Name

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

?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.

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 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 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.

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 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 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.

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.

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.

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.

?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.

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.

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.

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.

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.

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.

decreased osteoclast cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased osteoclast cell number 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.

decreased eosinophil cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased memory t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cochlear hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased transitional stage t2 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased transitional stage t2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased trophoblast glycogen cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased plasma cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased respiratory mucosa goblet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased t-helper 17 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased amacrine cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased nk t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased double-negative t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased common myeloid progenitor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased common myeloid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased b-1b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased b-1b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased germ cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased pancreatic beta cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cajal-retzius cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cerebellar granule cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased single-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased t-helper 2 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic delta cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased dn1 thymic pro-t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased dn1 thymic pro-t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pp cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased b-1a cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased b-1a cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased satellite cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased gamma-delta t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased mature b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased immature b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased macrophage cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased pancreatic acinar cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased transitional stage b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased transitional stage b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased erythroid progenitor cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased sebocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased primordial germ cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased hematopoietic stem cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased memory b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased t helper 1 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased t helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vascular endothelial cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased transitional stage t1 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased transitional stage t1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased lactotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased monocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased lymphatic vessel endothelial cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lymphatic vessel endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased pro-b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased organ of corti supporting cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased organ of corti supporting cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mast cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased platelet cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased gonadotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased purkinje cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased basophil cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased enterocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased pre-b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased b-1 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased b-1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased megakaryocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased double-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cerebral cortex pyramidal cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cerebral cortex pyramidal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neuronal precursor cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased leukocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased leukocyte cell number 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.

decreased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased plasmacytoid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased germinal center b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased germinal center b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased outer hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased follicular dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cd4-positive, alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd4-positive, alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pre-pro b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pre-pro b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased inner hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased hippocampus pyramidal cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased naive b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased fetal derived definitive erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased activated t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased neutrophil cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased thyrotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased somatotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased t follicular helper cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased clara cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cd8-positive, gamma-delta intraepithelial t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd8-positive, gamma-delta intraepithelial t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic epsilon cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased hematopoietic cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased thecal cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased uterine nk cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased brown fat cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased gamma-delta intraepithelial t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased trophoblast giant cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased schwann cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased osteoblast cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cd4-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased corticotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased mature gamma-delta t cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white fat cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white fat cell number 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.

decreased lymphocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased spinal cord ventral horn cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spinal cord ventral horn cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased marginal zone b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased marginal zone b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased transitional stage t3 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased transitional stage t3 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic alpha cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased male germ cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased nk cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased cd8-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased langerhans cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased myeloid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vestibular hair cell number 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.

decreased solitary pulmonary neuroendocrine cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased solitary pulmonary neuroendocrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vestibular hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vestibular hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased b-2 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased b-2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased follicular b cell number Gene Set

From MPO Gene-Phenotype Associations

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

decreased schwann cell precursor number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased schwann cell precursor number phenotype in transgenic mice from the MPO Gene-Phenotype 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.

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.

decreased number of sweat glands Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased numbers of nephrons Gene Set

From HPO Gene-Disease Associations

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

decreased number of cd8+ t cells Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of cd8+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased number of small peripheral myelinated nerve fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased number of large peripheral myelinated nerve fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased number of cd4+ t cells Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of cd4+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased number of peripheral myelinated nerve fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased oocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased glomerular capillary number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased glomerular capillary number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased number of peritubular myoid cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased number of peritubular myoid cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neuron number Gene Set

From MPO Gene-Phenotype Associations

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

decreased secondary ovarian follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased number of pulmonary neuroendocrine bodies Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased oligodendrocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased lymph node number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lymph node number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased keratohyalin granule number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased keratohyalin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased hepatoblast number Gene Set

From MPO Gene-Phenotype Associations

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

decreased chondrocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased prostate gland duct number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased prostate gland duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased otolith number Gene Set

From MPO Gene-Phenotype Associations

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

decreased primordial ovarian follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased lumbar vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic islet number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased rib number Gene Set

From MPO Gene-Phenotype Associations

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

decreased kidney collecting duct number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased sebaceous gland number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased erythroblast number Gene Set

From MPO Gene-Phenotype Associations

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

decreased vertebrae number Gene Set

From MPO Gene-Phenotype Associations

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

decreased myocardial fiber number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased myocardial fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mitochondria number Gene Set

From MPO Gene-Phenotype Associations

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

decreased molar number Gene Set

From MPO Gene-Phenotype Associations

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

decreased metatarsal bone number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased metatarsal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased hair follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased splenocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased caudal vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased caudal vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased hepatocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased granulocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased somatotroph secretory granule number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased somatotroph secretory granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased muscle spindle number Gene Set

From MPO Gene-Phenotype Associations

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

decreased primary ovarian follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased primary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased corpora lutea number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased corpora lutea number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased dopaminergic neuron number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased dopaminergic neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased motor neuron number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased thymocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased sternebra number Gene Set

From MPO Gene-Phenotype Associations

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

decreased tracheal cartilage ring number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased tracheal cartilage ring number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mature ovarian follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mature ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle fiber number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased embryonic cilium number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased embryonic cilium number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spleen germinal center number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spleen germinal center number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased melanocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased dn2 thymocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased dn2 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased brown fat lipid droplet number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased presacral vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased presacral vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased oligodendrocyte progenitor number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased oligodendrocyte progenitor number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased alveolar lamellar body number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased renal glomerulus number Gene Set

From MPO Gene-Phenotype Associations

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

decreased sensory neuron number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensory neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased nephron number Gene Set

From MPO Gene-Phenotype Associations

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

decreased endometrial gland number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased metacarpal bone number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased metacarpal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased respiratory motile cilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased respiratory motile cilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cervical vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cervical vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased type i pneumocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased type i pneumocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased thoracic vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased dn4 thymocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased dn4 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone trabecula number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone trabecula number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased podocyte number Gene Set

From MPO Gene-Phenotype Associations

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

decreased peyer's patch number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased peyer's patch number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased dn3 thymocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased dn3 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased type ii pneumocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased type ii pneumocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations 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 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.

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.

cone cell pedicle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cone cell pedicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cone cell pedicle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

cone cell pedicle Gene Set

From GO Cellular Component Annotations

proteins localized to the cone cell pedicle cellular component from the curated GO Cellular Component Annotations dataset.

Sema4D induced cell migration and growth-cone collapse Gene Set

From Reactome Pathways

proteins participating in the Sema4D induced cell migration and growth-cone collapse pathway from the Reactome Pathways dataset.

adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 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 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.

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.

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 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.

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.

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 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.

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 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.

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 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 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.

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.

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 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 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 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.

Cone-rod dystrophy 19 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 18 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 16 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 11 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone dystrophy 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 9 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 7 Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Enhanced s-cone syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Enhanced s-cone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone monochromatism Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

CONE DYSTROPHY 5, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

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

Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy amelogenesis imperfecta Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy 20 Gene Set

From ClinVar Gene-Phenotype Associations

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

growth cone membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

axonal growth cone Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the axonal growth cone cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

growth cone Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the growth cone cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

dendritic growth cone Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the dendritic growth cone cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

growth cone membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

axonal growth cone Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

growth cone Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

dendritic growth cone Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

investment cone Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Enhanced S-Cone Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Enhanced S-Cone Syndrome from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 8 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 7 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 5 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 13 Gene Set

From CTD Gene-Disease Associations

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

Cone Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Cone Dystrophy 4 Gene Set

From CTD Gene-Disease Associations

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

CONE-ROD DYSTROPHY 9 Gene Set

From CTD Gene-Disease Associations

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

CONE-ROD DYSTROPHY 2 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 1 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 12 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 11 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 10 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Newfoundland Rod-Cone Dystrophy Gene Set

From CTD Gene-Disease Associations

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

CONE-ROD DYSTROPHY 15 Gene Set

From CTD Gene-Disease Associations

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

Blue cone monochromatism Gene Set

From CTD Gene-Disease Associations

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

cone-rod dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cone-rod dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blue cone monochromacy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cone dystrophy Gene Set

From GAD Gene-Disease Associations

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

cone-rod dystrophy Gene Set

From GAD Gene-Disease Associations

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

cone degeneration Gene Set

From GAD Gene-Disease Associations

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

cone-rod dystrophy; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

recessive cone-rod dystrophy Gene Set

From GAD Gene-Disease Associations

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

cone Gene Set

From GeneRIF Biological Term Annotations

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

growth cone membrane Gene Set

From GO Cellular Component Annotations

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

axonal growth cone Gene Set

From GO Cellular Component Annotations

proteins localized to the axonal growth cone cellular component from the curated GO Cellular Component Annotations dataset.

growth cone Gene Set

From GO Cellular Component Annotations

proteins localized to the growth cone cellular component from the curated GO Cellular Component Annotations dataset.

dendritic growth cone Gene Set

From GO Cellular Component Annotations

proteins localized to the dendritic growth cone cellular component from the curated GO Cellular Component Annotations dataset.

abnormal rod and cone electroretinograms Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive cone degeneration Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphysis Gene Set

From HPO Gene-Disease Associations

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

cone-rod dystrophy Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of phalanges 2 to 5 Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of phalanges 2 to 5 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent rod-and cone-mediated responses on erg Gene Set

From HPO Gene-Disease Associations

genes associated with the absent rod-and cone-mediated responses on erg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphysis of the 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

blue cone monochromacy Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cone-shaped capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cone-mediated electroretinogram Gene Set

From HPO Gene-Disease Associations

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

cone monochromacy Gene Set

From HPO Gene-Disease Associations

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

cone-shaped metacarpal epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped metacarpal epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Progressive rod-cone degeneration protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Progressive rod-cone degeneration protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-cone Gene Set

From InterPro Predicted Protein Domain Annotations

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

absent ectoplacental cone Gene Set

From MPO Gene-Phenotype Associations

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

small ectoplacental cone Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ectoplacental cone morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cone electrophysiology Gene Set

From MPO Gene-Phenotype Associations

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

newfoundland rod-cone dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the newfoundland rod-cone dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

enhanced s-cone syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the enhanced s-cone syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy, x-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 6, 60177 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 6, 60177 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

blue cone monochromacy Gene Set

From OMIM Gene-Disease Associations

genes associated with the blue cone monochromacy phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy with central cone involvement Gene Set

From OMIM Gene-Disease Associations

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

cone dystrophy, progressive x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystropy, x-linked, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystropy, x-linked, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

?cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

EPHA-mediated growth cone collapse Gene Set

From Reactome Pathways

proteins participating in the EPHA-mediated growth cone collapse pathway from the Reactome Pathways dataset.

ectoplacental cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

male cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

female cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

maintenance of cell number Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of cell number biological process from the curated GO Biological Process Annotations dataset.

abnormal neutrophil cell number Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of b cell number Gene Set

From HPO Gene-Disease Associations

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

increased number of cd4-/cd8- t cells expressing alpha/beta t-cell receptors Gene Set

From HPO Gene-Disease Associations

genes associated with the increased number of cd4-/cd8- t cells expressing alpha/beta t-cell receptors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increase in t cell number Gene Set

From HPO Gene-Disease Associations

genes associated with the increase in t cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of t cell number Gene Set

From HPO Gene-Disease Associations

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

abnormal neutrophil cell number Gene Set

From HPO Gene-Disease Associations

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

increase in b cell number Gene Set

From HPO Gene-Disease Associations

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

abnormal fetal derived definitive erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased white fat cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased brown fat cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased nk cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal purkinje cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased pre-pro b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased pre-pro b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased t-helper 17 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasmacytoid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased eosinophil cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased gonadotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal plasma cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased platelet cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal nk t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal nk t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased organ of corti supporting cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased organ of corti supporting cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mast cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased hippocampus pyramidal cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased b-1 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased b-1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased t-helper 2 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased salivary gland mucosal cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased salivary gland mucosal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased activated t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased pp cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased transitional stage t1 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased transitional stage t1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal organ of corti supporting cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal organ of corti supporting cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal reticulocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal reticulocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased macrophage cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased neutrophil cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased lactotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal amacrine cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brown fat cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal b-1 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal b-1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal osteoclast cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal osteoclast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased immature b cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased late pro-b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased late pro-b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal myeloid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal myeloid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cd4-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased dn1 thymic pro-t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased dn1 thymic pro-t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased plasma cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal klrg1-positive nk cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal klrg1-positive nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased vascular endothelial cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased pancreatic epsilon cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased thyrotroph cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal white fat cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased leukocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased pancreatic alpha cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased basophil cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal t follicular helper cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal t follicular helper cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased transitional stage b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased transitional stage b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal leukocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased marginal zone b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased marginal zone b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased transitional stage t2 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased transitional stage t2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased monocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased megakaryocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd4-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal nk cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased osteoclast cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal effector memory cd4-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal effector memory cd4-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal monocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal monocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal t-helper 2 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased klrg1+ cd4 alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased klrg1+ cd4 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bronchioalveolar stem cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased clara cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased nucleated erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased amacrine cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased hematopoietic stem cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased purkinje cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pancreatic delta cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased osteoblast cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased b-2 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased b-2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skin cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skin cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased effector memory cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased effector memory cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased myeloid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased uterine nk cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal klrg1+ cd4 alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal klrg1+ cd4 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased memory t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased mature b cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal memory b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased thecal cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal osteoblast cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal osteoblast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thecal cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal thecal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased nk t cell number Gene Set

From MPO Gene-Phenotype Associations

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

low mean erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the low mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased macrophage derived foam cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased macrophage derived foam cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pre-b cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased respiratory mucosa goblet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased germinal center b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased germinal center b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased klrg1-positive nk cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased klrg1-positive nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enterocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enterocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased plasmacytoid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased effector memory cd4-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased effector memory cd4-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

high mean erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the high mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased transitional stage t3 b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased transitional stage t3 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basophil cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal basophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased t cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal intraepithelial t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intraepithelial t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal klrg1+ cd8 alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal klrg1+ cd8 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mature gamma-delta t cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cd4-positive, alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive, alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal nucleated erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal nucleated erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased deiters cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased double-negative t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased lymphocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased hematopoietic cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased b cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal gamma-delta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd8-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased satellite cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eosinophil cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eosinophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased b-1a cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased b-1a cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased erythroid progenitor cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal t-helper 17 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased solitary pulmonary neuroendocrine cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased solitary pulmonary neuroendocrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pancreatic beta cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal langerhans cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal langerhans cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neutrophil cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neutrophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased single-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal single-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal t-helper 1 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal t-helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pancreatic acinar cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased schwann cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pro-b cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal effector memory cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal effector memory cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased t-helper 1 cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased t-helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased trophoblast giant cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased mast cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased gamma-delta t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased follicular b cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hematopoietic cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hematopoietic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased enterocyte cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal precursor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased b-1b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased b-1b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cd8-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased gamma-delta intraepithelial t cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal macrophage cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal macrophage cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased double-positive t cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased trophoblast glycogen cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased cd4-positive, alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd4-positive, alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased klrg1+ cd8 alpha beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased klrg1+ cd8 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased t follicular helper cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased neuronal precursor cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased fetal derived definitive erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set

From GAD Gene-Disease Associations

genes associated with the disease b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell-cell signaling involved in cell-cell junction organization Gene Set

From GO Biological Process Annotations

genes participating in the cell-cell signaling involved in cell-cell junction organization biological process from the curated GO Biological Process Annotations dataset.

non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

decreased t cell activation Gene Set

From HPO Gene-Disease Associations

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

decreased mast cell degranulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mast cell degranulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased nk cell degranulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased nk cell degranulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neuronal stem cell self-renewal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pulmonary endothelial cell surface Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pulmonary endothelial cell surface phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased t cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased activation-induced b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cell mass Gene Set

