| Name |
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viii Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term viii in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Pyramus (VIII) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pyramus (VIII) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Pyramus (VIII), molecular layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pyramus (VIII), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Pyramus (VIII), granular layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pyramus (VIII), granular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V and factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
collagen type viii trimer Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the collagen type viii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
collagen type viii trimer Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen type viii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
myosin viii complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the myosin viii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
bisindolylmaleimide VIII Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bisindolylmaleimide VIII from the curated CTD Gene-Chemical Interactions dataset. |
Ehlers-Danlos Syndrome, Type VIII Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VIII from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset. |
Osteogenesis imperfecta, type VIII Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Osteogenesis imperfecta, type VIII from the curated CTD Gene-Disease Associations dataset. |
glycogen storage disease viii Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen storage disease viii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
factor viii deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factor viii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
factor viii and factor ix genes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor viii and factor ix genes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high plasma factor viii: c levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high plasma factor viii: c levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
collagen type viii trimer Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the collagen type viii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
factor viii deficiency Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease factor viii deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
reduced factor viii activity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the reduced factor viii activity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
reduced factor viii activity Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced factor viii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Endonuclease VIII-like 1, DNA binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Endonuclease VIII-like 1, DNA binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Annexin, type VIII Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Annexin, type VIII protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase subunit VIII/photosystem I reaction centre subunit IX Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit VIII/photosystem I reaction centre subunit IX protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal cerebellum vermis lobule viii morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule viii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear viii nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear viii nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating factor viii level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating factor viii level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating factor viii level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating factor viii level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cerebellum vermis lobule viii Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cerebellum vermis lobule viii phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
maturity-onset diabetes of the young, type viii Gene SetFrom OMIM Gene-Disease Associations genes associated with the maturity-onset diabetes of the young, type viii phenotype from the curated OMIM Gene-Disease Associations dataset. |
osteogenesis imperfecta, type viii Gene SetFrom OMIM Gene-Disease Associations genes associated with the osteogenesis imperfecta, type viii phenotype from the curated OMIM Gene-Disease Associations dataset. |
ehlers-danlos syndrome, type viii Gene SetFrom OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome, type viii phenotype from the curated OMIM Gene-Disease Associations dataset. |
factor v and factor viii, combined deficiency of Gene SetFrom OMIM Gene-Disease Associations genes associated with the factor v and factor viii, combined deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset. |
combined factor v and viii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the combined factor v and viii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
Severe Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mild Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mild Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Haemophilia A With Anti Factor Viii Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Haemophilia A With Anti Factor Viii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor Viii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor Viii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor V And Factor Viii, Combined Deficiency Of Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor V And Factor Viii, Combined Deficiency Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Moderate Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Moderate Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor Viii Inactivation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor Viii Inactivation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor Viii Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Factor Viii Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Factor Viii (East Hartford) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Factor Viii (East Hartford) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Factor Viii (Okayama) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Factor Viii (Okayama) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Factor Viii Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Factor Viii Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
collagen type VIII trimer Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the collagen type VIII trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal cochlear VIII nucleus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear VIII nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cerebellum vermis lobule VIII Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellum vermis lobule VIII phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating factor VIII level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating factor VIII level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear VIII nucleus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear VIII nucleus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating factor VIII level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating factor VIII level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cerebellum vermis lobule VIII morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule VIII morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Defective factor VIII causes hemophilia A Gene Setproteins participating in the Defective factor VIII causes hemophilia A pathway from the Reactome Pathways 2024 dataset. |
collagen type VIII trimer Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the collagen type VIII trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Factor VIII deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Factor VIII deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Glycogen storage disease VIII Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycogen storage disease VIII in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Collagen type VIII trimer Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Collagen type VIII trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Myosin VIII complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Myosin VIII complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
FACTOR VIII Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the FACTOR VIII phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Factor VIII levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Factor VIII levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
AKT INHIBITOR VIII Gene Setinteracting proteins for the AKT INHIBITOR VIII drug from theDGIdb Drug Targets 2026 dataset. |
JH-VIII-49 Gene Setinteracting proteins for the JH-VIII-49 drug from theDGIdb Drug Targets 2026 dataset. |
JNK INHIBITOR VIII Gene Setinteracting proteins for the JNK INHIBITOR VIII drug from theDGIdb Drug Targets 2026 dataset. |
FACTOR VIII Gene Setinteracting proteins for the FACTOR VIII drug from theDGIdb Drug Targets 2026 dataset. |