Name

Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.

?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2S Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy, limb-girdle, type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.

Limb-Girdle Muscular Dystrophy, Type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy, limb-girdle, type 2r Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2q Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2s Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2g Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2l Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2j Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

limb-girdle muscular dystrophy, type 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophies; muscular dystrophies, limb-girdle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies; muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

limb-girdle muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

limb-girdle muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

limb-girdle muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

Muscular Dystrophies, Limb-Girdle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophies, Limb-Girdle from the curated CTD Gene-Disease Associations dataset.

muscular dystrophies, limb-girdle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Muscular Dystrophies, Limb-Girdle Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

muscular dystrophy-dystroglycanopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Myasthenia, limb-girdle, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenia, limb-girdle, with tubular aggregates Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenia, limb-girdle, with tubular aggregates phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

limb-girdle muscle atrophy Gene Set

From HPO Gene-Disease Associations

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

limb-girdle muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the limb-girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

myasthenia, limb-girdle, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenia, limb-girdle, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

muscular dystrophy, congenital, megaconial type Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular atrophy, spinal; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

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

polycythemia vera(c15.378.190.636.753)/enzymology; polycythemia(c15.378.738)/enzymology Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycythemia vera(c15.378.190.636.753)/enzymology; polycythemia(c15.378.738)/enzymology in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Duchenne muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Merosin deficient congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Walker-Warburg congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Becker muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Facioscapulohumeral muscular dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ullrich congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Miyoshi Muscular Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Miyoshi Muscular Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

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

Facioscapulohumeral muscular dystrophy 1a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy congenital, merosin negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.

Scleroatonic muscular dystrophy Gene Set

From CTD Gene-Disease Associations

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

Muscular Dystrophy, Emery-Dreifuss Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Oculopharyngeal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Merosin-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.

Facioscapulohumeral Muscular Dystrophy 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Duchenne Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Lmna-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

ullrich congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

distal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ullrich congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

becker muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

duchenne muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy, oculopharyngeal Gene Set

From GAD Gene-Disease Associations

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

ullrich congenital muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

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

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

congenital muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

Muscular Dystrophy, Emery-Dreifuss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Dystrophy, Duchenne Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

fascioscapulohumeral muscular dystrophy 2, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, rigid spine, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, merosin-positive Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.

ullrich congenital muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

tibial muscular dystrophy, tardive Gene Set

From OMIM Gene-Disease Associations

genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

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

duchenne muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 3, ar Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with rimmed vacuoles Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 6, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with epidermolysis bullosa simplex Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

becker muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 7, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital merosin-deficient Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.

Emery-Dreifuss muscular dystrophy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

dystroglycanopathy Gene Set

From GeneRIF Biological Term Annotations

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

Spinal muscular atrophy, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, Jerash type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.

disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy, jokela type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, late-onset, finkel type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.

{spinal muscular atrophy, type iii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

girdle Gene Set

From GeneRIF Biological Term Annotations

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

abnormality of pelvic girdle bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

pelvic girdle muscle atrophy Gene Set

From HPO Gene-Disease Associations

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

shoulder girdle muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the shoulder girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hip-girdle musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of pelvic girdle bone morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the shoulder girdle musculature Gene Set

From HPO Gene-Disease Associations

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

pelvic girdle amyotrophy Gene Set

From HPO Gene-Disease Associations

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

pelvic girdle muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the pelvic girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shoulder girdle muscle atrophy Gene Set

From HPO Gene-Disease Associations

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

abnormal pectoral girdle bone morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pelvic girdle bone morphology Gene Set

From MPO Gene-Phenotype Associations

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

albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy type 3A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal endothelial dystrophy type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal endothelial dystrophy type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Groenouw corneal dystrophy type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular dystrophy, retinal, 1, North Carolina type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy Avellino type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset.

Lattice corneal dystrophy type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.

Bullous Dystrophy, Hereditary Macular Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset.