From MPO Gene-Phenotype Associations

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

decreased mast cell protease storage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mast cell protease storage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic endocrine progenitor cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cytotoxic t cell cytolysis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cytotoxic t cell cytolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased inner cell mass proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased t cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

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

decreased kidney cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased lung endothelial cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased hematopoietic stem cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cell migration 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.

decreased lung endothelial cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lung endothelial cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white fat cell size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white fat cell size 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.

decreased cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased single cell response threshold Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased single cell response threshold 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.

decreased cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased b cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

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

decreased fibroblast cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased fibroblast cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cell death Gene Set

From MPO Gene-Phenotype Associations

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

decreased lactotroph cell size Gene Set

From MPO Gene-Phenotype Associations

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

decreased brown fat cell size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mast cell histamine storage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mast cell histamine storage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic beta cell mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pancreatic beta cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreatic beta cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased fat cell size Gene Set

From MPO Gene-Phenotype Associations

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

decreased corticotroph cell size Gene Set

From MPO Gene-Phenotype Associations

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

decreased embryonic epiblast cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased brown fat cell lipid droplet size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased somatotroph cell size Gene Set

From MPO Gene-Phenotype Associations

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

decreased trophectoderm cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased sertoli cell phagocytosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sertoli cell phagocytosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white fat cell lipid droplet size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased embryonic neuroepithelial cell proliferation Gene Set

From MPO Gene-Phenotype Associations

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

decreased mesenchymal cell proliferation involved in lung development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mesenchymal cell proliferation involved in lung development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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.

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.

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.

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.

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 Detachment Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Detachment 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 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 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.

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 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.

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 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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

?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 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.

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.

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.

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 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 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.

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.

increased number of circulating vldl and idl particles Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased number of circulating vldl and idl particles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

numbers Gene Set

From GeneRIF Biological Term Annotations

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

number Gene Set

From GeneRIF Biological Term Annotations

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

homeostasis of number of cells Gene Set

From GO Biological Process Annotations

genes participating in the homeostasis of number of cells biological process from the curated GO Biological Process Annotations dataset.

homeostasis of number of cells in a free-living population Gene Set

From GO Biological Process Annotations

genes participating in the homeostasis of number of cells in a free-living population biological process from the curated GO Biological Process Annotations dataset.

homeostasis of number of cells within a tissue Gene Set

From GO Biological Process Annotations

genes participating in the homeostasis of number of cells within a tissue biological process from the curated GO Biological Process Annotations dataset.

Primary tooth development (number of teeth) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Primary tooth development (number of teeth) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormal number of teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

reduced number of teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the reduced number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal number of vertebrae Gene Set

From HPO Gene-Disease Associations

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

increased number of teeth Gene Set

From HPO Gene-Disease Associations

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

reduced number of intrahepatic bile ducts Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced number of intrahepatic bile ducts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of incisors Gene Set

From HPO Gene-Disease Associations

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

increased number of peripheral cd3+ t cells Gene Set

From HPO Gene-Disease Associations

genes associated with the increased number of peripheral cd3+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced number of corneal endothelial cells Gene Set

From HPO Gene-Disease Associations

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

abnormal number of permanent teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal number of teeth Gene Set

From HPO Gene-Disease Associations

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

abnormal number of erythroid precursors Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced number of teeth Gene Set

From HPO Gene-Disease Associations

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

fatty acid β-oxidation (unsaturated, odd number) Gene Set

From HumanCyc Pathways

proteins participating in the fatty acid β-oxidation (unsaturated, odd number) pathway from the HumanCyc Pathways dataset.

abnormal primordial ovarian follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sebaceous gland number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuron number Gene Set

From MPO Gene-Phenotype Associations

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

increased lumbar vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sacral vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sacral vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pancreatic islet number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased hemangioblast number Gene Set

From MPO Gene-Phenotype Associations

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

increased oligodendrocyte progenitor number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased oligodendrocyte progenitor number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased thymocyte number Gene Set

From MPO Gene-Phenotype Associations

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

increased skeletal muscle fiber number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hemangioblast number Gene Set

From MPO Gene-Phenotype Associations

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

increased corpora lutea number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased corpora lutea number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset