Disease Associations

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

retinal exudate Gene Set

From HPO Gene-Disease Associations

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

retinal hamartoma Gene Set

From HPO Gene-Disease Associations

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

angioid streaks of the retina Gene Set

From HPO Gene-Disease Associations

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

cystic retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

progressive retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

retinal vascular proliferation Gene Set

From HPO Gene-Disease Associations

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

attenuation of retinal blood vessels Gene Set

From HPO Gene-Disease Associations

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

neovascularization of peripheral and posterior retina Gene Set

From HPO Gene-Disease Associations

genes associated with the neovascularization of peripheral and posterior retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral traction retinal detachment Gene Set

From HPO Gene-Disease Associations

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

retinal hemangioblastoma Gene Set

From HPO Gene-Disease Associations

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

retinal atrophy Gene Set

From HPO Gene-Disease Associations

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

Retinal Detachment Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Artery Occlusion Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Dystrophies Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Degeneration Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Vein Occlusion Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Drusen Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Vasculitis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Neovascularization Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Perforations Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal pigment epithelium GPCR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal pigment epithelium GPCR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal-specific ATP-binding cassette transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal-specific ATP-binding cassette transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal protein C2orf71 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal protein C2orf71 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cellular retinaldehyde binding/alpha-tocopherol transport Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cellular retinaldehyde binding/alpha-tocopherol transport protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal cGMP phosphodiesterase, gamma subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal cGMP phosphodiesterase, gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Visual pigments (opsins) retinal binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Visual pigments (opsins) retinal binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal degeneration protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal retinal photoreceptor layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal inner nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal melanocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

retina microaneurysm Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal rod cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal ganglion cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

calcified retina Gene Set

From MPO Gene-Phenotype Associations

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

absent retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal neuronal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal neuronal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal outer nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal rod cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal rod cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal cone cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retina Gene Set

From MPO Gene-Phenotype Associations

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

increased total retina thickness Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal rod cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal degeneration Gene Set

From MPO Gene-Phenotype Associations

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

retinal pigment epithelium atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal layers Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal photoreceptor morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total retina thickness Gene Set

From MPO Gene-Phenotype Associations

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

increased retinal ganglion cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal pigment epithelium hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal pigment epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retina morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal progenitor cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal deposits Gene Set

From MPO Gene-Phenotype Associations

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

abnormal induced retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal ganglion layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased retinal photoreceptor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal photoreceptor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal ischemia Gene Set

From MPO Gene-Phenotype Associations

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

retinal outer nuclear layer degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal rod cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal detachment Gene Set

From MPO Gene-Phenotype Associations

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

retinal cone cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal gliosis Gene Set

From MPO Gene-Phenotype Associations

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

thin retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal apoptosis Gene Set

From MPO Gene-Phenotype Associations

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

thin retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal vasculature morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retina outer limiting membrane morphology Gene Set

From MPO Gene-Phenotype Associations

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

retina coloboma Gene Set

From MPO Gene-Phenotype Associations

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

retinal ganglion cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal ganglion cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal ganglion cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal hemorrhage Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal outer plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal ganglion cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal ganglion cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal cone cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal cone cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal spots Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal blood vessel pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal rod cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal rod cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased susceptibility to induced retinal damage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal nerve fiber layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal nerve fiber layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal photoreceptor degeneration Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal outer plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal outer nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased ventral retina size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal pigment epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retina inner limiting membrane morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased retinal cone cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal outer plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal inner plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal inner nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal total retina thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

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

retina hyperplasia Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retina hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{retinal disease in usher syndrome type iia, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {retinal disease in usher syndrome type iia, modifier of} 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.

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.

retinal degeneration, late-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, late-onset, autosomal dominant 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.

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.

[fleck retina, familial benign] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fleck retina, familial benign] 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.

retinal nonattachment, nonsyndromic congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal nonattachment, nonsyndromic congenital 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.

gyrate atrophy of choroid and retina with or without ornithinemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.

doyne honeycomb degeneration of retina Gene Set

From OMIM Gene-Disease Associations

genes associated with the doyne honeycomb degeneration of retina phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal arterial macroaneurysm with supravalvular pulmonic stenosis 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.

infantile cerebellar-retinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

cavernous malformations of cns and retina Gene Set

From OMIM Gene-Disease Associations

genes associated with the cavernous malformations of cns and retina phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, autosomal recessive, clumped pigment type 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.

vasculopathy, retinal, with cerebral leukodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

retina Gene Set

From Phosphosite Textmining Biological Term Annotations

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

retina Gene Set

From ProteomicsDB Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in retina relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.

Biosynthesis of A2E, implicated in retinal degradation Gene Set

From Reactome Pathways

proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways dataset.

retinal rod Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal cone Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retina Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retina Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

retinal microvascular endothelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal ganglion cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal rod Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retina Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal ganglion cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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