Name

FAD-linked oxidoreductase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidoreductase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-linked oxidase-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidase-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, FAD/NAD(P)-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, FAD/NAD(P)-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, FAD-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, FAD-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD dependent oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD dependent oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-dependent pyridine nucleotide-disulphide oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-dependent pyridine nucleotide-disulphide oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase FAD/NAD(P)-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase FAD/NAD(P)-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD linked oxidase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD linked oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD/NAD-linked reductase, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD/NAD-linked reductase, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-linked oxidase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CO dehydrogenase flavoprotein-like, FAD-binding, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CO dehydrogenase flavoprotein-like, FAD-binding, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DHS-like NAD/FAD-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DHS-like NAD/FAD-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, subunit 1/F420H2 oxidoreductase subunit H Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit 1/F420H2 oxidoreductase subunit H protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription elongation factor A-like/Brain expressed X-linked-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription elongation factor A-like/Brain expressed X-linked-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase subunit E-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase subunit E-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase-like, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase-like, 20kDa subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase-like, 20kDa subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

fad Gene Set

From GeneRIF Biological Term Annotations

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

fad biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the fad biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

fad metabolic process Gene Set

From GO Biological Process Annotations

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

fad transmembrane transport Gene Set

From GO Biological Process Annotations

genes participating in the fad transmembrane transport biological process from the curated GO Biological Process Annotations dataset.

fad transport Gene Set

From GO Biological Process Annotations

genes participating in the fad transport biological process from the curated GO Biological Process Annotations dataset.

protein-fad linkage Gene Set

From GO Biological Process Annotations

genes participating in the protein-fad linkage biological process from the curated GO Biological Process Annotations dataset.

fad transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the fad transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

fad binding Gene Set

From GO Molecular Function Annotations

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

fad-amp lyase (cyclizing) activity Gene Set

From GO Molecular Function Annotations

genes performing the fad-amp lyase (cyclizing) activity molecular function from the curated GO Molecular Function Annotations dataset.

FAD Gene Set

From HMDB Metabolites of Enzymes

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

UBA/THIF-type NAD/FAD binding fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UBA/THIF-type NAD/FAD binding fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-binding, type 2, subdomain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-binding, type 2, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-binding 8 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-binding 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA photolyase, FAD-binding/Cryptochrome, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA photolyase, FAD-binding/Cryptochrome, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdopterin dehydrogenase, FAD-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdopterin dehydrogenase, FAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-binding, type 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-binding, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-binding, type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-binding, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fumarate reductase/succinate dehydrogenase, FAD-binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fumarate reductase/succinate dehydrogenase, FAD-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-dependent glycerol-3-phosphate dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-dependent glycerol-3-phosphate dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADPH-cytochrome p450 reductase, FAD-binding, alpha-helical domain-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADPH-cytochrome p450 reductase, FAD-binding, alpha-helical domain-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ferredoxin reductase-type FAD-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ferredoxin reductase-type FAD-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Monooxygenase, FAD-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Monooxygenase, FAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD synthetase with the MoaB/Mog domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD synthetase with the MoaB/Mog domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Asparagine-linked glycosylation protein 1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Asparagine-linked glycosylation protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

insulin-like growth factor-1; insulin-like growth factor-3 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-1; insulin-like growth factor-3 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

EGF-like repeat and discoidin I-like domain-containing protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EGF-like repeat and discoidin I-like domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thrombomodulin-like, EGF-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thrombomodulin-like, EGF-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAUS augmin-like complex subunit 7-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAUS augmin-like complex subunit 7-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) Gene Set

From Reactome Pathways

proteins participating in the Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) pathway from the Reactome Pathways dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

oxidoreductase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the oxidoreductase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

oxidoreductase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

cytochrome p450 oxidoreductase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytochrome p450 oxidoreductase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oxidoreductase Gene Set

From GeneRIF Biological Term Annotations

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

sulfide oxidation, using sulfide:quinone oxidoreductase Gene Set

From GO Biological Process Annotations

genes participating in the sulfide oxidation, using sulfide:quinone oxidoreductase biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations dataset.

oxidoreductase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the oxidoreductase complex cellular component from the curated GO Cellular Component Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors molecular function from the curated GO Molecular Function Annotations dataset.

n1-acetylspermidine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity Gene Set

From GO Molecular Function Annotations

genes performing the n1-acetylspermidine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations dataset.

sn-glycerol-3-phosphate:ubiquinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the sn-glycerol-3-phosphate:ubiquinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on superoxide radicals as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on superoxide radicals as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

aminoacetone:oxygen oxidoreductase(deaminating) activity Gene Set

From GO Molecular Function Annotations

genes performing the aminoacetone:oxygen oxidoreductase(deaminating) activity molecular function from the curated GO Molecular Function Annotations dataset.

intramolecular oxidoreductase activity, interconverting aldoses and ketoses Gene Set

From GO Molecular Function Annotations

genes performing the intramolecular oxidoreductase activity, interconverting aldoses and ketoses molecular function from the curated GO Molecular Function Annotations dataset.

n1-acetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity Gene Set

From GO Molecular Function Annotations

genes performing the n1-acetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations dataset.

peptide disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the peptide disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity Gene Set

From GO Molecular Function Annotations

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

oxidoreductase activity, acting on iron-sulfur proteins as donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch or ch2 groups, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch or ch2 groups, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on diphenols and related substances as donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen molecular function from the curated GO Molecular Function Annotations dataset.

glutathione disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the glutathione disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on peroxide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on peroxide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors molecular function from the curated GO Molecular Function Annotations dataset.

n1-acetylspermine:oxygen oxidoreductase (n1-acetylspermidine-forming) activity Gene Set

From GO Molecular Function Annotations

genes performing the n1-acetylspermine:oxygen oxidoreductase (n1-acetylspermidine-forming) activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h molecular function from the curated GO Molecular Function Annotations dataset.

intramolecular oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the intramolecular oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, oxidizing metal ions with flavin as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, oxidizing metal ions with flavin as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

alditol:nadp+ 1-oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the alditol:nadp+ 1-oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors molecular function from the curated GO Molecular Function Annotations dataset.

sn-glycerol-3-phosphate:ubiquinone-8 oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the sn-glycerol-3-phosphate:ubiquinone-8 oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

n(1),n(12)-diacetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity Gene Set

From GO Molecular Function Annotations

genes performing the n(1),n(12)-diacetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch or ch2 groups Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch or ch2 groups molecular function from the curated GO Molecular Function Annotations dataset.

sulfide:quinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfide:quinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

spermine:oxygen oxidoreductase (spermidine-forming) activity Gene Set

From GO Molecular Function Annotations

genes performing the spermine:oxygen oxidoreductase (spermidine-forming) activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

intramolecular oxidoreductase activity, transposing c=c bonds Gene Set

From GO Molecular Function Annotations

genes performing the intramolecular oxidoreductase activity, transposing c=c bonds molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, oxidizing metal ions, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, oxidizing metal ions, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

tryptamine:oxygen oxidoreductase (deaminating) activity Gene Set

From GO Molecular Function Annotations

genes performing the tryptamine:oxygen oxidoreductase (deaminating) activity molecular function from the curated GO Molecular Function Annotations dataset.

protein disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the protein disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

glutathione oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the glutathione oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

norspermine:oxygen oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the norspermine:oxygen oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a heme group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a heme group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h, nad(p) as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h, nad(p) as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, oxidizing metal ions, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, oxidizing metal ions, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

intramolecular oxidoreductase activity, transposing s-s bonds Gene Set

From GO Molecular Function Annotations

genes performing the intramolecular oxidoreductase activity, transposing s-s bonds molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, oxidizing metal ions Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, oxidizing metal ions molecular function from the curated GO Molecular Function Annotations dataset.

nadph:sulfur oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the nadph:sulfur oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

spermidine:oxygen oxidoreductase (3-aminopropanal-forming) activity Gene Set

From GO Molecular Function Annotations

genes performing the spermidine:oxygen oxidoreductase (3-aminopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch or ch2 groups, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch or ch2 groups, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch-oh group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch-oh group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on diphenols and related substances as donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

intramolecular oxidoreductase activity, interconverting keto- and enol-groups Gene Set

From GO Molecular Function Annotations

genes performing the intramolecular oxidoreductase activity, interconverting keto- and enol-groups molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

phenethylamine:oxygen oxidoreductase (deaminating) activity Gene Set

From GO Molecular Function Annotations

genes performing the phenethylamine:oxygen oxidoreductase (deaminating) activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on phosphorus or arsenic in donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on phosphorus or arsenic in donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch or ch2 groups, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch or ch2 groups, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch or ch2 groups, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch or ch2 groups, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

glyceraldehyde oxidoreductase activity Gene Set

From GO Molecular Function Annotations

genes performing the glyceraldehyde oxidoreductase activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h, heme protein as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h, heme protein as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set

From HPO Gene-Disease Associations

genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

NADH:quinone oxidoreductase/Mrp antiporter, membrane subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:quinone oxidoreductase/Mrp antiporter, membrane subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH ubiquinone oxidoreductase, F subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH ubiquinone oxidoreductase, F subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase intermediate-associated protein 30 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase intermediate-associated protein 30 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, molybdopterin-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, molybdopterin-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, 49kDa subunit, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, 49kDa subunit, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, iron-sulphur subunit 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, iron-sulphur subunit 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, 51kDa subunit, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, 51kDa subunit, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase subunit B14.5a Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase subunit B14.5a protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdopterin oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdopterin oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, subunit NDUFB4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit NDUFB4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, 30kDa subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, 30kDa subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, NDUFB5/SGDH subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, NDUFB5/SGDH subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Moybdenum cofactor oxidoreductase, dimerisation Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Moybdenum cofactor oxidoreductase, dimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NAD(P)H-quinone oxidoreductase subunit D/H Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NAD(P)H-quinone oxidoreductase subunit D/H protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, 42kDa subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, 42kDa subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone/plastoquinone oxidoreductase, chain 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone/plastoquinone oxidoreductase, chain 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, NAD-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, NAD-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, subunit G Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit G protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, 75kDa subunit, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, 75kDa subunit, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, class I, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, class I, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, subunit 1, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit 1, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase 51 kDa subunit, iron-sulphur binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase 51 kDa subunit, iron-sulphur binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase 51 kDa subunit, FMN-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase 51 kDa subunit, FMN-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, MNLL subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, MNLL subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, subunit b14.5b Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit b14.5b protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase, 20 Kd subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase, 20 Kd subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, 30kDa subunit, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, 30kDa subunit, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein-ubiquinone oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein-ubiquinone oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Quinone oxidoreductase/zeta-crystallin, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Quinone oxidoreductase/zeta-crystallin, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone/plastoquinone oxidoreductase, chain 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone/plastoquinone oxidoreductase, chain 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, chain G, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, chain G, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, subunit G, iron-sulphur binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit G, iron-sulphur binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, chain M/4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, chain M/4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, class-II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, class-II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, chain 4, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, chain 4, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, subunit D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, subunit D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, ESSS subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, ESSS subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase, subunit 10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase, subunit 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, chain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, chain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-plastoquinone oxidoreductase, chain 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-plastoquinone oxidoreductase, chain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Malic oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Malic oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eukaryotic molybdopterin oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eukaryotic molybdopterin oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, chain I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, chain I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase flavoprotein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase flavoprotein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADP-dependent oxidoreductase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADP-dependent oxidoreductase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Multi-copper polyphenol oxidoreductase, laccase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Multi-copper polyphenol oxidoreductase, laccase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase chain 4L/K Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase chain 4L/K protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH:ubiquinone oxidoreductase, B18 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:ubiquinone oxidoreductase, B18 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, molybdopterin binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, molybdopterin binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Quinone oxidoreductase PIG3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Quinone oxidoreductase PIG3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADPH-dependent diflavin oxidoreductase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADPH-dependent diflavin oxidoreductase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-ubiquinone oxidoreductase 1 subunit C1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-ubiquinone oxidoreductase 1 subunit C1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transketolase, C-terminal/Pyruvate-ferredoxin oxidoreductase, domain II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transketolase, C-terminal/Pyruvate-ferredoxin oxidoreductase, domain II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdopterin oxidoreductase, 4Fe-4S domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdopterin oxidoreductase, 4Fe-4S domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set

From OMIM Gene-Disease Associations

genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset.

X-linked ichthyosis with steryl-sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked lissencephaly 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked lissencephaly 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 58 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 58 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrogenic diabetes insipidus, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrogenic diabetes insipidus, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Creatine deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Creatine deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Properdin deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Properdin deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic, Claes-Jensen type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic, Claes-Jensen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 63 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 63 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked severe combined immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, turner type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, turner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic X-linked ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypohidrotic X-linked ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, early-onset, severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked mental retardation 90 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked mental retardation 90 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked syndromic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked syndromic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dyskeratosis congenita X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dyskeratosis congenita X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndromic X-linked mental retardation 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndromic X-linked mental retardation 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderius X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nystagmus 6, congenital, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with marfanoid habitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Protoporphyria, erythropoietic, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Protoporphyria, erythropoietic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, idiopathic, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, X-linked 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, X-linked 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, X-linked 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, X-linked 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, X-linked 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, X-linked 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked infantile nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wilson-Turner X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondrodysplasia punctata 2 X-linked dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondrodysplasia punctata 2 X-linked dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, raymond type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, raymond type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hypoplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac valvular dysplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alport syndrome, X-linked recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alport syndrome, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked lymphoproliferative syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked lymphoproliferative syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked lymphoproliferative syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked lymphoproliferative syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked recessive hypophosphatemic rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked recessive hypophosphatemic rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 19 phenotype from the curated ClinVar Gene-Phenotype Associations 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.

Parkinsonism with spasticity, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinsonism with spasticity, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital short bowel syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ohdo syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ohdo syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ZNF711-Related X-linked Mental Retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe X-linked myotubular myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial exudative vitreoretinopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined immunodeficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined immunodeficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked myopathy with postural muscle atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hydrocephalus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tooth agenesis, selective, X-linked, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tooth agenesis, selective, X-linked, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONE DYSTROPHY 5, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked dominant scapuloperoneal myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked dominant scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

VACTERL association with hydrocephaly, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the VACTERL association with hydrocephaly, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 32 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, wu type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, wu type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked Mental Retardation 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked Mental Retardation 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, Hedera type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, Hedera type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked syndromic mental retardation, Nascimento type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked syndromic mental retardation, Nascimento type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 3, torsion, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 3, torsion, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked agammaglobulinemia with growth hormone deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked agammaglobulinemia with growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, X-linked, intermittent Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, X-linked, intermittent phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked periventricular heterotopia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked periventricular heterotopia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial atypical mycobacteriosis, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, childhood-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, high-frequency sensorineural, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, high-frequency sensorineural, X-linked 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.

X-linked agammaglobulinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked agammaglobulinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 93 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 93 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotaxy, visceral, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Heterotaxy, visceral, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 96 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 96 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 98 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 98 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 99 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 99 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 72 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 72 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.

X-linked hypospadias 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hypospadias 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hypospadias 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hypospadias 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondrodysplasia punctata 1, X-linked recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondrodysplasia punctata 1, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

lipid-linked oligosaccharides Gene Set

From CTD Gene-Chemical Interactions

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

Siderius X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Siderius X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Partington X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Partington X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac valvular dysplasia, X-linked from the curated CTD Gene-Disease Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

Properdin deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Properdin deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Opitz GBBB Syndrome, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Opitz GBBB Syndrome, X-Linked from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 34, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 34, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 30 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.

Nystagmus 1, congenital, X- linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 23 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 91 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 91 from the curated CTD Gene-Disease Associations dataset.

Keratosis Follicularis Spinulosa Decalvans, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Follicularis Spinulosa Decalvans, X-Linked from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Partial Agenesis of, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Partial Agenesis of, X-Linked from the curated CTD Gene-Disease Associations dataset.

Miles-Carpenter x-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miles-Carpenter x-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 95 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 95 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 9 from the curated CTD Gene-Disease Associations dataset.

Hydrocephalus, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hydrocephalus, X-linked from the curated CTD Gene-Disease Associations dataset.

Deafness, X-Linked 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, X-Linked 5 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Endothelial, X-Linked Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 77 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 77 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 13 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 12 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 14 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE from the curated CTD Gene-Disease Associations dataset.

Hypospadias 1, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypospadias 1, X-Linked from the curated CTD Gene-Disease Associations dataset.

Deafness, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

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

Charcot-Marie-Tooth disease, X-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Hairy Ears, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hairy Ears, Y-Linked from the curated CTD Gene-Disease Associations dataset.

Lissencephaly, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

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

Tooth Agenesis, Selective, X-Linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, X-Linked, 1 from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal Dysplasia Tarda, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal Dysplasia Tarda, X-Linked from the curated CTD Gene-Disease Associations dataset.

Lubs X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lubs X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Hypoparathyroidism, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoparathyroidism, X-Linked from the curated CTD Gene-Disease Associations dataset.

Bulbospinal neuronopathy, X-linked recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bulbospinal neuronopathy, X-linked recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 16, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 16, X-linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Short Stature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset.

Prostate Cancer, Hereditary, X-Linked 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, X-Linked 2 from the curated CTD Gene-Disease Associations dataset.

Creatine deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Creatine deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 20 from the curated CTD Gene-Disease Associations dataset.

Mental retardation X-linked syndromic 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation X-linked syndromic 7 from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 2, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 2, X-linked from the curated CTD Gene-Disease Associations dataset.

Scapuloperoneal Myopathy, X-Linked Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant from the curated CTD Gene-Disease Associations dataset.

Heterotaxy, visceral, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotaxy, visceral, X-linked from the curated CTD Gene-Disease Associations dataset.

Angioma serpiginosum, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angioma serpiginosum, X-linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 17 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset.

VACTERL association with hydrocephaly, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VACTERL association with hydrocephaly, X-linked from the curated CTD Gene-Disease Associations dataset.

Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.

X-linked mental retardation Gustavson type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked mental retardation Gustavson type from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 81 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 81 from the curated CTD Gene-Disease Associations dataset.

Episodic Muscle Weakness, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Muscle Weakness, X-Linked from the curated CTD Gene-Disease Associations dataset.

ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Sertoli cell-only syndrome, Y-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sertoli cell-only syndrome, Y-linked from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked 14 from the curated CTD Gene-Disease Associations dataset.

Mental retardation-hypotonic facies syndrome, x-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation-hypotonic facies syndrome, x-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Christianson Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Christianson Type from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 84 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 84 from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, syndromic 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, syndromic 5 from the curated CTD Gene-Disease Associations dataset.

ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

Deafness, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, X-Linked 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, X-Linked 5 from the curated CTD Gene-Disease Associations dataset.

HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 21 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, Y-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, Y-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 78 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 78 from the curated CTD Gene-Disease Associations dataset.

X-linked sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked from the curated CTD Gene-Disease Associations dataset.

Chondrodysplasia punctata 2, X-linked dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chondrodysplasia punctata 2, X-linked dominant from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 1 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.

Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 73 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 73 from the curated CTD Gene-Disease Associations dataset.

Abidi X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abidi X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Panhypopituitarism X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Panhypopituitarism X-linked from the curated CTD Gene-Disease Associations dataset.

Lymphoproliferative Syndrome, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

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

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 82 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 82 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.

AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 96 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 96 from the curated CTD Gene-Disease Associations dataset.

Genetic Diseases, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Genetic Diseases, X-Linked from the curated CTD Gene-Disease Associations dataset.

Frontotemporal Dementia, Chromosome 3-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Frontotemporal Dementia, Chromosome 3-Linked from the curated CTD Gene-Disease Associations dataset.

DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Myopathy, X-Linked, with Excessive Autophagy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, X-Linked, with Excessive Autophagy from the curated CTD Gene-Disease Associations dataset.

Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 5, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 5, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 49 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 49 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Panhypopituitarism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Panhypopituitarism from the curated CTD Gene-Disease Associations dataset.

PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, Y-Linked from the curated CTD Gene-Disease Associations dataset.

PROSTATE CANCER, HEREDITARY, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 52 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 52 from the curated CTD Gene-Disease Associations dataset.

Radial Ray Deficiency, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Radial Ray Deficiency, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 53 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 53 from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 6, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 6, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 4 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 3 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 58 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 58 from the curated CTD Gene-Disease Associations dataset.

Dystonia 3, Torsion, X-Linked Gene Set

From CTD Gene-Disease Associations

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

Neutropenia, Severe Congenital, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 63 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 63 from the curated CTD Gene-Disease Associations dataset.

Nephrolithiasis, X-Linked Recessive, with Renal Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephrolithiasis, X-Linked Recessive, with Renal Failure from the curated CTD Gene-Disease Associations dataset.

Arthrogryposis multiplex congenita, distal, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset.

MYOPATHY, CENTRONUCLEAR, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Hodgkin disease, X-linked pseudoautosomal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hodgkin disease, X-linked pseudoautosomal from the curated CTD Gene-Disease Associations dataset.

Armfield X-Linked Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Armfield X-Linked Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 42 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 42 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 93 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 93 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 94 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 94 from the curated CTD Gene-Disease Associations dataset.

X-Linked Combined Immunodeficiency Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-Linked Combined Immunodeficiency Diseases from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis congenital generalized X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.

GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Short Stature, Idiopathic, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Turner Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Turner Type from the curated CTD Gene-Disease Associations dataset.

Agammaglobulinemia, X-linked, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Agammaglobulinemia, X-linked, type 2 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTHEMIA, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTHEMIA, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 72 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 72 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.

Mental Retardation, X-Linked 45 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 45 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 46 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 46 from the curated CTD Gene-Disease Associations dataset.

Spermatogenic Failure, Nonobstructive, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spermatogenic Failure, Nonobstructive, Y-Linked from the curated CTD Gene-Disease Associations dataset.

Cleft palate X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleft palate X-linked from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Prieto X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prieto X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.

EXUDATIVE VITREORETINOPATHY 2, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EXUDATIVE VITREORETINOPATHY 2, X-LINKED from the curated CTD Gene-Disease Associations dataset.

ALPORT SYNDROME, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ALPORT SYNDROME, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 10 from the curated CTD Gene-Disease Associations dataset.

Hypospadias 2, X-Linked Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 50 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 50 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, X-Linked from the curated CTD Gene-Disease Associations dataset.

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, X-Linked from the curated CTD Gene-Disease Associations dataset.

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.

x-linked disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

x-linked sideroblastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

x-linked hypophosphatemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

non-specific x-linked mental retardation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-specific x-linked mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

x-linked disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked ichthyosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

x-linked hyper igm syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked hyper igm syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

x-linked nonsyndromic deafness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked myopathy with excessive autophagy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

agammaglobulinemia; genetic diseases, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease agammaglobulinemia; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, x-linked; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x linked juvenile retinoschisis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x linked juvenile retinoschisis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

non-syndromic x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked charcot-marie tooth disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked charcot-marie tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; rett syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, x-linked; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; genetic diseases, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypophosphatemic rickets, x-linked dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypophosphatemic rickets, x-linked dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ichthyosis, x-linked Gene Set

From GAD Gene-Disease Associations

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

x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked lymphoproliferative disease Gene Set

From GAD Gene-Disease Associations

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

x-linked severe combined immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked; syndrome Gene Set

From GAD Gene-Disease Associations

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

colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked adrenoleukodystrophy Gene Set

From GAD Gene-Disease Associations

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

linked Gene Set

From GeneRIF Biological Term Annotations

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

protein k33-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k33-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

histone h2a k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the histone h2a k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein k48-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein k48-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein c-linked glycosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein c-linked glycosylation biological process from the curated GO Biological Process Annotations dataset.

dolichol-linked oligosaccharide biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the dolichol-linked oligosaccharide biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of protein k48-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein k48-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of protein k48-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of protein k48-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k29-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k29-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

negative regulation of histone h2a k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of histone h2a k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked mannosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked mannosylation biological process from the curated GO Biological Process Annotations dataset.

regulation of histone h2a k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of histone h2a k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein c-linked glycosylation via 2'-alpha-mannosyl-l-tryptophan Gene Set

From GO Biological Process Annotations

genes participating in the protein c-linked glycosylation via 2'-alpha-mannosyl-l-tryptophan biological process from the curated GO Biological Process Annotations dataset.

protein k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k27-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k27-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

histone h2a k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the histone h2a k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked glycosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked glycosylation biological process from the curated GO Biological Process Annotations dataset.

protein k6-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k6-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k48-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k48-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked fucosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked fucosylation biological process from the curated GO Biological Process Annotations dataset.

protein c-linked glycosylation via tryptophan Gene Set

From GO Biological Process Annotations

genes participating in the protein c-linked glycosylation via tryptophan biological process from the curated GO Biological Process Annotations dataset.

protein k11-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k11-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein o-linked glycosylation via threonine Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked glycosylation via threonine biological process from the curated GO Biological Process Annotations dataset.

protein k48-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k48-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

carnitine metabolic process, coa-linked Gene Set

From GO Biological Process Annotations

genes participating in the carnitine metabolic process, coa-linked biological process from the curated GO Biological Process Annotations dataset.

protein n-linked glycosylation via asparagine Gene Set

From GO Biological Process Annotations

genes participating in the protein n-linked glycosylation via asparagine biological process from the curated GO Biological Process Annotations dataset.

protein k27-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k27-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k11-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k11-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k29-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k29-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

regulation of protein k63-linked deubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein k63-linked deubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k33-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k33-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

regulation of protein k63-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein k63-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

protein k6-linked ubiquitination Gene Set

From GO Biological Process Annotations

genes participating in the protein k6-linked ubiquitination biological process from the curated GO Biological Process Annotations dataset.

enzyme linked receptor protein signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the enzyme linked receptor protein signaling pathway biological process from the curated GO Biological Process Annotations dataset.

protein n-linked glycosylation Gene Set

From GO Biological Process Annotations

genes participating in the protein n-linked glycosylation biological process from the curated GO Biological Process Annotations dataset.

protein o-linked glycosylation via serine Gene Set

From GO Biological Process Annotations

genes participating in the protein o-linked glycosylation via serine biological process from the curated GO Biological Process Annotations dataset.

gpi-linked ephrin receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the gpi-linked ephrin receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

k63-linked polyubiquitin binding Gene Set

From GO Molecular Function Annotations

genes performing the k63-linked polyubiquitin binding molecular function from the curated GO Molecular Function Annotations dataset.

k6-linked polyubiquitin binding Gene Set

From GO Molecular Function Annotations

genes performing the k6-linked polyubiquitin binding molecular function from the curated GO Molecular Function Annotations dataset.

flavin-linked sulfhydryl oxidase activity Gene Set

From GO Molecular Function Annotations

genes performing the flavin-linked sulfhydryl oxidase activity molecular function from the curated GO Molecular Function Annotations dataset.

x-linked disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormal protein n-linked glycosylation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

x-linked dominant inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the x-linked dominant inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

x-linked recessive inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the x-linked recessive inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased urinary o-linked sialopeptides Gene Set

From HPO Gene-Disease Associations

genes associated with the increased urinary o-linked sialopeptides phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

x-linked inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the x-linked inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

y-linked inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the y-linked inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hypophosphatemic Rickets, X-Linked Dominant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hypophosphatemic Rickets, X-Linked Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ichthyosis, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Retardation, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mental Retardation, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Genetic Diseases, Y-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Genetic Diseases, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heat shock transcription factor, Y-linked Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heat shock transcription factor, Y-linked protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Integrin-linked protein kinase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Integrin-linked protein kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Heat shock transcription factor, X-linked Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heat shock transcription factor, X-linked protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain-expressed X-linked protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain-expressed X-linked protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{autism, susceptibility to, x-linked 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism, susceptibility to, x-linked 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 1, progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, x-linked 1, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 84 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 84 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 81 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 81 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 82 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 82 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 89 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 89 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-parkinsonism, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-parkinsonism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?olmsted syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?olmsted syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, snyder-robinson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, snyder-robinson type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 30/47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 30/47 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked syndromic 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked syndromic 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 40, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 40, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 16, x-linked, complicated Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 16, x-linked, complicated phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, x-linked dominant, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, x-linked dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, x-linked recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, x-linked recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, x-linked, with hyper-igm Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with hyper-igm phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, fraxe type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, fraxe type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoparathyroidism, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoparathyroidism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{graves disease, susceptibility to, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {graves disease, susceptibility to, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, y-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, y-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, intermittent Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, intermittent phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

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.

lissencephaly, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the lissencephaly, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with isolated growth hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic, hedera type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic, hedera type phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 91 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

lissencephaly, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

epilepsy, x-linked, with variable learning disabilities and behavior disorders Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, x-linked, with variable learning disabilities and behavior disorders phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 90 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 90 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 98 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 98 phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, shashi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, shashi type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-hypotonic facies syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-hypotonic facies syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spermatogenic failure, y-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spermatogenic failure, y-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spermatogenic failure, y-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spermatogenic failure, y-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

exudative vitreoretinopathy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the exudative vitreoretinopathy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, x-linked, with postural muscle atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

hypospadias 1, x-linked Gene Set

From OMIM Gene-Disease Associations

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

{autism susceptibility, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 78 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 78 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 72 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 72 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

chondrodysplasia punctata, x-linked dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrodysplasia punctata, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 52 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 52 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 53 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 53 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 50 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 50 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 58 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 58 phenotype from the curated OMIM Gene-Disease Associations dataset.

properdin deficiency, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the properdin deficiency, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, claes-jensen type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, claes-jensen type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, nascimento-type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, nascimento-type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 21/34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 21/34 phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, x-linked 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, x-linked 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 1, hypohidrotic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 1, hypohidrotic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 2, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

keratosis follicularis spinulosa decalvans, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratosis follicularis spinulosa decalvans, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia with beta-thalassemia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia with beta-thalassemia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?stocco dos santos x-linked mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stocco dos santos x-linked mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

ohdo syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

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

neutropenia, severe congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 77 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 77 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, congenital, with fiber-type disproportion, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{asperger syndrome susceptibility, x-linked 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asperger syndrome susceptibility, x-linked 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 15 (cabezas type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 15 (cabezas type) phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, x-linked 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, x-linked 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, reducing body, x-linked, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with short stature Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, chudley-schwartz type, Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, chudley-schwartz type, phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 92 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 92 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 93 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 93 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 96 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 96 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 97 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 97 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 94 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 94 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 95 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 99 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 99 phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypospadias 4, x-linked, susceptibilty to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypospadias 4, x-linked, susceptibilty to} phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 34, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 34, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy, progressive x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked syndromic, raymond type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, raymond type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, endothelial, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

vacterl association, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the vacterl association, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

combined immunodeficiency, x-linked, moderate Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined immunodeficiency, x-linked, moderate phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus, infantile periodic alternating, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal myopathy, x-linked dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal myopathy, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

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

agammaglobulinemia, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

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

agammaglobulinemia, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

chondrodysplasia punctata, x-linked recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrodysplasia punctata, x-linked recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 1, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 1, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoproliferative syndrome, x-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoproliferative syndrome, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphoproliferative syndrome, x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoproliferative syndrome, x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic muscle weakness, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic muscle weakness, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocythemia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocythemia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 34, mycobacteriosis, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 34, mycobacteriosis, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, abidi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, abidi type phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

myotubular myopathy, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the myotubular myopathy, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

protoporphyria, erythropoietic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the protoporphyria, erythropoietic, x-linked 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.

spermatogenic failure, x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spermatogenic failure, x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular degeneration, x-linked atrophic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular degeneration, x-linked atrophic phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

subcortical laminal heteropia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the subcortical laminal heteropia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, y-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, y-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{autism susceptibility, x-linked 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {autism susceptibility, x-linked 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypophosphatemic rickets, x-linked dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatemic rickets, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac valvular dysplasia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac valvular dysplasia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect 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.

?mental retardation, x-linked 101 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 101 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 100 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 100 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, turner type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, turner type 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.

mental retardation, x-linked 49 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 49 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, lubs type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, lubs type phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 6, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 6, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, x-linked 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

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

deafness, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

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

deafness, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

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

panhypopituitarism, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the panhypopituitarism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 29 and others Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 29 and others phenotype from the curated OMIM Gene-Disease Associations dataset.

?parkinsonism with spasticity, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?parkinsonism with spasticity, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa, x-linked recessive, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa, x-linked recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis congenita, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskeratosis congenita, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{mycobacerium tuberculosis, susceptibility, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {mycobacerium tuberculosis, susceptibility, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypospadias 2, x-linked Gene Set

From OMIM Gene-Disease Associations

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

myopathy, reducing body, x-linked, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?hairy ears, y-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hairy ears, y-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus 5, congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus 5, congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{asperger syndrome susceptibility, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asperger syndrome susceptibility, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{diabetes mellitus, insulin-dependent, x-linked} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {diabetes mellitus, insulin-dependent, x-linked} phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodysregulation, polyendocrinopathy, and enteropathy, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodysregulation, polyendocrinopathy, and enteropathy, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, christianson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, christianson type phenotype from the curated OMIM Gene-Disease Associations dataset.

Coenzyme A linked carnitine metabolism Gene Set

From PANTHER Pathways

proteins participating in the Coenzyme A linked carnitine metabolism pathway from the PANTHER Pathways dataset.

Integrin-linked kinase signaling Gene Set

From PID Pathways

proteins participating in the Integrin-linked kinase signaling pathway from the PID Pathways dataset.

Asparagine N-linked glycosylation Gene Set

From Reactome Pathways

proteins participating in the Asparagine N-linked glycosylation pathway from the Reactome Pathways dataset.

O-linked glycosylation Gene Set

From Reactome Pathways

proteins participating in the O-linked glycosylation pathway from the Reactome Pathways dataset.

O-linked glycosylation of mucins Gene Set

From Reactome Pathways

proteins participating in the O-linked glycosylation of mucins pathway from the Reactome Pathways dataset.

Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set

From Reactome Pathways

proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways dataset.

Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Set

From Reactome Pathways

proteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways dataset.

X-linked hypophosphatemia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease X-linked hypophosphatemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

X-linked agammaglobulinaemia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease X-linked agammaglobulinaemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Striatum-like amygdalar nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

toll-like receptor pathway Gene Set

From Biocarta Pathways

proteins participating in the toll-like receptor pathway pathway from the Biocarta Pathways dataset.

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

C-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the C-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Weill-Marchesani-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Weill-Marchesani-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nijmegen breakage syndrome-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-like growth factor 1 resistance to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-like growth factor 1 resistance to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pitt-Hopkins-like syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pitt-Hopkins-like syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pitt-Hopkins-like syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pitt-Hopkins-like syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Townes-Brocks-branchiootorenal-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Townes-Brocks-branchiootorenal-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Band-like calcification with simplified gyration and polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephronophthisis-like nephropathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephronophthisis-like nephropathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-like growth factor I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-like growth factor I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylocheirodysplasia, Ehlers-Danlos syndrome-like Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylocheirodysplasia, Ehlers-Danlos syndrome-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prader-Willi-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prader-Willi-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wolfram-like syndrome, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wolfram-like syndrome, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Marden Walker like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Marden Walker like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

insulin-like growth factor binding protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the insulin-like growth factor binding protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

insulin-like growth factor ternary complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

elg1 rfc-like complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the elg1 rfc-like complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ctf18 rfc-like complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ctf18 rfc-like complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

insulin-like growth factor binding protein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the insulin-like growth factor binding protein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

insulin-like growth factor binary complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

rad17 rfc-like complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the rad17 rfc-like complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

lewy body-like hyaline inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the lewy body-like hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

skein-like inclusion Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

slik (saga-like) complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the slik (saga-like) complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

digoxin-like factors Gene Set

From CTD Gene-Chemical Interactions

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

hirulog-like peptide Gene Set

From CTD Gene-Chemical Interactions

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

Vaccines, Virus-Like Particle Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Vaccines, Virus-Like Particle from the curated CTD Gene-Chemical Interactions dataset.

Huntington Disease-Like 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, gelatinous drop-like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

Larsen-Like Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Larsen-Like Syndrome from the curated CTD Gene-Disease Associations dataset.

BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.

Seborrhea-Like Dermatitis with Psoriasiform Elements Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Seborrhea-Like Dermatitis with Psoriasiform Elements from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 3 Gene Set

From CTD Gene-Disease Associations

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

Insulin-Like Growth Factor I, Resistance To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insulin-Like Growth Factor I, Resistance To from the curated CTD Gene-Disease Associations dataset.

Cowden-Like Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cowden-Like Syndrome from the curated CTD Gene-Disease Associations dataset.

Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like from the curated CTD Gene-Disease Associations dataset.

ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.

Nijmegen Breakage Syndrome-Like Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nijmegen Breakage Syndrome-Like Disorder from the curated CTD Gene-Disease Associations dataset.

Weill-Marchesani-Like Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Weill-Marchesani-Like Syndrome from the curated CTD Gene-Disease Associations dataset.

Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.

NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 from the curated CTD Gene-Disease Associations dataset.

Insulin-Like Growth Factor I Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insulin-Like Growth Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.

Cataract, Coppock-Like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Coppock-Like from the curated CTD Gene-Disease Associations dataset.

Insulin-Like Growth Factor Binding Protein 5 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Insulin-Like Growth Factor Binding Protein 5 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Insulin-Like Growth Factor Binding Protein 4 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Insulin-Like Growth Factor Binding Protein 4 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Insulin-Like Growth Factor I Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Insulin-Like Growth Factor I in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

lymphoepithelioma-like thymic carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lymphoepithelioma-like carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

insulin-like growth factor-1; estrogen metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-1; estrogen metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor binding protein 4 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor binding protein 4 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor-3; retinol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-3; retinol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder-like phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder-like phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autosomal dominant coral-like cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autosomal dominant coral-like cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast cancer; insulin-like growth factor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast cancer; insulin-like growth factor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pituitary anomalies and holoprosencephaly-like features. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pituitary anomalies and holoprosencephaly-like features. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile endogenous attack-like psychoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile endogenous attack-like psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin-like growth factor binding protein 5 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor binding protein 5 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

like Gene Set

From GeneRIF Biological Term Annotations

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

like1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term like1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

likely Gene Set

From GeneRIF Biological Term Annotations

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

likelihood Gene Set

From GeneRIF Biological Term Annotations

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

likewise Gene Set

From GeneRIF Biological Term Annotations

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

likeliness Gene Set

From GeneRIF Biological Term Annotations

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

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 5 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 5 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of myd88-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of myd88-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 8 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 8 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor tlr1:tlr2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor tlr1:tlr2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of myd88-independent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of myd88-independent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor tlr6:tlr2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor tlr6:tlr2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 5 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 5 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 7 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 7 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tirap-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tirap-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

myd88-independent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the myd88-independent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tram-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tram-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 10 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 10 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 5 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 5 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 7 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 7 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 1 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 1 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

myd88-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the myd88-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tram-dependent toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tram-dependent toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 7 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 7 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

tirap-dependent toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the tirap-dependent toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of insulin-like growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of insulin-like growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

response to insulin-like growth factor stimulus Gene Set

From GO Biological Process Annotations

genes participating in the response to insulin-like growth factor stimulus biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

cellular response to insulin-like growth factor stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to insulin-like growth factor stimulus biological process from the curated GO Biological Process Annotations dataset.

regulation of toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 3 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 3 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of toll-like receptor 9 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of toll-like receptor 9 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 2 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 2 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

trif-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the trif-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 6 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 6 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of myd88-dependent toll-like receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of myd88-dependent toll-like receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

toll-like receptor 4 signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the toll-like receptor 4 signaling pathway biological process from the curated GO Biological Process Annotations dataset.

insulin-like growth factor binding protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the insulin-like growth factor binding protein complex cellular component from the curated GO Cellular Component Annotations dataset.

ctf18 rfc-like complex Gene Set

From GO Cellular Component Annotations

proteins localized to the ctf18 rfc-like complex cellular component from the curated GO Cellular Component Annotations dataset.

x11-like protein binding Gene Set

From GO Molecular Function Annotations

genes performing the x11-like protein binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

toll-like receptor 2 binding Gene Set

From GO Molecular Function Annotations

genes performing the toll-like receptor 2 binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor-activated receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor-activated receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein conjugating enzyme activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein-specific isopeptidase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein-specific isopeptidase activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein transferase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein transferase activity molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein binding Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein binding molecular function from the curated GO Molecular Function Annotations dataset.

receptor tyrosine kinase-like orphan receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the receptor tyrosine kinase-like orphan receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein ligase binding Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein ligase binding molecular function from the curated GO Molecular Function Annotations dataset.

natural killer cell lectin-like receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the natural killer cell lectin-like receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor ii binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor ii binding molecular function from the curated GO Molecular Function Annotations dataset.

ring-like zinc finger domain binding Gene Set

From GO Molecular Function Annotations

genes performing the ring-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein conjugating enzyme binding Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein-specific protease activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein-specific protease activity molecular function from the curated GO Molecular Function Annotations dataset.

toll-like receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the toll-like receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

toll-like receptor 4 binding Gene Set

From GO Molecular Function Annotations

genes performing the toll-like receptor 4 binding molecular function from the curated GO Molecular Function Annotations dataset.

insulin-like growth factor i binding Gene Set

From GO Molecular Function Annotations

genes performing the insulin-like growth factor i binding molecular function from the curated GO Molecular Function Annotations dataset.

ubiquitin-like protein ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitin-like protein ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

Social autistic-like traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Social autistic-like traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Insulin-like growth factors Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Insulin-like growth factors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

madelung-like forearm deformities Gene Set

From HPO Gene-Disease Associations

genes associated with the madelung-like forearm deformities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

conjunctival whitish salt-like deposits Gene Set

From HPO Gene-Disease Associations

genes associated with the conjunctival whitish salt-like deposits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bird-like facies Gene Set

From HPO Gene-Disease Associations

genes associated with the bird-like facies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

doll-like facies Gene Set

From HPO Gene-Disease Associations

genes associated with the doll-like facies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

confetti-like hypopigmented macules Gene Set

From HPO Gene-Disease Associations

genes associated with the confetti-like hypopigmented macules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mask-like facies Gene Set

From HPO Gene-Disease Associations

genes associated with the mask-like facies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reye syndrome-like episodes Gene Set

From HPO Gene-Disease Associations

genes associated with the reye syndrome-like episodes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular, rachitic-like metaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular, rachitic-like metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

swan neck-like deformities of the fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the swan neck-like deformities of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

stroke-like episodes Gene Set

From HPO Gene-Disease Associations

genes associated with the stroke-like episodes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disc-like vertebral bodies Gene Set

From HPO Gene-Disease Associations

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

slit-like opening of the exterior auditory meatus Gene Set

From HPO Gene-Disease Associations

genes associated with the slit-like opening of the exterior auditory meatus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scheuermann-like vertebral changes Gene Set

From HPO Gene-Disease Associations

genes associated with the scheuermann-like vertebral changes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

PHF5-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PHF5-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Class I glutamine amidotransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Class I glutamine amidotransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Putative Bcl-2 like protein of testis Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Putative Bcl-2 like protein of testis protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Riboflavin synthase-like beta-barrel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Riboflavin synthase-like beta-barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ferritin- like diiron domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ferritin- like diiron domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vesicle tethering protein p115-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vesicle tethering protein p115-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Restriction endonuclease type II-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Restriction endonuclease type II-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoporin, Nup133/Nup155-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoporin, Nup133/Nup155-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kringle-like fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kringle-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Microcephalin-like Gene Set

From InterPro Predicted Protein Domain Annotations

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

Thiolase-like, subgroup Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thiolase-like, subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase, mitochondrial-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase, mitochondrial-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ssl1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ssl1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cystatin-9 like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cystatin-9 like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kelch-like protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kelch-like protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Signal-induced proliferation-associated 1-like protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Signal-induced proliferation-associated 1-like protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Galactose mutarotase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Galactose mutarotase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-like domain of Spt6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

SPOC like C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the SPOC like C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Acid sphingomyelinase-like phosphodiesterase, predicted Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acid sphingomyelinase-like phosphodiesterase, predicted protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transferrin receptor-like, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transferrin receptor-like, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RuvA domain 2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RuvA domain 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Genetic suppressor element-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Genetic suppressor element-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosducin, thioredoxin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosducin, thioredoxin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleoporin, Nup153-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleoporin, Nup153-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Steroidogenic acute regulatory protein-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Steroidogenic acute regulatory protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fringe-like Gene Set

From InterPro Predicted Protein Domain Annotations

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

ASX-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ASX-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ASX-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ASX-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thrombospondin, type 3-like repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thrombospondin, type 3-like repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Threonine synthase-like 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Threonine synthase-like 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcriptional regulator TACO1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcriptional regulator TACO1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HbrB-like Gene Set

From InterPro Predicted Protein Domain Annotations

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

Myelin protein zero-like protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin protein zero-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myelin protein zero-like protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin protein zero-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Myelin protein zero-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin protein zero-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Rossmann-like alpha/beta/alpha sandwich fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rossmann-like alpha/beta/alpha sandwich fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Enolase N-terminal domain-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Enolase N-terminal domain-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ORM1-like protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ORM1-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tudor-like, plant