Name

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.

cerebral cortex pyramidal cell degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cerebral cortex pyramidal cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebral cortex pyramidal cell morphology 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.

ectopic cerebral cortex pyramidal cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ectopic cerebral cortex pyramidal cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease 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.

cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex tangential migration using cell-axon interactions Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex tangential migration using cell-axon interactions biological process from the curated GO Biological Process Annotations dataset.

extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex radially oriented cell migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex radially oriented cell migration biological process from the curated GO Biological Process Annotations dataset.

cell motility involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the cell motility involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex cell migration Gene Set

From GO Biological Process Annotations

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

negative regulation of cell motility involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cell motility involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; hypertension Gene Set

From GAD Gene-Disease Associations

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

apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct; cerebral arteriopathy Gene Set

From GAD Gene-Disease Associations

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

apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension Gene Set

From GAD Gene-Disease Associations

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

abnormal hippocampus pyramidal cell layer Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hippocampus pyramidal cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

hippocampus pyramidal cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hippocampus pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype 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 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.

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 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 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 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 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 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 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 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.

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.

Cerebral cortex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Frontal pole, cerebral cortex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Frontal pole, cerebral cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cerebral cortex neuron differentiation Gene Set

From GO Biological Process Annotations

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

cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex tangential migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex development Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex development biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex regionalization Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex regionalization biological process from the curated GO Biological Process Annotations dataset.

neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

layer formation in cerebral cortex Gene Set

From GO Biological Process Annotations

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

substrate-dependent cerebral cortex tangential migration Gene Set

From GO Biological Process Annotations

genes participating in the substrate-dependent cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex gabaergic interneuron fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex gabaergic interneuron fate commitment biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex gabaergic interneuron migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex gabaergic interneuron migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex gabaergic interneuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex gabaergic interneuron differentiation biological process from the curated GO Biological Process Annotations dataset.

abnormality of the cerebral cortex Gene Set

From GWASdb SNP-Phenotype Associations

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

cerebral cortex Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in cerebral cortex relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

small cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

thick cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

neuronal loss in the cerebral cortex Gene Set

From HPO Gene-Disease Associations

genes associated with the neuronal loss in the cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

delaminated cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

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

thin cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

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

thickened cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

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

abnormal stratification in cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal stratification in cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebral cortex morphology Gene Set

From MPO Gene-Phenotype Associations

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

cerebral-cortex Gene Set

From Phosphosite Textmining Biological Term Annotations

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

cerebral cortex Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cerebral cortex Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

embryonic cerebral cortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral cortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

pyramidal layer of S Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Field CA2, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Field CA2, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

pyramidal layer of IG Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Piriform area, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Piriform area, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Nucleus of the lateral olfactory tract, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Nucleus of the lateral olfactory tract, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

pyramidal layer of taenia tecta Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in pyramidal layer of taenia tecta relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Olfactory tubercle, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Olfactory tubercle, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Field CA3, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Field CA3, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Piriform-amygdalar area, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Piriform-amygdalar area, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Subiculum, dorsal part, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Field CA1, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Field CA1, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Subiculum, ventral part, pyramidal layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

pyramidal cells of rostral CA4 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pyramidal cells of rostral CA4 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

pyramidal layer of caudal subiculum Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pyramidal layer of caudal subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

pyramidal cells of caudal CA4 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pyramidal cells of caudal CA4 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

pyramidal layer of rostral subiculum Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pyramidal layer of rostral subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

pyramidal Gene Set

From GeneRIF Biological Term Annotations

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

pyramidal neuron development Gene Set

From GO Biological Process Annotations

genes participating in the pyramidal neuron development biological process from the curated GO Biological Process Annotations dataset.

pyramidal neuron differentiation Gene Set

From GO Biological Process Annotations

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

aplasia/hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

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

abnormal pyramidal signs Gene Set

From HPO Gene-Disease Associations

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

pyramidal skinfold extending from the base to the top of the nails Gene Set

From HPO Gene-Disease Associations

genes associated with the pyramidal skinfold extending from the base to the top of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

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

ectopic hippocampus pyramidal cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ectopic hippocampus pyramidal cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pyramidal decussation morphology Gene Set

From MPO Gene-Phenotype Associations

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

pyramidal neuron Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hippocampal pyramidal layer Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

decreased cerebral infarction size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cerebral infarction size 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.

primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

SG in posterior frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in SG in posterior frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

IZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in IZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

SP in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in SP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

MZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in MZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

adrenal cortex neoplasms; tumors of adrenal cortex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal cortex neoplasms; tumors of adrenal cortex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal cortex neoplasms; adrenal cortical adenoma; adrenocortical adenoma; hyperaldosteronism; tumors of adrenal cortex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal cortex neoplasms; adrenal cortical adenoma; adrenocortical adenoma; hyperaldosteronism; tumors of adrenal cortex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal cortex neoplasms; adrenocortical carcinoma; tumors of adrenal cortex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal cortex neoplasms; adrenocortical carcinoma; tumors of adrenal cortex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

cerebral giant cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral granule cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebral granule cell 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 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 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 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.

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.

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 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.

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.

cell cortex part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

cell cortex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

cell cortex part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

cell cortex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

adrenal cortex neoplasms; cell transformation, neoplastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal cortex neoplasms; cell transformation, neoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein localization to cell cortex Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to cell cortex biological process from the curated GO Biological Process Annotations dataset.

cell cortex part Gene Set

From GO Cellular Component Annotations

proteins localized to the cell cortex part cellular component from the curated GO Cellular Component Annotations dataset.

cell cortex Gene Set

From GO Cellular Component Annotations

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

brain cortex cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

adrenal cortex cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

brain cortex cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

embryonic brain cortex cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Cerebral nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral folate deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination, global cerebral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination, global cerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral cavernous malformations 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral cavernous malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral cavernous malformations 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral cavernous malformations 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cerebral amyloid angiopathy, Icelandic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular hypertrophy-cerebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral hemorrhage with amyloidosis, hereditary, Dutch type from the curated CTD Gene-Disease Associations dataset.

Cerebral Infarction Gene Set

From CTD Gene-Disease Associations

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

Cerebral Amyloid Angiopathy, App-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, App-Related 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.

Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.

Infarction, Middle Cerebral Artery Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Infarction, Middle Cerebral Artery from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy, Ataxic, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Ataxic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy, Spastic Quadriplegic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 2 from the curated CTD Gene-Disease Associations dataset.

Diffuse Cerebral Sclerosis of Schilder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diffuse Cerebral Sclerosis of Schilder from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy Gene Set

From CTD Gene-Disease Associations

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

Cerebral Cavernous Malformations 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Cavernous Malformations 2 from the curated CTD Gene-Disease Associations dataset.

Hypomyelination, Global Cerebral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomyelination, Global Cerebral from the curated CTD Gene-Disease Associations dataset.

Cerebral Amyloid Angiopathy Gene Set

From CTD Gene-Disease Associations

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

Cerebral Cavernous Malformations 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Cavernous Malformations 3 from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy, Spastic Quadriplegic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 1 from the curated CTD Gene-Disease Associations dataset.

Cerebral Hemorrhage Gene Set

From CTD Gene-Disease Associations

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

Cerebral Amyloid Angiopathy, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

cerebral degeneration Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cerebral arterial disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

cerebral angioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral primitive neuroectodermal tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral sarcoidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle cerebral artery infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral atherosclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ataxic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral malaria Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral convexity meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral creatine deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

transient cerebral ischemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anterior cerebral artery infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral neuroblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral arteritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral arterial disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral falx meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral ventricle cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dyskinetic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral lipidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral amyloid angiopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral amyloid angiopathy-related hemorrhage. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy-related hemorrhage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy Gene Set

From GAD Gene-Disease Associations

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

anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; memory disorders; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; memory disorders; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral cavernous malformations Gene Set

From GAD Gene-Disease Associations

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

cerebral atherosclerosis Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct; stroke, lacunar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarct; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; thrombosis Gene Set

From GAD Gene-Disease Associations

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

hypertension; cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

microangiopathy- related cerebral damage (marcd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microangiopathy- related cerebral damage (marcd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, malaria related; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy; hemiplegia Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, cerebral; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

cerebral arteriopathy Gene Set

From GAD Gene-Disease Associations

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

cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

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

cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

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

cerebral circulation Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral ischemia Gene Set

From GAD Gene-Disease Associations

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

cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

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

cerebral ischemic events Gene Set

From GAD Gene-Disease Associations

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

apoplexy; atherosclerosis; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; cerebral infarction; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; cerebral infarction; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; lipoprotein; cerebral infarct Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; lipoprotein; cerebral infarct in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; Gene Set

From GAD Gene-Disease Associations

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

cerebral small-vessel disease Gene Set

From GAD Gene-Disease Associations

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

toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral aging Gene Set

From GAD Gene-Disease Associations

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

antithrombin iii deficiency; cerebral infarction; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; cerebral infarction; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; intracranial arteriovenous malformations Gene Set

From GAD Gene-Disease Associations

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

cerebral amyloid angiopathy; senile plaques Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; senile plaques in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cerebral arterial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral white matter hyperintensities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral white matter hyperintensities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

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

malarial anemia and cerebral malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malarial anemia and cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; intracranial embolism and thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; intracranial embolism and thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy; hemiplegia; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; hemiplegia; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; pregnancy complications, infectious; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; pregnancy complications, infectious; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; cerebral arterial diseases; intracranial embolism; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral arterial diseases; intracranial embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy. Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherothrombotic cerebral infarction. Gene Set

From GAD Gene-Disease Associations

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

cerebral malaria Gene Set

From GAD Gene-Disease Associations

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

cerebral amyloid angiopathy; plaque, amyloid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; plaque, amyloid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct, atherothrombotic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarct, atherothrombotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cadasil; cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cadasil; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; leukomalacia, periventricular; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; leukomalacia, periventricular; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral arteriopathy; leukoencephalopathy Gene Set

From GAD Gene-Disease Associations

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

birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; infarction, middle cerebral artery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral white matter lesions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral circulation in smokers Gene Set

From GAD Gene-Disease Associations

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

brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; recurrence; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; hypertension Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction, atherosclerotic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction, atherosclerotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; infarction, middle cerebral artery; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; hypoxia-ischemia, brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction. Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; hypertension; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; cerebral arterial diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebral arterial diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, cerebral Gene Set

From GAD Gene-Disease Associations

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

infarction, middle cerebral artery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral Gene Set

From GeneRIF Biological Term Annotations

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

White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

cerebral arterial disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of the cerebral subcortex Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cerebral artery Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral white matter Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

hypointensity of cerebral white matter on mri Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the hypointensity of cerebral white matter on mri phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

diffuse cerebral sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the diffuse cerebral sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

cerebral ischemia Gene Set

From GWASdb SNP-Phenotype Associations

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

cerebral aneurysm Gene Set

From GWASdb SNP-Phenotype Associations

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

cerebral palsy Gene Set

From HPO Gene-Disease Associations

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

cerebral edema Gene Set

From HPO Gene-Disease Associations

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

cerebral aneurysm Gene Set

From HPO Gene-Disease Associations

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

cerebral white matter atrophy Gene Set

From HPO Gene-Disease Associations

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

cerebral venous thrombosis Gene Set

From HPO Gene-Disease Associations

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

abnormality of cerebral artery Gene Set

From HPO Gene-Disease Associations

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

cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

recurrent cerebral hemorrhage Gene Set

From HPO Gene-Disease Associations

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

diffuse demyelination of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse demyelination of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

cerebral amyloid angiopathy Gene Set

From HPO Gene-Disease Associations

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

diffuse swelling of cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse swelling of cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral calcification Gene Set

From HPO Gene-Disease Associations

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

cerebral ischemia Gene Set

From HPO Gene-Disease Associations

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

arteriosclerosis of small cerebral arteries Gene Set

From HPO Gene-Disease Associations

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

subcortical cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

tortuous cerebral arteries Gene Set

From HPO Gene-Disease Associations

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

cerebral vasculitis Gene Set

From HPO Gene-Disease Associations

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

increased cerebral lipofuscin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral vasculature Gene Set

From HPO Gene-Disease Associations

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

cerebral hypomyelination Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral subcortex Gene Set

From HPO Gene-Disease Associations

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

cerebral degeneration Gene Set

From HPO Gene-Disease Associations

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

cerebral cortical neurodegeneration Gene Set

From HPO Gene-Disease Associations

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

diffuse cerebral sclerosis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral ventricles Gene Set

From HPO Gene-Disease Associations

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

cerebral hamartomata Gene Set

From HPO Gene-Disease Associations

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

cerebral hemorrhage Gene Set

From HPO Gene-Disease Associations

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

multifocal cerebral white matter abnormalities Gene Set

From HPO Gene-Disease Associations

genes associated with the multifocal cerebral white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral cortical atrophy Gene Set

From HPO Gene-Disease Associations

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

cerebral dysmyelination Gene Set

From HPO Gene-Disease Associations

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

generalized cerebral atrophy/hypoplasia Gene Set

From HPO Gene-Disease Associations

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

diffuse cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

cerebral hypoplasia Gene Set

From HPO Gene-Disease Associations

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

cerebral inclusion bodies Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

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

frontotemporal cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

hypointensity of cerebral white matter on mri Gene Set

From HPO Gene-Disease Associations

genes associated with the hypointensity of cerebral white matter on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cerebral Hemorrhage, Traumatic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Infarction Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Malaria, Cerebral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Infarction, Middle Cerebral Artery Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infarction, Middle Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Toxoplasmosis, Cerebral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Arterial Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Diffuse Cerebral Sclerosis of Schilder Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Diffuse Cerebral Sclerosis of Schilder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Dominance, Cerebral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Palsy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Amyloid Angiopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Infarction, Anterior Cerebral Artery Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infarction, Anterior Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cerebral Ventricle Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

cerebral edema Gene Set

From MPO Gene-Phenotype Associations

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

cerebral arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cerebral aqueduct morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebral aqueduct Gene Set

From MPO Gene-Phenotype Associations

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

cerebral aqueductal stenosis Gene Set

From MPO Gene-Phenotype Associations

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

increased cerebral infarction size Gene Set

From MPO Gene-Phenotype Associations

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

{malaria, cerebral, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, cerebral, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral cavernous malformations 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral cavernous malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral amyloid angiopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral amyloid angiopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, dystonia, and cerebral hypomyelination Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral cavernous malformations-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral cavernous malformations-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral cavernous malformations-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral cavernous malformations-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral amyloid angiopathy, prnp-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral amyloid angiopathy, prnp-related phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, cerebral, reduced risk of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, cerebral, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral palsy, spastic quadriplegic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral palsy, spastic quadriplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination, global cerebral Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination, global cerebral phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral-cerebellar-coloboma syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{cerebral infarction, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {cerebral infarction, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration due to cerebral folate transport deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral palsy, spastic quadriplegic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral palsy, spastic quadriplegic, 2 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.

cerebral lobe Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cerebral hemisphere Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cerebral lobe Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral peduncle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral gyrus Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral hemisphere Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

right middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral gyrus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral peduncle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral cortical neuron Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral gray matter Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral white matter Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

left middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral subcortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral hemisphere Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

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