Name

arginine and proline metabolism Gene Set

From KEGG Pathways

proteins participating in the arginine and proline metabolism pathway from the KEGG Pathways dataset.

peptidyl-proline hydroxylation to 3-hydroxy-l-proline Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-proline hydroxylation to 3-hydroxy-l-proline biological process from the curated GO Biological Process Annotations dataset.

peptidyl-proline hydroxylation to 4-hydroxy-l-proline Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-proline hydroxylation to 4-hydroxy-l-proline biological process from the curated GO Biological Process Annotations dataset.

Arginine/Asparagine/Proline hydroxylase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine/Asparagine/Proline hydroxylase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

peptidyl-arginine methylation, to symmetrical-dimethyl arginine Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine methylation, to symmetrical-dimethyl arginine biological process from the curated GO Biological Process Annotations dataset.

peptidyl-arginine methylation, to asymmetrical-dimethyl arginine Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine methylation, to asymmetrical-dimethyl arginine biological process from the curated GO Biological Process Annotations dataset.

d arginine and d ornithine metabolism Gene Set

From KEGG Pathways

proteins participating in the d arginine and d ornithine metabolism pathway from the KEGG Pathways dataset.

abnormality of proline metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of arginine metabolism Gene Set

From HPO Gene-Disease Associations

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

Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

fluvoxamine metabolism; omeprazole metabolism Gene Set

From GAD Gene-Disease Associations

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

acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

omeprazole metabolism; sulfone metabolism Gene Set

From GAD Gene-Disease Associations

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

Proline dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

procollagen-proline 4-dioxygenase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the procollagen-proline 4-dioxygenase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

N-(3-propylcarbamoyloxirane-2-carbonyl)-isoleucyl-proline Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical N-(3-propylcarbamoyloxirane-2-carbonyl)-isoleucyl-proline from the curated CTD Gene-Chemical Interactions dataset.

histidyl-proline diketopiperazine Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical histidyl-proline diketopiperazine from the curated CTD Gene-Chemical Interactions dataset.

1-((5-(1-aminoethyl)-2-(8-methoxy-2-(triflurormethyl)-5-quinolinyl)-4-oxazolyl) carbonyl)-4-((cyclopropylcarbonyl)amino)proline ethyl ester Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 1-((5-(1-aminoethyl)-2-(8-methoxy-2-(triflurormethyl)-5-quinolinyl)-4-oxazolyl) carbonyl)-4-((cyclopropylcarbonyl)amino)proline ethyl ester from the curated CTD Gene-Chemical Interactions dataset.

L-N(Omega)-Nitroarginine-(4r)-Amino-L-Proline Amide Gene Set

From DrugBank Drug Targets

interacting proteins for the L-N(Omega)-Nitroarginine-(4r)-Amino-L-Proline Amide drug from the curated DrugBank Drug Targets dataset.

L-PROLINE, 1-[(2S)-3-MERCAPTO-2-METHYL-1-OXOPROPYL]-4-(PHENYLTHIO)-, 4S Gene Set

From DrugBank Drug Targets

interacting proteins for the L-PROLINE, 1-[(2S)-3-MERCAPTO-2-METHYL-1-OXOPROPYL]-4-(PHENYLTHIO)-, 4S drug from the curated DrugBank Drug Targets dataset.

D-Proline Gene Set

From DrugBank Drug Targets

interacting proteins for the D-Proline drug from the curated DrugBank Drug Targets dataset.

L-Proline Gene Set

From DrugBank Drug Targets

interacting proteins for the L-Proline drug from the curated DrugBank Drug Targets dataset.

N-(3-Propylcarbamoyloxirane-2-Carbonyl)-Isoleucyl-Proline Gene Set

From DrugBank Drug Targets

interacting proteins for the N-(3-Propylcarbamoyloxirane-2-Carbonyl)-Isoleucyl-Proline drug from the curated DrugBank Drug Targets dataset.

N-({(2S,3S)-3-[(BENZYLAMINO)CARBONYL]OXIRAN-2-YL}CARBONYL)-L-ISOLEUCYL-L-PROLINE Gene Set

From DrugBank Drug Targets

interacting proteins for the N-({(2S,3S)-3-[(BENZYLAMINO)CARBONYL]OXIRAN-2-YL}CARBONYL)-L-ISOLEUCYL-L-PROLINE drug from the curated DrugBank Drug Targets dataset.

proline Gene Set

From GeneRIF Biological Term Annotations

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

l-proline biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the l-proline biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

proline transmembrane transport Gene Set

From GO Biological Process Annotations

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

n-terminal peptidyl-proline dimethylation Gene Set

From GO Biological Process Annotations

genes participating in the n-terminal peptidyl-proline dimethylation biological process from the curated GO Biological Process Annotations dataset.

proline catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the proline catabolic process biological process from the curated GO Biological Process Annotations dataset.

proline catabolic process to glutamate Gene Set

From GO Biological Process Annotations

genes participating in the proline catabolic process to glutamate biological process from the curated GO Biological Process Annotations dataset.

proline metabolic process Gene Set

From GO Biological Process Annotations

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

n-terminal peptidyl-proline methylation Gene Set

From GO Biological Process Annotations

genes participating in the n-terminal peptidyl-proline methylation biological process from the curated GO Biological Process Annotations dataset.

peptidyl-proline modification Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-proline modification biological process from the curated GO Biological Process Annotations dataset.

proline biosynthetic process Gene Set

From GO Biological Process Annotations

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

proline transport Gene Set

From GO Biological Process Annotations

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

peptidyl-proline hydroxylation Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-proline hydroxylation biological process from the curated GO Biological Process Annotations dataset.

procollagen-proline 4-dioxygenase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the procollagen-proline 4-dioxygenase complex cellular component from the curated GO Cellular Component Annotations dataset.

l-proline transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

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

proline-rich region binding Gene Set

From GO Molecular Function Annotations

genes performing the proline-rich region binding molecular function from the curated GO Molecular Function Annotations dataset.

proline dehydrogenase activity Gene Set

From GO Molecular Function Annotations

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

proline:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the proline:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

proline racemase activity Gene Set

From GO Molecular Function Annotations

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

peptidyl-proline 3-dioxygenase activity Gene Set

From GO Molecular Function Annotations

genes performing the peptidyl-proline 3-dioxygenase activity molecular function from the curated GO Molecular Function Annotations dataset.

procollagen-proline dioxygenase activity Gene Set

From GO Molecular Function Annotations

genes performing the procollagen-proline dioxygenase activity molecular function from the curated GO Molecular Function Annotations dataset.

procollagen-proline 4-dioxygenase activity Gene Set

From GO Molecular Function Annotations

genes performing the procollagen-proline 4-dioxygenase activity molecular function from the curated GO Molecular Function Annotations dataset.

peptidyl-proline 4-dioxygenase activity Gene Set

From GO Molecular Function Annotations

genes performing the peptidyl-proline 4-dioxygenase activity molecular function from the curated GO Molecular Function Annotations dataset.

procollagen-proline 3-dioxygenase activity Gene Set

From GO Molecular Function Annotations

genes performing the procollagen-proline 3-dioxygenase activity molecular function from the curated GO Molecular Function Annotations dataset.

proline-trna ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the proline-trna ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

peptidyl-proline dioxygenase activity Gene Set

From GO Molecular Function Annotations

genes performing the peptidyl-proline dioxygenase activity molecular function from the curated GO Molecular Function Annotations dataset.

diphosphoglycolyl proline Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the diphosphoglycolyl proline ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

L-Proline Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the L-Proline metabolite from the curated HMDB Metabolites of Enzymes dataset.

3-Hydroxy-L-proline Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3-Hydroxy-L-proline metabolite from the curated HMDB Metabolites of Enzymes dataset.

4-Hydroxy-L-proline Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-Hydroxy-L-proline metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Proline Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Proline metabolite from the curated HMDB Metabolites of Enzymes dataset.

Trans-3-hydroxy-L-proline Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Trans-3-hydroxy-L-proline metabolite from the curated HMDB Metabolites of Enzymes dataset.

cis-4-Hydroxy-D-proline Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the cis-4-Hydroxy-D-proline metabolite from the curated HMDB Metabolites of Enzymes dataset.

proline biosynthesis Gene Set

From HumanCyc Pathways

proteins participating in the proline biosynthesis pathway from the HumanCyc Pathways dataset.

proline degradation Gene Set

From HumanCyc Pathways

proteins participating in the proline degradation pathway from the HumanCyc Pathways dataset.

Proline-rich protein PRCC Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich protein PRCC protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich acidic protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich acidic protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich nuclear receptor coactivator 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich nuclear receptor coactivator 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline/serine-rich coiled-coil protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline/serine-rich coiled-coil protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small proline-rich protein/late cornified envelope protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich protein Gene Set

From InterPro Predicted Protein Domain Annotations

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

Proline-tRNA ligase, class IIa, archaeal-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-tRNA ligase, class IIa, archaeal-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-serine-threonine phosphatase-interacting protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-serine-threonine phosphatase-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-tRNA ligase, class IIa Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-tRNA ligase, class IIa protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Late cornified envelope-like proline-rich protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Late cornified envelope-like proline-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small proline-rich protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small proline-rich protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PSP, proline-rich Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PSP, proline-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich nuclear receptor coactivator 1/2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich nuclear receptor coactivator 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline racemase family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline racemase family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline oxidase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich protein 15 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich protein 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline dehydrogenase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline dehydrogenase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich membrane anchor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich membrane anchor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-tRNA ligase, class II, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-tRNA ligase, class II, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosome receptor lysine/proline rich Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosome receptor lysine/proline rich protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich protein 14 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-rich protein 19 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proline-rich protein 19 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

proline-rich Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Proline catabolism Gene Set

From Reactome Pathways

proteins participating in the Proline catabolism pathway from the Reactome Pathways dataset.

Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha Gene Set

From Reactome Pathways

proteins participating in the Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha pathway from the Reactome Pathways dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

Arginine:glycine amidinotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arginine:glycine amidinotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

phenylalanyl-prolyl-arginine methyl chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical phenylalanyl-prolyl-arginine methyl chloride from the curated CTD Gene-Chemical Interactions dataset.

Arginine Vasopressin Gene Set

From CTD Gene-Chemical Interactions

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

Deamino Arginine Vasopressin Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Deamino Arginine Vasopressin from the curated CTD Gene-Chemical Interactions dataset.

valyl-prolyl-aspartyl-prolyl-arginine Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical valyl-prolyl-aspartyl-prolyl-arginine from the curated CTD Gene-Chemical Interactions dataset.

Arginine:Glycine Amidinotransferase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arginine:Glycine Amidinotransferase Deficiency from the curated CTD Gene-Disease Associations dataset.

L-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the L-Arginine drug from the curated DrugBank Drug Targets dataset.

N-Omega-Hydroxy-L-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the N-Omega-Hydroxy-L-Arginine drug from the curated DrugBank Drug Targets dataset.

Nor-N-Omega-Hydroxy-L-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the Nor-N-Omega-Hydroxy-L-Arginine drug from the curated DrugBank Drug Targets dataset.

5-N-Allyl-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the 5-N-Allyl-Arginine drug from the curated DrugBank Drug Targets dataset.

Benzoyl-Arginine-Alanine-Methyl Ketone Gene Set

From DrugBank Drug Targets

interacting proteins for the Benzoyl-Arginine-Alanine-Methyl Ketone drug from the curated DrugBank Drug Targets dataset.

Descarboxy-nor-N(Omega)-Hydroxy-L-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the Descarboxy-nor-N(Omega)-Hydroxy-L-Arginine drug from the curated DrugBank Drug Targets dataset.

N-Omega-Propyl-L-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the N-Omega-Propyl-L-Arginine drug from the curated DrugBank Drug Targets dataset.

Dinor-N(Omega)-Hydroxy-L-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the Dinor-N(Omega)-Hydroxy-L-Arginine drug from the curated DrugBank Drug Targets dataset.

D-Arginine Gene Set

From DrugBank Drug Targets

interacting proteins for the D-Arginine drug from the curated DrugBank Drug Targets dataset.

arginine Gene Set

From GeneRIF Biological Term Annotations

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

regulation of l-arginine import Gene Set

From GO Biological Process Annotations

genes participating in the regulation of l-arginine import biological process from the curated GO Biological Process Annotations dataset.

peptidyl-arginine n-methylation Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine n-methylation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of arginine catabolic process Gene Set

From GO Biological Process Annotations

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

regulation of arginine metabolic process Gene Set

From GO Biological Process Annotations

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

l-arginine transport Gene Set

From GO Biological Process Annotations

genes participating in the l-arginine transport biological process from the curated GO Biological Process Annotations dataset.

l-arginine import Gene Set

From GO Biological Process Annotations

genes participating in the l-arginine import biological process from the curated GO Biological Process Annotations dataset.

arginine transport Gene Set

From GO Biological Process Annotations

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

peptidyl-arginine omega-n-methylation Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine omega-n-methylation biological process from the curated GO Biological Process Annotations dataset.

histone arginine methylation Gene Set

From GO Biological Process Annotations

genes participating in the histone arginine methylation biological process from the curated GO Biological Process Annotations dataset.

arginine transmembrane transport Gene Set

From GO Biological Process Annotations

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

regulation of arginine catabolic process Gene Set

From GO Biological Process Annotations

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

peptidyl-arginine methylation Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine methylation biological process from the curated GO Biological Process Annotations dataset.

arginine metabolic process Gene Set

From GO Biological Process Annotations

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

arginine catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the arginine catabolic process biological process from the curated GO Biological Process Annotations dataset.

l-arginine import across plasma membrane Gene Set

From GO Biological Process Annotations

genes participating in the l-arginine import across plasma membrane biological process from the curated GO Biological Process Annotations dataset.

arginine biosynthetic process Gene Set

From GO Biological Process Annotations

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

l-arginine transmembrane transport Gene Set

From GO Biological Process Annotations

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

l-arginine import into cell Gene Set

From GO Biological Process Annotations

genes participating in the l-arginine import into cell biological process from the curated GO Biological Process Annotations dataset.

histone arginine demethylation Gene Set

From GO Biological Process Annotations

genes participating in the histone arginine demethylation biological process from the curated GO Biological Process Annotations dataset.

arginine biosynthetic process via ornithine Gene Set

From GO Biological Process Annotations

genes participating in the arginine biosynthetic process via ornithine biological process from the curated GO Biological Process Annotations dataset.

arginine import Gene Set

From GO Biological Process Annotations

genes participating in the arginine import biological process from the curated GO Biological Process Annotations dataset.

putrescine biosynthetic process from arginine Gene Set

From GO Biological Process Annotations

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

peptidyl-arginine modification Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine modification biological process from the curated GO Biological Process Annotations dataset.

protein-arginine deiminase activity Gene Set

From GO Molecular Function Annotations

genes performing the protein-arginine deiminase activity molecular function from the curated GO Molecular Function Annotations dataset.

protein-arginine n-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the protein-arginine n-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

arginine n-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the arginine n-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

arginine-trna ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the arginine-trna ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

nad(p)+-protein-arginine adp-ribosyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the nad(p)+-protein-arginine adp-ribosyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

[myelin basic protein]-arginine n-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the [myelin basic protein]-arginine n-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

arginine binding Gene Set

From GO Molecular Function Annotations

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

protein-arginine omega-n symmetric methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the protein-arginine omega-n symmetric methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

protein-arginine omega-n monomethyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the protein-arginine omega-n monomethyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

protein-arginine omega-n asymmetric methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the protein-arginine omega-n asymmetric methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

arginine deiminase activity Gene Set

From GO Molecular Function Annotations

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

high-affinity arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

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

histone-arginine n-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the histone-arginine n-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity l-arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity l-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

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

Nωpropyl-L-arginine Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the Nωpropyl-L-arginine ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

L-arginine Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the L-arginine ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

L-Arginine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the L-Arginine metabolite from the curated HMDB Metabolites of Enzymes dataset.

ADP-Ribosyl-L-arginine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the ADP-Ribosyl-L-arginine metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Arginine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Arginine metabolite from the curated HMDB Metabolites of Enzymes dataset.

beta-Alanyl-L-arginine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the beta-Alanyl-L-arginine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Dimethyl-L-arginine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Dimethyl-L-arginine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Homo-L-arginine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Homo-L-arginine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Arginine-tRNA ligase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine-tRNA ligase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Serine/arginine-rich splicing factor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Serine/arginine-rich splicing factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Serine/arginine-rich splicing factor 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Serine/arginine-rich splicing factor 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein arginine N-methyltransferase PRMT7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein arginine N-methyltransferase PRMT7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein arginine N-methyltransferase PRMT5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein arginine N-methyltransferase PRMT5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-arginine deiminase (PAD) N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-arginine deiminase (PAD) N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Serine/arginine repetitive matrix protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Serine/arginine repetitive matrix protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arginine/serine-rich protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine/serine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arginine-tRNA-protein transferase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

Protein arginine N-methyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein arginine N-methyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Histone-arginine methyltransferase CARM1, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Histone-arginine methyltransferase CARM1, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NAD:arginine ADP-ribosyltransferase, ART Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NAD:arginine ADP-ribosyltransferase, ART protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-arginine deiminase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

Arginine repressor C-terminal-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine repressor C-terminal-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-arginine deiminase (PAD), central domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-arginine deiminase (PAD), central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-arginine deiminase Gene Set

From InterPro Predicted Protein Domain Annotations

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

Arginine N-methyltransferase 2-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine N-methyltransferase 2-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arginine-tRNA-protein transferase 1, eukaryotic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine-tRNA-protein transferase 1, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arginine vasopressin-induced protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine vasopressin-induced protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arginine-tRNA-protein transferase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

Arginine biosynthesis Gene Set

From PANTHER Pathways

proteins participating in the Arginine biosynthesis pathway from the PANTHER Pathways dataset.

arginine Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

genetically deficient metabolism of debrisoquine and other drugs Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetically deficient metabolism of debrisoquine and other drugs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lead and mercury metabolism Gene Set

From GAD Gene-Disease Associations

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

homocysteine metabolism, cognition, and white matter lesions Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism and adiposity Gene Set

From GAD Gene-Disease Associations

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

thyroid hormone metabolism II (via conjugation and/or degradation) Gene Set

From HumanCyc Pathways

proteins participating in the thyroid hormone metabolism II (via conjugation and/or degradation) pathway from the HumanCyc Pathways dataset.

sphingosine and sphingosine-1-phosphate metabolism Gene Set

From HumanCyc Pathways

proteins participating in the sphingosine and sphingosine-1-phosphate metabolism pathway from the HumanCyc Pathways dataset.

thyronamine and iodothyronamine metabolism Gene Set

From HumanCyc Pathways

proteins participating in the thyronamine and iodothyronamine metabolism pathway from the HumanCyc Pathways dataset.

androgen and estrogen metabolism Gene Set

From KEGG Pathways

proteins participating in the androgen and estrogen metabolism pathway from the KEGG Pathways dataset.

d glutamine and d glutamate metabolism Gene Set

From KEGG Pathways

proteins participating in the d glutamine and d glutamate metabolism pathway from the KEGG Pathways dataset.

glyoxylate and dicarboxylate metabolism Gene Set

From KEGG Pathways

proteins participating in the glyoxylate and dicarboxylate metabolism pathway from the KEGG Pathways dataset.

glycine serine and threonine metabolism Gene Set

From KEGG Pathways

proteins participating in the glycine serine and threonine metabolism pathway from the KEGG Pathways dataset.

urea cycle and metabolism of amino groups Gene Set

From KEGG Pathways

proteins participating in the urea cycle and metabolism of amino groups pathway from the KEGG Pathways dataset.

taurine and hypotaurine metabolism Gene Set

From KEGG Pathways

proteins participating in the taurine and hypotaurine metabolism pathway from the KEGG Pathways dataset.

starch and sucrose metabolism Gene Set

From KEGG Pathways

proteins participating in the starch and sucrose metabolism pathway from the KEGG Pathways dataset.

nicotinate and nicotinamide metabolism Gene Set

From KEGG Pathways

proteins participating in the nicotinate and nicotinamide metabolism pathway from the KEGG Pathways dataset.

fructose and mannose metabolism Gene Set

From KEGG Pathways

proteins participating in the fructose and mannose metabolism pathway from the KEGG Pathways dataset.

porphyrin and chlorophyll metabolism Gene Set

From KEGG Pathways

proteins participating in the porphyrin and chlorophyll metabolism pathway from the KEGG Pathways dataset.

ascorbate and aldarate metabolism Gene Set

From KEGG Pathways

proteins participating in the ascorbate and aldarate metabolism pathway from the KEGG Pathways dataset.

alanine and aspartate metabolism Gene Set

From KEGG Pathways

proteins participating in the alanine and aspartate metabolism pathway from the KEGG Pathways dataset.

microcephaly, short stature, and impaired glucose metabolism Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, short stature, and impaired glucose metabolism phenotype from the curated OMIM Gene-Disease Associations dataset.

Vitamin D metabolism and pathway Gene Set

From PANTHER Pathways

proteins participating in the Vitamin D metabolism and pathway pathway from the PANTHER Pathways dataset.

Abacavir transport and metabolism Gene Set

From Reactome Pathways

proteins participating in the Abacavir transport and metabolism pathway from the Reactome Pathways dataset.

Neurotransmitter uptake and Metabolism In Glial Cells Gene Set

From Reactome Pathways

proteins participating in the Neurotransmitter uptake and Metabolism In Glial Cells pathway from the Reactome Pathways dataset.

Biotin transport and metabolism Gene Set

From Reactome Pathways

proteins participating in the Biotin transport and metabolism pathway from the Reactome Pathways dataset.

Retinoid metabolism and transport Gene Set

From Reactome Pathways

proteins participating in the Retinoid metabolism and transport pathway from the Reactome Pathways dataset.

Metabolism of folate and pterines Gene Set

From Reactome Pathways

proteins participating in the Metabolism of folate and pterines pathway from the Reactome Pathways dataset.

Metabolism of steroid hormones and vitamin D Gene Set

From Reactome Pathways

proteins participating in the Metabolism of steroid hormones and vitamin D pathway from the Reactome Pathways dataset.

alpha-linolenic (omega3) and linoleic (omega6) acid metabolism Gene Set

From Reactome Pathways

proteins participating in the alpha-linolenic (omega3) and linoleic (omega6) acid metabolism pathway from the Reactome Pathways dataset.

Pyruvate metabolism and Citric Acid (TCA) cycle Gene Set

From Reactome Pathways

proteins participating in the Pyruvate metabolism and Citric Acid (TCA) cycle pathway from the Reactome Pathways dataset.

Astrocytic Glutamate-Glutamine Uptake And Metabolism Gene Set

From Reactome Pathways

proteins participating in the Astrocytic Glutamate-Glutamine Uptake And Metabolism pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Metabolism of water-soluble vitamins and cofactors Gene Set

From Reactome Pathways

proteins participating in the Metabolism of water-soluble vitamins and cofactors pathway from the Reactome Pathways dataset.

Metabolism of lipids and lipoproteins Gene Set

From Reactome Pathways

proteins participating in the Metabolism of lipids and lipoproteins pathway from the Reactome Pathways dataset.

Metabolism of vitamins and cofactors Gene Set

From Reactome Pathways

proteins participating in the Metabolism of vitamins and cofactors pathway from the Reactome Pathways dataset.

Cobalamin (Cbl, vitamin B12) transport and metabolism Gene Set

From Reactome Pathways

proteins participating in the Cobalamin (Cbl, vitamin B12) transport and metabolism pathway from the Reactome Pathways dataset.

Fatty acid, triacylglycerol, and ketone body metabolism Gene Set

From Reactome Pathways

proteins participating in the Fatty acid, triacylglycerol, and ketone body metabolism pathway from the Reactome Pathways dataset.

Metabolism of amino acids and derivatives Gene Set

From Reactome Pathways

proteins participating in the Metabolism of amino acids and derivatives pathway from the Reactome Pathways dataset.

Bile acid and bile salt metabolism Gene Set

From Reactome Pathways

proteins participating in the Bile acid and bile salt metabolism pathway from the Reactome Pathways dataset.

Vitamin A and Carotenoid Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Vitamin A and Carotenoid Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Trans-sulfuration and one carbon metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Trans-sulfuration and one carbon metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Glutathione and one carbon metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Glutathione and one carbon metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

One carbon metabolism and related pathways(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the One carbon metabolism and related pathways(Mus musculus) pathway from the Wikipathways Pathways dataset.

Selenium Metabolism and Selenoproteins(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Selenium Metabolism and Selenoproteins(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Urea cycle and metabolism of amino groups(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Urea cycle and metabolism of amino groups(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Alanine and aspartate metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Alanine and aspartate metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Alanine and aspartate metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Alanine and aspartate metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Nuclear receptors in lipid metabolism and toxicity(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Nuclear receptors in lipid metabolism and toxicity(Mus musculus) pathway from the Wikipathways Pathways dataset.

Codeine and Morphine Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Codeine and Morphine Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) pathway from the Wikipathways Pathways dataset.

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

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

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy 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.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

metabolism of anandamide an endogenous cannabinoid Gene Set

From Biocarta Pathways

proteins participating in the metabolism of anandamide an endogenous cannabinoid pathway from the Biocarta Pathways dataset.

eicosanoid metabolism Gene Set

From Biocarta Pathways

proteins participating in the eicosanoid metabolism pathway from the Biocarta Pathways dataset.

Thyroid hormone metabolism, abnormal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Debrisoquine, poor metabolism of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Debrisoquine, poor metabolism of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mephenytoin, poor metabolism of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mephenytoin, poor metabolism of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Drug Metabolism, Poor, CYP2D6-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug Metabolism, Poor, CYP2D6-Related from the curated CTD Gene-Disease Associations dataset.

Drug Metabolism, Poor, CYP2C19-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug Metabolism, Poor, CYP2C19-Related from the curated CTD Gene-Disease Associations dataset.

Lipid Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Pyruvate Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

Iron Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iron Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Purine-Pyrimidine Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Purine-Pyrimidine Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Metabolism, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset.

Lipid Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipid Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Amino Acid Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amino Acid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Glucose Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glucose Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 2 from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 4 from the curated CTD Gene-Disease Associations dataset.

Phosphorus Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Phosphorus Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 3 from the curated CTD Gene-Disease Associations dataset.

Carbohydrate Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carbohydrate Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Metabolism Gene Set

From dbGAP Gene-Trait Associations

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

Lipid Metabolism Gene Set

From dbGAP Gene-Trait Associations

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

metal metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

glycogen metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

carbohydrate metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

mitochondrial metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

plasma protein metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

gamma-amino butyric acid metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease gamma-amino butyric acid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

histidine metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

mineral metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

glucose metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

phosphorus metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

disease of metabolism Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

lipid metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

iron metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

carbohydrate metabolism disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

glucose metabolism disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

mineral metabolism disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

disease of metabolism Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

lipid metabolism disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

iron metabolism disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

mitochondrial metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lipid metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

iron metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mineral metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

calcium metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

glycogen metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

phosphorus metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

plasma protein metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

metal metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

histidine metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

carbohydrate metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

glucose metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

disease of metabolism Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gamma-amino butyric acid metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease gamma-amino butyric acid metabolism disorder 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.

omeprazole metabolism Gene Set

From GAD Gene-Disease Associations

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

catecholestrogen formation; catecholestrogen metabolism Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism disorders; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

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

altered b vitamin/thiol metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altered b vitamin/thiol metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

clomipramine metabolism Gene Set

From GAD Gene-Disease Associations

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

cardiovascular disease; lipid metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

diclofenac metabolism Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; body fat; lipid metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; body fat; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

leukemia; hemochromatosis; iron metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; hemochromatosis; iron metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal metabolism Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

1-carbon metabolism Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis, coronary; lipid metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

amino acid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amino acid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carisoprodol metabolism Gene Set

From GAD Gene-Disease Associations

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

iron metabolism Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism disorders; muscular diseases Gene Set

From GAD Gene-Disease Associations

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

phenytoin metabolism Gene Set

From GAD Gene-Disease Associations

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

serum low-density lipoprotein metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum low-density lipoprotein metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism Gene Set

From GAD Gene-Disease Associations

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

flubiprofen metabolism Gene Set

From GAD Gene-Disease Associations

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

tamoxifen, metabolism Gene Set

From GAD Gene-Disease Associations

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

alprazolam metabolism Gene Set

From GAD Gene-Disease Associations

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

gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcium metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

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

glucose tolerance; lipid metabolism Gene Set

From GAD Gene-Disease Associations

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

arsenic metabolism Gene Set

From GAD Gene-Disease Associations

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

citalopram metabolism Gene Set

From GAD Gene-Disease Associations

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

glucose metabolism disorders; obesity; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism disorders; obesity Gene Set

From GAD Gene-Disease Associations

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

glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

doxepin metabolism Gene Set

From GAD Gene-Disease Associations

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

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amitriptyline metabolism Gene Set

From GAD Gene-Disease Associations

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

hemochromatosis; iron metabolism disorders; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; iron metabolism disorders; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; insulin; metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; insulin; metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug metabolism Gene Set

From GAD Gene-Disease Associations

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

metabolism of toluene di-isocyanate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolism of toluene di-isocyanate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

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

metabolism Gene Set

From GAD Gene-Disease Associations

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

mephobarbital metabolism Gene Set

From GAD Gene-Disease Associations

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

iron metabolism disorders; iron overload Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism, inborn errors; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolism of benzo[a]pyrene (b[a]p) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolism of benzo[a]pyrene (b[a]p) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amino acid disorder, nos; amino acid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism Gene Set

From GAD Gene-Disease Associations

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

metabolism disorders; myocardial infarction; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolism disorders; myocardial infarction; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart rate; risperidone metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart rate; risperidone metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; metal metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; metal metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism disorders; hyperlipidemia Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolismreview Gene Set

From GeneRIF Biological Term Annotations

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

metabolisminsulin Gene Set

From GeneRIF Biological Term Annotations

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

metabolism Gene Set

From GeneRIF Biological Term Annotations

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

metabolismhomoeostasis Gene Set

From GeneRIF Biological Term Annotations

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

metabolismdependent Gene Set

From GeneRIF Biological Term Annotations

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

metabolisms Gene Set

From GeneRIF Biological Term Annotations

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

metabolismrelated Gene Set

From GeneRIF Biological Term Annotations

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

Arsenic metabolism Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Arsenic metabolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Lipid metabolism phenotypes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Lipid metabolism phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

calcium metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

metal metabolism disorder Gene Set

From GWASdb SNP-Disease Associations

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

carbohydrate metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

glucose metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

phosphorus metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

mineral metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

disease of metabolism Gene Set

From GWASdb SNP-Disease Associations

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

lipid metabolism disorder Gene Set

From GWASdb SNP-Disease Associations

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

iron metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of vitamin metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin d metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of glycolipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin a metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin b metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of aromatic amino acid family metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of homocysteine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of tryptophan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cholesterol metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of liposaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of unsaturated fatty acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of fatty-acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of proteoglycan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of carbohydrate metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vitamin b12 metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of sulfur amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carboxylic acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of glycoprotein metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin e metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of polysaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nucleobase metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of purine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of glycolipid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycoprotein metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of prostaglandin metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of alanine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of cysteine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of ganglioside metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of tyrosine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of carbohydrate metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycosaminoglycan metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of orotic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of dicarboxylic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of leucine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of proteoglycan metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of vitamin k metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of amino acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of pyruvate family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pyruvate family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of fatty-acid anion metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of fatty-acid anion metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of vitamin e metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of purine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of xanthine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of phytanic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of unsaturated fatty acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of unsaturated fatty acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glutamine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of histidine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of mitochondrial metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycosphingolipid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of citrulline metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of serine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of lysine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycoside metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of vitamin d metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of galactoside metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of liposaccharide metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of pyrimidine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of homocysteine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of branched chain family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of branched chain family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of carboxylic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of long-chain fatty-acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of long-chain fatty-acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of aspartate family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of aspartate family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lipid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of vitamin metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of mucopolysaccharide metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of threonine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of sulfur amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of sulfur amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of superoxide metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of polysaccharide metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of cerebrosidase metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of carnitine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of monocarboxylic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of lysosomal metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of phenylalanine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of methionine metabolism Gene Set

From HPO Gene-Disease Associations

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

impairment of galactose metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the impairment of galactose metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of serine family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of serine family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of ornithine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of cholesterol metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of krebs cycle metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of calcium-phosphate metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of vitamin b metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the vitamin b12 metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vitamin b12 metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impairment of fructose metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the impairment of fructose metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of aromatic amino acid family metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of aromatic amino acid family metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of creatine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of glutamine family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glutamine family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of fatty-acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of nucleobase metabolism Gene Set

From HPO Gene-Disease Associations

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

Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Lipid Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lipid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Iron Metabolism Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Purine-Pyrimidine Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Purine-Pyrimidine Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Steroid Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Steroid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lipid Metabolism Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Amino Acid Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Amino Acid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Glucose Metabolism Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Metal Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Metal Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Carbohydrate Metabolism, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Carbohydrate Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Calcium Metabolism Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

D-myo-inositol-5-phosphate metabolism Gene Set

From HumanCyc Pathways

proteins participating in the D-myo-inositol-5-phosphate metabolism pathway from the HumanCyc Pathways dataset.

acyl carrier protein metabolism Gene Set

From HumanCyc Pathways

proteins participating in the acyl carrier protein metabolism pathway from the HumanCyc Pathways dataset.

sphingomyelin metabolism/ceramide salvage Gene Set

From HumanCyc Pathways

proteins participating in the sphingomyelin metabolism/ceramide salvage pathway from the HumanCyc Pathways dataset.

thyroid hormone metabolism I (via deiodination) Gene Set

From HumanCyc Pathways

proteins participating in the thyroid hormone metabolism I (via deiodination) pathway from the HumanCyc Pathways dataset.

superpathway of D-myo-inositol (1,4,5)-trisphosphate metabolism Gene Set

From HumanCyc Pathways

proteins participating in the superpathway of D-myo-inositol (1,4,5)-trisphosphate metabolism pathway from the HumanCyc Pathways dataset.

Membrane associated eicosanoid/glutathione metabolism-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane associated eicosanoid/glutathione metabolism-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/pantothenate metabolism flavoprotein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/pantothenate metabolism flavoprotein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Membrane-associated, eicosanoid/glutathione metabolism (MAPEG) protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane-associated, eicosanoid/glutathione metabolism (MAPEG) protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cys/Met metabolism, pyridoxal phosphate-dependent enzyme Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cys/Met metabolism, pyridoxal phosphate-dependent enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset.

arachidonic acid metabolism Gene Set

From KEGG Pathways

proteins participating in the arachidonic acid metabolism pathway from the KEGG Pathways dataset.

nucleotide sugars metabolism Gene Set

From KEGG Pathways

proteins participating in the nucleotide sugars metabolism pathway from the KEGG Pathways dataset.

lipoic acid metabolism Gene Set

From KEGG Pathways

proteins participating in the lipoic acid metabolism pathway from the KEGG Pathways dataset.

riboflavin metabolism Gene Set

From KEGG Pathways

proteins participating in the riboflavin metabolism pathway from the KEGG Pathways dataset.

glutamate metabolism Gene Set

From KEGG Pathways

proteins participating in the glutamate metabolism pathway from the KEGG Pathways dataset.

phenylalanine metabolism Gene Set

From KEGG Pathways

proteins participating in the phenylalanine metabolism pathway from the KEGG Pathways dataset.

sulfur metabolism Gene Set

From KEGG Pathways

proteins participating in the sulfur metabolism pathway from the KEGG Pathways dataset.

thiamine metabolism Gene Set

From KEGG Pathways

proteins participating in the thiamine metabolism pathway from the KEGG Pathways dataset.

cysteine metabolism Gene Set

From KEGG Pathways

proteins participating in the cysteine metabolism pathway from the KEGG Pathways dataset.

linoleic acid metabolism Gene Set

From KEGG Pathways

proteins participating in the linoleic acid metabolism pathway from the KEGG Pathways dataset.

methionine metabolism Gene Set

From KEGG Pathways

proteins participating in the methionine metabolism pathway from the KEGG Pathways dataset.

beta alanine metabolism Gene Set

From KEGG Pathways

proteins participating in the beta alanine metabolism pathway from the KEGG Pathways dataset.

metabolism of xenobiotics by cytochrome p450 Gene Set

From KEGG Pathways

proteins participating in the metabolism of xenobiotics by cytochrome p450 pathway from the KEGG Pathways dataset.

selenoamino acid metabolism Gene Set

From KEGG Pathways

proteins participating in the selenoamino acid metabolism pathway from the KEGG Pathways dataset.

aminophosphonate metabolism Gene Set

From KEGG Pathways

proteins participating in the aminophosphonate metabolism pathway from the KEGG Pathways dataset.

glutathione metabolism Gene Set

From KEGG Pathways

proteins participating in the glutathione metabolism pathway from the KEGG Pathways dataset.

nitrogen metabolism Gene Set

From KEGG Pathways

proteins participating in the nitrogen metabolism pathway from the KEGG Pathways dataset.

retinol metabolism Gene Set

From KEGG Pathways

proteins participating in the retinol metabolism pathway from the KEGG Pathways dataset.

glycerophospholipid metabolism Gene Set

From KEGG Pathways

proteins participating in the glycerophospholipid metabolism pathway from the KEGG Pathways dataset.

histidine metabolism Gene Set

From KEGG Pathways

proteins participating in the histidine metabolism pathway from the KEGG Pathways dataset.

caffeine metabolism Gene Set

From KEGG Pathways

proteins participating in the caffeine metabolism pathway from the KEGG Pathways dataset.

c5 branched dibasic acid metabolism Gene Set

From KEGG Pathways

proteins participating in the c5 branched dibasic acid metabolism pathway from the KEGG Pathways dataset.

fatty acid metabolism Gene Set

From KEGG Pathways

proteins participating in the fatty acid metabolism pathway from the KEGG Pathways dataset.

c21 steroid hormone metabolism Gene Set

From KEGG Pathways

proteins participating in the c21 steroid hormone metabolism pathway from the KEGG Pathways dataset.

tryptophan metabolism Gene Set

From KEGG Pathways

proteins participating in the tryptophan metabolism pathway from the KEGG Pathways dataset.

aminosugars metabolism Gene Set

From KEGG Pathways

proteins participating in the aminosugars metabolism pathway from the KEGG Pathways dataset.

sphingolipid metabolism Gene Set

From KEGG Pathways

proteins participating in the sphingolipid metabolism pathway from the KEGG Pathways dataset.

tyrosine metabolism Gene Set

From KEGG Pathways

proteins participating in the tyrosine metabolism pathway from the KEGG Pathways dataset.

inositol metabolism Gene Set

From KEGG Pathways

proteins participating in the inositol metabolism pathway from the KEGG Pathways dataset.

butanoate metabolism Gene Set

From KEGG Pathways

proteins participating in the butanoate metabolism pathway from the KEGG Pathways dataset.

glycerolipid metabolism Gene Set

From KEGG Pathways

proteins participating in the glycerolipid metabolism pathway from the KEGG Pathways dataset.

propanoate metabolism Gene Set

From KEGG Pathways

proteins participating in the propanoate metabolism pathway from the KEGG Pathways dataset.

pyruvate metabolism Gene Set

From KEGG Pathways

proteins participating in the pyruvate metabolism pathway from the KEGG Pathways dataset.

purine metabolism Gene Set

From KEGG Pathways

proteins participating in the purine metabolism pathway from the KEGG Pathways dataset.

ether lipid metabolism Gene Set

From KEGG Pathways

proteins participating in the ether lipid metabolism pathway from the KEGG Pathways dataset.

methane metabolism Gene Set

From KEGG Pathways

proteins participating in the methane metabolism pathway from the KEGG Pathways dataset.

cyanoamino acid metabolism Gene Set

From KEGG Pathways

proteins participating in the cyanoamino acid metabolism pathway from the KEGG Pathways dataset.

pyrimidine metabolism Gene Set

From KEGG Pathways

proteins participating in the pyrimidine metabolism pathway from the KEGG Pathways dataset.

inositol phosphate metabolism Gene Set

From KEGG Pathways

proteins participating in the inositol phosphate metabolism pathway from the KEGG Pathways dataset.

biotin metabolism Gene Set

From KEGG Pathways

proteins participating in the biotin metabolism pathway from the KEGG Pathways dataset.

alpha linolenic acid metabolism Gene Set

From KEGG Pathways

proteins participating in the alpha linolenic acid metabolism pathway from the KEGG Pathways dataset.

galactose metabolism Gene Set

From KEGG Pathways

proteins participating in the galactose metabolism pathway from the KEGG Pathways dataset.

vitamin b6 metabolism Gene Set

From KEGG Pathways

proteins participating in the vitamin b6 metabolism pathway from the KEGG Pathways dataset.

abnormal retinol metabolism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lipid metabolism Gene Set

From MPO Gene-Phenotype Associations

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

homeostasis/metabolism phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the homeostasis/metabolism phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vitamin metabolism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal response/metabolism to endogenous compounds Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal response/metabolism to endogenous compounds phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vitamin a metabolism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vitamin a metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cellular cholesterol metabolism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cellular cholesterol metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ethanol metabolism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal nucleotide metabolism Gene Set

From MPO Gene-Phenotype Associations

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

increased basal metabolism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal metabolism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vitamin or vitamin cofactor metabolism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vitamin or vitamin cofactor metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basal metabolism Gene Set

From MPO Gene-Phenotype Associations

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

thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

thyroid hormone metabolism, abnormal Gene Set

From OMIM Gene-Disease Associations

genes associated with the thyroid hormone metabolism, abnormal phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.

surfactant metabolism dysfunction, pulmonary, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

efavirenz, poor metabolism of Gene Set

From OMIM Gene-Disease Associations

genes associated with the efavirenz, poor metabolism of phenotype from the curated OMIM Gene-Disease Associations dataset.

surfactant metabolism dysfunction, pulmonary, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

surfactant metabolism dysfunction, pulmonary, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

surfactant metabolism dysfunction, pulmonary, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

surfactant metabolism dysfunction, pulmonary, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

Triacylglycerol metabolism Gene Set

From PANTHER Pathways

proteins participating in the Triacylglycerol metabolism pathway from the PANTHER Pathways dataset.

Thiamine metabolism Gene Set

From PANTHER Pathways

proteins participating in the Thiamine metabolism pathway from the PANTHER Pathways dataset.

Vitamin B6 metabolism Gene Set

From PANTHER Pathways

proteins participating in the Vitamin B6 metabolism pathway from the PANTHER Pathways dataset.

Purine metabolism Gene Set

From PANTHER Pathways

proteins participating in the Purine metabolism pathway from the PANTHER Pathways dataset.

Fructose galactose metabolism Gene Set

From PANTHER Pathways

proteins participating in the Fructose galactose metabolism pathway from the PANTHER Pathways 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.

N-acetylglucosamine metabolism Gene Set

From PANTHER Pathways

proteins participating in the N-acetylglucosamine metabolism pathway from the PANTHER Pathways dataset.

Pyrimidine Metabolism Gene Set

From PANTHER Pathways

proteins participating in the Pyrimidine Metabolism pathway from the PANTHER Pathways dataset.

Pyruvate metabolism Gene Set

From PANTHER Pathways

proteins participating in the Pyruvate metabolism pathway from the PANTHER Pathways dataset.

Mannose metabolism Gene Set

From PANTHER Pathways

proteins participating in the Mannose metabolism pathway from the PANTHER Pathways dataset.

Carnitine metabolism Gene Set

From PANTHER Pathways

proteins participating in the Carnitine metabolism pathway from the PANTHER Pathways dataset.

Metabolism of nucleotides Gene Set

From Reactome Pathways

proteins participating in the Metabolism of nucleotides pathway from the Reactome Pathways dataset.

Peptide hormone metabolism Gene Set

From Reactome Pathways

proteins participating in the Peptide hormone metabolism pathway from the Reactome Pathways dataset.

Ketone body metabolism Gene Set

From Reactome Pathways

proteins participating in the Ketone body metabolism pathway from the Reactome Pathways dataset.

Metabolism of nitric oxide Gene Set

From Reactome Pathways

proteins participating in the Metabolism of nitric oxide pathway from the Reactome Pathways dataset.

Vitamin D (calciferol) metabolism Gene Set

From Reactome Pathways

proteins participating in the Vitamin D (calciferol) metabolism pathway from the Reactome Pathways dataset.

Defects in cobalamin (B12) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in cobalamin (B12) metabolism pathway from the Reactome Pathways dataset.

Regulation of lipid metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha) Gene Set

From Reactome Pathways

proteins participating in the Regulation of lipid metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha) pathway from the Reactome Pathways dataset.

Glyoxylate metabolism Gene Set

From Reactome Pathways

proteins participating in the Glyoxylate metabolism pathway from the Reactome Pathways dataset.

Sulfur amino acid metabolism Gene Set

From Reactome Pathways

proteins participating in the Sulfur amino acid metabolism pathway from the Reactome Pathways dataset.

Vitamin C (ascorbate) metabolism Gene Set

From Reactome Pathways

proteins participating in the Vitamin C (ascorbate) metabolism pathway from the Reactome Pathways dataset.

Glucose metabolism Gene Set

From Reactome Pathways

proteins participating in the Glucose metabolism pathway from the Reactome Pathways dataset.

Pyruvate metabolism Gene Set

From Reactome Pathways

proteins participating in the Pyruvate metabolism pathway from the Reactome Pathways dataset.

Vitamin B2 (riboflavin) metabolism Gene Set

From Reactome Pathways

proteins participating in the Vitamin B2 (riboflavin) metabolism pathway from the Reactome Pathways dataset.

Integration of energy metabolism Gene Set

From Reactome Pathways

proteins participating in the Integration of energy metabolism pathway from the Reactome Pathways dataset.

Linoleic acid (LA) metabolism Gene Set

From Reactome Pathways

proteins participating in the Linoleic acid (LA) metabolism pathway from the Reactome Pathways dataset.

Vitamin B1 (thiamin) metabolism Gene Set

From Reactome Pathways

proteins participating in the Vitamin B1 (thiamin) metabolism pathway from the Reactome Pathways dataset.

Arachidonic acid metabolism Gene Set

From Reactome Pathways

proteins participating in the Arachidonic acid metabolism pathway from the Reactome Pathways dataset.

Glycosaminoglycan metabolism Gene Set

From Reactome Pathways

proteins participating in the Glycosaminoglycan metabolism pathway from the Reactome Pathways dataset.

Metabolism of Angiotensinogen to Angiotensins Gene Set

From Reactome Pathways

proteins participating in the Metabolism of Angiotensinogen to Angiotensins pathway from the Reactome Pathways dataset.

Metabolism Gene Set

From Reactome Pathways

proteins participating in the Metabolism pathway from the Reactome Pathways dataset.

Abacavir metabolism Gene Set

From Reactome Pathways

proteins participating in the Abacavir metabolism pathway from the Reactome Pathways dataset.

Purine metabolism Gene Set

From Reactome Pathways

proteins participating in the Purine metabolism pathway from the Reactome Pathways dataset.

Hyaluronan metabolism Gene Set

From Reactome Pathways

proteins participating in the Hyaluronan metabolism pathway from the Reactome Pathways dataset.

Pyrimidine metabolism Gene Set

From Reactome Pathways

proteins participating in the Pyrimidine metabolism pathway from the Reactome Pathways dataset.

Abnormal metabolism in phenylketonuria Gene Set

From Reactome Pathways

proteins participating in the Abnormal metabolism in phenylketonuria pathway from the Reactome Pathways dataset.

Diseases associated with glycosaminoglycan metabolism Gene Set

From Reactome Pathways

proteins participating in the Diseases associated with glycosaminoglycan metabolism pathway from the Reactome Pathways dataset.

Sialic acid metabolism Gene Set

From Reactome Pathways

proteins participating in the Sialic acid metabolism pathway from the Reactome Pathways dataset.

Sphingolipid metabolism Gene Set

From Reactome Pathways

proteins participating in the Sphingolipid metabolism pathway from the Reactome Pathways dataset.

Vitamin B5 (pantothenate) metabolism Gene Set

From Reactome Pathways

proteins participating in the Vitamin B5 (pantothenate) metabolism pathway from the Reactome Pathways dataset.

Glycosphingolipid metabolism Gene Set

From Reactome Pathways

proteins participating in the Glycosphingolipid metabolism pathway from the Reactome Pathways dataset.

Chondroitin sulfate/dermatan sulfate metabolism Gene Set

From Reactome Pathways

proteins participating in the Chondroitin sulfate/dermatan sulfate metabolism pathway from the Reactome Pathways dataset.

Keratan sulfate/keratin metabolism Gene Set

From Reactome Pathways

proteins participating in the Keratan sulfate/keratin metabolism pathway from the Reactome Pathways dataset.

Metabolism of non-coding RNA Gene Set

From Reactome Pathways

proteins participating in the Metabolism of non-coding RNA pathway from the Reactome Pathways dataset.

Metabolism of polyamines Gene Set

From Reactome Pathways

proteins participating in the Metabolism of polyamines pathway from the Reactome Pathways dataset.

PI Metabolism Gene Set

From Reactome Pathways

proteins participating in the PI Metabolism pathway from the Reactome Pathways dataset.

Defects in biotin (Btn) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in biotin (Btn) metabolism pathway from the Reactome Pathways dataset.

alpha-linolenic acid (ALA) metabolism Gene Set

From Reactome Pathways

proteins participating in the alpha-linolenic acid (ALA) metabolism pathway from the Reactome Pathways dataset.

Metabolism of porphyrins Gene Set

From Reactome Pathways

proteins participating in the Metabolism of porphyrins pathway from the Reactome Pathways dataset.

Metabolism of serotonin Gene Set

From Reactome Pathways

proteins participating in the Metabolism of serotonin pathway from the Reactome Pathways dataset.

Creatine metabolism Gene Set

From Reactome Pathways

proteins participating in the Creatine metabolism pathway from the Reactome Pathways dataset.

Lipoprotein metabolism Gene Set

From Reactome Pathways

proteins participating in the Lipoprotein metabolism pathway from the Reactome Pathways dataset.

Metabolism of carbohydrates Gene Set

From Reactome Pathways

proteins participating in the Metabolism of carbohydrates pathway from the Reactome Pathways dataset.

Phospholipid metabolism Gene Set

From Reactome Pathways

proteins participating in the Phospholipid metabolism pathway from the Reactome Pathways dataset.

Peroxisomal lipid metabolism Gene Set

From Reactome Pathways

proteins participating in the Peroxisomal lipid metabolism pathway from the Reactome Pathways dataset.

Metabolism of proteins Gene Set

From Reactome Pathways

proteins participating in the Metabolism of proteins pathway from the Reactome Pathways dataset.

Inositol phosphate metabolism Gene Set

From Reactome Pathways

proteins participating in the Inositol phosphate metabolism pathway from the Reactome Pathways dataset.

Heparan sulfate/heparin (HS-GAG) metabolism Gene Set

From Reactome Pathways

proteins participating in the Heparan sulfate/heparin (HS-GAG) metabolism pathway from the Reactome Pathways dataset.

Nicotinate metabolism Gene Set

From Reactome Pathways

proteins participating in the Nicotinate metabolism pathway from the Reactome Pathways dataset.

Glycogen Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Glycogen Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Sphingolipid Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Sphingolipid Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Tamoxifen metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Tamoxifen metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Vitamin D Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Vitamin D Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Felbamate Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Felbamate Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Dopamine metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Dopamine metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Estrogen metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Estrogen metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Nucleotide Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Nucleotide Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Selenium metabolism/Selenoproteins(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Selenium metabolism/Selenoproteins(Mus musculus) pathway from the Wikipathways Pathways dataset.

Glycogen Metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Glycogen Metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Tryptophan metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Tryptophan metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

One Carbon Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the One Carbon Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Glutathione metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Glutathione metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Globo Sphingolipid Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Globo Sphingolipid Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Glycine Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Glycine Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Retinol metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Retinol metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Estrogen metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Estrogen metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

One Carbon Metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the One Carbon Metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Nicotine Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Nicotine Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Iron metabolism in placenta(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Iron metabolism in placenta(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Glutathione metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Glutathione metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Aflatoxin B1 metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Aflatoxin B1 metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Glucocorticoid & Mineralcorticoid Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Glucocorticoid & Mineralcorticoid Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Benzo(a)pyrene metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Benzo(a)pyrene metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Arylamine metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Arylamine metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Ganglio Sphingolipid Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Ganglio Sphingolipid Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Amino Acid metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Amino Acid metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Lidocaine metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Lidocaine metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Vitamin B12 Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Vitamin B12 Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Folate Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Folate Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Tryptophan metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Tryptophan metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Aflatoxin B1 metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Aflatoxin B1 metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Purine metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Purine metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Nucleotide Metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Nucleotide Metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sinoatrial node dysfunction and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss 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.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 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.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mullerian aplasia and hyperandrogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Knuckle pads, deafness AND leukonychia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multicentric osteolysis, nodulosis and arthropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stapes ankylosis with broad thumb and toes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal 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.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Bone fragility with contractures, arterial rupture, and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Paragangliomas and Pheochromocytomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary Paragangliomas and Pheochromocytomas 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.

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.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Microcephaly, epilepsy, and diabetes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 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.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, deafness, and narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Juvenile macular degeneration and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, hiatal hernia and nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Jervell and Lange-Nielsen syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined malonic and methylmalonic aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis Gyrata syndrome of Beare and Stevenson Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation 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.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebroretinal microangiopathy with calcifications and cysts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, normal intelligence and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Calcification of joints and arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis and recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diabetes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Morbid obesity and spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory and autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of factor V and factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, cochlear, with myopia and intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of sialidase AND beta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of sialidase AND beta galactosidase 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.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial sorting and assembly machinery co