| Name |
|---|
thick skull base Gene SetFrom HPO Gene-Disease Associations genes associated with the thick skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Thick Skull Base Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
skull base chordoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull base chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
skull base meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull base meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
skull base neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull base neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sclerosis of skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the sclerosis of skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sclerosis of skull base Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive sclerosis of skull base Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cleft in skull base Gene SetFrom HPO Gene-Disease Associations genes associated with the cleft in skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the skull base Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Skull Base Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Skull Base Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Skull Base Chordoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skull Base Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skull Base Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skull Base Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Skull Base Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cleft In Skull Base Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft In Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Sclerosis Of Skull Base Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Sclerosis Of Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skull base meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull base meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Skull base cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull base cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Skull base chordoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull base chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
base-excision repair, AP site formation via deaminated base removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the base-excision repair, AP site formation via deaminated base removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
base-excision repair, AP site formation via deaminated base removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the base-excision repair, AP site formation via deaminated base removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
skull cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
skull Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term skull in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Bone mineral density (paediatric, skull) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Bone mineral density (paediatric, skull) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
cloverleaf skull Gene SetFrom HPO Gene-Disease Associations genes associated with the cloverleaf skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skull ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased skull ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the increased skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skull size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skull size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skull defect Gene SetFrom HPO Gene-Disease Associations genes associated with the skull defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skull asymmetry Gene SetFrom HPO Gene-Disease Associations genes associated with the skull asymmetry phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the skull Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased skull ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the skull Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad skull Gene SetFrom HPO Gene-Disease Associations genes associated with the broad skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Skull Fractures Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Skull Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Calvarial Skull Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Calvarial Skull Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Defect Of Skull And Scalp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of Skull And Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Doughnut Lesions Of Skull, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Doughnut Lesions Of Skull, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Skull Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Skull in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Skull Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Skull in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cloverleaf Skull Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cloverleaf Skull in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Asymmetrical Skull Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Asymmetrical Skull in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Skull Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Skull Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skull cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bone mineral density (paediatric, skull) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (paediatric, skull) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
proteasome regulatory particle, base subcomplex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proteasome regulatory particle, base subcomplex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytosolic trna wobble base thiouridylase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytosolic trna wobble base thiouridylase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Bandrowski's base Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bandrowski's base from the curated CTD Gene-Chemical Interactions dataset. |
base Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term base in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
rrna base methylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the rrna base methylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
trna wobble base modification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the trna wobble base modification biological process from the curated GO Biological Process Annotations 2015 dataset. |
base conversion or substitution editing Gene SetFrom GO Biological Process Annotations 2015 genes participating in the base conversion or substitution editing biological process from the curated GO Biological Process Annotations 2015 dataset. |
base-excision repair, ap site formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the base-excision repair, ap site formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
base-excision repair, gap-filling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the base-excision repair, gap-filling biological process from the curated GO Biological Process Annotations 2015 dataset. |
base-excision repair, dna ligation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the base-excision repair, dna ligation biological process from the curated GO Biological Process Annotations 2015 dataset. |
base-excision repair Gene SetFrom GO Biological Process Annotations 2015 genes participating in the base-excision repair biological process from the curated GO Biological Process Annotations 2015 dataset. |
proteasome regulatory particle, base subcomplex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the proteasome regulatory particle, base subcomplex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
ciliary base Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the ciliary base cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
pyrimidine-specific mismatch base pair dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the pyrimidine-specific mismatch base pair dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidized base lesion dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidized base lesion dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mismatch base pair dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mismatch base pair dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
deaminated base dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the deaminated base dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
site-specific endodeoxyribonuclease activity, specific for altered base Gene SetFrom GO Molecular Function Annotations 2015 genes performing the site-specific endodeoxyribonuclease activity, specific for altered base molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
purine-specific mismatch base pair dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the purine-specific mismatch base pair dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
single base insertion or deletion binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype 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. |
pyramidal skinfold extending from the base to the top of the nails Gene SetFrom HPO Gene-Disease Associations genes associated with the pyramidal skinfold extending from the base to the top of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
wide nasal base Gene SetFrom HPO Gene-Disease Associations genes associated with the wide nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased cranial base ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cranial base ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of acid-base homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Helix-turn-helix, base-excision DNA repair, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Helix-turn-helix, base-excision DNA repair, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Schiff base-forming aldolase, active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Schiff base-forming aldolase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal base-excision repair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal base-excision repair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Base-free sugar-phosphate removal via the single-nucleotide replacement pathway Gene Setproteins participating in the Base-free sugar-phosphate removal via the single-nucleotide replacement pathway pathway from the Reactome Pathways dataset. |
Base-Excision Repair, AP Site Formation Gene Setproteins participating in the Base-Excision Repair, AP Site Formation pathway from the Reactome Pathways dataset. |
Base Excision Repair Gene Setproteins participating in the Base Excision Repair pathway from the Reactome Pathways dataset. |
leaf base Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue leaf base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
shoot base Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue shoot base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Pyramidal Skinfold Extending From The Base To The Top Of The Nails Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Skinfold Extending From The Base To The Top Of The Nails in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carcinoma Of Base Of Tongue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma Of Base Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Wide Nasal Base Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Nasal Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Cranial Base Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cranial Base Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Narrow Nasal Base Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Nasal Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
rRNA base methylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the rRNA base methylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
base-excision repair Gene SetFrom GO Biological Process Annotations 2023 genes participating in the base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset. |
base-excision repair, gap-filling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the base-excision repair, gap-filling biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of base-excision repair Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of base-excision repair Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset. |
telomere maintenance via base-excision repair Gene SetFrom GO Biological Process Annotations 2023 genes participating in the telomere maintenance via base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset. |
base-excision repair, AP site formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the base-excision repair, AP site formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
base-excision repair, DNA ligation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the base-excision repair, DNA ligation biological process from the curated GO Biological Process Annotations 2023 dataset. |
base conversion or substitution editing Gene SetFrom GO Biological Process Annotations 2023 genes participating in the base conversion or substitution editing biological process from the curated GO Biological Process Annotations 2023 dataset. |
tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
tRNA wobble base cytosine methylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tRNA wobble base cytosine methylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
tRNA wobble base modification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tRNA wobble base modification biological process from the curated GO Biological Process Annotations 2023 dataset. |
pyrimidine-specific mismatch base pair DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the pyrimidine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
purine-specific mismatch base pair DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the purine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
site-specific endodeoxyribonuclease activity, specific for altered base Gene SetFrom GO Molecular Function Annotations 2023 genes performing the site-specific endodeoxyribonuclease activity, specific for altered base molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
single base insertion or deletion binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidized base lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized base lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
mismatch base pair DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
deaminated base DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the deaminated base DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal base-excision repair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal base-excision repair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Crypt-base columnar cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Crypt-base columnar cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Crypt base columnar(CBC) cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Crypt base columnar(CBC) cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Base excision repair Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Base excision repair pathway from the WikiPathways Pathways 2024 dataset. |
Base Excision Repair Gene Setproteins participating in the Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
Base-Excision Repair, AP Site Formation Gene Setproteins participating in the Base-Excision Repair, AP Site Formation pathway from the Reactome Pathways 2024 dataset. |
Defective Base Excision Repair Associated with MUTYH Gene Setproteins participating in the Defective Base Excision Repair Associated with MUTYH pathway from the Reactome Pathways 2024 dataset. |
Defective Base Excision Repair Associated with NEIL1 Gene Setproteins participating in the Defective Base Excision Repair Associated with NEIL1 pathway from the Reactome Pathways 2024 dataset. |
Defective Base Excision Repair Associated with NEIL3 Gene Setproteins participating in the Defective Base Excision Repair Associated with NEIL3 pathway from the Reactome Pathways 2024 dataset. |
Defective Base Excision Repair Associated with NTHL1 Gene Setproteins participating in the Defective Base Excision Repair Associated with NTHL1 pathway from the Reactome Pathways 2024 dataset. |
Defective Base Excision Repair Associated with OGG1 Gene Setproteins participating in the Defective Base Excision Repair Associated with OGG1 pathway from the Reactome Pathways 2024 dataset. |
Diseases of Base Excision Repair Gene Setproteins participating in the Diseases of Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
PCNA-Dependent Long Patch Base Excision Repair Gene Setproteins participating in the PCNA-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
POLB-Dependent Long Patch Base Excision Repair Gene Setproteins participating in the POLB-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
rRNA base methylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the rRNA base methylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
base-excision repair Gene SetFrom GO Biological Process Annotations 2025 genes participating in the base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset. |
base-excision repair, gap-filling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the base-excision repair, gap-filling biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of base-excision repair Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of base-excision repair Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset. |
telomere maintenance via base-excision repair Gene SetFrom GO Biological Process Annotations 2025 genes participating in the telomere maintenance via base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset. |
base-excision repair, AP site formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the base-excision repair, AP site formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
base conversion or substitution editing Gene SetFrom GO Biological Process Annotations 2025 genes participating in the base conversion or substitution editing biological process from the curated GO Biological Process Annotations 2025 dataset. |
tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
tRNA wobble base cytosine methylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tRNA wobble base cytosine methylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
tRNA wobble base modification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tRNA wobble base modification biological process from the curated GO Biological Process Annotations 2025 dataset. |
pyrimidine-specific mismatch base pair DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the pyrimidine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
purine-specific mismatch base pair DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the purine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
site-specific endodeoxyribonuclease activity, specific for altered base Gene SetFrom GO Molecular Function Annotations 2025 genes performing the site-specific endodeoxyribonuclease activity, specific for altered base molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
single base insertion or deletion binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidized base lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized base lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
mismatch base pair DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
deaminated base DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the deaminated base DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Leaf base Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Leaf base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Shoot base Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Shoot base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ciliary base Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Ciliary base cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Stereocilium base Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Stereocilium base cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Proteasome regulatory particle, base subcomplex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proteasome regulatory particle, base subcomplex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cytosolic tRNA wobble base thiouridylase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cytosolic tRNA wobble base thiouridylase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Ciliary base Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Ciliary base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mating projection base Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mating projection base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Stereocilium base Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Stereocilium base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cytosolic tRNA wobble base thiouridylase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytosolic tRNA wobble base thiouridylase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Phagocytic cup base Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Phagocytic cup base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Proteasome regulatory particle, base subcomplex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proteasome regulatory particle, base subcomplex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Base excision repair Gene SetFrom KEGG Pathways 2026 proteins participating in the Base excision repair pathway from the KEGG Pathways 2026 dataset. |
SEL120-34A FREE BASE Gene Setinteracting proteins for the SEL120-34A FREE BASE drug from theDGIdb Drug Targets 2026 dataset. |
CEFAMANDOLE NAFATE FREE BASE Gene Setinteracting proteins for the CEFAMANDOLE NAFATE FREE BASE drug from theDGIdb Drug Targets 2026 dataset. |
DS-3801B FREE BASE Gene Setinteracting proteins for the DS-3801B FREE BASE drug from theDGIdb Drug Targets 2026 dataset. |
AV-412 FREE BASE Gene Setinteracting proteins for the AV-412 FREE BASE drug from theDGIdb Drug Targets 2026 dataset. |
striated muscle myosin thick filament Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the striated muscle myosin thick filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
thick Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term thick in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
striated muscle myosin thick filament assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the striated muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric thick ascending limb development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric thick ascending limb development biological process from the curated GO Biological Process Annotations 2015 dataset. |
thick ascending limb development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the thick ascending limb development biological process from the curated GO Biological Process Annotations 2015 dataset. |
skeletal muscle myosin thick filament assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
striated muscle myosin thick filament Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the striated muscle myosin thick filament cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
thick eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the thick eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick anterior alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the thick anterior alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the thick corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick cerebral cortex Gene SetFrom HPO Gene-Disease Associations genes associated with the thick cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick hair Gene SetFrom HPO Gene-Disease Associations genes associated with the thick hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick upper lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the thick upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the thick nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick nail Gene SetFrom HPO Gene-Disease Associations genes associated with the thick nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick vermilion border Gene SetFrom HPO Gene-Disease Associations genes associated with the thick vermilion border phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick lower lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the thick lower lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick mitral valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick mitral valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick epidermis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick epidermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick myocardium Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick myocardium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick retinal ganglion layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick lung-associated mesenchyme Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick lung-associated mesenchyme phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick epidermis stratum spinosum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick epidermis stratum spinosum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick epidermis stratum granulosum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick epidermis stratum granulosum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick embryonic epiblast Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick embryonic epiblast phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick apical ectodermal ridge Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick apical ectodermal ridge phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick heart valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick heart valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick hair follicle outer rooth sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick dermal layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick dermal layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick aortic valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick epidermis stratum basale Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick epidermis stratum basale phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick mitral valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick mitral valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal loop of henle ascending limb thick segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal loop of henle ascending limb thick segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick pulmonary interalveolar septum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick pulmonary interalveolar septum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick pulmonary valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick pulmonary valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick eyelids Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick eyelids phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick hippocampus stratum oriens Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick hippocampus stratum oriens phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick ears Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick ears phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick tricuspid valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick tricuspid valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick placenta labyrinth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick placenta labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick hypodermis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick hypodermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick ventricular wall Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick ventricular wall phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick epidermis suprabasal layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick epidermis suprabasal layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick sperm flagellum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick sperm flagellum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick hippocampus stratum radiatum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick hippocampus stratum radiatum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick pulmonary valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick pulmonary valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick skin Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick tail Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick diaphragm muscle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick diaphragm muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick interventricular septum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick interventricular septum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Thick Cerebral Cortex Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thick Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thick Lower Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Lower Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Eyebrow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Nasal Alae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Nasal Alae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Skin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Upper Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Vermilion Border Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Vermilion Border in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Anterior Alveolar Ridges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Anterior Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Rib Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Rib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Corpus Callosum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Nasal Septum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Nasal Septum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Ear Helices Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Ear Helices in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
skeletal muscle myosin thick filament assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric thick ascending limb development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric thick ascending limb development biological process from the curated GO Biological Process Annotations 2023 dataset. |
striated muscle myosin thick filament assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the striated muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
thick ascending limb development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the thick ascending limb development biological process from the curated GO Biological Process Annotations 2023 dataset. |
thick lung-associated mesenchyme Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick lung-associated mesenchyme phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick myocardium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick myocardium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick ventricular wall Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick ventricular wall phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick aortic valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick mitral valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick mitral valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick skin Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick skin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick tail Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick tail phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick dermal layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick dermal layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick epidermis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick epidermis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick neurocranium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick neurocranium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick pulmonary interalveolar septum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick pulmonary interalveolar septum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick pulmonary valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick pulmonary valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick embryonic epiblast Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick embryonic epiblast phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick interventricular septum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick interventricular septum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal loop of Henle ascending limb thick segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal loop of Henle ascending limb thick segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick apical ectodermal ridge Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick apical ectodermal ridge phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick hypodermis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick hypodermis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick mitral valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick mitral valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick tricuspid valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick tricuspid valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick epidermis stratum granulosum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick epidermis stratum granulosum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick diaphragm muscle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick diaphragm muscle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick pulmonary valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick pulmonary valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick eyelids Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick eyelids phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick ears Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick ears phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick hair follicle outer root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick hair follicle outer root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick retina ganglion layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick retina ganglion layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick epidermis stratum basale Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick epidermis stratum basale phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick epidermis stratum spinosum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick epidermis stratum spinosum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick heart valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick heart valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick sperm flagellum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick sperm flagellum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick nasal septum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick nasal septum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick placenta labyrinth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick placenta labyrinth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick retina inner plexiform layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick epidermis suprabasal layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick epidermis suprabasal layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick tricuspid valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick tricuspid valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick skin Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the thick skin phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
thick ventricular wall Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the thick ventricular wall phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Kidney - L1 - Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Cortical Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Medullary Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Medullary Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Medullary Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Medullary Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Thick Ascending Limb cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Thick Ascending Limb cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Thick Ascending Limb cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Thick Ascending Limb cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Loop of Henle thick ascending limb cell (TAL)_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Loop of Henle thick ascending limb cell (TAL)_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Thick ascending loop of Henle(TALH) cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Thick ascending loop of Henle(TALH) cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical thick ascending limb cell (CTAL cell)_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical thick ascending limb cell (CTAL cell)_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medullary thick ascending limb limb cell (MTAL limb cell)_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medullary thick ascending limb limb cell (MTAL limb cell)_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Kidney_CT1_Medullary Thick Ascending Limb Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Medullary Thick Ascending Limb Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Cortical Thick Ascending Limb Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Cortical Thick Ascending Limb Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Cortical Thick Ascending Limb Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Cortical Thick Ascending Limb Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Medullary Thick Ascending Limb Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Medullary Thick Ascending Limb Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
skeletal muscle myosin thick filament assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric thick ascending limb development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric thick ascending limb development biological process from the curated GO Biological Process Annotations 2025 dataset. |
striated muscle myosin thick filament assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the striated muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
thick ascending limb development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the thick ascending limb development biological process from the curated GO Biological Process Annotations 2025 dataset. |
Striated muscle myosin thick filament Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Striated muscle myosin thick filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Striated muscle myosin thick filament Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Striated muscle myosin thick filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Thick vs thin eyebrows Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thick vs thin eyebrows phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |