| Name |
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abnormal enzyme/coenzyme activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enzyme/coenzyme activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Enzyme/Coenzyme Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Enzyme/Coenzyme Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enzyme/coenzyme activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal enzyme/ coenzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enzyme/ coenzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enzyme/coenzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enzyme/coenzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Ribosomal S6 modification enzyme RimK/Lysine biosynthesis enzyme LysX Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal S6 modification enzyme RimK/Lysine biosynthesis enzyme LysX protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal angiotensin i-converting enzyme activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal angiotensin i-converting enzyme activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal angiotensin I-converting enzyme activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal angiotensin I-converting enzyme activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
coenzyme transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the coenzyme transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
coenzyme a transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the coenzyme a transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
coenzyme A transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the coenzyme A transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
acyl-coenzyme A diphosphatase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the acyl-coenzyme A diphosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
coenzyme A diphosphatase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the coenzyme A diphosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
coenzyme A transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the coenzyme A transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
abnormal circulating enzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating enzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine enzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine enzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating enzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating enzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine enzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine enzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Abnormal circulating enzyme concentration Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal circulating enzyme concentration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Impdh2 enzyme activity, variation in Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Impdh2 enzyme activity, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
enzyme activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease enzyme activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
undetectable glucose-6-phosphate dehydrogenase enzyme activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease undetectable glucose-6-phosphate dehydrogenase enzyme activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angiotensin-converting enzyme activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angiotensin-converting enzyme activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sulfotransferases enzyme activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sulfotransferases enzyme activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fat10 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the fat10 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
radical sam enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the radical sam enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
sumo activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the sumo activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
atg8 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the atg8 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
enzyme activator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the enzyme activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ubiquitin-like protein conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ubiquitin-like protein conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
sumo conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the sumo conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
urm1 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the urm1 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ufm1 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ufm1 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
enzyme regulator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the enzyme regulator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ubiquitin conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ubiquitin conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
udp-n-acetylglucosamine-lysosomal-enzyme n-acetylglucosaminephosphotransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the udp-n-acetylglucosamine-lysosomal-enzyme n-acetylglucosaminephosphotransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
atg12 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the atg12 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ubiquitin activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ubiquitin activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small protein activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
malic enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the malic enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
isg15 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the isg15 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna lariat debranching enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna lariat debranching enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
1,4-alpha-glucan branching enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the 1,4-alpha-glucan branching enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
glycogen debranching enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the glycogen debranching enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
enzyme inhibitor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the enzyme inhibitor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
nedd8 activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the nedd8 activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Angiotensin-converting enzyme activity Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Angiotensin-converting enzyme activity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
decreased angiotensin i-converting enzyme activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased angiotensin i-converting enzyme activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased angiotensin i-converting enzyme activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased angiotensin i-converting enzyme activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[impdh2 enzyme activity, variation in] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [impdh2 enzyme activity, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Impdh2 Enzyme Activity, Variation In Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impdh2 Enzyme Activity, Variation In in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enzyme Activity Finding Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enzyme Activity Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
ubiquitin conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ubiquitin conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
malic enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the malic enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SUMO conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the SUMO conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
1,4-alpha-glucan branching enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the 1,4-alpha-glucan branching enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
NEDD8 conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the NEDD8 conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
RNA lariat debranching enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the RNA lariat debranching enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
UFM1 conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the UFM1 conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
RNA lariat debranching enzyme activator activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the RNA lariat debranching enzyme activator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
ubiquitin-like protein conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ubiquitin-like protein conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
decreased angiotensin I-converting enzyme activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased angiotensin I-converting enzyme activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased angiotensin I-converting enzyme activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased angiotensin I-converting enzyme activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ubiquitin conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ubiquitin conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
malic enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the malic enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
SUMO conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the SUMO conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
1,4-alpha-glucan branching enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the 1,4-alpha-glucan branching enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
NEDD8 conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the NEDD8 conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Atg12 conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the Atg12 conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Atg8-family conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the Atg8-family conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
RNA lariat debranching enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the RNA lariat debranching enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
UFM1 conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the UFM1 conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
RNA lariat debranching enzyme activator activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the RNA lariat debranching enzyme activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ubiquitin-like protein conjugating enzyme activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ubiquitin-like protein conjugating enzyme activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Enzyme activity finding Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Enzyme activity finding phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Angiotensin-converting enzyme activity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Angiotensin-converting enzyme activity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 6 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
methyl-tetrahydromethanopterin:coenzyme m methyltransferase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the methyl-tetrahydromethanopterin:coenzyme m methyltransferase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Acyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Acyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
succinyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical succinyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
lauroyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical lauroyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
linoleoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical linoleoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
oleoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical oleoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
nafenopin-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical nafenopin-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
coenzyme Q10 Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical coenzyme Q10 from the curated CTD Gene-Chemical Interactions dataset. |
arachidoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical arachidoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
stearoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical stearoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
ciprofibrate-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical ciprofibrate-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
arachidonyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical arachidonyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Palmitoyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Palmitoyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
S-tetradecanoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical S-tetradecanoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Malonyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Malonyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
decanoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical decanoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
glutaryl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical glutaryl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
valproyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical valproyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
hexanoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical hexanoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Acetyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Acetyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COENZYME Q10 DEFICIENCY, PRIMARY, 1 from the curated CTD Gene-Disease Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset. |
coenzyme q10 deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease coenzyme q10 deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Coenzyme A Gene Setinteracting proteins for the Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Octanoyl-Coenzyme A Gene Setinteracting proteins for the Octanoyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Alpha-Fluoro-Carboxymethyldethia Coenzyme a Complex Gene Setinteracting proteins for the Alpha-Fluoro-Carboxymethyldethia Coenzyme a Complex drug from the curated DrugBank Drug Targets dataset. |
Hexanoyl-Coenzyme A Gene Setinteracting proteins for the Hexanoyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Nitromethyldethia Coenzyme A Gene Setinteracting proteins for the Nitromethyldethia Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Coenzyme a Persulfide Gene Setinteracting proteins for the Coenzyme a Persulfide drug from the curated DrugBank Drug Targets dataset. |
Methacrylyl-Coenzyme A Gene Setinteracting proteins for the Methacrylyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
3-Thiaoctanoyl-Coenzyme A Gene Setinteracting proteins for the 3-Thiaoctanoyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
3-Hydroxybutyryl-Coenzyme A Gene Setinteracting proteins for the 3-Hydroxybutyryl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Sinapoyl Coenzyme A Gene Setinteracting proteins for the Sinapoyl Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Trifluoroacetonyl Coenzyme A Gene Setinteracting proteins for the Trifluoroacetonyl Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Feruloyl Coenzyme A Gene Setinteracting proteins for the Feruloyl Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Acetoacetyl-Coenzyme A Gene Setinteracting proteins for the Acetoacetyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coenzyme Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term coenzyme in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
oxidoreduction coenzyme metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the oxidoreduction coenzyme metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of coenzyme metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of coenzyme metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the coenzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Coenzyme Q10 Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coenzyme Q10 metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Coenzyme Q9 Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coenzyme Q9 metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Cervonyl coenzyme A Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Cervonyl coenzyme A metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Coenzyme A Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coenzyme A metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Tetracosapentaenoyl coenzyme A, n-6 Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Tetracosapentaenoyl coenzyme A, n-6 metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Dihomo-gamma-linolenyl coenzyme A Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Dihomo-gamma-linolenyl coenzyme A metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
coenzyme A biosynthesis Gene SetFrom HumanCyc Pathways proteins participating in the coenzyme A biosynthesis pathway from the HumanCyc Pathways dataset. |
Acetyl-coenzyme A transporter 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AmpG-like permease/Acetyl-coenzyme A transporter 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AmpG-like permease/Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-coenzyme A synthase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-coenzyme A synthase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-coenzyme A synthase C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-coenzyme A synthase C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acetyl-coenzyme A carboxyltransferase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-coenzyme A carboxyltransferase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coenzyme A transferase binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coenzyme A transferase binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-coenzyme A synthase, active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-coenzyme A synthase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coenzyme A transferase active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coenzyme A transferase active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acyl-coenzyme A oxidase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-coenzyme A oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acetyl-coenzyme A carboxyltransferase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-coenzyme A carboxyltransferase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
2-amino-3-ketobutyrate coenzyme A ligase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 2-amino-3-ketobutyrate coenzyme A ligase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coenzyme A transferase family I Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coenzyme A transferase family I protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
coenzyme q10 deficiency, primary, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Coenzyme A linked carnitine metabolism Gene SetFrom PANTHER Pathways proteins participating in the Coenzyme A linked carnitine metabolism pathway from the PANTHER Pathways dataset. |
Coenzyme A biosynthesis Gene SetFrom PANTHER Pathways proteins participating in the Coenzyme A biosynthesis pathway from the PANTHER Pathways dataset. |
Coenzyme A biosynthesis Gene Setproteins participating in the Coenzyme A biosynthesis pathway from the Reactome Pathways dataset. |
Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coenzyme Q10 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coenzyme Q10 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coenzyme A Synthase Protein Associated Neurodegeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coenzyme A Synthase Protein Associated Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Succinate-Coenzyme Q Reductase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Succinate-Coenzyme Q Reductase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Methylmalonyl-Coenzyme A Mutase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Methylmalonyl-Coenzyme A Mutase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
coenzyme A catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitochondrial coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitochondrial coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the coenzyme A binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Coenzyme A Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Coenzyme A metabolite from the MW Gene Metabolite Associations dataset. |
Cobamide coenzyme Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Cobamide coenzyme metabolite from the MW Gene Metabolite Associations dataset. |
Coenzyme A biosynthesis Gene Setproteins participating in the Coenzyme A biosynthesis pathway from the Reactome Pathways 2024 dataset. |
coenzyme A catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondrial coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondrial coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
Coenzyme Q10 deficiency disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Coenzyme Q10 deficiency disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Coenzyme Q10 deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Coenzyme Q10 deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Methyl coenzyme M reductase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Methyl coenzyme M reductase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
methyl-tetrahydromethanopterin:coenzyme M methyltransferase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the methyl-tetrahydromethanopterin:coenzyme M methyltransferase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Coenzyme Q10 levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coenzyme Q10 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bifunctional peroxisomal enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiotensin i-converting enzyme, benign serum increase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiotensin i-converting enzyme, benign serum increase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ubiquitin conjugating enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the ubiquitin conjugating enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
sumo activating enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the sumo activating enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the tricarboxylic acid cycle enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
apolipoprotein b mrna editing enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the apolipoprotein b mrna editing enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
ubiquitin conjugating enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ubiquitin conjugating enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
sumo activating enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the sumo activating enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the tricarboxylic acid cycle enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
udp-n-acetylglucosamine-lysosomal-enzyme n-acetylglucosaminephosphotransferase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the udp-n-acetylglucosamine-lysosomal-enzyme n-acetylglucosaminephosphotransferase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
apolipoprotein b mrna editing enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the apolipoprotein b mrna editing enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial tricarboxylic acid cycle enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Raf1-PP2A core enzyme complex (Ppp2r1a, Ppp2ca), untreated Gene Setproteins in the Raf1-PP2A core enzyme complex (Ppp2r1a, Ppp2ca), untreated protein complex from the CORUM Protein Complexes dataset. |
Ksr1-PP2A core enzyme complex (Ppp2r1a, Ppp2ca), untreated Gene Setproteins in the Ksr1-PP2A core enzyme complex (Ppp2r1a, Ppp2ca), untreated protein complex from the CORUM Protein Complexes dataset. |
Enzyme Inhibitors Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Enzyme Inhibitors from the curated CTD Gene-Chemical Interactions dataset. |
Angiotensin-Converting Enzyme Inhibitors Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Angiotensin-Converting Enzyme Inhibitors from the curated CTD Gene-Chemical Interactions dataset. |
Angiotensin-Converting Enzyme Inhibitors Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Angiotensin-Converting Enzyme Inhibitors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
angiotensin-converting enzyme inhibitor-related cough Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angiotensin-converting enzyme inhibitor-related cough in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angiotensin-converting enzyme gene polymorphism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angiotensin-converting enzyme gene polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cough, angiotensin-converting enzyme; inhibitor-related Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cough, angiotensin-converting enzyme; inhibitor-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease and antioxidant enzyme defense Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease and antioxidant enzyme defense in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiproteinuric effect of angiotensin i-converting enzyme inhibitors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiproteinuric effect of angiotensin i-converting enzyme inhibitors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angiotensin-converting enzyme genotype Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angiotensin-converting enzyme genotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angiotensin i converting enzyme and cytokine gene polymorphisms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angiotensin i converting enzyme and cytokine gene polymorphisms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angiotensin-converting enzyme inhibitors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angiotensin-converting enzyme inhibitors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dramatically increased serum enzyme levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dramatically increased serum enzyme levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
enzyme Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term enzyme in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
enzyme-directed rrna 2'-o-methylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the enzyme-directed rrna 2'-o-methylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
recruitment of mrna capping enzyme to rna polymerase ii holoenzyme complex Gene SetFrom GO Biological Process Annotations 2015 genes participating in the recruitment of mrna capping enzyme to rna polymerase ii holoenzyme complex biological process from the curated GO Biological Process Annotations 2015 dataset. |
enzyme active site formation via l-cysteine sulfinic acid Gene SetFrom GO Biological Process Annotations 2015 genes participating in the enzyme active site formation via l-cysteine sulfinic acid biological process from the curated GO Biological Process Annotations 2015 dataset. |
enzyme active site formation via l-cysteine persulfide Gene SetFrom GO Biological Process Annotations 2015 genes participating in the enzyme active site formation via l-cysteine persulfide biological process from the curated GO Biological Process Annotations 2015 dataset. |
enzyme active site formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the enzyme active site formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
enzyme linked receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the enzyme linked receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
ubiquitin conjugating enzyme complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the ubiquitin conjugating enzyme complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
sumo activating enzyme complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the sumo activating enzyme complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
tricarboxylic acid cycle enzyme complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the tricarboxylic acid cycle enzyme complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
apolipoprotein b mrna editing enzyme complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the apolipoprotein b mrna editing enzyme complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
mitochondrial tricarboxylic acid cycle enzyme complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small protein activating enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ubiquitin conjugating enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ubiquitin conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase core enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase core enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ubiquitin-like protein conjugating enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ubiquitin-like protein conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Liver enzyme levels (gamma-glutamyl transferase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Liver enzyme levels (gamma-glutamyl transferase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Liver enzyme levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Liver enzyme levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Liver enzyme levels (alanine transaminase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Liver enzyme levels (alanine transaminase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Liver enzyme levels (aspartate transaminase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Liver enzyme levels (aspartate transaminase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Liver enzyme levels (alkaline phosphatase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Liver enzyme levels (alkaline phosphatase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
mitochondrial malic enzyme reduced Gene SetFrom HPO Gene-Disease Associations genes associated with the mitochondrial malic enzyme reduced phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating enzyme level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating enzyme level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Thiamine pyrophosphate enzyme, C-terminal TPP-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, C-terminal TPP-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-like 1 activating enzyme, catalytic cysteine domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-like 1 activating enzyme, catalytic cysteine domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AMP-binding enzyme C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AMP-binding enzyme C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MiaB-like tRNA modifying enzyme, archaeal-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MiaB-like tRNA modifying enzyme, archaeal-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Scavenger mRNA decapping enzyme DcpS/DCS2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Scavenger mRNA decapping enzyme DcpS/DCS2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Thiolase, acyl-enzyme intermediate active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiolase, acyl-enzyme intermediate active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-activating enzyme repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-activating enzyme repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Malic enzyme, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Malic enzyme, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin/SUMO-activating enzyme ubiquitin-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin/SUMO-activating enzyme ubiquitin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase A1, beta-site APP cleaving enzyme 1, BACE 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase A1, beta-site APP cleaving enzyme 1, BACE 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Atrial natriuretic peptide-converting enzyme corin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Atrial natriuretic peptide-converting enzyme corin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-activating enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-activating enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SUMO-conjugating enzyme Ubc9 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SUMO-conjugating enzyme Ubc9 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
mRNA capping enzyme, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the mRNA capping enzyme, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
mRNA capping enzyme, bifunctional Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the mRNA capping enzyme, bifunctional protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
1,4-alpha-glucan-branching enzyme, GlgB Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 1,4-alpha-glucan-branching enzyme, GlgB protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Malic enzyme, NAD-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Malic enzyme, NAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-activating enzyme e1, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-activating enzyme e1, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Thiamine pyrophosphate enzyme, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycogen debranching enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycogen debranching enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TPP-binding enzyme, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TPP-binding enzyme, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
tRNA-i(6)A37 modification enzyme MiaB Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the tRNA-i(6)A37 modification enzyme MiaB protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycogen debranching enzyme, metazoa Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycogen debranching enzyme, metazoa protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Endothelin-converting enzyme 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Endothelin-converting enzyme 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Endothelin-converting enzyme 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Endothelin-converting enzyme 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-activating enzyme, E1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-activating enzyme, E1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-fold modifier-conjugating enzyme 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-fold modifier-conjugating enzyme 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Endothelin-converting enzyme-like 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Endothelin-converting enzyme-like 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-conjugating enzyme E2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-conjugating enzyme E2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
mRNA capping enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the mRNA capping enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Eukaryotic glycogen debranching enzyme, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Eukaryotic glycogen debranching enzyme, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mandelate racemase/muconate lactonizing enzyme/methylaspartate ammonia-lyase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mandelate racemase/muconate lactonizing enzyme/methylaspartate ammonia-lyase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cobalamin (vitamin B12)-dependent enzyme, catalytic Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-dependent enzyme, catalytic protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-activating enzyme, E1, active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-activating enzyme, E1, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CDK5 and ABL1 enzyme substrate 1/2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CDK5 and ABL1 enzyme substrate 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase A1, beta-site APP cleaving enzyme, BACE Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase A1, beta-site APP cleaving enzyme, BACE protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Prohormone convertase enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Prohormone convertase enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-conjugating enzyme/RWD-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-conjugating enzyme/RWD-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mandelate racemase/muconate lactonizing enzyme, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mandelate racemase/muconate lactonizing enzyme, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-conjugating enzyme E2-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-conjugating enzyme E2-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Thiamine pyrophosphate enzyme, N-terminal TPP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, N-terminal TPP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mandelate racemase/muconate lactonizing enzyme, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mandelate racemase/muconate lactonizing enzyme, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Scavenger mRNA decapping enzyme, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Scavenger mRNA decapping enzyme, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lariat debranching enzyme, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lariat debranching enzyme, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mandelate racemase/muconate lactonizing enzyme, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mandelate racemase/muconate lactonizing enzyme, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA breaking-rejoining enzyme, catalytic core Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA breaking-rejoining enzyme, catalytic core protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-like modifier-activating enzyme Atg7 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-like modifier-activating enzyme Atg7 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin/SUMO-activating enzyme E1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin/SUMO-activating enzyme E1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin activating enzyme, alpha domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin activating enzyme, alpha domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutathione-dependent formaldehyde-activating enzyme/centromere protein V Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutathione-dependent formaldehyde-activating enzyme/centromere protein V protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin-conjugating enzyme, active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin-conjugating enzyme, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase A1, beta-site APP cleaving enzyme 2, BACE 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase A1, beta-site APP cleaving enzyme 2, BACE 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Malic enzyme, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Malic enzyme, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cobalamin (vitamin B12)-dependent enzyme, catalytic subdomain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cobalamin (vitamin B12)-dependent enzyme, catalytic subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tryptophan synthase beta subunit-like PLP-dependent enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tryptophan synthase beta subunit-like PLP-dependent enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cys/Met metabolism, pyridoxal phosphate-dependent enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cys/Met metabolism, pyridoxal phosphate-dependent enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sulfatase-modifying factor enzyme Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sulfatase-modifying factor enzyme protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased lysosomal enzyme secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lysosomal enzyme secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lysosomal enzyme secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lysosomal enzyme secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[angiotensin i-converting enzyme, benign serum increase] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [angiotensin i-converting enzyme, benign serum increase] phenotype from the curated OMIM Gene-Disease Associations dataset. |
enzyme-inhibitors Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term enzyme-inhibitors in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
tissues, cell types and enzyme sources Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue tissues, cell types and enzyme sources from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
tissues, cell types and enzyme sources Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue tissues, cell types and enzyme sources in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
tissues, cell types and enzyme sources Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tissues, cell types and enzyme sources in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Combined Molybdoflavoprotein Enzyme Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Combined Molybdoflavoprotein Enzyme Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fast Acetylator Due To N-Acetyltransferase Enzyme Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fast Acetylator Due To N-Acetyltransferase Enzyme Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Slow Acetylator Due To N-Acetyltransferase Enzyme Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Slow Acetylator Due To N-Acetyltransferase Enzyme Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitochondrial Enzyme Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Enzyme Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Finding Of Liver Enzyme Levels Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finding Of Liver Enzyme Levels in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Measurement Of Liver Enzyme Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Measurement Of Liver Enzyme in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Circulating Enzyme Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Circulating Enzyme Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Angiotensin I-Converting Enzyme, Benign Serum Increase Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Angiotensin I-Converting Enzyme, Benign Serum Increase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enzyme Inhibition Disorder Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enzyme Inhibition Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bifunctional Peroxisomal Enzyme Deficiency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifunctional Peroxisomal Enzyme Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mitochondrial Malic Enzyme Reduced Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mitochondrial Malic Enzyme Reduced in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
enzyme-linked receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the enzyme-linked receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
enzyme-directed rRNA pseudouridine synthesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the enzyme-directed rRNA pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
recruitment of mRNA capping enzyme to RNA polymerase II holoenzyme complex Gene SetFrom GO Biological Process Annotations 2023 genes participating in the recruitment of mRNA capping enzyme to RNA polymerase II holoenzyme complex biological process from the curated GO Biological Process Annotations 2023 dataset. |
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
ubiquitin-like protein conjugating enzyme binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ubiquitin-like protein conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
