Small muscular protein Chisel

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Results for "Small muscular protein Chisel": 1001 gene sets

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Small muscular protein Chisel Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small muscular protein Chisel protein domain from the InterPro Predicted Protein Domain Annotations dataset.
[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ <small>Dsmall>-Tic⁹]OT Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ <small>Dsmall>-Tic⁹]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO₂H Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO₂H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷]OT Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ Aib⁹]OT Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ Aib⁹]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO₂H Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO₂H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
becker muscular dystrophy; duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophies; muscular dystrophies, limb-girdle Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophies; muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
protein modification by small protein conjugation Gene Set From GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset.
protein modification by small protein removal Gene Set From GO Biological Process Annotations 2015 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2015 dataset.
protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 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.
protein modification by small protein conjugation Gene Set From GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2023 dataset.
protein modification by small protein removal Gene Set From GO Biological Process Annotations 2023 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset.
protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset.
protein modification by small protein conjugation Gene Set From GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2025 dataset.
protein modification by small protein removal Gene Set From GO Biological Process Annotations 2025 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset.
protein modification by small protein conjugation or removal Gene Set From GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset.
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d[<small>Dsmall>-Phe²]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Phe²]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr² Val⁴ Arg⁶ Arg-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr² Val⁴ Arg⁶ Arg-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[<small>Dsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Bpa⁵ Ile¹³]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[tBaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Arg-NH₂⁸ des-Gly⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [tBaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Arg-NH₂⁸ des-Gly⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[His⁵ <small>Dsmall>-Tyr⁶]GnRH Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [His⁵ <small>Dsmall>-Tyr⁶]GnRH ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[<small>Lsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Lsmall>-Bpa⁵ Ile¹³]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Tyr-NH₂⁸ des-Gly⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Tyr-NH₂⁸ des-Gly⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Sar <small>Dsmall>-Phe⁸ des-Arg⁹]bradykinin Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Sar <small>Dsmall>-Phe⁸ des-Arg⁹]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d[<small>Dsmall>-Pal²]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Pal²]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr(Me)² Arg⁶ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr(Me)² Arg⁶ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Ile⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Ile⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[<small>Dsmall>-Lys¹ des-Arg¹⁰]kallidin Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Lys¹ des-Arg¹⁰]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
<small>Dsmall>-Lys⁰-[des-Arg¹⁰]kallidin Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the <small>Dsmall>-Lys⁰-[des-Arg¹⁰]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr(Et)² Lys⁶ des-Gly⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr(Et)² Lys⁶ des-Gly⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I][des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I][des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' protein domain from the InterPro Predicted Protein Domain Annotations dataset.
non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Muscular LMNA-interacting protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscular LMNA-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
SNAPc (small nuclear RNA-activating protein) complex Gene Set From CORUM Protein Complexes proteins in the SNAPc (small nuclear RNA-activating protein) complex protein complex from the CORUM Protein Complexes dataset.
small protein activating enzyme binding Gene Set From GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
small protein activating enzyme activity Gene Set From GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTP-binding protein domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTP-binding protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small acidic protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U3 small nucleolar RNA-associated protein 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small membrane A-kinase anchor protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small membrane A-kinase anchor protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U3 small nucleolar RNA-associated protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 6 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.
U3 small nucleolar RNA-associated protein 15, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 15, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small integral membrane protein 15 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small integral membrane protein 19 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 19 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small integral membrane protein 10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small acidic protein-like domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
lipid modification by small protein conjugation Gene Set From GO Biological Process Annotations 2023 genes participating in the lipid modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2023 dataset.
small protein activating enzyme binding Gene Set From GO Molecular Function Annotations 2023 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
lipid modification by small protein conjugation Gene Set From GO Biological Process Annotations 2025 genes participating in the lipid modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2025 dataset.
small protein activating enzyme binding Gene Set From GO Molecular Function Annotations 2025 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Duchenne muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2S Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, X-linked 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, autosomal recessive 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miyoshi Muscular Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral muscular dystrophy 1a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy, Jerash type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophies, Limb-Girdle Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophies, Limb-Girdle from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Animal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Scleroatonic muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scleroatonic muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy with respiratory distress 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophies from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Oculopharyngeal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.
Muscular Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Diseases from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophies of Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Merosin-Positive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy, limb-girdle, type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Lmna-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.
Muscular Diseases Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Muscular Diseases in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
atrophic muscular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease atrophic muscular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease muscular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease muscular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
atrophic muscular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophic muscular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease emery-dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
survival motor neuron spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophies, limb-girdle Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; glucose intolerance; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, oculopharyngeal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism disorders; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease ullrich congenital muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophies of childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophies Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain diseases; muscular dystrophies Gene Set From GAD Gene-Disease Associations genes associated with the disease brain diseases; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular disorders, atrophic Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular disorders, atrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; hypercholesterolemia; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; hypercholesterolemia; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term muscular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
muscular septum morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the muscular septum morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
muscular atrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
muscular disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease muscular disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
muscular hypotonia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the muscular hypotonia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
limb-girdle muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital muscular torticollis Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular torticollis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
extrapyramidal muscular rigidity Gene Set From HPO Gene-Disease Associations genes associated with the extrapyramidal muscular rigidity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular edema Gene Set From HPO Gene-Disease Associations genes associated with the muscular edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular hypotonia of the trunk Gene Set From HPO Gene-Disease Associations genes associated with the muscular hypotonia of the trunk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the severe muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscular appearance from birth Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Muscular Dystrophies, Limb-Girdle Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophies, Limb-Girdle phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Disorders, Atrophic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Disorders, Atrophic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophies Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Facioscapulohumeral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Muscular Atrophies of Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Duchenne phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal interventricular septum muscular part morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal interventricular septum muscular part morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fascioscapulohumeral muscular dystrophy 2, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, megaconial type Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2c Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, chronic distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to itga7 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy, limb-girdle, type 2r Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, rigid spine, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, merosin-positive Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2q Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2s Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2d Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2g Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2l Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2j Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, jokela type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal spinal muscular atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
tibial muscular dystrophy, tardive Gene Set From OMIM Gene-Disease Associations genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, late-onset, finkel type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
{spinal muscular atrophy, type iii, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 3, ar Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
limb-girdle muscular dystrophy, type 1g Gene Set From OMIM Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with rimmed vacuoles Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 6, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with epidermolysis bullosa simplex Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 1, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, x-linked 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
becker muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal and bulbar muscular atrophy of kennedy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 7, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital merosin-deficient Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular system Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
vertebrate muscular system Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue vertebrate muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
muscular system Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
vertebrate muscular system Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue vertebrate muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
muscular coat Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue muscular coat in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
muscular system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
invertebrate muscular system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue invertebrate muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
vertebrate muscular system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue vertebrate muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Emery-Dreifuss muscular dystrophy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Or Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Or Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eichsfeld Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eichsfeld Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne And Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne And Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Walker-Warburg Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Walker-Warburg Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fukuyama Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fukuyama Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Muscular, Spinobulbar Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Muscular, Spinobulbar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Ventricular Septum Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ullrich Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ullrich Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Hypertrophy-Cerebral Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Hypertrophy-Cerebral Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Limb Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Limb Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy, Tardive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy, Tardive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hereditary Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hereditary Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intermediate Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intermediate Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe [Duchenne] Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe [Duchenne] Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophies Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophies Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ocular Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ocular Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Sarcoidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Sarcoidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngeal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonprogressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Muscular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Hypotonia Of The Trunk Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Hypotonia Of The Trunk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Stiffness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Muscular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Extrapyramidal Muscular Rigidity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extrapyramidal Muscular Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscular Appearance From Birth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscular Appearance From Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Fasciculation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Fasciculation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurogenic Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurogenic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Marked Muscular Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Marked Muscular Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Muscular Rigidity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Muscular Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
muscular septum morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the muscular septum morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
muscular ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal interventricular septum muscular part morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interventricular septum muscular part morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptibility to induced muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Affected pathways in Duchenne muscular dystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Affected pathways in Duchenne muscular dystrophy pathway from the WikiPathways Pathways 2024 dataset.
muscular septum morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the muscular septum morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
Muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Muscular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Emery-Dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital merosin-deficient muscular dystrophy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Miyoshi muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy-dystroglycanopathy type A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy-dystroglycanopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Tibial muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Tibial muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked spinal muscular atrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with lower extremity predominant from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Atrophic muscular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Atrophic muscular disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy due to LMNA mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Muscular disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Muscular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Emery-Dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2S Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2S in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2M Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2M in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2K Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2K in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital merosin-deficient muscular dystrophy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to LMNA mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megaconial type congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megaconial type congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type C8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type C8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2X Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2X in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2J Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tibial muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tibial muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked Emery-Dreifuss muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked Emery-Dreifuss muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2L Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrophic muscular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophic muscular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2Q Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2Q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked Emery-Dreifuss muscular dystrophy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked Emery-Dreifuss muscular dystrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant Emery-Dreifuss muscular dystrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant Emery-Dreifuss muscular dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive Emery-Dreifuss muscular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive Emery-Dreifuss muscular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epidermolysis bullosa simplex with muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epidermolysis bullosa simplex with muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2Y Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2Y in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2W Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2W in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rigid spine muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rigid spine muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked distal spinal muscular atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinal muscular atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Miyoshi muscular dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Miyoshi muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to integrin alpha-7 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy with cataracts and intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy with cataracts and intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2T Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2T in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2O Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2O in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2N Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2N in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2U Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2U in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy type 1H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant limb-girdle muscular dystrophy type 1H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2P Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2P in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy A7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy A7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy, Jokela type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy, Jokela type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type B4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type B4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular dystrophy-dystroglycanopathy type C12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular dystrophy-dystroglycanopathy type C12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Facioscapulohumeral muscular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Facioscapulohumeral muscular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ullrich congenital muscular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ullrich congenital muscular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy type 2Z Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive limb-girdle muscular dystrophy type 2Z in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy type 0 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy type 0 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular system Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Vertebrate muscular system Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Vertebrate muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Muscular system Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Vertebrate muscular system Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Vertebrate muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Vertebrate muscular system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Vertebrate muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Muscular system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Invertebrate muscular system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Invertebrate muscular system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Muscular coat Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Muscular coat in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Autosomal recessive limb-girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive limb-girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Miyoshi muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Miyoshi muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ANO5-related muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ANO5-related muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Emery-Dreifuss muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Muscular dystrophy-dystroglycanopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscular dystrophy-dystroglycanopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb-girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FKRP-related muscular dystrophy-dystroglycanopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FKRP-related muscular dystrophy-dystroglycanopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Eichsfeld muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Eichsfeld muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Facioscapulohumeral muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Facioscapulohumeral muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MUSCULAR DYSTRO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MUSCULAR DYSTRO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked Emery-Dreifuss muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked Emery-Dreifuss muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Duchenne muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tibial muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tibial muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LAMA2-related muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the LAMA2-related muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital Muscular Dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital Muscular Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to LMNA mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant limb-girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant limb-girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular alpha-dystroglycanopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular alpha-dystroglycanopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to integrin alpha-7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intermediate muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intermediate muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oculopharyngeal muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oculopharyngeal muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb-girdle muscular dystrophy due to POMK deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscular dystrophy due to POMK deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Megaconial muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Megaconial muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Duchenne and Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Duchenne and Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked scapuloperoneal muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked scapuloperoneal muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapulohumeral muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapulohumeral muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe muscular hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe muscular hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Muscular channelopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscular channelopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
protein c deficiency; protein s deficiency; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of g-protein coupled receptor protein signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
protein maturation by protein folding Gene Set From GO Biological Process Annotations 2015 genes participating in the protein maturation by protein folding biological process from the curated GO Biological Process Annotations 2015 dataset.
protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of g-protein coupled receptor protein signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset.
activation of signaling protein activity involved in unfolded protein response Gene Set From GO Biological Process Annotations 2015 genes participating in the activation of signaling protein activity involved in unfolded protein response biological process from the curated GO Biological Process Annotations 2015 dataset.
desensitization of g-protein coupled receptor protein signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of g-protein coupled receptor protein signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2015 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset.
protein kinase c-activating g-protein coupled receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the protein kinase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
desensitization of g-protein coupled receptor protein signaling pathway by arrestin Gene Set From GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway by arrestin biological process from the curated GO Biological Process Annotations 2015 dataset.
protein binding involved in protein folding Gene Set From GO Molecular Function Annotations 2015 genes performing the protein binding involved in protein folding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Vacuolar protein sorting-associated protein 54 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 54 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myelin protein zero-like protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myelin protein zero-like protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myelin protein zero-like protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tumour protein p53-inducible nuclear protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour protein p53-inducible nuclear protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ADP-ribosylation factor-like protein 6-interacting protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ADP-ribosylation factor-like protein 6-interacting protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dyslexia-associated protein KIAA0319-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dyslexia-associated protein KIAA0319-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein kinase A anchor protein, RI-RII subunit-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, RI-RII subunit-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Guanine nucleotide binding protein (G-protein), alpha subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Guanine nucleotide binding protein (G-protein), alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein transport protein SecG/Sec61-beta/Sbh Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein transport protein SecG/Sec61-beta/Sbh protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein of unknown function DUF3669, zinc finger protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3669, zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
50S ribosomal protein L18Ae/60S ribosomal protein L20 and L18a Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the 50S ribosomal protein L18Ae/60S ribosomal protein L20 and L18a protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cleft lip and palate transmembrane protein 1-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cleft lip and palate transmembrane protein 1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pre-rRNA-processing protein IPI1/Testis-expressed sequence 10 protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pre-rRNA-processing protein IPI1/Testis-expressed sequence 10 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tumor protein p53-inducible protein 11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
V-set and transmembrane domain-containing protein 2-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the V-set and transmembrane domain-containing protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Actin-related protein 2/3 complex subunit 5-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 2/3 complex subunit 5-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 13 domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
EH domain-binding protein 1-like protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the EH domain-binding protein 1-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
SWR1-complex protein 5/Craniofacial development protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 5/Craniofacial development protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DMRT/protein doublesex/protein male abnormal 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting protein 36, GLUE domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 36, GLUE domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
UV radiation resistance protein/autophagy-related protein 14 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the UV radiation resistance protein/autophagy-related protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Four-jointed box protein 1/four-jointed protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Four-jointed box protein 1/four-jointed protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
G protein-coupled receptor kinase-interacting protein 1 C term Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the G protein-coupled receptor kinase-interacting protein 1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coiled-coil domain-containing protein 18/Cytoskeletal protein Sojo Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coiled-coil domain-containing protein 18/Cytoskeletal protein Sojo protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 13A N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13A N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting protein 26 related Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 26 related protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tumor protein p53-inducible nuclear protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 41 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 41 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Bone morphogenetic protein 1/tolloid-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Bone morphogenetic protein 1/tolloid-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synaptonemal complex protein 2/protein 2-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex protein 2/protein 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sterol regulatory element-binding protein cleavage-activating protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sterol regulatory element-binding protein cleavage-activating protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Polyadenylate-binding protein/Hyperplastic disc protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Polyadenylate-binding protein/Hyperplastic disc protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Uncharacterised protein family WW domain-binding protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised protein family WW domain-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Receptor-transporting protein/CXXC-type zinc finger protein 11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor-transporting protein/CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Receptor tyrosine-protein phosphatase C-associated protein CD45-AP Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor tyrosine-protein phosphatase C-associated protein CD45-AP protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 8, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 8, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Growth arrest/ DNA-damage-inducible protein-interacting protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth arrest/ DNA-damage-inducible protein-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 16 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vesicle-associated membrane protein-associated protein B Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein B protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vesicle-associated membrane protein-associated protein A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein LIN-9/Protein ALWAYS EARLY Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Steroid receptor RNA activator-protein/coat protein complex II, Sec31 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Steroid receptor RNA activator-protein/coat protein complex II, Sec31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 35, Vps35 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 35, Vps35 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tumor protein p53-inducible nuclear protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein of unknown function DUF3697, ubiquitin-associated protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3697, ubiquitin-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinoic acid-induced protein 2/sine oculis-binding protein homologue Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinoic acid-induced protein 2/sine oculis-binding protein homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tetracycline resistance protein, TetA/multidrug resistance protein MdtG Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tetracycline resistance protein, TetA/multidrug resistance protein MdtG protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TYRO protein tyrosine kinase-binding protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TYRO protein tyrosine kinase-binding protein protein domain from the InterPro Predicted Protein Domain Annotations 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.
Usher syndrome type-1C protein-binding protein 1, PDZ domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Usher syndrome type-1C protein-binding protein 1, PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal protein L1/ribosomal biogenesis protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L1/ribosomal biogenesis protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Actin-related protein 8/Plant actin-related protein 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 8/Plant actin-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Regulator of G-protein signalling 9-binding protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of G-protein signalling 9-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 13 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vesicle-associated membrane-protein-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane-protein-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting protein 11, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 11, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
cAMP-responsive element-binding protein 3-like protein 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
cAMP-responsive element-binding protein 3-like protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
cAMP-responsive element-binding protein 3-like protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
cAMP-responsive element-binding protein 3-like protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 33 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 33 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein kinase A anchor protein, nuclear localisation signal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, nuclear localisation signal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Spermatogenesis-associated protein 2-like protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
A-kinase anchor protein 6/Centrosomal protein of 68kDa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the A-kinase anchor protein 6/Centrosomal protein of 68kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
PodNet: protein-protein interactions in the podocyte(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the PodNet: protein-protein interactions in the podocyte(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
protein kinase C-activating G protein-coupled receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the protein kinase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2023 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
protein initiator methionine removal involved in protein maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the protein initiator methionine removal involved in protein maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset.
Protein-protein interactions at synapses Gene Set From Reactome Pathways 2024 proteins participating in the Protein-protein interactions at synapses pathway from the Reactome Pathways 2024 dataset.
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2025 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of protein processing involved in protein targeting to mitochondrion Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset.
Non-small cell lung cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brain small vessel disease with hemorrhage Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
mitochondrial small ribosomal subunit Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
preribosome, small subunit precursor Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the preribosome, small subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
small nuclear ribonucleoprotein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nuclear ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
small nucleolar ribonucleoprotein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
organellar small ribosomal subunit Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the organellar small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
small ribosomal subunit Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
gamma-tubulin small complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the gamma-tubulin small complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cytosolic small ribosomal subunit Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytosolic small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
small-subunit processome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small-subunit processome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial small ribosomal subunit Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
preribosome, small subunit precursor Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the preribosome, small subunit precursor cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
small nuclear ribonucleoprotein complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small nuclear ribonucleoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
small nucleolar ribonucleoprotein complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small nucleolar ribonucleoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chloroplast small ribosomal subunit Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chloroplast small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
organellar small ribosomal subunit Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the organellar small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
small ribosomal subunit Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
gamma-tubulin small complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the gamma-tubulin small complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cytosolic small ribosomal subunit Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytosolic small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
plastid small ribosomal subunit Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plastid small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
small-subunit processome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small-subunit processome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Carcinoma, Small Cell Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Small Cell from the curated CTD Gene-Disease Associations dataset.
Brain Small Vessel Disease with Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Carcinoma, Non-Small-Cell Lung Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Non-Small-Cell Lung from the curated CTD Gene-Disease Associations dataset.
Small Cell Lung Carcinoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Small Cell Lung Carcinoma from the curated CTD Gene-Disease Associations dataset.
Desmoplastic Small Round Cell Tumor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Desmoplastic Small Round Cell Tumor from the curated CTD Gene-Disease Associations dataset.
Carcinoma, Non-Small-Cell Lung Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Carcinoma, Non-Small-Cell Lung in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
non-small cell lung carcinoma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease non-small cell lung carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
small intestine cancer Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease small intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
ureter small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ureter small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small cell osteogenic sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell osteogenic sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine neuroendocrine neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
prostate small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prostate small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gallbladder small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gallbladder small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine leiomyoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung combined type small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung combined type small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
laryngeal small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease laryngeal small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung mixed small cell and squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine leiomyosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypercalcemic type ovarian small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypercalcemic type ovarian small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gastric small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small cell sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
non-small cell lung carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-small cell lung carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestinal sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestinal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cervix small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cervix small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
endometrial small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung small cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small intestine cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urinary bladder small cell neuroendocrine carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary bladder small cell neuroendocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small for gestational age infant Gene Set From GAD Gene-Disease Associations genes associated with the disease small for gestational age infant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; exanthema; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; exanthema; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-small-cell lung cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease non-small-cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral small-vessel disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-small cell lung carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, lacunar; small-vessel disease Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, lacunar; small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
small artery compliance Gene Set From GAD Gene-Disease Associations genes associated with the disease small artery compliance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-small cell lung cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease non-small cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, small fiber Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, small fiber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel Gene Set From GAD Gene-Disease Associations genes associated with the disease vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
small for gestational age Gene Set From GAD Gene-Disease Associations genes associated with the disease small for gestational age in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
differential expansion rates of small abdominal aortic aneurysms Gene Set From GAD Gene-Disease Associations genes associated with the disease differential expansion rates of small abdominal aortic aneurysms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
small Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term small in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Adenoma of small intestine_Intestinal Epithelium_GSE422 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Adenoma of small intestine_Intestinal Epithelium_GSE422 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PDX1_KO_GDS4348_360_mouse_Proximal small intestine Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PDX1_KO_GDS4348_360_mouse_Proximal small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
amoxicillin_rattus norvegicus_gpl341_distal small intestine_gds1273 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the amoxicillin_rattus norvegicus_gpl341_distal small intestine_gds1273 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
amoxicillin_rattus norvegicus_gpl341_proximal small intestine_gds1273 Gene Set From GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the amoxicillin_rattus norvegicus_gpl341_proximal small intestine_gds1273 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
regulation of small gtpase mediated signal transduction Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of small gtpase mediated signal transduction Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset.
small molecule catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the small molecule catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
ribosomal small subunit biogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit biogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of small gtpase mediated signal transduction Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset.
production of small rna involved in gene silencing by rna Gene Set From GO Biological Process Annotations 2015 genes participating in the production of small rna involved in gene silencing by rna biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleobase-containing small molecule catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of production of small rna involved in gene silencing by rna Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of production of small rna involved in gene silencing by rna biological process from the curated GO Biological Process Annotations 2015 dataset.
small gtpase mediated signal transduction Gene Set From GO Biological Process Annotations 2015 genes participating in the small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset.
small molecule biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the small molecule biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleobase-containing small molecule interconversion Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule interconversion biological process from the curated GO Biological Process Annotations 2015 dataset.
small rna loading onto risc Gene Set From GO Biological Process Annotations 2015 genes participating in the small rna loading onto risc biological process from the curated GO Biological Process Annotations 2015 dataset.
ribosomal small subunit export from nucleus Gene Set From GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit export from nucleus biological process from the curated GO Biological Process Annotations 2015 dataset.
small nucleolar ribonucleoprotein complex assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the small nucleolar ribonucleoprotein complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleobase-containing small molecule metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
small molecule metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the small molecule metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
ribosomal small subunit assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
mitochondrial small ribosomal subunit Gene Set From GO Cellular Component Annotations 2015 proteins localized to the mitochondrial small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.
preribosome, small subunit precursor Gene Set From GO Cellular Component Annotations 2015 proteins localized to the preribosome, small subunit precursor cellular component from the curated GO Cellular Component Annotations 2015 dataset.
small nuclear ribonucleoprotein complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the small nuclear ribonucleoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
small nucleolar ribonucleoprotein complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
organellar small ribosomal subunit Gene Set From GO Cellular Component Annotations 2015 proteins localized to the organellar small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.
small ribosomal subunit Gene Set From GO Cellular Component Annotations 2015 proteins localized to the small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.
gamma-tubulin small complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the gamma-tubulin small complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cytosolic small ribosomal subunit Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cytosolic small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset.
small-subunit processome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the small-subunit processome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
small molecule binding Gene Set From GO Molecular Function Annotations 2015 genes performing the small molecule binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
small gtpase binding Gene Set From GO Molecular Function Annotations 2015 genes performing the small gtpase binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
small conductance calcium-activated potassium channel activity Gene Set From GO Molecular Function Annotations 2015 genes performing the small conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
small gtpase regulator activity Gene Set From GO Molecular Function Annotations 2015 genes performing the small gtpase regulator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
ribosomal small subunit binding Gene Set From GO Molecular Function Annotations 2015 genes performing the ribosomal small subunit binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
small ribosomal subunit rrna binding Gene Set From GO Molecular Function Annotations 2015 genes performing the small ribosomal subunit rrna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
small intestine Gene Set From GTEx Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.
Response to irinotecan in non-small-cell lung cancer Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to irinotecan in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Non-small cell lung cancer (survival) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Non-small cell lung cancer (survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Non-small cell lung cancer Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to platinum-based chemotherapy in non-small-cell lung cancer Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
non-small cell lung carcinoma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
small intestine neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease small intestine neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
lung small cell carcinoma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease lung small cell carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of the small intestine Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
small intestine Gene Set From HPA Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.
small intestine Gene Set From HPA Tissue Protein Expression Profiles proteins with high or low expression in small intestine relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.
small cerebral cortex Gene Set From HPO Gene-Disease Associations genes associated with the small cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small nail Gene Set From HPO Gene-Disease Associations genes associated with the small nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small pituitary gland Gene Set From HPO Gene-Disease Associations genes associated with the small pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small proximal tibial epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the small proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small sella turcica Gene Set From HPO Gene-Disease Associations genes associated with the small sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypotrophy of the small hand muscles Gene Set From HPO Gene-Disease Associations genes associated with the hypotrophy of the small hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neoplasm of the small intestine Gene Set From HPO Gene-Disease Associations genes associated with the neoplasm of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small foramen magnum Gene Set From HPO Gene-Disease Associations genes associated with the small foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small anterior fontanelle Gene Set From HPO Gene-Disease Associations genes associated with the small anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the small epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of small peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
arteriosclerosis of small cerebral arteries Gene Set From HPO Gene-Disease Associations genes associated with the arteriosclerosis of small cerebral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small, conical teeth Gene Set From HPO Gene-Disease Associations genes associated with the small, conical teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small earlobe Gene Set From HPO Gene-Disease Associations genes associated with the small earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small forehead Gene Set From HPO Gene-Disease Associations genes associated with the small forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple small vertebral fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small distal femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the small distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small cervical vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the small cervical vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small intestine carcinoid Gene Set From HPO Gene-Disease Associations genes associated with the small intestine carcinoid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small intestinal polyposis Gene Set From HPO Gene-Disease Associations genes associated with the small intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small hypothenar eminence Gene Set From HPO Gene-Disease Associations genes associated with the small hypothenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of small intestinal villus morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of small intestinal villus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small vessel vasculitis Gene Set From HPO Gene-Disease Associations genes associated with the small vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small intestinal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the small intestinal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small thenar eminence Gene Set From HPO Gene-Disease Associations genes associated with the small thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small placenta Gene Set From HPO Gene-Disease Associations genes associated with the small placenta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ankylosis of feet small joints Gene Set From HPO Gene-Disease Associations genes associated with the ankylosis of feet small joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small hand Gene Set From HPO Gene-Disease Associations genes associated with the small hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the small intestine Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple small medullary renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
brain very small Gene Set From HPO Gene-Disease Associations genes associated with the brain very small phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small face Gene Set From HPO Gene-Disease Associations genes associated with the small face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small for gestational age Gene Set From HPO Gene-Disease Associations genes associated with the small for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
calcification of the small brain vessels Gene Set From HPO Gene-Disease Associations genes associated with the calcification of the small brain vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small abnormally formed scapulae Gene Set From HPO Gene-Disease Associations genes associated with the small abnormally formed scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Carcinoma, Small Cell Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Small Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Carcinoma, Non-Small-Cell Lung Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Non-Small-Cell Lung phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Small Cell Lung Carcinoma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Small Cell Lung Carcinoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Desmoplastic Small Round Cell Tumor Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Desmoplastic Small Round Cell Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Large neutral amino acids transporter small subunit 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Large neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small-subunit processome, Utp21 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp21 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
GyrI-like small molecule binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the GyrI-like small molecule binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U2 auxiliary factor small subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U2 auxiliary factor small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, Ras type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Ras type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U3 small nucleolar ribonucleoprotein complex, subunit Mpp10 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar ribonucleoprotein complex, subunit Mpp10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, Rho type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Rho type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U1 small nuclear ribonucleoprotein of 70kDa N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein of 70kDa N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, mitochondrial Rho Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, mitochondrial Rho protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U4/U6 small nuclear ribonucleoprotein Prp31 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small nuclear RNA activating complex subunit 2-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear RNA activating complex subunit 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U1 small nuclear ribonucleoprotein C Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein C protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Clathrin adaptor complex, small chain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Clathrin adaptor complex, small chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small nuclear RNA activating complex (SNAPc), subunit SNAP43 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear RNA activating complex (SNAPc), subunit SNAP43 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal RNA small subunit methyltransferase H Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA small subunit methyltransferase H protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small nuclear ribonucleoprotein Sm D2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear ribonucleoprotein Sm D2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, GEM/REM/Rad Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, GEM/REM/Rad protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA polymerase delta/II small subunit family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase delta/II small subunit family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small-subunit processome, Utp13 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small-subunit processome, Utp12 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small-subunit processome, Utp11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small-subunit processome, Utp14 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Carbamoyl-phosphate synthase, small subunit N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, small subunit N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small ribonucleoprotein associated, SmB/SmN Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ribonucleoprotein associated, SmB/SmN protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribonucleotide reductase small subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribonucleotide reductase small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Methyltransferase small domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Methyltransferase small domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small nuclear ribonucleoprotein E Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear ribonucleoprotein E protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Iron hydrogenase, small subunit-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase, small subunit-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Xanthine dehydrogenase, small subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Xanthine dehydrogenase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U4/U6 small nuclear ribonucleoprotein Prp4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
U4/U6 small nuclear ribonucleoprotein Prp3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aconitase A/isopropylmalate dehydratase small subunit, swivel Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitase A/isopropylmalate dehydratase small subunit, swivel protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Citrate synthase-like, small alpha subdomain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Citrate synthase-like, small alpha subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small ubiquitin-related modifier, chordates Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ubiquitin-related modifier, chordates protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small subunit of serine palmitoyltransferase-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small subunit of serine palmitoyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA primase, small subunit, eukaryotic/archaeal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, small subunit, eukaryotic/archaeal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, ARF type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, ARF type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, SAR1-type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, SAR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Small GTPase superfamily, ARF/SAR type Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, ARF/SAR type protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA primase, small subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Harmonizome 3.0

Small muscular protein Chisel Gene Set

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H Gene Set

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT Gene Set

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H Gene Set

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

carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene Set

muscular atrophy, spinal; spinal muscular atrophy Gene Set

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

muscular dystrophies; muscular dystrophies, limb-girdle Gene Set

protein modification by small protein conjugation Gene Set

negative regulation of protein modification by small protein conjugation or removal Gene Set

positive regulation of protein modification by small protein conjugation or removal Gene Set

regulation of protein modification by small protein conjugation or removal Gene Set

protein modification by small protein removal Gene Set

protein modification by small protein conjugation or removal Gene Set

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

protein modification by small protein conjugation Gene Set

protein modification by small protein removal Gene Set

regulation of protein modification by small protein conjugation or removal Gene Set

positive regulation of protein modification by small protein conjugation or removal Gene Set

negative regulation of protein modification by small protein conjugation or removal Gene Set

protein modification by small protein conjugation or removal Gene Set

protein modification by small protein conjugation Gene Set

protein modification by small protein removal Gene Set

regulation of protein modification by small protein conjugation or removal Gene Set

positive regulation of protein modification by small protein conjugation or removal Gene Set

negative regulation of protein modification by small protein conjugation or removal Gene Set

protein modification by small protein conjugation or removal Gene Set

adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene Set

d[<small>Dsmall>-Phe2]AVP Gene Set

[125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene Set

[Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP Gene Set

[<small>Dsmall>-Bpa5 Ile13]motilin (human) Gene Set

[tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP Gene Set

[His5 <small>Dsmall>-Tyr6]GnRH Gene Set

[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP Gene Set

[<small>Lsmall>-Bpa5 Ile13]motilin (human) Gene Set

[des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene Set

[Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP Gene Set

[Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin Gene Set

d[<small>Dsmall>-Pal2]AVP Gene Set

d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP Gene Set

[Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP Gene Set

[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP Gene Set

[<small>Dsmall>-Lys1 des-Arg10]kallidin Gene Set

[125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene Set

<small>Dsmall>-Lys0-[des-Arg10]kallidin Gene Set

[Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP Gene Set

[125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene Set

U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene Set

non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set

Muscular LMNA-interacting protein Gene Set

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

SNAPc (small nuclear RNA-activating protein) complex Gene Set

small protein activating enzyme binding Gene Set

small protein activating enzyme activity Gene Set

U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 Gene Set

Small GTP-binding protein domain Gene Set

Small acidic protein Gene Set

U3 small nucleolar RNA-associated protein 10 Gene Set

Small membrane A-kinase anchor protein Gene Set

U3 small nucleolar RNA-associated protein 6 Gene Set

Small proline-rich protein 2 Gene Set

U3 small nucleolar RNA-associated protein 15, C-terminal Gene Set

Small integral membrane protein 15 Gene Set

Small integral membrane protein 19 Gene Set

Small integral membrane protein 10 Gene Set

Small acidic protein-like domain Gene Set

lipid modification by small protein conjugation Gene Set

[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ <small>Dsmall>-Tic⁹]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO₂H Gene Set

[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷]OT Gene Set

[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ Aib⁹]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO₂H Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set

d[<small>Dsmall>-Phe²]AVP Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set

[Phaa¹ <small>Dsmall>-Tyr² Val⁴ Arg⁶ Arg-NH₂⁹]AVP Gene Set

[<small>Dsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set

[tBaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Arg-NH₂⁸ des-Gly⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂⁹]AVP Gene Set

[His⁵ <small>Dsmall>-Tyr⁶]GnRH Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴]AVP Gene Set

[<small>Lsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set

[des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set

[Phaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Tyr-NH₂⁸ des-Gly⁹]AVP Gene Set

[Sar <small>Dsmall>-Phe⁸ des-Arg⁹]bradykinin Gene Set

d[<small>Dsmall>-Pal²]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂]AVP Gene Set

[Phaa¹ <small>Dsmall>-Tyr(Me)² Arg⁶ Tyr-NH₂⁹]AVP Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Ile⁴ Tyr-NH₂⁹]AVP Gene Set

[<small>Dsmall>-Lys¹ des-Arg¹⁰]kallidin Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set

<small>Dsmall>-Lys⁰-[des-Arg¹⁰]kallidin Gene Set

[Phaa¹ <small>Dsmall>-Tyr(Et)² Lys⁶ des-Gly⁹]AVP Gene Set

[¹²⁵I][des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set