Name

pigmented Gene Set

From GeneRIF Biological Term Annotations

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

p2 portion of the parabrachial pigmented nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in p2 portion of the parabrachial pigmented nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

p1 part of parabrachial pigmented nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in p1 part of parabrachial pigmented nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

p3 portion of parabrachial pigmented nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in p3 portion of parabrachial pigmented nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pigmented nodular adrenocortical disease, primary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amelogenesis imperfecta pigmented hypomaturation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amelogenesis imperfecta pigmented hypomaturation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset.

Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.

Pigmented Nodular Adrenocortical Disease, Primary, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 2 from the curated CTD Gene-Disease Associations dataset.

Amelogenesis imperfecta pigmented hypomaturation type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis imperfecta pigmented hypomaturation type from the curated CTD Gene-Disease Associations dataset.

Pigmented Paravenous Chorioretinal Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.

pigmented villonodular synovitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pigmented basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

conjunctival neoplasms; melanoma; melanosis; nevus, pigmented; uveal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conjunctival neoplasms; melanoma; melanosis; nevus, pigmented; uveal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microsatellite instability; nevus, pigmented; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microsatellite instability; nevus, pigmented; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pigmented basal cell carcinoma Gene Set

From GWASdb SNP-Disease Associations

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

numerous pigmented freckles Gene Set

From HPO Gene-Disease Associations

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

pigmented micronodular adrenocortical disease Gene Set

From HPO Gene-Disease Associations

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

profuse pigmented skin lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the profuse pigmented skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pigmented paravenous chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

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

Nevus, Pigmented Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

non-pigmented tail tip Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the non-pigmented tail tip phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pigmented parathyroid gland Gene Set

From MPO Gene-Phenotype Associations

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

pigmented nodular adrenocortical disease, primary, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

pigmented nodular adrenocortical disease, primary, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pigmented nodular adrenocortical disease, primary, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

pigmented paravenous chorioretinal atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

pigmented nodular adrenocortical disease, primary, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented nodular adrenocortical disease, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.