ubiquitin conjugating enzyme binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ubiquitin conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
small protein activating enzyme binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
RNA polymerase core enzyme binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the RNA polymerase core enzyme binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
decreased lysosomal enzyme secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased lysosomal enzyme secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased lysosomal enzyme secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased lysosomal enzyme secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enzyme-linked receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the enzyme-linked receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
enzyme-directed rRNA pseudouridine synthesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the enzyme-directed rRNA pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
ubiquitin-like protein conjugating enzyme binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ubiquitin-like protein conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ubiquitin conjugating enzyme binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ubiquitin conjugating enzyme binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
small protein activating enzyme binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
RNA polymerase core enzyme binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the RNA polymerase core enzyme binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
tissues, cell types and enzyme sources Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue tissues, cell types and enzyme sources from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
tissues, cell types and enzyme sources Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue tissues, cell types and enzyme sources in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
tissues, cell types and enzyme sources Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue tissues, cell types and enzyme sources in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Tricarboxylic acid cycle enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Apolipoprotein B mRNA editing enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Apolipoprotein B mRNA editing enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
SUMO activating enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the SUMO activating enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Ubiquitin conjugating enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Ubiquitin conjugating enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Apolipoprotein B mRNA editing enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apolipoprotein B mRNA editing enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Tricarboxylic acid cycle enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial tricarboxylic acid cycle enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial tricarboxylic acid cycle enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
SUMO activating enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the SUMO activating enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Ubiquitin conjugating enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Ubiquitin conjugating enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Ubiquitin activating enzyme complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Ubiquitin activating enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Glycogen storage disease due to glycogen branching enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glycogen branching enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined molybdoflavoprotein enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined molybdoflavoprotein enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bifunctional peroxisomal enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cough in response to angiotensin-converting enzyme inhibitor drugs Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cough in response to angiotensin-converting enzyme inhibitor drugs phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cerebrospinal fluid beta-site APP cleaving enzyme levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal fluid beta-site APP cleaving enzyme levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver enzyme levels (alanine transaminase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver enzyme levels (alanine transaminase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver enzyme levels (aspartate transaminase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver enzyme levels (aspartate transaminase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver enzyme levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver enzyme levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver enzyme levels (gamma-glutamyl transferase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver enzyme levels (gamma-glutamyl transferase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver enzyme levels (alkaline phosphatase) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver enzyme levels (alkaline phosphatase) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Angiotensin-converting enzyme inhibitor intolerance Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Angiotensin-converting enzyme inhibitor intolerance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ENZYME INHIBITOR Gene Setinteracting proteins for the ENZYME INHIBITOR drug from theDGIdb Drug Targets 2026 dataset. |
abnormal activity of mitochondrial respiratory chain Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hormone-sensitive lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hormone-sensitive lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glucokinase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glucokinase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal redox activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal redox activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alkaline phosphatase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alkaline phosphatase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renin activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renin activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glyceraldehyde-3-phosphate dehydrogenase (nad+) (phosphorylating) activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glyceraldehyde-3-phosphate dehydrogenase (nad+) (phosphorylating) activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peroxidase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peroxidase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zone of polarizing activity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zone of polarizing activity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glutathione peroxidase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glutathione peroxidase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triglyceride lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triglyceride lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purine-nucleoside phosphorylase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purine-nucleoside phosphorylase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ornithine carbamoyltransferase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ornithine carbamoyltransferase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertical activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertical activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipoprotein lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal catalase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal catalase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Lactate Dehydrogenase Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lactate Dehydrogenase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eeg With Persistent Abnormal Rhythmic Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Persistent Abnormal Rhythmic Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Activity Of Mitochondrial Respiratory Chain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Activity Of Mitochondrial Respiratory Chain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal zone of polarizing activity morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zone of polarizing activity morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal renin activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renin activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal redox activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal redox activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal catalase activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal catalase activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Physical activity (moderate intensity activity duration) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Physical activity (moderate intensity activity duration) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Physical activity (overall physical activity time) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Physical activity (overall physical activity time) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal maternal serum screening Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rod and cone electroretinograms Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal albumin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enchondral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet membrane protein expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondria in muscle tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal placental size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet granules Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lung lobation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal flash visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine phosphate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal drinking behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal fear/anxiety-related behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal humeral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delayed hypersensitivity skin test Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein n-linked glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal echocardiogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum ferritin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal calcification of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal testosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal speech discrimination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal genital system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal trabecular bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metacarpal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal t3/t4 ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal posturing Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal monocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrial arrangement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrial arrangement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating renin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal folds Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pancreas size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine sodium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine sodium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vestibulo-ocular reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral pedicle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tendon morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tendon morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal leukocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spermatogenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine potassium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine potassium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary light reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pyramidal signs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pyramidal signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pigmentation of the oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of incisors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal localization of kidney Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal localization of kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal elasticity of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet volume Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vas deferens morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vas deferens morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle tone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle tone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lower motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ciliary motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metatarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal st segment Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sweat homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal base Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pelvis bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal isoelectric focusing of serum transferrin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hemoglobin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hemoglobin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal concentration of calcium in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal epiphyseal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine cytology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine cytology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal palmar dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal palmar dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal csf lactate level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal csf lactate level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal joint morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral segmentation and fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal oral glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone collagen fibril morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delivery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal middle ear reflexes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cervical curvature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cervical curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal location of ears Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cns myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eating behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eating behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ventriculo-arterial connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ventriculo-arterial connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anterior horn cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal form of the vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine output Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal blistering of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal diaphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal diaphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine citrate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine citrate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of the palpebral fissures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair quantity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anatomic location of the heart Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iron deposition in mitochondria Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating aldosterone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating creatinine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine chloride concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine chloride concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal heart morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal heart morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair laboratory examination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lymphocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pulmonary lymphatics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pattern of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair whorl Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal connection of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage collagen Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical stump bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical stump bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal social behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical gyration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum iron Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sex determination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal prolactin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal prolactin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory epithelium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axonemal organization of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal foot bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neutrophil cell number Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cone-mediated electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cone-mediated electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal basal ganglia mri signal intensity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sensory nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle glycogen content Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal appendicular skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of erythroid precursors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine magnesium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine magnesium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ekg Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ekg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal levels of creatine kinase in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ejaculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ejaculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary electrolyte concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary electrolyte concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal trabeculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical cord blood vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal head movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal head movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facility in opposing the shoulders Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facility in opposing the shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal migration of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the frontal region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the frontal region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary sulfate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary sulfate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spatial orientation of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rib ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sternal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the occiput Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the occiput phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal vascular invasion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal vascular invasion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral action potential amplitude Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reflex, Abnormal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex, Abnormal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spindle assembly abnormal protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle assembly abnormal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male abnormal 21-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abnormal spindle-like microcephaly-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal clitoris morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal clitoris morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung volume Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basilar membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basilar membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural fold elevation formation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory capabilities/reflexes/nociception Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory capabilities/reflexes/nociception phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to anesthetic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal trigeminal ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal trigeminal ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response waveform shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal photoreceptor layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bradykinin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bradykinin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal derived definitive erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paravertebral ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paravertebral ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasal cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasal cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary sex determination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus stratum lacunosum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus stratum lacunosum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ectomesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ectomesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona glomerulosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona glomerulosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum fastigial nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum fastigial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal social/conspecific interaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal social/conspecific interaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tooth morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vomer bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vomer bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endplate potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endplate potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sagittal suture morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sagittal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal semicircular canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal semicircular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal estrous cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive t cell differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive t cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron innervation pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanosome transport Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanosome transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inferior colliculus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inferior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tongue muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tongue muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner nuclear layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to methamphetamine Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to methamphetamine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage derived foam cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage derived foam cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left atrium weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal malleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal malleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala vestibuli morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala vestibuli morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pupillary reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pupillary reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interdigital cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal protein reabsorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal habenula morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal habenula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal laryngeal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal laryngeal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneocyte envelope morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneocyte envelope morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primordial ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland dorsolateral lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular nerve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal melanocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parametrial fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parametrial fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal effector t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal effector t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal roof plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal roof plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone healing Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rhombomere 4 morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rhombomere 4 morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal snout morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal snout morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic disc morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blinking Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blinking phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellar molecular layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal efferent ductules of testis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal efferent ductules of testis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal periocular mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal periocular mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal frontonasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal frontonasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gas homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis papillary layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis papillary layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular replicative senescence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal throat morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal throat morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal loop of henle descending limb morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visual acuity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parturition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala tympani morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala tympani morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external urethral orifice morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external urethral orifice morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chorioallantoic fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell dendrite morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell dendrite morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lens development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lens development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary diverticulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary diverticulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal arteriole morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal arteriole morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outer hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rosenthal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rosenthal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal glomerulus basement membrane thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal superior vagus ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal superior vagus ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanoblast morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanoblast morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal single cell response threshold Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal single cell response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis reticular layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis reticular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body height Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic stalk morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural tube mantle layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal tubule epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intramembranous bone ossification Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal maxillary sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal otic vesicle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node b cell domain morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node b cell domain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal rod cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory summating potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse inhibition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal ganglion cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postnatal growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal miniature inhibitory postsynaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axillary lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axillary lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal costal cartilage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal costal cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thalamus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medulla air spaces Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zigzag hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pons morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pons morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somite size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic acinar cell zymogen granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal meibomian gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum vermis lobule ii morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tubuloglomerular feedback response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b wave amplitude Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine organic cation level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory bulb granule cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lumbar dorsal root ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lumbar dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensorimotor gating Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensorimotor gating phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatic sensory system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatic sensory system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coccygeal vertebrae morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coccygeal vertebrae morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell chemotaxis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell chemotaxis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axon pruning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axon pruning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pinna reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pinna reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glomerular capillary morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glomerular capillary morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hind foot hair pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spinal cord dorsal column morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coronary vessel morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coronary vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mucous neck cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mucous neck cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pre-pro b cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pre-pro b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sertoli cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sertoli cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior primitive streak morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior primitive streak morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endolymphatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endolymphatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary respiratory rate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gestational length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gestational length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thymus medulla morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thymus medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal cone cell inner segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood gas level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal suprachiasmatic nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal suprachiasmatic nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cortical plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cortical plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male germ cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male germ cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal epididymis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal epididymis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal object recognition memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal catecholamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal catecholamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basal lamina morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basal lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal respiration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal respiration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vagina development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vagina development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeletal muscle fiber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeletal muscle fiber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal forced expiratory flow rates Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal forced expiratory flow rates phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal right lung morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lateral nasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lateral nasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sarcolemma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sarcolemma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertebral lamina morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine crypts of lieberkuhn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postimplantation uterine environment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postimplantation uterine environment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spinal cord white matter morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal cone bipolar cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placenta size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cajal body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cajal body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd8-positive, gamma-delta intraepithelial t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd8-positive, gamma-delta intraepithelial t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cornea morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cornea morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteoblast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoblast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auchene hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auchene hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 17 cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 17 cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterine horn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterine horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body temperature Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal atrium myocardium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal atrium myocardium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hyperactivated sperm motility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hyperactivated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endometrium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eosinophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eosinophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating estradiol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anxiety-related response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anxiety-related response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal conditioned emotional response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal conditioned emotional response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neurocranium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neurocranium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucagon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal functional residual capacity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal functional residual capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mesendoderm development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mesendoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pyruvate kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pyruvate kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intraepithelial t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intraepithelial t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune system organ morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune system organ morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal right lung middle lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung middle lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal survival Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal survival phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovulation cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovulation cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct intercalated cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct intercalated cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mucociliary clearance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mucociliary clearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hyoid bone body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hyoid bone body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic beta cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic beta cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal transitional stage t1 b cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal transitional stage t1 b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona fasciculata morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona fasciculata morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary vitreous morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary vitreous morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin absorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulp cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulp cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dosage compensation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dosage compensation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymphatic vessel morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphatic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular extravasation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular extravasation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myeloid leukocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myeloid leukocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interferon secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interferon secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motor nerve collateral sprouting Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motor nerve collateral sprouting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal submandibular gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal submandibular gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skin condition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skin condition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycogen homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycogen homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dosage compensation, by inactivation of x chromosome Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dosage compensation, by inactivation of x chromosome phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse facilitation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse facilitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary vascular resistance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal manchette morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal manchette morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrial proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peripheral nervous system regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peripheral nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thromboxane level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thromboxane level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal type iv hypersensitivity reaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal type iv hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal conotruncal ridge morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal conotruncal ridge morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain white matter morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone structure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adaptive immunity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adaptive immunity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear endolymph ionic homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear endolymph ionic homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen secondary b follicle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen secondary b follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal epicardium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal epicardium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adrenergic neuron morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adrenergic neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal penis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal penis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle telogen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sperm capacitation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sperm capacitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal partial thromboplastin time Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal partial thromboplastin time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating prothrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating prothrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala media morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala media morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |