| Name |
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apolipoprotein e mutation [apolipoprotein e (delta149 leu)] Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein e mutation [apolipoprotein e (delta149 leu)] in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Leu-Ser-Lys-Leu peptide Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Leu-Ser-Lys-Leu peptide from the curated CTD Gene-Chemical Interactions dataset. |
bombesin (6-14), Tpi(6)-Leu(13)-psi(CH2NH)-Leu(14)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bombesin (6-14), Tpi(6)-Leu(13)-psi(CH2NH)-Leu(14)- from the curated CTD Gene-Chemical Interactions dataset. |
CBZ-LEU-LEU-TYR-CH2F Gene Setinteracting proteins for the CBZ-LEU-LEU-TYR-CH2F drug from the curated DrugBank Drug Targets dataset. |
Met-Met-Trp-Leu-Leu Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the Met-Met-Trp-Leu-Leu ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[D-Tpi6 Leu13 ψ(CH2NH)-Leu14]bombesin-(6-14) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [D-Tpi6 Leu13 ψ(CH2NH)-Leu14]bombesin-(6-14) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Met-Trp-Leu-Leu Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Met-Trp-Leu-Leu ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
FMET-MET-TRP-LEU-LEU Gene Setinteracting proteins for the FMET-MET-TRP-LEU-LEU drug from theDGIdb Drug Targets 2026 dataset. |
MET-MET-TRP-LEU-LEU Gene Setinteracting proteins for the MET-MET-TRP-LEU-LEU drug from theDGIdb Drug Targets 2026 dataset. |
Ratio of apolipoprotein A1 to apolipoprotein B Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ratio of apolipoprotein A1 to apolipoprotein B phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LHRH, Leu(6)-des-Et-GlyNH2(10)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical LHRH, Leu(6)-des-Et-GlyNH2(10)- from the curated CTD Gene-Chemical Interactions dataset. |
bradykinin, Lys-Leu(8)-desArg(9)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bradykinin, Lys-Leu(8)-desArg(9)- from the curated CTD Gene-Chemical Interactions dataset. |
enkephalin-Leu, Ala(2)-melphalan methyl ester- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical enkephalin-Leu, Ala(2)-melphalan methyl ester- from the curated CTD Gene-Chemical Interactions dataset. |
Phe-Leu boronic acid Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Phe-Leu boronic acid from the curated CTD Gene-Chemical Interactions dataset. |
neuropeptide Y, Leu(31)-Pro(34)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical neuropeptide Y, Leu(31)-Pro(34)- from the curated CTD Gene-Chemical Interactions dataset. |
vasoactive intestinal peptide, 4-chloro-Phe(6)-Leu(17)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical vasoactive intestinal peptide, 4-chloro-Phe(6)-Leu(17)- from the curated CTD Gene-Chemical Interactions dataset. |
enkephalin, Ser(2), Leu(5), Thr(6)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical enkephalin, Ser(2), Leu(5), Thr(6)- from the curated CTD Gene-Chemical Interactions dataset. |
bradykinin, Leu(8)-des-Arg(9)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bradykinin, Leu(8)-des-Arg(9)- from the curated CTD Gene-Chemical Interactions dataset. |
cyclo(Trp-Asp-Pro-Val-Leu) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical cyclo(Trp-Asp-Pro-Val-Leu) from the curated CTD Gene-Chemical Interactions dataset. |
enkephalin-Leu, Ala(2)-Arg(6)- Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical enkephalin-Leu, Ala(2)-Arg(6)- from the curated CTD Gene-Chemical Interactions dataset. |
cyclo(Gln-Trp-Phe-Gly-Leu-Met) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical cyclo(Gln-Trp-Phe-Gly-Leu-Met) from the curated CTD Gene-Chemical Interactions dataset. |
leu Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term leu in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
fMet-Ile-Val-Ile-Leu Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Ile-Val-Ile-Leu ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Leu-Phe-Glu Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Leu-Phe-Glu ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu9 des-Arg10]kallidin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu9 des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
des-His1-[Leu4-Glu9]glucagon-NH2 Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the des-His1-[Leu4-Glu9]glucagon-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Leu-Phe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Leu-Phe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu14 ψ 13-14)]bombesin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu14 ψ 13-14)]bombesin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[Leu4]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[Leu4]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[D-Arg1 D-Trp7 9 Leu11]substance P Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [D-Arg1 D-Trp7 9 Leu11]substance P ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu31 Pro34]NPY Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu31 Pro34]NPY ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu31 Pro34]NPY (pig) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu31 Pro34]NPY (pig) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu31 Pro34]PYY (pig) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu31 Pro34]PYY (pig) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[19Lys 26Leu]-galparan Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [19Lys 26Leu]-galparan ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu31 Pro34]PYY (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu31 Pro34]PYY (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Met-Tyr-Ala-Leu-Phe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Met-Tyr-Ala-Leu-Phe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Lys15 Arg16 Leu27]VIP-(1–7)/GRF-(8–27)-NH2 Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Lys15 Arg16 Leu27]VIP-(1–7)/GRF-(8–27)-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu13]motilin (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu8 des-Arg9]bradykinin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu8 des-Arg9]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Leu8]-phyllolitorin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Leu8]-phyllolitorin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I][Leu31 Pro34]NPY Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I][Leu31 Pro34]NPY ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
i-Boc-Met-Leu-Phe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the i-Boc-Met-Leu-Phe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
t-Boc-Met-Leu-Phe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the t-Boc-Met-Leu-Phe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Ile-Val-Thr-Leu-Phe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Ile-Val-Thr-Leu-Phe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[Leu4]LVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[Leu4]LVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phe3 Leu13]motilin (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phe3 Leu13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Lys5 Me-Leu9 Nle10]NKA-(4-10) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Lys5 Me-Leu9 Nle10]NKA-(4-10) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[Leu4 Dap8]VP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[Leu4 Dap8]VP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Leu-Phe-Ile-Ile-Lys-FITC Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Leu-Phe-Ile-Ile-Lys-FITC ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
Z-Arg-Leu-Val-Agly-Ile-Val-OMe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the Z-Arg-Leu-Val-Agly-Ile-Val-OMe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[D-Arg1 D-Phe5 D-Trp7 9 Leu11]substance P Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [D-Arg1 D-Phe5 D-Trp7 9 Leu11]substance P ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Ala11 D-Leu15]orexin-B Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Ala11 D-Leu15]orexin-B ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
Ac-Lys-[MeAla6 Leu8 des-Arg9]bradykinin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the Ac-Lys-[MeAla6 Leu8 des-Arg9]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
fMet-Ile-Phe-Leu Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the fMet-Ile-Phe-Leu ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Ac-D-2Nal1 D4CPA2 D-3Pal3 6 Leu8 D-Ala10]GnRH-II Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Ac-D-2Nal1 D4CPA2 D-3Pal3 6 Leu8 D-Ala10]GnRH-II ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[3H]Lys-[Leu8][des-Arg9]BK Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [3H]Lys-[Leu8][des-Arg9]BK ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[3H]fMet-Leu-Phe Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [3H]fMet-Leu-Phe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
HMB-Val-Ser-Leu-VE Gene SetFrom DeepCoverMOA Drug Mechanisms of Action proteins with high or low expression in HMB-Val-Ser-Leu-VE relative to other proteins from the DeepCoverMOA Drug Mechanisms of Action dataset. |
Z-ARG-LEU-VAL-AGLY-ILE-VAL-OME Gene Setinteracting proteins for the Z-ARG-LEU-VAL-AGLY-ILE-VAL-OME drug from theDGIdb Drug Targets 2026 dataset. |
FMET-ILE-PHE-LEU Gene Setinteracting proteins for the FMET-ILE-PHE-LEU drug from theDGIdb Drug Targets 2026 dataset. |
FMET-ILE-VAL-ILE-LEU Gene Setinteracting proteins for the FMET-ILE-VAL-ILE-LEU drug from theDGIdb Drug Targets 2026 dataset. |
FMET-ILE-VAL-THR-LEU-PHE Gene Setinteracting proteins for the FMET-ILE-VAL-THR-LEU-PHE drug from theDGIdb Drug Targets 2026 dataset. |
FMET-LEU-PHE Gene Setinteracting proteins for the FMET-LEU-PHE drug from theDGIdb Drug Targets 2026 dataset. |
FMET-LEU-PHE-ILE-ILE Gene Setinteracting proteins for the FMET-LEU-PHE-ILE-ILE drug from theDGIdb Drug Targets 2026 dataset. |
FMET-MET-TYR-ALA-LEU-PHE Gene Setinteracting proteins for the FMET-MET-TYR-ALA-LEU-PHE drug from theDGIdb Drug Targets 2026 dataset. |
I-BOC-MET-LEU-PHE Gene Setinteracting proteins for the I-BOC-MET-LEU-PHE drug from theDGIdb Drug Targets 2026 dataset. |
T-BOC-MET-LEU-PHE Gene Setinteracting proteins for the T-BOC-MET-LEU-PHE drug from theDGIdb Drug Targets 2026 dataset. |
[3H]FMET-LEU-PHE Gene Setinteracting proteins for the [3H]FMET-LEU-PHE drug from theDGIdb Drug Targets 2026 dataset. |
[LEU]ENKEPHALIN Gene Setinteracting proteins for the [LEU]ENKEPHALIN drug from theDGIdb Drug Targets 2026 dataset. |
[3H]LEU-N/OFQ Gene Setinteracting proteins for the [3H]LEU-N/OFQ drug from theDGIdb Drug Targets 2026 dataset. |
MULTI-LEU (ML)-PEPTIDE Gene Setinteracting proteins for the MULTI-LEU (ML)-PEPTIDE drug from theDGIdb Drug Targets 2026 dataset. |
g130v mutation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease g130v mutation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high frequency of factor v leiden mutation. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high frequency of factor v leiden mutation. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cys39arg mutation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cys39arg mutation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
germline brca1 mutation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease germline brca1 mutation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cftr mutation spectrum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cftr mutation spectrum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heteroallelic ceruloplasmin gene mutation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heteroallelic ceruloplasmin gene mutation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
LHX1_NULL MUTATION - Ablation_GDS1748_748_mouse_Embryonic kidneys (from day E14.5) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LHX1_NULL MUTATION - Ablation_GDS1748_748_mouse_Embryonic kidneys (from day E14.5) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
LHX1_NULL MUTATION - Ablation_GDS1748_749_mouse_Embryonic kidneys (from day E18.5) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LHX1_NULL MUTATION - Ablation_GDS1748_749_mouse_Embryonic kidneys (from day E18.5) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
somatic diversification of immune receptors via somatic mutation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the somatic diversification of immune receptors via somatic mutation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Ovarian cancer in BRCA1 mutation carriers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Ovarian cancer in BRCA1 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Breast Cancer in BRCA1 mutation carriers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Breast Cancer in BRCA1 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Breast cancer in BRCA2 mutation carriers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Breast cancer in BRCA2 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
somatic mutation Gene SetFrom HPO Gene-Disease Associations genes associated with the somatic mutation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
autosomal dominant somatic cell mutation Gene SetFrom HPO Gene-Disease Associations genes associated with the autosomal dominant somatic cell mutation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mutation-missense Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term mutation-missense in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Ldlr Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ldlr Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor V Leiden Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor V Leiden Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Density Lipoprotein Receptor Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Density Lipoprotein Receptor Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prothrombin G20210A Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prothrombin G20210A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitochondrial Dna Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Dna Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Desmoid Tumor Caused By Somatic Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Desmoid Tumor Caused By Somatic Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Methylenetetrahydrofolate Reductase Gene Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Methylenetetrahydrofolate Reductase Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility With Teratozoospermia Due To Single Gene Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Teratozoospermia Due To Single Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polg Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polg Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Midline Glioma, Point Mutation K27M In Histone H3 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Midline Glioma, Point Mutation K27M In Histone H3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heterozygous Factor V Leiden Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heterozygous Factor V Leiden Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Homozygous Factor V Leiden Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Homozygous Factor V Leiden Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor Ii Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor Ii Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heterozygous Prothrombin G20210A Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heterozygous Prothrombin G20210A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mutation-Negative Lynch Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mutation-Negative Lynch Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Density Lipoprotein Receptor Adaptor Protein 1 Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Density Lipoprotein Receptor Adaptor Protein 1 Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biallelic Rpe65 Mutation Associated Retinal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biallelic Rpe65 Mutation Associated Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Somatic Mutation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Somatic Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prothrombin Gene Mutation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prothrombin Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Caused By Mutation In The Tbc1 Domain Family, Member 24 Gene (Tbc1D24, 613577.0004) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Tbc1 Domain Family, Member 24 Gene (Tbc1D24, 613577.0004) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Caused By Mutation In The Transportin 3 Gene (Tnpo3, 610032.0001) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Transportin 3 Gene (Tnpo3, 610032.0001) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Effects of MFN2 mutation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Effects of MFN2 mutation pathway from the WikiPathways Pathways 2024 dataset. |
Severe congenital encephalopathy due to MECP2 mutation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital encephalopathy due to MECP2 mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital muscular dystrophy due to LMNA mutation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy due to LMNA mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital muscular dystrophy due to LMNA mutation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to LMNA mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital encephalopathy due to MECP2 mutation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital encephalopathy due to MECP2 mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acute myeloid leukemia with biallelic mutation of CEBPA Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute myeloid leukemia with biallelic mutation of CEBPA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lissencephaly due to TUBA1A mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to TUBA1A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital bilateral aplasia of vas deferens from CFTR mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bilateral aplasia of vas deferens from CFTR mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alagille syndrome due to a JAG1 point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alagille syndrome due to a JAG1 point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lissencephaly due to LIS1 mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to LIS1 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lissencephaly due to doublecortin gene mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to doublecortin gene mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital muscular dystrophy due to LMNA mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to LMNA mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary familial polycythemia due to EPO receptor mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary familial polycythemia due to EPO receptor mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Desmoid tumor caused by somatic mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Desmoid tumor caused by somatic mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Caused by mutation in the TBC1 domain family Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Caused by mutation in the TBC1 domain family phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to SLC37A4 mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to SLC37A4 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alagille syndrome due to a NOTCH2 point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alagille syndrome due to a NOTCH2 point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Syndrome of entercolitis and autoinflmmation caused by mutation of NLRC4 Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndrome of entercolitis and autoinflmmation caused by mutation of NLRC4 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neurofibromatosis due to NF1 mutation or intragenic deletion Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurofibromatosis due to NF1 mutation or intragenic deletion phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DeSanto-Shinawi syndrome due to WAC point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DeSanto-Shinawi syndrome due to WAC point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Beckwith-Wiedemann syndrome due to CDKN1C mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Beckwith-Wiedemann syndrome due to CDKN1C mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Caused by mutation in the tafazzin gene Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Caused by mutation in the tafazzin gene phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SIN3A-related intellectual disability syndrome due to a point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SIN3A-related intellectual disability syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
POLE Exonuclease Domain Mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the POLE Exonuclease Domain Mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Kleefstra syndrome due to a point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Kleefstra syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hao-Fountain syndrome due to USP7 mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hao-Fountain syndrome due to USP7 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adult diffuse glioma (IDH mutation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adult diffuse glioma (IDH mutation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Adult diffuse glioma (IDH mutation, 1p/19q non-codeleted) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adult diffuse glioma (IDH mutation, 1p/19q non-codeleted) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Adult diffuse glioma (TERT mutation only) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adult diffuse glioma (TERT mutation only) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
EGFR mutation-positive lung adenocarcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the EGFR mutation-positive lung adenocarcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Frontotemporal dementia with GRN mutation (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Frontotemporal dementia with GRN mutation (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Frontotemporal dementia with GRN mutation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Frontotemporal dementia with GRN mutation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parkinson's disease in GBA mutation carriers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease in GBA mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in BRCA2 mutation carriers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in BRCA2 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hereditary hemochromatosis-related traits (HFE mutation homozygotes) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hereditary hemochromatosis-related traits (HFE mutation homozygotes) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
BRCA1 mutation in breast cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the BRCA1 mutation in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Amyotrophic lateral sclerosis (C9orf72 mutation interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Amyotrophic lateral sclerosis (C9orf72 mutation interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Amyotrophic lateral sclerosis in C9orf72 mutation negative individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Amyotrophic lateral sclerosis in C9orf72 mutation negative individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Amyotrophic lateral sclerosis in C9orf72 mutation positive individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Amyotrophic lateral sclerosis in C9orf72 mutation positive individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast Cancer in BRCA1 mutation carriers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast Cancer in BRCA1 mutation carriers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PMC7305081-10120_2020_1045_MOESM1_ESM.xlsx-Tab2-Mutation-MAF_MAF Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC7305081-10120_2020_1045_MOESM1_ESM.xlsx-Tab2-Mutation-MAF_MAF transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
Apolipoprotein a-i deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Apolipoprotein a-i deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 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. |
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. |
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset. |
Apolipoprotein A-I Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Apolipoprotein A-I in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
familial defective apolipoprotein b100. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma high density lipoprotein cholesterol and apolipoprotein ai Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma high density lipoprotein cholesterol and apolipoprotein ai in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum lipoprotein lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum lipoprotein lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial defective apolipoprotein b Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apolipoprotein[a] null allele Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein[a] null allele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced expression of the apolipoprotein a-i gene and resolution of disputed paternity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced expression of the apolipoprotein a-i gene and resolution of disputed paternity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apolipoprotein a-i levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein a-i levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial defective apolipoprotein b-100 in a chinese man Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apolipoprotein a-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein a-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma total and ldl-apolipoprotein b Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma total and ldl-apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
elevated serum apolipoprotein ai levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease elevated serum apolipoprotein ai levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
altered brain levels of apolipoprotein e Gene SetFrom GAD Gene-Disease Associations genes associated with the disease altered brain levels of apolipoprotein e in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apolipoprotein b gene polymorphism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein b gene polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased production rate of apolipoprotein a-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased production rate of apolipoprotein a-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apolipoprotein c3 haplotype specified by the ssti polymorphism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein c3 haplotype specified by the ssti polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apolipoprotein Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term apolipoprotein in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of apolipoprotein binding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of apolipoprotein binding biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of apolipoprotein binding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of apolipoprotein binding biological process from the curated GO Biological Process Annotations 2015 dataset. |
apolipoprotein a-i-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the apolipoprotein a-i-mediated signaling pathway biological process from the curated GO Biological Process 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. |
apolipoprotein a-i receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the apolipoprotein a-i receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
apolipoprotein binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the apolipoprotein binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
apolipoprotein a-i receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the apolipoprotein a-i receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
apolipoprotein receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the apolipoprotein receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
apolipoprotein receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the apolipoprotein receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
apolipoprotein a-i binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the apolipoprotein a-i binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Apolipoprotein Levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Apolipoprotein Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Apolipoprotein B receptor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein B receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein A/E Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein A/E protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein C-IV Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein C-IV protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein C-II Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein C-II protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein D Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein D protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein M Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein M protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein L Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein L protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein F Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein F protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein O Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein O protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein CIII Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein CIII protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein C-I Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein C-I protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein A-II (ApoA-II) Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein A-II (ApoA-II) protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein D, vertebrates Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein D, vertebrates protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Apolipoprotein B100 C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Apolipoprotein B100 C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal circulating apolipoprotein e level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating apolipoprotein e level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating apolipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating apolipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal apolipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal apolipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
apolipoprotein a-ii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the apolipoprotein a-ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
apolipoprotein c-iii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the apolipoprotein c-iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Apolipoprotein C-Ii Deficiency (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Apolipoprotein C-Ii Deficiency (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Apolipoprotein C-Ii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Apolipoprotein C-Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Apolipoprotein C-Iii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Apolipoprotein C-Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Apolipoprotein A-I Deficiency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apolipoprotein A-I Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Apolipoprotein A-Iv Polymorphism, Apoa4*1/Apoa4*2 Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apolipoprotein A-Iv Polymorphism, Apoa4*1/Apoa4*2 Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Apolipoprotein B Assay Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apolipoprotein B Assay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Apolipoprotein C-Ii (Wakayama) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apolipoprotein C-Ii (Wakayama) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Apolipoprotein C-Ii Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apolipoprotein C-Ii Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Apolipoprotein C-Iii, Nonglycosylated Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apolipoprotein C-Iii, Nonglycosylated Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Apolipoprotein Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Apolipoprotein Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Apolipoprotein A-Ii Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Apolipoprotein A-Ii Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Apolipoprotein B Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Apolipoprotein B Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
apolipoprotein A-I-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the apolipoprotein A-I-mediated signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
apolipoprotein A-I binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the apolipoprotein A-I binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
apolipoprotein receptor binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the apolipoprotein receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
apolipoprotein A-I receptor binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the apolipoprotein A-I receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal circulating apolipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating apolipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating apolipoprotein E level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating apolipoprotein E level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal apolipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal apolipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
apolipoprotein A-I-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the apolipoprotein A-I-mediated signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
apolipoprotein A-I binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the apolipoprotein A-I binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
apolipoprotein receptor binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the apolipoprotein receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
apolipoprotein A-I receptor binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the apolipoprotein A-I receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Familial apolipoprotein C-II deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial apolipoprotein C-II deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Apolipoprotein C-III deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Apolipoprotein C-III deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Apolipoprotein A-IV associated amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Apolipoprotein A-IV associated amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation 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. |
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. |
APOLIPOPROTEIN C-II Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the APOLIPOPROTEIN C-II phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial apolipoprotein C-II deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial apolipoprotein C-II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
APOLIPOPROTEIN A-IV POLYMORPH Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the APOLIPOPROTEIN A-IV POLYMORPH phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
APOLIPOPROTEIN A-I Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the APOLIPOPROTEIN A-I phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Apolipoprotein A-II deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Apolipoprotein A-II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Apolipoprotein c-III deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Apolipoprotein c-III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lipoprotein(a) levels adjusted for apolipoprotein(a) isoforms Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein(a) levels adjusted for apolipoprotein(a) isoforms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Apolipoprotein A1 levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Apolipoprotein A1 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Apolipoprotein B levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Apolipoprotein B levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Apolipoprotein Levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Apolipoprotein Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Apolipoprotein A-IV levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Apolipoprotein A-IV levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |