Name

mhc class ii deficiency, complementation group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the mhc class ii deficiency, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset.

MHC class II-associated invariant chain/CLIP, MHC II-interacting Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II-associated invariant chain/CLIP, MHC II-interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor deficiency, complementation group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Molybdenum cofactor deficiency, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Molybdenum cofactor deficiency, complementation group B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Molybdenum cofactor deficiency, complementation group B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Molybdenum cofactor deficiency, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Molybdenum cofactor deficiency, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

mhc class ii deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mhc class i deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

bare lymphocyte syndrome, type ii, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

Fanconi anemia, complementation group O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, complementation group b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, complementation group b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group D2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group D2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP C from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP E from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP F from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group J from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group B from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group N Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group N from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP D2 from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group C from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group B from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group E from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group D from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group G from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group F from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group I from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP O Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP O from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group D1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group D1 from the curated CTD Gene-Disease Associations dataset.

fanconi anemia, complementation group p Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group p phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group q Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group q phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group i Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group i phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group j Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group j phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group l Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group l phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group m Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group m phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group n Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group n phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group o Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group o phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group f Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group f phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group g Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group g phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group d1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group d1 phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group d2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group d2 phenotype from the curated OMIM Gene-Disease Associations dataset.

trichothiodystrophy, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichothiodystrophy, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

mhc class ib protein binding, via antigen binding groove Gene Set

From GO Molecular Function Annotations

genes performing the mhc class ib protein binding, via antigen binding groove molecular function from the curated GO Molecular Function Annotations dataset.

mhc class ii protein binding, via antigen binding groove Gene Set

From GO Molecular Function Annotations

genes performing the mhc class ii protein binding, via antigen binding groove molecular function from the curated GO Molecular Function Annotations dataset.

positive regulation of mhc class i biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mhc class i biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

mhc class ii biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the mhc class ii biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mhc class ii biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mhc class ii biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mhc class ii biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mhc class ii biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of mhc class i biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mhc class i biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of mhc class ii biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mhc class ii biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

mhc class ii protein binding Gene Set

From GO Molecular Function Annotations

genes performing the mhc class ii protein binding molecular function from the curated GO Molecular Function Annotations dataset.

mhc class ib protein binding Gene Set

From GO Molecular Function Annotations

genes performing the mhc class ib protein binding molecular function from the curated GO Molecular Function Annotations dataset.

mhc class i protein binding Gene Set

From GO Molecular Function Annotations

genes performing the mhc class i protein binding molecular function from the curated GO Molecular Function Annotations dataset.

mhc class i protein complex binding Gene Set

From GO Molecular Function Annotations

genes performing the mhc class i protein complex binding molecular function from the curated GO Molecular Function Annotations dataset.

mhc class ii protein complex binding Gene Set

From GO Molecular Function Annotations

genes performing the mhc class ii protein complex binding molecular function from the curated GO Molecular Function Annotations dataset.

MHC class II, beta chain, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II, beta chain, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class II, alpha/beta chain, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II, alpha/beta chain, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

mhc class ii protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mhc class ii protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mhc class i peptide loading complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mhc class i peptide loading complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mhc class i protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mhc class i protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mhc class ii protein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mhc class i peptide loading complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mhc class i protein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mhc class ib protein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

antigen processing and presentation, endogenous lipid antigen via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation, endogenous lipid antigen via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of exogenous peptide antigen via mhc class i Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of exogenous peptide antigen via mhc class i biological process from the curated GO Biological Process Annotations dataset.

negative regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of endogenous peptide antigen via mhc class i via er pathway Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of endogenous peptide antigen via mhc class i via er pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of antigen processing and presentation of peptide antigen via mhc class i Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of antigen processing and presentation of peptide antigen via mhc class i biological process from the curated GO Biological Process Annotations dataset.

negative regulation of antigen processing and presentation of peptide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of antigen processing and presentation of peptide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

regulation of antigen processing and presentation of peptide antigen via mhc class i Gene Set

From GO Biological Process Annotations

genes participating in the regulation of antigen processing and presentation of peptide antigen via mhc class i biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of peptide antigen via mhc class i Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of peptide antigen via mhc class i biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of endogenous peptide antigen via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of endogenous peptide antigen via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

peptide antigen assembly with mhc class ii protein complex Gene Set

From GO Biological Process Annotations

genes participating in the peptide antigen assembly with mhc class ii protein complex biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of exogenous peptide antigen via mhc class i, tap-dependent Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of exogenous peptide antigen via mhc class i, tap-dependent biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of lipid antigen via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of lipid antigen via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

mhc class ii protein complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mhc class ii protein complex assembly biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

polysaccharide assembly with mhc class ii protein complex Gene Set

From GO Biological Process Annotations

genes participating in the polysaccharide assembly with mhc class ii protein complex biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of endogenous peptide antigen via mhc class ib via er pathway, tap-dependent Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of endogenous peptide antigen via mhc class ib via er pathway, tap-dependent biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of peptide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of peptide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of peptide antigen via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of peptide antigen via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of endogenous peptide antigen via mhc class ib via er pathway Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of endogenous peptide antigen via mhc class ib via er pathway biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of endogenous peptide antigen via mhc class i Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of endogenous peptide antigen via mhc class i biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of endogenous peptide antigen via mhc class i via er pathway, tap-dependent Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of endogenous peptide antigen via mhc class i via er pathway, tap-dependent biological process from the curated GO Biological Process Annotations dataset.

positive regulation of antigen processing and presentation of peptide antigen via mhc class i Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of antigen processing and presentation of peptide antigen via mhc class i biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of exogenous peptide antigen via mhc class i, tap-independent Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of exogenous peptide antigen via mhc class i, tap-independent biological process from the curated GO Biological Process Annotations dataset.

positive regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

peptide antigen assembly with mhc class i protein complex Gene Set

From GO Biological Process Annotations

genes participating in the peptide antigen assembly with mhc class i protein complex biological process from the curated GO Biological Process Annotations dataset.

positive regulation of antigen processing and presentation of peptide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of antigen processing and presentation of peptide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of exogenous protein antigen via mhc class ib, tap-dependent Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of exogenous protein antigen via mhc class ib, tap-dependent biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of exogenous peptide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of exogenous peptide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation of exogenous peptide antigen via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation of exogenous peptide antigen via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

antigen processing and presentation, exogenous lipid antigen via mhc class ib Gene Set

From GO Biological Process Annotations

genes participating in the antigen processing and presentation, exogenous lipid antigen via mhc class ib biological process from the curated GO Biological Process Annotations dataset.

regulation of antigen processing and presentation of peptide antigen via mhc class ii Gene Set

From GO Biological Process Annotations

genes participating in the regulation of antigen processing and presentation of peptide antigen via mhc class ii biological process from the curated GO Biological Process Annotations dataset.

mhc class ii protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mhc class ii protein complex cellular component from the curated GO Cellular Component Annotations dataset.

mhc class i peptide loading complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mhc class i peptide loading complex cellular component from the curated GO Cellular Component Annotations dataset.

mhc class ib protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mhc class ib protein complex cellular component from the curated GO Cellular Component Annotations dataset.

mhc class i protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mhc class i protein complex cellular component from the curated GO Cellular Component Annotations dataset.

activating mhc class i receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the activating mhc class i receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

hla-a specific inhibitory mhc class i receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the hla-a specific inhibitory mhc class i receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

hla-b specific inhibitory mhc class i receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the hla-b specific inhibitory mhc class i receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

mhc class i receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the mhc class i receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

hla-a specific activating mhc class i receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the hla-a specific activating mhc class i receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

mhc class ii receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the mhc class ii receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

inhibitory mhc class i receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the inhibitory mhc class i receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

MHC class II-associated invariant chain, trimerisation Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II-associated invariant chain, trimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class II, alpha chain, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II, alpha chain, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class II transactivator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II transactivator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class I alpha chain, alpha1 alpha2 domains Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class I alpha chain, alpha1 alpha2 domains protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class I-like antigen recognition Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class I-like antigen recognition protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class I alpha chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class I alpha chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class I, alpha chain, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class I, alpha chain, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

MHC class II-associated invariant chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC class II-associated invariant chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal antigen presentation via mhc class i Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal antigen presentation via mhc class i phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal antigen presentation via mhc class ii Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal antigen presentation via mhc class ii phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

MHC class II antigen presentation Gene Set

From Reactome Pathways

proteins participating in the MHC class II antigen presentation pathway from the Reactome Pathways dataset.

Class I MHC mediated antigen processing & presentation Gene Set

From Reactome Pathways

proteins participating in the Class I MHC mediated antigen processing & presentation pathway from the Reactome Pathways dataset.

Nef mediated downregulation of MHC class I complex cell surface expression Gene Set

From Reactome Pathways

proteins participating in the Nef mediated downregulation of MHC class I complex cell surface expression pathway from the Reactome Pathways dataset.

Antigen Presentation: Folding, assembly and peptide loading of class I MHC Gene Set

From Reactome Pathways

proteins participating in the Antigen Presentation: Folding, assembly and peptide loading of class I MHC pathway from the Reactome Pathways dataset.

Cytochrome P450, E-class, group I, CYP1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2D-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2D-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2J-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2J-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group IV Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group IV protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2B-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2B-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2A-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2A-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2E-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2E-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

regulation of dna damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the regulation of dna damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator biological process from the curated GO Biological Process Annotations dataset.

dna damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the dna damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator biological process from the curated GO Biological Process Annotations dataset.

positive regulation of dna damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of dna damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator biological process from the curated GO Biological Process Annotations dataset.

Peptide chain release factor class I/class II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide chain release factor class I/class II protein domain from the InterPro Predicted Protein Domain Annotations 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.

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.

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.

phospholipase a2, group iv a, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the phospholipase a2, group iv a, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From CTD Gene-Disease Associations

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

complementation Gene Set

From GeneRIF Biological Term Annotations

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

homocystinuria-megaloblastic anemia, cblg complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria-megaloblastic anemia, cblg complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

regulation of t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell Gene Set

From GO Biological Process Annotations

genes participating in the regulation of t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations dataset.

negative regulation of t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations dataset.

positive regulation of t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations dataset.

t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell Gene Set

From GO Biological Process Annotations

genes participating in the t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations dataset.

mhc protein complex binding Gene Set

From GO Molecular Function Annotations

genes performing the mhc protein complex binding molecular function from the curated GO Molecular Function Annotations dataset.

mhc protein binding Gene Set

From GO Molecular Function Annotations

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

MHC binding peptide Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the MHC binding peptide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mhc protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

mhc protein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mhc Gene Set

From GeneRIF Biological Term Annotations

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

mhc protein complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mhc protein complex assembly biological process from the curated GO Biological Process Annotations dataset.

peptide antigen assembly with mhc protein complex Gene Set

From GO Biological Process Annotations

genes participating in the peptide antigen assembly with mhc protein complex biological process from the curated GO Biological Process Annotations dataset.

mhc protein complex Gene Set

From GO Cellular Component Annotations

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

MHC classes I/II-like antigen recognition protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MHC classes I/II-like antigen recognition protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal mhc ii cell surface expression on macrophages Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mhc ii cell surface expression on macrophages phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Neuraminidase deficiency with beta-galactosidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD 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.

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

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.

anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

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

choline deficiency; dna damage; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia 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.

folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload 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.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.

Fructose-1,6-bisphosphatase class 1/Sedoheputulose-1,7-bisphosphatase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fructose-1,6-bisphosphatase class 1/Sedoheputulose-1,7-bisphosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Blood group, john milton hagen system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, john milton hagen system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WALDNER TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WALDNER TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cromer blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cromer blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Radin blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Radin blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, junior system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, junior system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, gerbich system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, gerbich system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--OK Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--OK phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antigen in Scianna blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antigen in Scianna blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Langereis blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Langereis blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--FROESE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--FROESE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--LUTHERAN INHIBITOR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--LUTHERAN INHIBITOR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, dombrock system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, dombrock system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WRIGHT ANTIGEN Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WRIGHT ANTIGEN phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

blood group incompatibility Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

2-Bromoacetyl Group Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-Bromoacetyl Group drug from the curated DrugBank Drug Targets dataset.

blood group incompatibility; rh isoimmunization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood group incompatibility; rh isoimmunization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; blood group incompatibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; blood group incompatibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

i/d ace gene polymorphism and abo blood group system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease i/d ace gene polymorphism and abo blood group system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prosthetic group binding Gene Set

From GO Molecular Function Annotations

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

quaternary ammonium group binding Gene Set

From GO Molecular Function Annotations

genes performing the quaternary ammonium group binding molecular function from the curated GO Molecular Function Annotations dataset.

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Blood Group Incompatibility Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Group Incompatibility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Pre-SET zinc-binding sub-group Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pre-SET zinc-binding sub-group protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group box domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Blood group Rhesus C/E/D polypeptide Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Blood group Rhesus C/E/D polypeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group nucleosome-binding domain-containing family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group nucleosome-binding domain-containing family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kell blood group glycoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kell blood group glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bacterial Ig-like, group 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bacterial Ig-like, group 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group box domain 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group box domain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

[blood group, swann] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, swann] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rodgers] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rodgers] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, colton] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, colton] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, knops system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, knops system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[junior blood group system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [junior blood group system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, raph] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, raph] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group gil] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group gil] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, dombrock] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, dombrock] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, waldner] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, waldner] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, scianna system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, scianna system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, mn] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, mn] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, xg system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, xg system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lutheran system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, abo system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, abo system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ok] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ok] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, auberger system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, auberger system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, indian system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, indian system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, froese] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, froese] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, landsteiner-wiener] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, landsteiner-wiener] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rhesus] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rhesus] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, globoside system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, globoside system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran null] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lutheran null] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, kell] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, kell] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, radin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, radin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, kidd] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, kidd] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, yt system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, yt system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p(k) phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p(k) phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

blood group--lutheran inhibitor Gene Set

From OMIM Gene-Disease Associations

genes associated with the blood group--lutheran inhibitor phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, vel system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, vel system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ss] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ss] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, stoltzfus system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, stoltzfus system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lewis] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lewis] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, diego] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, diego] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ii] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ii] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, langereis system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, langereis system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, gerbich] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, gerbich] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, wright] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, wright] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group cromer] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group cromer] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, john-milton-hagen system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, john-milton-hagen system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p(2) phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p(2) phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, duffy system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, duffy system] phenotype from the curated OMIM Gene-Disease Associations dataset.

peroxisome membrane class-1 targeting sequence binding Gene Set

From GO Molecular Function Annotations

genes performing the peroxisome membrane class-1 targeting sequence binding molecular function from the curated GO Molecular Function Annotations dataset.

tfiib-class binding transcription factor activity Gene Set

From GO Molecular Function Annotations

genes performing the tfiib-class binding transcription factor activity molecular function from the curated GO Molecular Function Annotations dataset.

tfiib-class transcription factor binding Gene Set

From GO Molecular Function Annotations

genes performing the tfiib-class transcription factor binding molecular function from the curated GO Molecular Function Annotations dataset.

tbp-class protein binding Gene Set

From GO Molecular Function Annotations

genes performing the tbp-class protein binding molecular function from the curated GO Molecular Function Annotations dataset.

tfiid-class transcription factor binding Gene Set

From GO Molecular Function Annotations

genes performing the tfiid-class transcription factor binding molecular function from the curated GO Molecular Function Annotations dataset.

erbb-2 class receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the erbb-2 class receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

erbb-3 class receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the erbb-3 class receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

tfiiic-class transcription factor binding Gene Set

From GO Molecular Function Annotations

genes performing the tfiiic-class transcription factor binding molecular function from the curated GO Molecular Function Annotations dataset.

Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxymethylglutaryl-CoA reductase, class I/II, NAD/NADP-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA reductase, class I/II, NAD/NADP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutamyl/glutaminyl-tRNA synthetase, class Ib, anti-codon binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutamyl/glutaminyl-tRNA synthetase, class Ib, anti-codon binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fructose-bisphosphate aldolase, class-I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fructose-bisphosphate aldolase, class-I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Prolyl-tRNA synthetase, class IIa, bacterial-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Prolyl-tRNA synthetase, class IIa, bacterial-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class 1a, anticodon-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class 1a, anticodon-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alanine-tRNA ligase, class IIc, anti-codon-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alanine-tRNA ligase, class IIc, anti-codon-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phenylalanyl-tRNA synthetase, class IIc, beta subunit, archae/euk cytosolic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phenylalanyl-tRNA synthetase, class IIc, beta subunit, archae/euk cytosolic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferases, class-I, pyridoxal-phosphate-binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferases, class-I, pyridoxal-phosphate-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class I, anticodon-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class I, anticodon-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fructose-bisphosphate aldolase class-I active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fructose-bisphosphate aldolase class-I active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class I, anticodon-binding domain, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class I, anticodon-binding domain, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase, class-II, pyridoxal-phosphate binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase, class-II, pyridoxal-phosphate binding site 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.

Hydroxymethylglutaryl-CoA reductase, class I/II, substrate-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA reductase, class I/II, substrate-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Helix-hairpin-helix DNA-binding motif, class 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Helix-hairpin-helix DNA-binding motif, class 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase class-V, pyridoxal-phosphate binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase class-V, pyridoxal-phosphate binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fructose-bisphosphate aldolase class-I, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fructose-bisphosphate aldolase class-I, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aspartate-tRNA ligase, class IIb, bacterial/mitochondrial-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aspartate-tRNA ligase, class IIb, bacterial/mitochondrial-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphatidylinositol-glycan biosynthesis class S protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphatidylinositol-glycan biosynthesis class S protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutamyl/glutaminyl-tRNA synthetase, class Ib, alpha-bundle domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutamyl/glutaminyl-tRNA synthetase, class Ib, alpha-bundle domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

gigantocellular group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gigantocellular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central medullary reticular group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

rostral group of intralaminar nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

caudal group of intralaminar nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in caudal group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

rostral group of intralaminar nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral medullary reticular group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

caudal group of intralaminar nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in caudal group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, left, ventral division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, left, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

gigantocellular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gigantocellular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, right, ventral division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, right, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cortico-medial group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cortico-medial group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral medullary reticular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cortico-medial group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cortico-medial group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, left, dorsal division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, left, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, right, dorsal division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, right, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central medullary reticular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior digastric muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Geniculate group, ventral thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Geniculate group, ventral thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medial group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medial group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

A4 noradrenergic cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in A4 noradrenergic cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

temporal muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in temporal muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Geniculate group, dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Geniculate group, dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Ventral group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Ventral group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Dopaminergic A13 group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Dopaminergic A13 group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r5 part of A5 noradrenergic cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r5 part of A5 noradrenergic cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

pterigoid muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in pterigoid muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

temporotympanic muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in temporotympanic muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Midline group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Midline group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

rostral ventral respiratory cell group Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral ventral respiratory cell group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

central nuclear group Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central nuclear group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Xeroderma pigmentosum, group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monoisopropyl Ester Phosphonic Acid Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Monoisopropyl Ester Phosphonic Acid Group drug from the curated DrugBank Drug Targets dataset.

Diisopropylphosphono Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Diisopropylphosphono Group drug from the curated DrugBank Drug Targets dataset.

4-Methylpiperazin-1-Yl Carbonyl Group Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-Methylpiperazin-1-Yl Carbonyl Group drug from the curated DrugBank Drug Targets dataset.

(1S)-MENTHYL HEXYL PHOSPHONATE GROUP Gene Set

From DrugBank Drug Targets

interacting proteins for the (1S)-MENTHYL HEXYL PHOSPHONATE GROUP drug from the curated DrugBank Drug Targets dataset.

Methylphosphonic Acid Ester Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Methylphosphonic Acid Ester Group drug from the curated DrugBank Drug Targets dataset.

(1R)-MENTHYL HEXYL PHOSPHONATE GROUP Gene Set

From DrugBank Drug Targets

interacting proteins for the (1R)-MENTHYL HEXYL PHOSPHONATE GROUP drug from the curated DrugBank Drug Targets dataset.

Pyruvoyl Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Pyruvoyl Group drug from the curated DrugBank Drug Targets dataset.

Diethylphosphono Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Diethylphosphono Group drug from the curated DrugBank Drug Targets dataset.

group Gene Set

From GeneRIF Biological Term Annotations

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

quaternary ammonium group transport Gene Set

From GO Biological Process Annotations

genes participating in the quaternary ammonium group transport biological process from the curated GO Biological Process Annotations dataset.

prosthetic group metabolic process Gene Set

From GO Biological Process Annotations

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

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

From GO Molecular Function Annotations

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

phosphotransferase activity, phosphate group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, phosphate group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

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

From GO Molecular Function Annotations

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

quaternary ammonium group transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

phosphotransferase activity, nitrogenous group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

group ii metabotropic glutamate receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the group ii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

group iii metabotropic glutamate receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the group iii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

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

From GO Molecular Function Annotations

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

phosphotransferase activity, carboxyl group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, carboxyl group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

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

From GO Molecular Function Annotations

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

phosphotransferase activity, alcohol group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

group E 1682-2106 [PMID:16118363] Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the group E 1682-2106 [PMID:16118363] ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Psychotherapy, Group Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

G-protein alpha subunit, group I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G-protein alpha subunit, group S Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group S protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G-protein alpha subunit, group Q Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group Q protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anaemia group C protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anaemia group C protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Xeroderma pigmentosum group D protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Xeroderma pigmentosum group D protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G-protein alpha subunit, group 12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anemia group I protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anemia group I protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi Anaemia group E protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi Anaemia group E protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group, HMG-I/HMG-Y Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group, HMG-I/HMG-Y protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phospholipase A2, group XII secretory Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phospholipase A2, group XII secretory protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alanine racemase/group IV decarboxylase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alanine racemase/group IV decarboxylase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anaemia group A protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anaemia group A protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

xeroderma pigmentosum, group g/cockayne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group g/cockayne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group b phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group c phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group a phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group f Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group f phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group g Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group g phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group d phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group e, ddb-negative subtype Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group e, ddb-negative subtype phenotype from the curated OMIM Gene-Disease Associations dataset.

Metabotropic glutamate receptor group I pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group I pathway pathway from the PANTHER Pathways dataset.

Metabotropic glutamate receptor group III pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group III pathway pathway from the PANTHER Pathways dataset.

Metabotropic glutamate receptor group II pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group II pathway pathway from the PANTHER Pathways dataset.

phosphotransferases-alcohol-group-acceptor Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Human immunodeficiency virus type 1 group M subtype B (isolate MN) Gene Set

From Virus MINT Protein-Virus Interactions

interacting proteins for the virus Human immunodeficiency virus type 1 group M subtype B (isolate MN) from the Virus MINT Protein-Virus Interactions dataset.

phosphatidylinositol 3-kinase complex, class iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the phosphatidylinositol 3-kinase complex, class iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class i Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the phosphatidylinositol 3-kinase complex, class i cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class ib Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the phosphatidylinositol 3-kinase complex, class ib cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class ia Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the phosphatidylinositol 3-kinase complex, class ia cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class iii, type ii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class iii, type ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class ib Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class ib cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class ia Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class ia cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class iii, type i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class iii, type i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Class C Vps complex (VPS11, VPS18, STX7) Gene Set

From CORUM Protein Complexes

proteins in the Class C Vps complex (VPS11, VPS18, STX7) protein complex from the CORUM Protein Complexes dataset.

Class C Vps complex (VPS11, VPS18, VPS16) Gene Set

From CORUM Protein Complexes

proteins in the Class C Vps complex (VPS11, VPS18, VPS16) protein complex from the CORUM Protein Complexes dataset.

Class C VPS/HOPS complex Gene Set

From CORUM Protein Complexes

proteins in the Class C VPS/HOPS complex protein complex from the CORUM Protein Complexes dataset.

class Gene Set

From GeneRIF Biological Term Annotations

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

regulation of signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the regulation of signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

dna damage response, signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the dna damage response, signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

negative regulation of dna damage response, signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of dna damage response, signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

negative regulation of signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

positive regulation of signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

regulation of intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the regulation of intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

regulation of intrinsic apoptotic signaling pathway by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the regulation of intrinsic apoptotic signaling pathway by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

negative regulation of intrinsic apoptotic signaling pathway by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of intrinsic apoptotic signaling pathway by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

intrinsic apoptotic signaling pathway by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the intrinsic apoptotic signaling pathway by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

positive regulation of dna damage response, signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of dna damage response, signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

5s class rrna transcription from rna polymerase iii type 1 promoter Gene Set

From GO Biological Process Annotations

genes participating in the 5s class rrna transcription from rna polymerase iii type 1 promoter biological process from the curated GO Biological Process Annotations dataset.

negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

dna damage response, signal transduction by p53 class mediator resulting in cell cycle arrest Gene Set

From GO Biological Process Annotations

genes participating in the dna damage response, signal transduction by p53 class mediator resulting in cell cycle arrest biological process from the curated GO Biological Process Annotations dataset.

intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

positive regulation of intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

negative regulation of intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

regulation of dna damage response, signal transduction by p53 class mediator Gene Set

From GO Biological Process Annotations

genes participating in the regulation of dna damage response, signal transduction by p53 class mediator biological process from the curated GO Biological Process Annotations dataset.

phosphatidylinositol 3-kinase complex, class iii Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class iii cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class i Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class i cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class iii, type i Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class iii, type i cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class iii, type ii Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class iii, type ii cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class ib Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class ib cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class ia Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class ia cellular component from the curated GO Cellular Component Annotations dataset.

impaired ig class switch recombination Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired ig class switch recombination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Malocclusion, Angle Class II Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Malocclusion, Angle Class II phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Malocclusion, Angle Class I Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Malocclusion, Angle Class I phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Class I glutamine amidotransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Class I glutamine amidotransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dihydroorotate dehydrogenase, class 1/ 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dihydroorotate dehydrogenase, class 1/ 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxymethylglutaryl-CoA reductase, class I/II, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA reductase, class I/II, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Class II glutamine amidotransferase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Class II glutamine amidotransferase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

LDLR class B repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the LDLR class B repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, receptor class V, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, receptor class V, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, receptor class III, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, receptor class III, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phenylalanyl-tRNA synthetase, class IIc, alpha subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phenylalanyl-tRNA synthetase, class IIc, alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase, class IV Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase, class IV protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alcohol dehydrogenase family, zinc-type, class-V subfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-V subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alanyl-tRNA synthetase, class IIc, core domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alanyl-tRNA synthetase, class IIc, core domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class II (D/K/N) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class II (D/K/N) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Leucyl-tRNA synthetase, class Ia, archaeal/eukaryotic cytosolic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Leucyl-tRNA synthetase, class Ia, archaeal/eukaryotic cytosolic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

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

From InterPro Predicted Protein Domain Annotations

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

Tyrosine-protein kinase, receptor class II, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, receptor class II, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

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

From InterPro Predicted Protein Domain Annotations

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

Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

POU, class 2, associating factor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the POU, class 2, associating factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Iroquois-class homeodomain protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Iroquois-class homeodomain protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phenylalanyl-tRNA synthetase, class IIc, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phenylalanyl-tRNA synthetase, class IIc, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class II (D/K/N)-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class II (D/K/N)-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proline-tRNA ligase, class IIa Gene Set

From InterPro Predicted Protein Domain Annotations

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

Ribonucleotide reductase, class I , alpha subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonucleotide reductase, class I , alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

N6 adenine-specific DNA methyltransferase, D21 class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the N6 adenine-specific DNA methyltransferase, D21 class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase class V domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase class V domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome c, class IA/ IB Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c, class IA/ IB protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aspartyl/Asparaginyl-tRNA synthetase, class IIb Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aspartyl/Asparaginyl-tRNA synthetase, class IIb protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase, class I/classII Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase, class I/classII protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Carbonic anhydrase, alpha-class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbonic anhydrase, alpha-class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, class-II Gene Set

From InterPro Predicted Protein Domain Annotations

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

Alcohol dehydrogenase family, zinc-type, class-IV subfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-IV subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutathione S-transferase, Mu class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutathione S-transferase, Mu class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sirtuin, class I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sirtuin, class I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase class-III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase class-III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lysine-tRNA ligase, class II Gene Set

From InterPro Predicted Protein Domain Annotations

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

Hydroxymethylglutaryl-CoA reductase, class I/II, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA reductase, class I/II, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Galactose-1-phosphate uridyl transferase, class I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Galactose-1-phosphate uridyl transferase, class I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Histone deacetylase class II, eukaryotic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Histone deacetylase class II, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low-density lipoprotein (LDL) receptor class A, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low-density lipoprotein (LDL) receptor class A, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class Ia Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class Ia protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class Ic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class Ic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

N6 adenine-specific DNA methyltransferase, N12 class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the N6 adenine-specific DNA methyltransferase, N12 class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sirtuin, class II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sirtuin, class II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, CYP3A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, CYP3A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleotidyltransferase, class I, C-terminal-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleotidyltransferase, class I, C-terminal-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenylyl cyclase class-3/4/guanylyl cyclase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenylyl cyclase class-3/4/guanylyl cyclase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase, class IV, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase, class IV, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutathione S-transferase, alpha class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutathione S-transferase, alpha class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Helix-hairpin-helix motif, class 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Helix-hairpin-helix motif, class 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Threonyl/alanyl tRNA synthetase, class II-like, putative editing domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Threonyl/alanyl tRNA synthetase, class II-like, putative editing domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

POU-domain transcription factor, class 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the POU-domain transcription factor, class 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class II (G/ H/ P/ S), conserved domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class II (G/ H/ P/ S), conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

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

From InterPro Predicted Protein Domain Annotations

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

Carbonic anhydrase, alpha-class, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbonic anhydrase, alpha-class, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Threonine-tRNA ligase, class IIa Gene Set

From InterPro Predicted Protein Domain Annotations

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

Lysyl-tRNA synthetase, class II, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

Alanyl-tRNA synthetase, class IIc, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alanyl-tRNA synthetase, class IIc, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminoacyl-tRNA synthetase, class I, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminoacyl-tRNA synthetase, class I, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutathione S-transferase, Pi class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutathione S-transferase, Pi class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sirtuin, class III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sirtuin, class III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Prolyl-tRNA synthetase, class II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Prolyl-tRNA synthetase, class II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Galactose-1-phosphate uridyl transferase, class I His-active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Galactose-1-phosphate uridyl transferase, class I His-active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

POU domain-containing protein, class 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the POU domain-containing protein, class 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fumarate hydratase, class II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fumarate hydratase, class II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low-density lipoprotein (LDL) receptor class A repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low-density lipoprotein (LDL) receptor class A repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alcohol dehydrogenase family, zinc-type, class-II subfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-II subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenylyl cyclase class-3/4/guanylyl cyclase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenylyl cyclase class-3/4/guanylyl cyclase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxymethylglutaryl-CoA reductase, class I/II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA reductase, class I/II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dihydroorotate dehydrogenase, class 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dihydroorotate dehydrogenase, class 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutamyl/glutaminyl-tRNA synthetase, class Ib, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutamyl/glutaminyl-tRNA synthetase, class Ib, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alanine-tRNA ligase, class IIc Gene Set

From InterPro Predicted Protein Domain Annotations

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

Glutathione S-transferase, omega-class Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutathione S-transferase, omega-class protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Class II aldolase/adducin N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Class II aldolase/adducin N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased level of surface class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased level of surface class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective assembly of class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective assembly of class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective assembly of class ii molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective assembly of class ii molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal level of surface class ii molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal level of surface class ii molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased level of surface class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased level of surface class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal level of surface class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal level of surface class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

defective intracellular transport of class i molecules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the defective intracellular transport of class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal class switch recombination Gene Set

From MPO Gene-Phenotype Associations

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

Class I PI3K signaling events mediated by Akt Gene Set

From PID Pathways

proteins participating in the Class I PI3K signaling events mediated by Akt pathway from the PID Pathways dataset.

Class I PI3K signaling events Gene Set

From PID Pathways

proteins participating in the Class I PI3K signaling events pathway from the PID Pathways dataset.

Signaling events mediated by HDAC Class II Gene Set

From PID Pathways

proteins participating in the Signaling events mediated by HDAC Class II pathway from the PID Pathways dataset.

Signaling events mediated by HDAC Class I Gene Set

From PID Pathways

proteins participating in the Signaling events mediated by HDAC Class I pathway from the PID Pathways dataset.

Class IB PI3K non-lipid kinase events Gene Set

From PID Pathways

proteins participating in the Class IB PI3K non-lipid kinase events pathway from the PID Pathways dataset.

Signaling events mediated by HDAC Class III Gene Set

From PID Pathways

proteins participating in the Signaling events mediated by HDAC Class III pathway from the PID Pathways dataset.

Class C/3 (Metabotropic glutamate/pheromone receptors) Gene Set

From Reactome Pathways

proteins participating in the Class C/3 (Metabotropic glutamate/pheromone receptors) pathway from the Reactome Pathways dataset.

Class II GLUTs Gene Set

From Reactome Pathways

proteins participating in the Class II GLUTs pathway from the Reactome Pathways dataset.

Scavenging by Class A Receptors Gene Set

From Reactome Pathways

proteins participating in the Scavenging by Class A Receptors pathway from the Reactome Pathways dataset.

Class A/1 (Rhodopsin-like receptors) Gene Set

From Reactome Pathways

proteins participating in the Class A/1 (Rhodopsin-like receptors) pathway from the Reactome Pathways dataset.

Class B/2 (Secretin family receptors) Gene Set

From Reactome Pathways

proteins participating in the Class B/2 (Secretin family receptors) pathway from the Reactome Pathways dataset.

Scavenging by Class H Receptors Gene Set

From Reactome Pathways

proteins participating in the Scavenging by Class H Receptors pathway from the Reactome Pathways dataset.

Scavenging by Class B Receptors Gene Set

From Reactome Pathways

proteins participating in the Scavenging by Class B Receptors pathway from the Reactome Pathways dataset.

Scavenging by Class F Receptors Gene Set

From Reactome Pathways

proteins participating in the Scavenging by Class F Receptors pathway from the Reactome Pathways dataset.

GPCRs, Class B Secretin-like(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the GPCRs, Class B Secretin-like(Mus musculus) pathway from the Wikipathways Pathways dataset.

GPCRs, Class B Secretin-like(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the GPCRs, Class B Secretin-like(Homo sapiens) pathway from the Wikipathways Pathways dataset.

GPCRs, Class A Rhodopsin-like(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the GPCRs, Class A Rhodopsin-like(Homo sapiens) pathway from the Wikipathways Pathways dataset.

GPCRs, Class C Metabotropic glutamate, pheromone(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the GPCRs, Class C Metabotropic glutamate, pheromone(Mus musculus) pathway from the Wikipathways Pathways dataset.

GPCRs, Class A Rhodopsin-like(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the GPCRs, Class A Rhodopsin-like(Mus musculus) pathway from the Wikipathways Pathways dataset.

GPCRs, Class C Metabotropic glutamate, pheromone(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the GPCRs, Class C Metabotropic glutamate, pheromone(Homo sapiens) pathway from the Wikipathways Pathways dataset.

alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Bifunctional peroxisomal enzyme deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Galactosylceramide beta-galactosidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Galactosylceramide beta-galactosidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Birbeck granule deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Testosterone 17-beta-dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testosterone 17-beta-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Biotinidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Deficiency of butyryl-CoA dehydrogenase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of butyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corticosteroid-binding globulin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corticosteroid-binding globulin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Branched-chain ketoacid dehydrogenase kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Branched-chain ketoacid dehydrogenase kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase E3-binding protein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase E3-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of steroid 11-beta-monooxygenase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of steroid 11-beta-monooxygenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dopamine beta hydroxylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dopamine beta hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Butyrylcholinesterase deficiency, fluoride-resistant, japanese type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Butyrylcholinesterase deficiency, fluoride-resistant, japanese type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase E1-beta deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase E1-beta deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3 beta-Hydroxysteroid dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3 beta-Hydroxysteroid dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mannose-binding protein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mannose-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fructose-biphosphatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Beta-hydroxyisobutyryl-CoA deacylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Beta-hydroxyisobutyryl-CoA deacylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of butyrylcholine esterase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of butyrylcholine esterase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of sialidase AND beta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of beta-ureidopropionase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of beta-ureidopropionase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Beta ketothiolase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Beta ketothiolase deficiency from the curated CTD Gene-Disease Associations dataset.

dopamine beta hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease dopamine beta hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset.

D-BIFUNCTIONAL PROTEIN DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease D-BIFUNCTIONAL PROTEIN DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Biotinidase Deficiency Gene Set

From CTD Gene-Disease Associations

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

Corticosteroid-Binding Globulin Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corticosteroid-Binding Globulin Deficiency from the curated CTD Gene-Disease Associations dataset.

Pyruvate Dehydrogenase E3-Binding Protein Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Dehydrogenase E3-Binding Protein Deficiency from the curated CTD Gene-Disease Associations dataset.

Beta-Ureidopropionase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Beta-Ureidopropionase Deficiency from the curated CTD Gene-Disease Associations dataset.

BISPHOSPHOGLYCERATE MUTASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BISPHOSPHOGLYCERATE MUTASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Beta-Hydroxyisobutyryl CoA Deacylase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Beta-Hydroxyisobutyryl CoA Deacylase Deficiency from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Lysosomal beta-mannosidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lysosomal beta-mannosidase deficiency from the curated CTD Gene-Disease Associations dataset.

Butyrylcholinesterase deficiency Gene Set

From CTD Gene-Disease Associations

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

Split-hand/foot malformation with long bone deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset.

biotinidase deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

beta-ketothiolase deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

fructose-1,6-bisphosphatase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease fructose-1,6-bisphosphatase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

vitamin b12 deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease vitamin b12 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

biotinidase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

beta-ketothiolase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tetrahydrobiopterin (bh4) deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tetrahydrobiopterin (bh4) deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiectasis; immunologic deficiency syndromes Gene Set

From GAD Gene-Disease Associations

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

erythrocyte band 4.2 deficiency. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease erythrocyte band 4.2 deficiency. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone resorption; vitamin k deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; vitamin k deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

biotinidase deficiency Gene Set

From GAD Gene-Disease Associations

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

hyperhomocystinemia; cystathionine beta-synthase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocystinemia; cystathionine beta-synthase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamin b12 deficiency Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease vitamin b12 deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

vitamin b12 deficiency Gene Set

From HPO Gene-Disease Associations

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

Biotinidase Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

pyruvate dehydrogenase e1-beta deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyruvate dehydrogenase e1-beta deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

3-beta-hydroxysteroid dehydrogenase, type ii, deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the 3-beta-hydroxysteroid dehydrogenase, type ii, deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?[birbeck granule deficiency] Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?[birbeck granule deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.

beta-ureidopropionase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the beta-ureidopropionase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

d-bifunctional protein deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the d-bifunctional protein deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

dopamine beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dopamine beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

biotinidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the biotinidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

17-beta-hydroxysteroid dehydrogenase x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the 17-beta-hydroxysteroid dehydrogenase x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

fructose-1,6-bisphosphatase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the fructose-1,6-bisphosphatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocytosis due to bisphosphoglycerate mutase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

platelet plc beta-2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the platelet plc beta-2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

corticosteroid-binding globulin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the corticosteroid-binding globulin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

branched-chain ketoacid dehydrogenase kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the branched-chain ketoacid dehydrogenase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective BTD causes biotidinase deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective BTD causes biotidinase deficiency pathway from the Reactome Pathways dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked ichthyosis with steryl-sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Phosphoglycerate dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Isolated 17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Isolated 17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Endplate acetylcholinesterase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Sepiapterin reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Methionine adenosyltransferase deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase E2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase E2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coenzyme Q10 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of ribose-5-phosphate isomerase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of ribose-5-phosphate isomerase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kininogen deficiency, total Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kininogen deficiency, total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

6-pyruvoyl-tetrahydropterin synthase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 6-pyruvoyl-tetrahydropterin synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

N-terminal acetyltransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the N-terminal acetyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Creatine deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

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

Glucocorticoid deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucocorticoid deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucocorticoid deficiency 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucocorticoid deficiency 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Properdin deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

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

PROPERDIN DEFICIENCY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PROPERDIN DEFICIENCY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement factor d deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement factor d deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methylmalonyl-CoA epimerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methylmalonyl-CoA epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 8 deficiency type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 8 deficiency type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acyl-CoA dehydrogenase family, member 9, deficiency of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acyl-CoA dehydrogenase family, member 9, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of 2-methylbutyryl-CoA dehydrogenase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of 2-methylbutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of isobutyryl-CoA dehydrogenase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of isobutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral folate deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Phosphoserine aminotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Severe combined immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carnitine acylcarnitine translocase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carnitine acylcarnitine translocase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Partial hypoxanthine-guanine phosphoribosyltransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Partial hypoxanthine-guanine phosphoribosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Succinyl-CoA acetoacetate transferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Succinyl-CoA acetoacetate transferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carnitine palmitoyltransferase I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carnitine palmitoyltransferase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HNSHA due to aldolase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-activating factor acetylhydrolase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-activating factor acetylhydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary C1 esterase inhibitor deficiency - dysfunctional factor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipase deficiency combined Gene Set

From ClinVar Gene-Phenotype Associations

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

5-Oxoprolinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 5-Oxoprolinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucocorticoid deficiency with achalasia Gene Set

From ClinVar Gene-Phenotype Associations

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

Proopiomelanocortin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Pituitary hormone deficiency, combined Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pituitary hormone deficiency, combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrinsic factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

21-hydroxylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 21-hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutaryl-CoA oxidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutaryl-CoA oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corticosterone methyloxidase type 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corticosterone methyloxidase type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thiopurine methyltransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

METHYLCOBALAMIN DEFICIENCY, cblG TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLCOBALAMIN DEFICIENCY, cblG TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carnitine palmitoyltransferase II deficiency, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lactate dehydrogenase b deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Combined oxidative phosphorylation deficiency 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of 3-hydroxyacyl-CoA dehydrogenase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of 3-hydroxyacyl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen deficiency, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen deficiency, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant isolated somatotropin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Deficiency of phosphoserine phosphatase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of phosphoserine phosphatase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Isolated growth hormone deficiency type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anhidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3 Methylcrotonyl-CoA carboxylase 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3 Methylcrotonyl-CoA carboxylase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of hyaluronoglucosaminidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of hyaluronoglucosaminidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sulfite oxidase deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sulfite oxidase deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen activator inhibitor type 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen activator inhibitor type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase phosphatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Combined oxidative phosphorylation deficiency 22 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monoamine oxidase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monoamine oxidase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor V deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenine phosphoribosyltransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutamate formiminotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypoglycemia with deficiency of glycogen synthetase in the liver Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoglycemia with deficiency of glycogen synthetase in the liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Follicle-stimulating hormone deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Follicle-stimulating hormone deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ganglioside sialidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

C1q deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Interferon gamma receptor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interferon gamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet glycoprotein IV deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet glycoprotein IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

N-acetylaspartate deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Adenylosuccinate lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Triosephosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Aromatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary factor II deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor xiii, a subunit, deficiency of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor xiii, a subunit, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylcrotonyl CoA carboxylase 2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylcrotonyl CoA carboxylase 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Combined oxidative phosphorylation deficiency 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corticosterone methyloxidase type 2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corticosterone methyloxidase type 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 9 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Holocarboxylase synthetase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

2,4-Dienoyl-CoA reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 2,4-Dienoyl-CoA reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of glycerate kinase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of glycerate kinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia with vitamin E deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of galactokinase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of galactokinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ACTH deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

PROPERDIN DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PROPERDIN DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carboxylesterase 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carboxylesterase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Purine-nucleoside phosphorylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Purine-nucleoside phosphorylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 6 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antithrombin III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Inosine triphosphatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Growth hormone deficiency with pituitary anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth hormone deficiency with pituitary anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase lipoic acid synthetase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocysteinemia due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of pyrroline-5-carboxylate reductase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of pyrroline-5-carboxylate reductase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to ficolin 3 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sarcosine dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

L-ferritin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arginase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Hepatic lipase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Factor X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor IX deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha-fetoprotein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypermethioninemia due to adenosine kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitamin k-dependent clotting factors, combined deficiency of, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of iodide peroxidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of iodide peroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycosylphosphatidylinositol deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Vitamin k-dependent clotting factors, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukocyte adhesion deficiency type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukocyte adhesion deficiency type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital lactase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Caspase-8 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Caspase-8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phosphoglycerate kinase 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phosphoglycerate kinase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anaphylotoxin inactivator deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cytochrome-c oxidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cytochrome-c oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Enterokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Coenzyme Q10 deficiency, primary, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coenzyme Q10 deficiency, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coenzyme Q10 deficiency, primary, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coenzyme Q10 deficiency, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coenzyme Q10 deficiency, primary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coenzyme Q10 deficiency, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coenzyme Q10 deficiency, primary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coenzyme Q10 deficiency, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocyte amp deaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocyte amp deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor VII deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Apolipoprotein a-i deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Apolipoprotein a-i deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glut1 deficiency syndrome 1, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-aminobutyric acid transaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-aminobutyric acid transaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myeloperoxidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Mitochondrial phosphate carrier deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial phosphate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor XI deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Porphobilinogen synthase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Very long chain acyl-CoA dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IRAK4 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IRAK4 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukocyte adhesion deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukocyte adhesion deficiency 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.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortisone reductase deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortisone reductase deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arginine:glycine amidinotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Pyruvate kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Methionine adenosyltransferase deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscle AMP deaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscle AMP deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dihydropyrimidinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Dimethylglycine dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Deficiency of hydroxymethylglutaryl-CoA lyase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of hydroxymethylglutaryl-CoA lyase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase E1-alpha deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase E1-alpha deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Isovaleryl-CoA dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Cd59 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cd59 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ornithine aminotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Sphingolipid activator protein 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sphingolipid activator protein 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of ferroxidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of ferroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lysosomal acid lipase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lysosomal acid lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

UDPglucose-4-epimerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the UDPglucose-4-epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of alpha-mannosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of alpha-mannosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-like growth factor I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-like growth factor I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pituitary hormone deficiency, combined 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pituitary hormone deficiency, combined 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pituitary hormone deficiency, combined 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pituitary hormone deficiency, combined 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pituitary hormone deficiency, combined 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pituitary hormone deficiency, combined 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pituitary hormone deficiency, combined 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pituitary hormone deficiency, combined 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate carboxylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Gluthathione synthetase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Fumarase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Deficiency of transaldolase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of transaldolase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial pyruvate carrier deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial pyruvate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MASP2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MASP2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Argininosuccinate lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Prekallikrein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Chitotriosidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prothrombin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial trifunctional protein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial trifunctional protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GTP cyclohydrolase I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GTP cyclohydrolase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of malonyl-CoA decarboxylase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of malonyl-CoA decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Succinate-semialdehyde dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked agammaglobulinemia with growth hormone deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Okt4 epitope deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Okt4 epitope deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of acetyl-CoA acetyltransferase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of acetyl-CoA acetyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mineralocorticoid deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement 1s deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement 1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dihydropteridine reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Glucose transporter type 1 deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myd88 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myd88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cd8 deficiency, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cd8 deficiency, familial 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.

Acid-labile subunit deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement factor B deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement factor B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, severe, due to leptin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor VIII deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proline dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

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

Factor H deficiency Gene Set