Corneal endothelial dystrophy type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal endothelial dystrophy type 2 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Thiel-Behnke type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset.

Groenouw type I corneal dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Lattice Type IIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy of Bowman layer, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, corneal type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset.

myotonic dystrophy type 1 Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

myotonic dystrophy type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

myotonic dystrophy type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

myotonic dystrophy type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myotonic dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lattice corneal dystrophy type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

corneal dystrophy, schnyder type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lattice type iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, north carolina type Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, north carolina type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, reis-bucklers type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, thiel-behnke type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, thiel-behnke type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lattice type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type i phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, groenouw type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, avellino type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset.

interstitial nucleus of the posterior limb of the anterior commissure Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in interstitial nucleus of the posterior limb of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb, layer 4 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb, layer 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, lower limb, layer 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, lower limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 4 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper limb region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in upper limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

lower limb region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lower limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anophthalmos with limb anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anophthalmos with limb anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Limb Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

Limb-mammary syndrome Gene Set

From CTD Gene-Disease Associations

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

mononeuritis of upper limb and mononeuritis multiplex Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

periodic limb movement disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mononeuritis of lower limb Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

limb deformities, congenital; rothmund-thomson syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease limb deformities, congenital; rothmund-thomson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

limb deficiency Gene Set

From GAD Gene-Disease Associations

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

limb Gene Set

From GeneRIF Biological Term Annotations

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

LAMA2_Deficiency_GDS3371_595_mouse_Hind limb skeletal muscle (4-week old dy3K/dy3K animals) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the LAMA2_Deficiency_GDS3371_595_mouse_Hind limb skeletal muscle (4-week old dy3K/dy3K animals) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

limb joint morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the limb joint morphogenesis biological process from the curated GO Biological Process Annotations dataset.

limb epidermis development Gene Set

From GO Biological Process Annotations

genes participating in the limb epidermis development biological process from the curated GO Biological Process Annotations dataset.

embryonic limb morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the embryonic limb morphogenesis biological process from the curated GO Biological Process Annotations dataset.

limb morphogenesis Gene Set

From GO Biological Process Annotations

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

metanephric descending thin limb development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric descending thin limb development biological process from the curated GO Biological Process Annotations dataset.

descending thin limb development Gene Set

From GO Biological Process Annotations

genes participating in the descending thin limb development biological process from the curated GO Biological Process Annotations dataset.

ascending thin limb development Gene Set

From GO Biological Process Annotations

genes participating in the ascending thin limb development biological process from the curated GO Biological Process Annotations dataset.

metanephric thick ascending limb development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric thick ascending limb development biological process from the curated GO Biological Process Annotations dataset.

metanephric ascending thin limb development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric ascending thin limb development biological process from the curated GO Biological Process Annotations dataset.

thick ascending limb development Gene Set

From GO Biological Process Annotations

genes participating in the thick ascending limb development biological process from the curated GO Biological Process Annotations dataset.

embryonic skeletal limb joint morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations dataset.

limb development Gene Set

From GO Biological Process Annotations

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

limb bud formation Gene Set

From GO Biological Process Annotations

genes participating in the limb bud formation biological process from the curated GO Biological Process Annotations dataset.

Bone mineral density (paediatric, upper limb) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, lower limb) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, lower limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of upper limb bone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lower limb Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the upper limb Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of lower limb joint Gene Set

From GWASdb SNP-Phenotype Associations

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

predominantly lower limb lymphedema Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the predominantly lower limb lymphedema phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of upper limb metaphysis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of lower limb bone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of limb bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

anomaly of the upper limb diaphyses Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anomaly of the upper limb diaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone Gene Set

From GWASdb SNP-Phenotype Associations

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

anomaly of the limb diaphyses Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anomaly of the limb diaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

limb hypertonia Gene Set

From HPO Gene-Disease Associations

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

limb pain Gene Set

From HPO Gene-Disease Associations

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

abnormality of lower limb bone Gene Set

From HPO Gene-Disease Associations

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

distal upper limb muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lower limb Gene Set

From HPO Gene-Disease Associations

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

upper limb metaphyseal widening Gene Set

From HPO Gene-Disease Associations

genes associated with the upper limb metaphyseal widening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper limb Gene Set

From HPO Gene-Disease Associations

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

generalized limb muscle atrophy Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

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

limb muscle weakness Gene Set

From HPO Gene-Disease Associations

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

lower limb peromelia Gene Set

From HPO Gene-Disease Associations

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

limb ataxia Gene Set

From HPO Gene-Disease Associations

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

lower limb hyperreflexia Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

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

limb dysmetria Gene Set

From HPO Gene-Disease Associations

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

abnormality of limb bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb joint Gene Set

From HPO Gene-Disease Associations

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

disproportionate short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hemihypotrophy of lower limb Gene Set

From HPO Gene-Disease Associations

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

lower limb hypertonia Gene Set

From HPO Gene-Disease Associations

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

limb dystonia Gene Set

From HPO Gene-Disease Associations

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

limb tremor Gene Set

From HPO Gene-Disease Associations

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

upper limb postural tremor Gene Set

From HPO Gene-Disease Associations

genes associated with the upper limb postural tremor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal lower limb amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lower-limb metaphyses Gene Set

From HPO Gene-Disease Associations

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

distal lower limb muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

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

limb undergrowth Gene Set

From HPO Gene-Disease Associations

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

upper limb phocomelia Gene Set

From HPO Gene-Disease Associations

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

limb fasciculations Gene Set

From HPO Gene-Disease Associations

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

upper limb spasticity Gene Set

From HPO Gene-Disease Associations

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

proximal upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the proximal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

limb duplication Gene Set

From HPO Gene-Disease Associations

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

lower limb muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lower limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

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

limb joint contracture Gene Set

From HPO Gene-Disease Associations

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

childhood onset short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lower limb amyotrophy Gene Set

From HPO Gene-Disease Associations

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

mesomelic/rhizomelic limb shortening Gene Set

From HPO Gene-Disease Associations

genes associated with the mesomelic/rhizomelic limb shortening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe short-limb dwarfism Gene Set

From HPO Gene-Disease Associations

genes associated with the severe short-limb dwarfism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lower limb undergrowth Gene Set

From HPO Gene-Disease Associations

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

flared upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the flared upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lower limb pain Gene Set

From HPO Gene-Disease Associations

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

abnormality of lower limb joint Gene Set

From HPO Gene-Disease Associations

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

upper limb muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lower limb spasticity Gene Set

From HPO Gene-Disease Associations

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

flared lower limb metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the flared lower limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lower-limb metaphyseal irregularity Gene Set

From HPO Gene-Disease Associations

genes associated with the lower-limb metaphyseal irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper limb undergrowth Gene Set

From HPO Gene-Disease Associations

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

anomaly of the limb diaphyses Gene Set

From HPO Gene-Disease Associations

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

predominantly lower limb lymphedema Gene Set

From HPO Gene-Disease Associations

genes associated with the predominantly lower limb lymphedema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

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

neonatal short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

proximal lower limb amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the proximal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe limb shortening Gene Set

From HPO Gene-Disease Associations

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

abnormality of limb bone morphology Gene Set

From HPO Gene-Disease Associations

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

lower limb asymmetry Gene Set

From HPO Gene-Disease Associations

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

upper limb muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

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

Limb Deformities, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Limb-bud-and-heart Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Limb-bud-and-heart protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Limb expression 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Limb expression 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal loop of henle descending limb morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal limb position Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb paddle morphology Gene Set

From MPO Gene-Phenotype Associations

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

small limb buds Gene Set

From MPO Gene-Phenotype Associations

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

absent limb buds Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb mesenchyme morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal loop of henle ascending limb thick segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal loop of henle ascending limb thick segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal limb bud morphology Gene Set

From MPO Gene-Phenotype Associations

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

broad limb buds Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb long bone morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal loop of henle ascending limb morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal loop of henle ascending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed limb development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb posture Gene Set

From MPO Gene-Phenotype Associations

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

impaired limb coordination Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal limb bone morphology Gene Set

From MPO Gene-Phenotype Associations

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

limb grasping Gene Set

From MPO Gene-Phenotype Associations

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

robin sequence with cleft mandible and limb anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the robin sequence with cleft mandible and limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

ulna and fibula, absence of, with severe limb deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ulna and fibula, absence of, with severe limb deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia with limb anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia with limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

limb-mammary syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the limb-mammary syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

limb Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

limb Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

limb bud Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Distal spinal muscular atrophy, X-linked 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant 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.

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy with respiratory distress 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.

Muscular Atrophy Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophies Gene Set

From CTD Gene-Disease Associations

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

Muscular Diseases Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophies of Childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.

Muscular Atrophy, Spinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.

Muscular Diseases Gene Set

From dbGAP Gene-Trait Associations

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

spinal muscular atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

atrophic muscular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

atrophic muscular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adult spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

juvenile spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intermediate spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

survival motor neuron spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

muscular atrophy; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism disorders; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid metabolism disorders; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; muscular diseases Gene Set

From GAD Gene-Disease Associations

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

spinal muscular atrophies of childhood Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular diseases Gene Set

From GAD Gene-Disease Associations

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

muscular atrophy, spinal Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

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

muscular dystrophies Gene Set

From GAD Gene-Disease Associations

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

als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

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

muscular disorders, atrophic Gene Set

From GAD Gene-Disease Associations

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

disorder of muscle, unspec; hypercholesterolemia; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; hypercholesterolemia; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular Gene Set

From GeneRIF Biological Term Annotations

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

Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

muscular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the muscular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

muscular atrophy Gene Set

From GWASdb SNP-Disease Associations

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

muscular disease Gene Set

From GWASdb SNP-Disease Associations

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

muscular hypotonia Gene Set

From GWASdb SNP-Phenotype Associations

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

congenital muscular torticollis Gene Set

From HPO Gene-Disease Associations

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

extrapyramidal muscular rigidity Gene Set

From HPO Gene-Disease Associations

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

muscular edema Gene Set

From HPO Gene-Disease Associations

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

muscular hypotonia Gene Set

From HPO Gene-Disease Associations

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

progressive distal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

infantile muscular hypotonia Gene Set

From HPO Gene-Disease Associations

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

nonprogressive muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

muscular hypotonia of the trunk Gene Set

From HPO Gene-Disease Associations

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

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

severe muscular hypotonia Gene Set

From HPO Gene-Disease Associations

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

generalized muscular appearance from birth Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Muscular Disorders, Atrophic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Dystrophies Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Muscular Atrophies of Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Atrophy, Spinal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular LMNA-interacting protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Muscular LMNA-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small muscular protein Chisel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small muscular protein Chisel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal interventricular septum muscular part morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interventricular septum muscular part morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

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

spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, x-linked 2, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, chronic distal, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal spinal muscular atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal and bulbar muscular atrophy of kennedy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, congenital nonprogressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

vertebrate muscular system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

muscular system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

vertebrate muscular system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

muscular coat Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

invertebrate muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

vertebrate muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

C1q deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the C1q deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ING4 complex (ING4, MYST2, C1orf149, PHF16) Gene Set

From CORUM Protein Complexes

proteins in the ING4 complex (ING4, MYST2, C1orf149, PHF16) protein complex from the CORUM Protein Complexes dataset.

ING4 complex (ING4, MYST2, C1orf149, PHF15) Gene Set

From CORUM Protein Complexes

proteins in the ING4 complex (ING4, MYST2, C1orf149, PHF15) protein complex from the CORUM Protein Complexes dataset.

C1D homodimer protein Gene Set

From CORUM Protein Complexes

proteins in the C1D homodimer protein protein complex from the CORUM Protein Complexes dataset.

ING4 complex (ING4, MYST2, C1orf149, PHF17) Gene Set

From CORUM Protein Complexes

proteins in the ING4 complex (ING4, MYST2, C1orf149, PHF17) protein complex from the CORUM Protein Complexes dataset.

C186 65 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical C186 65 from the curated CTD Gene-Chemical Interactions dataset.

COMPLEMENT COMPONENT C1r/C1s DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease COMPLEMENT COMPONENT C1r/C1s DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

parkinson disease(c10.228.140.079.862.500)/genetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson disease(c10.228.140.079.862.500)/genetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders(c10.228.140.546.399.750)/genetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders(c10.228.140.546.399.750)/genetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension(c14.907.489)/genetics; (c23.550.291.687.500) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension(c14.907.489)/genetics; (c23.550.291.687.500) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

c118t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c118t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1910ct Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1910ct in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1048ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1048ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c190t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c190t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1562t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1562t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c143ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c143ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1galt Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1galt in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1858t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1858t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qc3d Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qc3d in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c17391740insalu Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c17391740insalu in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c196gt Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c196gt in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1867 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1867 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1orf86 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1orf86 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c182dela Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c182dela in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1galt1vc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1galt1vc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c187tc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c187tc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf95rela Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf95rela in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c145 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c145 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1402c1402 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1402c1402 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1363ct Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1363ct in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1orf142 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1orf142 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1494t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1494t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c14orf1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c14orf1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c196 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c196 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1772t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1772t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1rlp Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1rlp in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1918cg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1918cg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qgc1qr Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qgc1qr in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c19mc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c19mc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12orf30 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12orf30 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf59 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf59 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1inh Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1inh in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1351gt Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1351gt in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c19orf12 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c19orf12 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1135ct Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1135ct in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1galt1330gt Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1galt1330gt in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1654t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1654t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11771178delaa Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11771178delaa in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf30 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf30 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1171ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1171ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf25 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf25 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1243ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1243ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12491251 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12491251 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c188 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c188 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1019t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1019t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf95mkl2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf95mkl2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1344delc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1344delc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf92c11orf93 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf92c11orf93 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1445ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1445ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1305 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1305 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c159t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c159t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1level Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1level in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1420t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1420t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c187g Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c187g in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1c4 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1c4 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1c1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1c1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1c2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1c2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c171cg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c171cg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c19 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c19 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c18 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c18 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c10 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c10 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c17 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c17 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c16 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c16 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c14 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c14 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1b Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1b in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1a Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1a in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1d Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1d in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1s Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1s in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1r Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1r in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1q Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1q in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1p Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1p in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1127c Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1127c in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c14orf166 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c14orf166 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1inhibitor Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1inhibitor in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c16orf35 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c16orf35 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1687ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1687ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c106a Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c106a in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qigg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qigg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c127 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c127 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1279ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1279ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf10 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf10 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12orf42 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12orf42 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1sc1rc1rc1s Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1sc1rc1rc1s in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1049gt Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1049gt in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12151218dupccga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12151218dupccga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c17t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c17t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c178 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c178 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1orf103 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1orf103 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c101918g Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c101918g in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1galt1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1galt1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1528gc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1528gc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12orf3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12orf3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1027 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1027 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c157160delgagg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c157160delgagg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c14orf28 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c14orf28 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c100211101113deltaag Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c100211101113deltaag in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c18ceramide Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c18ceramide in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c161t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c161t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c156157insalu Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c156157insalu in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qmediated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qmediated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c116 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c116 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1165cg Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1165cg in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c13nj Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c13nj in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1502 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1502 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c150t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c150t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c19ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c19ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1rc1s Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1rc1s in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c12orf51 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c12orf51 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1377ct Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1377ct in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1187ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1187ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c13 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c13 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c167delt Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c167delt in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1ag Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1ag in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1402t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1402t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c10orf97 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c10orf97 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1565 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1565 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1444t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1444t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1622at Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1622at in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c137ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c137ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qb Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qb in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qa Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qa in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1ten Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1ten in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qc4d Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qc4d in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1236t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1236t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c106 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c106 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c10x Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c10x in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qtnf Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qtnf in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c16ceramide Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c16ceramide in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c162165delaaga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c162165delaaga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1019g Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1019g in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c106t Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c106t in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1qrelated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1qrelated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11374g Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11374g in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c17315ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c17315ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1639ga Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1639ga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c1196ag Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c1196ag in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c11orf30lrrc32 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c11orf30lrrc32 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c152 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c152 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

c10orf90 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term c10orf90 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

complement component c1q binding Gene Set

From GO Molecular Function Annotations

genes performing the complement component c1q binding molecular function from the curated GO Molecular Function Annotations dataset.

AR-C126313 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the AR-C126313 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

AR-C118925XX Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the AR-C118925XX ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Decanoyl-CoA (n-C10:0CoA) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Decanoyl-CoA (n-C10:0CoA) metabolite from the curated HMDB Metabolites of Enzymes dataset.

Peptidase S1A, complement C1r/C1S/mannan-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase S1A, complement C1r/C1S/mannan-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

SPEC3/C1orf95 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the SPEC3/C1orf95 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C12, ubiquitin carboxyl-terminal hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C12, ubiquitin carboxyl-terminal hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

C1GALT1-specific chaperone 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the C1GALT1-specific chaperone 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C19, ubiquitin-specific peptidase, DUSP domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C19, ubiquitin-specific peptidase, DUSP domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DnaJ-like protein C11, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DnaJ-like protein C11, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed RNA polymerase, subunit C11/M/9 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase, subunit C11/M/9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C13, legumain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C13, legumain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C19, ubiquitin carboxyl-terminal hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C19, ubiquitin carboxyl-terminal hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transmembrane protein C12orf23, UPF0444 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transmembrane protein C12orf23, UPF0444 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1A, cathepsin K Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1A, cathepsin K protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UPF0722 protein C11orf88 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UPF0722 protein C11orf88 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14A, caspase precursor p45, core Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14A, caspase precursor p45, core protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UPF0505 protein C16ORF62 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UPF0505 protein C16ORF62 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, caspase non-catalytic subunit p10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, caspase non-catalytic subunit p10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Exosome-associated factor Rrp47/DNA strand repair C1D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Exosome-associated factor Rrp47/DNA strand repair C1D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1A, propeptide Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1A, propeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uncharacterised protein C12orf43 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uncharacterised protein C12orf43 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Centrosomal protein C10orf90 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Centrosomal protein C10orf90 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, ICE, catalytic subunit p20, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, ICE, catalytic subunit p20, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1B, bleomycin hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1B, bleomycin hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, caspase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, caspase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uncharacterised protein C1orf114 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uncharacterised protein C1orf114 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1A, cathepsin B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1A, cathepsin B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, ICE, catalytic subunit p20 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, ICE, catalytic subunit p20 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1A, papain C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1A, papain C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C15, pyroglutamyl peptidase I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C15, pyroglutamyl peptidase I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein C10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein C10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sas10/Utp3/C1D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sas10/Utp3/C1D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

C1GALT1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the C1GALT1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C15, pyroglutamyl peptidase I-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C15, pyroglutamyl peptidase I-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Complement C1q protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Complement C1q protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

C170 Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles

genes with high or low copy number in C170 relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.

C170 Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles

genes with high or low expression in C170 relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset.

C170 Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles

genes mutated in the C170 cell line from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles dataset.

BL1049 (C11orf30) Gene Set

From NURSA Protein Complexes

proteins in the BL1049 (C11orf30) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL2746 (C1D) Gene Set

From NURSA Protein Complexes

proteins in the BL2746 (C1D) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL2747 (C1D) Gene Set

From NURSA Protein Complexes

proteins in the BL2747 (C1D) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL8332 (C1orf55) Gene Set

From NURSA Protein Complexes

proteins in the BL8332 (C1orf55) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL8333 (C1orf55) Gene Set

From NURSA Protein Complexes

proteins in the BL8333 (C1orf55) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL3816 (C12orf5) Gene Set

From NURSA Protein Complexes

proteins in the BL3816 (C12orf5) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL7903 (C16orf53) Gene Set

From NURSA Protein Complexes

proteins in the BL7903 (C16orf53) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL1050 (C11orf30) Gene Set

From NURSA Protein Complexes

proteins in the BL1050 (C11orf30) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL9187 (C19orf62) Gene Set

From NURSA Protein Complexes

proteins in the BL9187 (C19orf62) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

ab81302 (C19orf21) Gene Set

From NURSA Protein Complexes

proteins in the ab81302 (C19orf21) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL2745 (C1D) Gene Set

From NURSA Protein Complexes

proteins in the BL2745 (C1D) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

CBC421 (C14orf43) Gene Set

From NURSA Protein Complexes

proteins in the CBC421 (C14orf43) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL2569 (C17orf71) Gene Set

From NURSA Protein Complexes

proteins in the BL2569 (C17orf71) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

BL4905 (C19orf2) Gene Set

From NURSA Protein Complexes

proteins in the BL4905 (C19orf2) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.

C1ORF112 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C1ORF112 from the NURSA Protein-Protein Interactions dataset.

C12ORF10 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C12ORF10 from the NURSA Protein-Protein Interactions dataset.

C17ORF75 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C17ORF75 from the NURSA Protein-Protein Interactions dataset.

C1ORF226 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C1ORF226 from the NURSA Protein-Protein Interactions dataset.

C11ORF30 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C11ORF30 from the NURSA Protein-Protein Interactions dataset.

C12ORF43 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C12ORF43 from the NURSA Protein-Protein Interactions dataset.

C17ORF59 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for C17ORF59 from the NURSA Protein-Protein Interactions dataset.

c1r/c1s deficiency, combined Gene Set

From OMIM Gene-Disease Associations

genes associated with the c1r/c1s deficiency, combined phenotype from the curated OMIM Gene-Disease Associations dataset.

c1q deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the c1q deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

c1s deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the c1s deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

C16orf13 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf13 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf119 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf119 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf95 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf95 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf1 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf26 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf26 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf25 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf25 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf16 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf16 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf70 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf70 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf72 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf72 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf78 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf78 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf35 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf35 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf48 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf48 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf40 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf40 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf41 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf41 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf43 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf43 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf31 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf31 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf10 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf10 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf58 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf58 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf59 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf59 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf54 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf54 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf53 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf53 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf52 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf52 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf50 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf50 from the Pathway Commons Protein-Protein Interactions dataset.

C1D Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1D from the Pathway Commons Protein-Protein Interactions dataset.

C1orf74 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf74 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf112 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf112 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf110 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf110 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf116 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf116 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf115 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf115 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf4 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf4 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf5 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf5 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf90 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf90 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf131 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf131 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf12 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf12 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf74 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf74 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf76 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf76 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf216 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf216 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf35 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf35 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf32 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf32 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf39 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf39 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf174 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf174 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf233 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf233 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf54 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf54 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf55 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf55 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf76 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf76 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf30 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf30 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf65 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf65 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf85 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf85 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf86 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf86 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf87 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf87 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf97 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf97 from the Pathway Commons Protein-Protein Interactions dataset.

C18orf25 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C18orf25 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf68 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf68 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf2 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf142 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf142 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf49 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf49 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf43 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf43 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf45 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf45 from the Pathway Commons Protein-Protein Interactions dataset.

C1QL3 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QL3 from the Pathway Commons Protein-Protein Interactions dataset.

C1QTNF1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QTNF1 from the Pathway Commons Protein-Protein Interactions dataset.

C1QTNF7 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QTNF7 from the Pathway Commons Protein-Protein Interactions dataset.

C1QTNF5 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QTNF5 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf70 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf70 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf75 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf75 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf53 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf53 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf52 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf52 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf57 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf57 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf54 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf54 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf49 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf49 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf45 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf45 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf82 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf82 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf169 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf169 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf29 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf29 from the Pathway Commons Protein-Protein Interactions dataset.

C1QBP Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QBP from the Pathway Commons Protein-Protein Interactions dataset.

C18orf8 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C18orf8 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf131 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf131 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf70 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf70 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf59 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf59 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf68 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf68 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf51 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf51 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf53 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf53 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf65 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf65 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf63 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf63 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf28 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf28 from the Pathway Commons Protein-Protein Interactions dataset.

C18orf21 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C18orf21 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf105 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf105 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf1 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf89 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf89 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf18 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf18 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf12 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf12 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf80 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf80 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf33 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf33 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf62 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf62 from the Pathway Commons Protein-Protein Interactions dataset.

C1QL1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QL1 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf27 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf27 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf88 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf88 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf59 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf59 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf57 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf57 from the Pathway Commons Protein-Protein Interactions dataset.

C15orf52 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C15orf52 from the Pathway Commons Protein-Protein Interactions dataset.

C1S Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1S from the Pathway Commons Protein-Protein Interactions dataset.

C1R Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1R from the Pathway Commons Protein-Protein Interactions dataset.

C16orf45 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf45 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf43 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf43 from the Pathway Commons Protein-Protein Interactions dataset.

C1QTNF9 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QTNF9 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf101 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf101 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf105 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf105 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf106 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf106 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf109 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf109 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf68 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf68 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf61 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf61 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf64 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf64 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf48 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf48 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf84 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf84 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf87 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf87 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf80 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf80 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf122 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf122 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf123 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf123 from the Pathway Commons Protein-Protein Interactions dataset.

C16orf87 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C16orf87 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf2 from the Pathway Commons Protein-Protein Interactions dataset.

C1GALT1C1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1GALT1C1 from the Pathway Commons Protein-Protein Interactions dataset.

C1QC Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QC from the Pathway Commons Protein-Protein Interactions dataset.

C1QB Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QB from the Pathway Commons Protein-Protein Interactions dataset.

C1QA Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1QA from the Pathway Commons Protein-Protein Interactions dataset.

C1orf168 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf168 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf166 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf166 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf60 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf60 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf57 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf57 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf10 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf10 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf228 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf228 from the Pathway Commons Protein-Protein Interactions dataset.

C1RL Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1RL from the Pathway Commons Protein-Protein Interactions dataset.

C14orf93 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf93 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf62 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf62 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf111 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf111 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf80 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf80 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf81 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf81 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf73 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf73 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf75 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf75 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf94 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf94 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf111 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf111 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf82 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf82 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf80 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf80 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf85 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf85 from the Pathway Commons Protein-Protein Interactions dataset.

C18orf32 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C18orf32 from the Pathway Commons Protein-Protein Interactions dataset.

C12orf57 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C12orf57 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf62 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf62 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf40 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf40 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf43 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf43 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf44 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf44 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf45 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf45 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf47 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf47 from the Pathway Commons Protein-Protein Interactions dataset.

C18orf54 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C18orf54 from the Pathway Commons Protein-Protein Interactions dataset.

C1GALT1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1GALT1 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf159 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf159 from the Pathway Commons Protein-Protein Interactions dataset.

C17orf49 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C17orf49 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf66 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf66 from the Pathway Commons Protein-Protein Interactions dataset.

C19orf67 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C19orf67 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf58 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf58 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf53 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf53 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf52 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf52 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf54 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf54 from the Pathway Commons Protein-Protein Interactions dataset.

C14orf178 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C14orf178 from the Pathway Commons Protein-Protein Interactions dataset.

C10orf10 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C10orf10 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf71 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf71 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf70 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf70 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf73 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf73 from the Pathway Commons Protein-Protein Interactions dataset.

C11orf74 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C11orf74 from the Pathway Commons Protein-Protein Interactions dataset.

C1orf198 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for C1orf198 from the Pathway Commons Protein-Protein Interactions dataset.

vero c1008 cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue vero c1008 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

c1r cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue c1r cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

c127i cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue c127i cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance 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.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyp