akap95 role in mitosis and chromosome dynamics

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Results for "akap95 role in mitosis and chromosome dynamics": 1001 gene sets

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akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
akap95 Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term akap95 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
A-kinase anchoring protein 95 (AKAP95) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the A-kinase anchoring protein 95 (AKAP95) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Intracellular signaling and cytoskeletal dynamics Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Intracellular signaling and cytoskeletal dynamics assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Cytoskeletal dynamics and intracellular transport Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Cytoskeletal dynamics and intracellular transport assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Cytoskeletal organization and cell adhesion dynamics Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Cytoskeletal organization and cell adhesion dynamics assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Mitochondrial dynamics and metabolism Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial dynamics and metabolism assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Regulation of Cytoskeletal Dynamics and Cell Morphology Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of Cytoskeletal Dynamics and Cell Morphology assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Regulation of Cytoskeletal Dynamics and Gene Expression Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of Cytoskeletal Dynamics and Gene Expression assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene Set From GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dynamics Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dynamics in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Regulation of actin dynamics for phagocytic cup formation Gene Set From Reactome Pathways 2014 proteins participating in the Regulation of actin dynamics for phagocytic cup formation pathway from the Reactome Pathways dataset.
Regulation of actin dynamics for phagocytic cup formation Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of actin dynamics for phagocytic cup formation pathway from the Reactome Pathways 2024 dataset.
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set From Reactome Pathways 2014 proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways dataset.
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set From Reactome Pathways 2024 proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways 2024 dataset.
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set From Reactome Pathways 2024 proteins participating in the FBXL7 down-regulates AURKA during mitotic entry and in early mitosis pathway from the Reactome Pathways 2024 dataset.
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proximal chromosome 9p to q and distal chromosome 9q Gene Set From GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
The role of Nef in HIV-1 replication and disease pathogenesis Gene Set From Reactome Pathways 2014 proteins participating in the The role of Nef in HIV-1 replication and disease pathogenesis pathway from the Reactome Pathways dataset.
Model for regulation of MSMP expression in cancer cells and its proangiogenic role in ovarian tumors Gene Set From WikiPathways Pathways 2024 proteins participating in the Model for regulation of MSMP expression in cancer cells and its proangiogenic role in ovarian tumors pathway from the WikiPathways Pathways 2024 dataset.
MAP3K1 role in promoting and blocking gonadal determination Gene Set From WikiPathways Pathways 2024 proteins participating in the MAP3K1 role in promoting and blocking gonadal determination pathway from the WikiPathways Pathways 2024 dataset.
The role of Nef in HIV-1 replication and disease pathogenesis Gene Set From Reactome Pathways 2024 proteins participating in the The role of Nef in HIV-1 replication and disease pathogenesis pathway from the Reactome Pathways 2024 dataset.
NEVER IN MITOSIS GENE A-RELATED KINASE 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEVER IN MITOSIS GENE A-RELATED KINASE 1 from the curated CTD Gene-Disease Associations dataset.
mitosis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mitosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of transcription from rna polymerase ii promoter during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription from rna polymerase ii promoter during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of transcription from rna polymerase ii promoter during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription from rna polymerase ii promoter during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of transcription during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of transcription on exit from mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription on exit from mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
microtubule cytoskeleton organization involved in mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the microtubule cytoskeleton organization involved in mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
exit from mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the exit from mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of transcription during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormal mitosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mitosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mitosis Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term mitosis in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2023 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2023 dataset.
exit from mitosis Gene Set From GO Biological Process Annotations 2023 genes participating in the exit from mitosis biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2023 dataset.
microtubule cytoskeleton organization involved in mitosis Gene Set From GO Biological Process Annotations 2023 genes participating in the microtubule cytoskeleton organization involved in mitosis biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of transcription involved in exit from mitosis Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of transcription involved in exit from mitosis biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal mitosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mitosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2025 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2025 dataset.
microtubule cytoskeleton organization involved in mitosis Gene Set From GO Biological Process Annotations 2025 genes participating in the microtubule cytoskeleton organization involved in mitosis biological process from the curated GO Biological Process Annotations 2025 dataset.
exit from mitosis Gene Set From GO Biological Process Annotations 2025 genes participating in the exit from mitosis biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of exit from mitosis Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of exit from mitosis biological process from the curated GO Biological Process Annotations 2025 dataset.
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene Set From GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; dna damage Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cadasil; chromosome aberrations; chromosome abnormality Gene Set From GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome deletion; dystonia; myoclonus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; lymphocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene Set From GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome inversion; leukemia, myeloid; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome inversion; leukemia, myeloid; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
homologous chromosome movement towards spindle pole involved in homologous chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the homologous chromosome movement towards spindle pole involved in homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome localization to nuclear envelope involved in homologous chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the chromosome localization to nuclear envelope involved in homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
Mosaic loss of chromosome Y (Y chromosome dosage) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosaic loss of chromosome Y (Y chromosome dosage) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
role of mal in rho-mediated activation of srf Gene Set From Biocarta Pathways proteins participating in the role of mal in rho-mediated activation of srf pathway from the Biocarta Pathways dataset.
role of erk5 in neuronal survival pathway Gene Set From Biocarta Pathways proteins participating in the role of erk5 in neuronal survival pathway pathway from the Biocarta Pathways dataset.
role of ran in mitotic spindle regulation Gene Set From Biocarta Pathways proteins participating in the role of ran in mitotic spindle regulation pathway from the Biocarta Pathways dataset.
role of egf receptor transactivation by gpcrs in cardiac hypertrophy Gene Set From Biocarta Pathways proteins participating in the role of egf receptor transactivation by gpcrs in cardiac hypertrophy pathway from the Biocarta Pathways dataset.
role of parkin in ubiquitin-proteasomal pathway Gene Set From Biocarta Pathways proteins participating in the role of parkin in ubiquitin-proteasomal pathway pathway from the Biocarta Pathways dataset.
role of mitochondria in apoptotic signaling Gene Set From Biocarta Pathways proteins participating in the role of mitochondria in apoptotic signaling pathway from the Biocarta Pathways dataset.
role of mef2d in t-cell apoptosis Gene Set From Biocarta Pathways proteins participating in the role of mef2d in t-cell apoptosis pathway from the Biocarta Pathways dataset.
role of nicotinic acetylcholine receptors in the regulation of apoptosis Gene Set From Biocarta Pathways proteins participating in the role of nicotinic acetylcholine receptors in the regulation of apoptosis pathway from the Biocarta Pathways dataset.
Role of Calcineurin-dependent NFAT signaling in lymphocytes Gene Set From PID Pathways proteins participating in the Role of Calcineurin-dependent NFAT signaling in lymphocytes pathway from the PID Pathways dataset.
Role of Abl in Robo-Slit signaling Gene Set From Reactome Pathways 2014 proteins participating in the Role of Abl in Robo-Slit signaling pathway from the Reactome Pathways dataset.
Role of DCC in regulating apoptosis Gene Set From Reactome Pathways 2014 proteins participating in the Role of DCC in regulating apoptosis pathway from the Reactome Pathways dataset.
Role of phospholipids in phagocytosis Gene Set From Reactome Pathways 2014 proteins participating in the Role of phospholipids in phagocytosis pathway from the Reactome Pathways dataset.
Role of second messengers in netrin-1 signaling Gene Set From Reactome Pathways 2014 proteins participating in the Role of second messengers in netrin-1 signaling pathway from the Reactome Pathways dataset.
Role of LAT2/NTAL/LAB on calcium mobilization Gene Set From Reactome Pathways 2014 proteins participating in the Role of LAT2/NTAL/LAB on calcium mobilization pathway from the Reactome Pathways dataset.
miRNA role in immune response in sepsis Gene Set From WikiPathways Pathways 2024 proteins participating in the miRNA role in immune response in sepsis pathway from the WikiPathways Pathways 2024 dataset.
SMC1 SMC3 role in DNA damage Cornelia de Lange Syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the SMC1 SMC3 role in DNA damage Cornelia de Lange Syndrome pathway from the WikiPathways Pathways 2024 dataset.
NIPBL role in DNA damage Cornelia de Lange syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the NIPBL role in DNA damage Cornelia de Lange syndrome pathway from the WikiPathways Pathways 2024 dataset.
Non classical role of vitamin D Gene Set From WikiPathways Pathways 2024 proteins participating in the Non classical role of vitamin D pathway from the WikiPathways Pathways 2024 dataset.
Role of ABL in ROBO-SLIT signaling Gene Set From Reactome Pathways 2024 proteins participating in the Role of ABL in ROBO-SLIT signaling pathway from the Reactome Pathways 2024 dataset.
Role of LAT2/NTAL/LAB on calcium mobilization Gene Set From Reactome Pathways 2024 proteins participating in the Role of LAT2/NTAL/LAB on calcium mobilization pathway from the Reactome Pathways 2024 dataset.
Role of phospholipids in phagocytosis Gene Set From Reactome Pathways 2024 proteins participating in the Role of phospholipids in phagocytosis pathway from the Reactome Pathways 2024 dataset.
Role of second messengers in netrin-1 signaling Gene Set From Reactome Pathways 2024 proteins participating in the Role of second messengers in netrin-1 signaling pathway from the Reactome Pathways 2024 dataset.
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain Gene Set From Reactome Pathways 2024 proteins participating in the TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain pathway from the Reactome Pathways 2024 dataset.
The role of GTSE1 in G2/M progression after G2 checkpoint Gene Set From Reactome Pathways 2024 proteins participating in the The role of GTSE1 in G2/M progression after G2 checkpoint pathway from the Reactome Pathways 2024 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
increased chromosome aberrations and higher lung cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease increased chromosome aberrations and higher lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; chromosome breakage; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; chromosome breakage; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; chromosome breakage; head and neck neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; chromosome breakage; head and neck neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome segregation and DNA repair Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Chromosome segregation and DNA repair assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Chromosome stability and DNA repair mechanisms Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Chromosome stability and DNA repair mechanisms assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Mitotic cell cycle and chromosome segregation regulators Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitotic cell cycle and chromosome segregation regulators assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chromosome 2q32-q33 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 1q43-q44 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome Xq28 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome Xq28 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 9q deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 9q deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cytoplasmic chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytoplasmic chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
sex chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the sex chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed chromosome inner kinetochore Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome inner kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed nuclear chromosome kinetochore Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed nuclear chromosome kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed nuclear chromosome outer kinetochore Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed nuclear chromosome outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed nuclear chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
nuclear chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
chromosome, centromeric core domain Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome, centromeric core domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed chromosome, centromeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
nuclear chromosome part Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear chromosome part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
y chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the y chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
chromosome, centromeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed chromosome kinetochore Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
nuclear chromosome, telomeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
chromosome, telomeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
x chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the x chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
chromosome passenger complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome passenger complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed chromosome outer kinetochore Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
condensed nuclear chromosome, centromeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed nuclear chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cytoplasmic chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytoplasmic chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
sex chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the sex chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed chromosome inner kinetochore Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed chromosome inner kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed nuclear chromosome kinetochore Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed nuclear chromosome kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed nuclear chromosome outer kinetochore Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed nuclear chromosome outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
polytene chromosome chromocenter Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the polytene chromosome chromocenter cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed nuclear chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed nuclear chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
polytene chromosome puff Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the polytene chromosome puff cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
w chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the w chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chloroplast chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chloroplast chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
y chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the y chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed chromosome, centromeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
nuclear chromosome part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear chromosome part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
polytene chromosome interband Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the polytene chromosome interband cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
plastid chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plastid chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
nuclear chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chromosome, centromeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitochondrial chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed chromosome kinetochore Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed chromosome kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
z chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the z chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chromosome segregation-directing complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromosome segregation-directing complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
nuclear chromosome, telomeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
polytene chromosome band Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the polytene chromosome band cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chromosome, telomeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
x chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the x chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
polytene chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the polytene chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chromosome passenger complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromosome passenger complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed chromosome outer kinetochore Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed chromosome outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
condensed nuclear chromosome, centromeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the condensed nuclear chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Chromosome 17 deletion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome 17 deletion from the curated CTD Gene-Disease Associations dataset.
Chromosome 2q37 deletion syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome 2q37 deletion syndrome from the curated CTD Gene-Disease Associations dataset.
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Chromosome Breakage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome Breakage from the curated CTD Gene-Disease Associations dataset.
TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 from the curated CTD Gene-Disease Associations dataset.
Chromosome Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome Disorders from the curated CTD Gene-Disease Associations dataset.
Frontotemporal Dementia, Chromosome 3-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Frontotemporal Dementia, Chromosome 3-Linked from the curated CTD Gene-Disease Associations dataset.
Chromosome Aberrations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome Aberrations from the curated CTD Gene-Disease Associations dataset.
Heterotopia, Periventricular, associated with Chromosome 5p Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heterotopia, Periventricular, associated with Chromosome 5p Anomalies from the curated CTD Gene-Disease Associations dataset.
Micronuclei, Chromosome-Defective Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Micronuclei, Chromosome-Defective from the curated CTD Gene-Disease Associations dataset.
Chromosome 3, monosomy 3p25 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome 3, monosomy 3p25 from the curated CTD Gene-Disease Associations dataset.
Heterotopia, Periventricular, Associated With Chromosome 5q Deletion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heterotopia, Periventricular, Associated With Chromosome 5q Deletion from the curated CTD Gene-Disease Associations dataset.
Chromosome Xp11.3 Deletion Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome Xp11.3 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.
chromosome aberrations; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; chromosome deletion; lung neoplasms; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; chromosome deletion; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility, male; sex chromosome aberrations Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility, male; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; chromosome disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; chromosome disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; leukemia, lymphocytic, chronic, b-cell Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; leukemia, myeloid, acute; primary myelofibrosis; thrombocythemia, essential; trisomy Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; leukemia, myeloid, acute; primary myelofibrosis; thrombocythemia, essential; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; chromosome breakage; dna damage; mammary neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chromosome breakage; dna damage; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; intestinal neoplasms; lymphoma; lymphoma, b-cell, marginal zone Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; intestinal neoplasms; lymphoma; lymphoma, b-cell, marginal zone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; chromosome breakage; mammary neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chromosome breakage; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brill-symmers disease; chromosome deletion; lymphoma, follicular Gene Set From GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; chromosome deletion; lymphoma, follicular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; digeorge syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; digeorge syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome breakage; dna damage; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome breakage; dna damage; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; leukemia, myeloid, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome inversion; hemophilia a Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome inversion; hemophilia a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; epilepsy, generalized; Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; epilepsy, generalized; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases in twins; sex chromosome aberrations Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases in twins; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
altitude sickness; chromosome deletion; pulmonary edema Gene Set From GAD Gene-Disease Associations genes associated with the disease altitude sickness; chromosome deletion; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
azoospermia; chromosome deletion Gene Set From GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; leukemia, myeloid, acute; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; leukemia, myeloid, acute; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; dna damage Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; chromosome aberrations; lung neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; chromosome aberrations; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; li-fraumeni syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; li-fraumeni syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
flushing; micronuclei, chromosome-defective Gene Set From GAD Gene-Disease Associations genes associated with the disease flushing; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome breakage Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome breakage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome breakage; leukemia, myelogenous, chronic, bcr-abl positive Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome breakage; leukemia, myelogenous, chronic, bcr-abl positive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; keratosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; keratosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cd3 epsilon locus on chromosome 11 Gene Set From GAD Gene-Disease Associations genes associated with the disease cd3 epsilon locus on chromosome 11 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; chromosome inversion; Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; chromosome inversion; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome breakage; cleft lip; cleft palate; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome breakage; cleft lip; cleft palate; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility, male; oligospermia; sex chromosome aberrations Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; leukemia, lymphocytic, chronic, b-cell Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term chromosome in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
chromosome separation Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome separation biological process from the curated GO Biological Process Annotations 2015 dataset.
mitotic chromosome movement towards spindle pole Gene Set From GO Biological Process Annotations 2015 genes participating in the mitotic chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations 2015 dataset.
random inactivation of x chromosome Gene Set From GO Biological Process Annotations 2015 genes participating in the random inactivation of x chromosome biological process from the curated GO Biological Process Annotations 2015 dataset.
meiotic chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the meiotic chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome movement towards spindle pole Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations 2015 dataset.
meiotic chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the meiotic chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
apoptotic chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the apoptotic chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome organization Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome organization biological process from the curated GO Biological Process Annotations 2015 dataset.
establishment of chromosome localization Gene Set From GO Biological Process Annotations 2015 genes participating in the establishment of chromosome localization biological process from the curated GO Biological Process Annotations 2015 dataset.
establishment of protein localization to chromosome Gene Set From GO Biological Process Annotations 2015 genes participating in the establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome attachment to the nuclear envelope Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome attachment to the nuclear envelope biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of establishment of protein localization to chromosome Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations 2015 dataset.
mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome passenger complex localization to kinetochore Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome passenger complex localization to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome passenger complex localization to spindle midzone Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome passenger complex localization to spindle midzone biological process from the curated GO Biological Process Annotations 2015 dataset.
protein localization to chromosome, centromeric region Gene Set From GO Biological Process Annotations 2015 genes participating in the protein localization to chromosome, centromeric region biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome organization involved in meiosis Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome organization involved in meiosis biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of chromosome organization Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of chromosome organization Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of chromosome organization Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of homologous chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-s10 phosphorylation involved in chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-s10 phosphorylation involved in chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
inactivation of x chromosome by dna methylation Gene Set From GO Biological Process Annotations 2015 genes participating in the inactivation of x chromosome by dna methylation biological process from the curated GO Biological Process Annotations 2015 dataset.
meiotic chromosome movement towards spindle pole Gene Set From GO Biological Process Annotations 2015 genes participating in the meiotic chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations 2015 dataset.
homologous chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
dosage compensation by inactivation of x chromosome Gene Set From GO Biological Process Annotations 2015 genes participating in the dosage compensation by inactivation of x chromosome biological process from the curated GO Biological Process Annotations 2015 dataset.
meiotic chromosome separation Gene Set From GO Biological Process Annotations 2015 genes participating in the meiotic chromosome separation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
male meiosis chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the male meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
male meiosis chromosome separation Gene Set From GO Biological Process Annotations 2015 genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome breakage Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome breakage biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset.
protein localization to chromosome Gene Set From GO Biological Process Annotations 2015 genes participating in the protein localization to chromosome biological process from the curated GO Biological Process Annotations 2015 dataset.
protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2015 genes participating in the protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome localization to nuclear envelope involved in synapsis Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome localization to nuclear envelope involved in synapsis biological process from the curated GO Biological Process Annotations 2015 dataset.
chromosome localization Gene Set From GO Biological Process Annotations 2015 genes participating in the chromosome localization biological process from the curated GO Biological Process Annotations 2015 dataset.
cytoplasmic chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cytoplasmic chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
sex chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the sex chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed chromosome inner kinetochore Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome inner kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed nuclear chromosome kinetochore Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed nuclear chromosome kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed nuclear chromosome outer kinetochore Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed nuclear chromosome outer kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed nuclear chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
nuclear chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
chromosome, centromeric core domain Gene Set From GO Cellular Component Annotations 2015 proteins localized to the chromosome, centromeric core domain cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed chromosome, centromeric region Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset.
nuclear chromosome part Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nuclear chromosome part cellular component from the curated GO Cellular Component Annotations 2015 dataset.
y chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the y chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
chromosome, centromeric region Gene Set From GO Cellular Component Annotations 2015 proteins localized to the chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
mitochondrial chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the mitochondrial chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed chromosome kinetochore Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset.
nuclear chromosome, telomeric region Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nuclear chromosome, telomeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset.
chromosome, telomeric region Gene Set From GO Cellular Component Annotations 2015 proteins localized to the chromosome, telomeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset.
x chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the x chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
chromosome passenger complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the chromosome passenger complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed chromosome outer kinetochore Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome outer kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset.
chromosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
condensed nuclear chromosome, centromeric region Gene Set From GO Cellular Component Annotations 2015 proteins localized to the condensed nuclear chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset.
abnormality of chromosome condensation Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased rate of premature chromosome condensation Gene Set From HPO Gene-Disease Associations genes associated with the increased rate of premature chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of chromosome segregation Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of chromosome segregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
endopolyploidy on chromosome studies of bone marrow Gene Set From HPO Gene-Disease Associations genes associated with the endopolyploidy on chromosome studies of bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of chromosome stability Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of chromosome stability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sex Chromosome Disorders of Sex Development Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sex Chromosome Disorders of Sex Development phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Fragility Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Fragility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Philadelphia Chromosome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Philadelphia Chromosome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Inversion Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Inversion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sex Chromosome Aberrations Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sex Chromosome Aberrations phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Deletion Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Deletion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Inversion, Chromosome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Inversion, Chromosome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Breakage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Breakage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Aberrations Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Aberrations phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Micronuclei, Chromosome-Defective Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Micronuclei, Chromosome-Defective phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Duplication Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Duplication phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Non-structural maintenance of chromosome element 4, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Non-structural maintenance of chromosome element 4, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mini-chromosome maintenance, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mini-chromosome maintenance, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mini-chromosome maintenance complex protein 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mini-chromosome maintenance complex protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Chromosome segregation protein Spc25 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Chromosome segregation protein Spc25 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myeloid transforming gene on chromosome 16 (MTG16) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myeloid transforming gene on chromosome 16 (MTG16) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mini-chromosome maintenance complex-binding protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mini-chromosome maintenance complex-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Chromosome transmission fidelity protein 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Chromosome transmission fidelity protein 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mini-chromosome maintenance, DNA-dependent ATPase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mini-chromosome maintenance, DNA-dependent ATPase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Regulator of chromosome condensation 1/beta-lactamase-inhibitor protein II Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of chromosome condensation 1/beta-lactamase-inhibitor protein II protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Regulator of chromosome condensation, RCC1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of chromosome condensation, RCC1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Chromosome passenger complex (CPC) protein INCENP N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Chromosome passenger complex (CPC) protein INCENP N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Myeloid transforming gene on chromosome 8 (MTG8) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myeloid transforming gene on chromosome 8 (MTG8) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal dosage compensation, by inactivation of x chromosome Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal dosage compensation, by inactivation of x chromosome phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mitochondrial chromosome morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial chromosome morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal chromosome morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal chromosome morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal chromosome pairing during meiosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal chromosome pairing during meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spontaneous chromosome breakage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spontaneous chromosome breakage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal chromosome number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal chromosome number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal chromosome stability Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal chromosome stability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
chromosome breakage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the chromosome breakage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
induced chromosome breakage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the induced chromosome breakage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal x-y chromosome synapsis during male meiosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal x-y chromosome synapsis during male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q21.31 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q21.31 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 4q21 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 4q21 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 6pter-p24 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 6pter-p24 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 15q26-qter deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 15q26-qter deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xp11.23-p11.22 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xp11.23-p11.22 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q12 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q12 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 18p deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 18p deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 2p16.1-p15 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 2p16.1-p15 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 2p12-p11.2 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 2p12-p11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
leri pleonosteosis chromosome duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the leri pleonosteosis chromosome duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 7q11.23 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1p36 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1p36 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1q21.1 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1q21.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 6q25-q25 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 6q25-q25 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q11.2 deletion syndrome, 1.4mb Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q11.2 deletion syndrome, 1.4mb phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 15q25 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 15q25 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1p32-p31 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1p32-p31 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 22q11.2 deletion syndrome, distal Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p11.2 deletion syndrome, 593kb Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p11.2 deletion syndrome, 593kb phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 15q13.3 microdeletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 15q13.3 microdeletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p11.2 deletion syndrome, 220kb Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p11.2 deletion syndrome, 220kb phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 11p15-p14 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 11p15-p14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xq28 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xq28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q23.1-q23.2 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q23.1-q23.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 22q13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 22q13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p12.2-p11.2 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p12.2-p11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p11.2 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p11.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xp11.3 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xp11.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p13.3 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 22q11.2 microduplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 22q11.2 microduplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16q22 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16q22 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xq27.3-q28 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xq27.3-q28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 18q deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 18q deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 8q21.11 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 8q21.11 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p13.3 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p13.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17p13.3 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
leukemia, philadelphia chromosome-positive, resistant to imatinib Gene Set From OMIM Gene-Disease Associations genes associated with the leukemia, philadelphia chromosome-positive, resistant to imatinib phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 2q31.1 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 2q31.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
radiation sensitivity/chromosome instability syndrome, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the radiation sensitivity/chromosome instability syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1q43-q44 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1q43-q44 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 13q14 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 13q14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 2q31.2 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 2q31.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 6q11-q14 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 6q11-q14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1q21.1 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1q21.1 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 15q11.2 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 15q11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 3q29 microduplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 3q29 microduplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 3q13.31 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 3q13.31 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 4q32.1-q32.2 triplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 4q32.1-q32.2 triplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 18 pericentric inversion Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 18 pericentric inversion phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 9p deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 9p deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q12 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q12 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xp21 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xp21 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 5q12 deletion sydrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 5q12 deletion sydrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 19p13.13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 19p13.13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1q41-q42 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1q41-q42 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 10q26 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 10q26 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 5p13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 5p13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 15q24 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 15q24 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 19p13.13 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 19p13.13 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q23.1-q23.2 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q23.1-q23.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 19q13.11 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 19q13.11 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 14q11-q22 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 14q11-q22 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 8p11 myeloproliferative syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 8p11 myeloproliferative syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 3q29 microdeletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 3q29 microdeletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17p13.1 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17p13.1 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 5q14.3 deletion syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 5q14.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term chromosome in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Chromosome Maintenance Gene Set From Reactome Pathways 2014 proteins participating in the Chromosome Maintenance pathway from the Reactome Pathways dataset.
Philadelphia Chromosome Positive Chronic Myelogenous Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Philadelphia Chromosome Positive Chronic Myelogenous Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 9, Trisomy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 9, Trisomy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Philadelphia Chromosome Negative Chronic Myelogenous Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Philadelphia Chromosome Negative Chronic Myelogenous Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 15Q, Tetrasomy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 15Q, Tetrasomy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isodicentric Chromosome 15 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isodicentric Chromosome 15 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xq26.3 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xq26.3 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 2, Trisomy 2P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 2, Trisomy 2P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 1, Monosomy 1P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 1, Monosomy 1P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 11P11.2 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 11P11.2 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 9, Partial Trisomy 9P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 9, Partial Trisomy 9P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 9P Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 9P Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 11Q Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 11Q Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 8, Monosomy 8P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 8, Monosomy 8P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 5, Trisomy 5Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 5, Trisomy 5Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 21 Monosomy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 21 Monosomy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 6Q24-Q25 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 6Q24-Q25 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 15Q, Trisomy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 15Q, Trisomy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Instability Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Instability Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 22Q11.2 Deletion Syndrome, Distal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 22Q11.2 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 8P11 Myeloproliferative Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 8P11 Myeloproliferative Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 12, 12P Trisomy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 12, 12P Trisomy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17 Trisomy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17 Trisomy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 1P36 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 1P36 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 3, Monosomy 3P25 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 3, Monosomy 3P25 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 7 Ring Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 7 Ring Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 10, Monosomy 10Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 10, Monosomy 10Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 2, Trisomy 2Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 2, Trisomy 2Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 3, Trisomy 3Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 3, Trisomy 3Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 6, Monosomy 6Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 6, Monosomy 6Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 10, Monosomy 10P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 10, Monosomy 10P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 8, Trisomy 8Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 8, Trisomy 8Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 8, Trisomy 8P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 8, Trisomy 8P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ring Chromosome 20 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ring Chromosome 20 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 15Q13.3 Microdeletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 15Q13.3 Microdeletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ring Chromosome 5 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ring Chromosome 5 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 16P13.3 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 16P13.3 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 11P Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 11P Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uniparental Disomy, Paternal, Chromosome 14 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uniparental Disomy, Paternal, Chromosome 14 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 3Q29 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 3Q29 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 9, Tetrasomy 9P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 9, Tetrasomy 9P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 2Q37 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 2Q37 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ring Chromosome 3 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ring Chromosome 3 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xq27.3-Q28 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xq27.3-Q28 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fragile X Chromosome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fragile X Chromosome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Deletions Of Part Of A Chromosome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Deletions Of Part Of A Chromosome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 8, Monosomy 8P23 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 8, Monosomy 8P23 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 18, Trisomy 18Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 18, Trisomy 18Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 18P Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 18P Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 18Q Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 18Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Deletion Of Long Arm Of Chromosome 18 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Deletion Of Long Arm Of Chromosome 18 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maternal Uniparental Disomy Of Chromosome 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maternal Uniparental Disomy Of Chromosome 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 7, Trisomy 7Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 7, Trisomy 7Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 4Q- Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 4Q- Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17Q12 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17Q12 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ring Chromosome 15 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ring Chromosome 15 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xp11.23-P11.22 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xp11.23-P11.22 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17 Deletion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17 Deletion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17Q21.31 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17Q21.31 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 12, Trisomy 12Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 12, Trisomy 12Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 2Q32-Q33 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 2Q32-Q33 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 15Q26-Qter Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 15Q26-Qter Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maternal Uniparental Disomy Of Chromosome 20 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maternal Uniparental Disomy Of Chromosome 20 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 15Q14 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 15Q14 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 6Pter-P24 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 6Pter-P24 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 1P32-P31 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 1P32-P31 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 5P13 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 5P13 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 5, Monosomy 5Q35 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 5, Monosomy 5Q35 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 2P16.3 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 2P16.3 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17P13.3 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17P13.3 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 7, Trisomy 7P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 7, Trisomy 7P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paternal Uniparental Disomy Of Chromosome 6 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paternal Uniparental Disomy Of Chromosome 6 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17, Trisomy 17P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17, Trisomy 17P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Trisomy Of Chromosome 17 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Trisomy Of Chromosome 17 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 13Q14 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 13Q14 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recombinant Chromosome 8 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recombinant Chromosome 8 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 16P11.2 Deletion Syndrome, 220-Kb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 16P11.2 Deletion Syndrome, 220-Kb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 16P11.2 Deletion Syndrome, 593-Kb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 16P11.2 Deletion Syndrome, 593-Kb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 3, Monosomy 3P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 3, Monosomy 3P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 22Q11.2 Microduplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 22Q11.2 Microduplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17Q23.1-Q23.2 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17Q23.1-Q23.2 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17Q23.1-Q23.2 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17Q23.1-Q23.2 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 7, Trisomy Mosaic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 7, Trisomy Mosaic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paternal Uniparental Disomy Of Chromosome 20 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paternal Uniparental Disomy Of Chromosome 20 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 16P13.2 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 16P13.2 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 12 Ring Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 12 Ring in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 10P12-P11 Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 10P12-P11 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 19Q13.11 Deletion Syndrome, Distal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 19Q13.11 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Micronuclei, Chromosome-Defective Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Micronuclei, Chromosome-Defective in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Chromosome Stability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Chromosome Stability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome Breakage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome Breakage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome 10Q23 Deletion Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome 10Q23 Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome Breaks Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome Breaks in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Endopolyploidy On Chromosome Studies Of Bone Marrow Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endopolyploidy On Chromosome Studies Of Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Chromosome Y Deletion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Chromosome Y Deletion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Chromosome Segregation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Chromosome Segregation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome 1Q21.1 Deletion Syndrome, 1.35-Mb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome 1Q21.1 Deletion Syndrome, 1.35-Mb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome 17P Deletion Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome 17P Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Rate Of Premature Chromosome Condensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Rate Of Premature Chromosome Condensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome Xq28 Duplication Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome Xq28 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome 2, Monosomy 2Q24 Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome 2, Monosomy 2Q24 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Chromosome Morphology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Chromosome Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome 15, Trisomy Mosaicism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome 15, Trisomy Mosaicism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
homologous chromosome segregation Gene Set From GO Biological Process Annotations 2023 genes participating in the homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2023 dataset.
dosage compensation by inactivation of X chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the dosage compensation by inactivation of X chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
inactivation of X chromosome by heterochromatin formation Gene Set From GO Biological Process Annotations 2023 genes participating in the inactivation of X chromosome by heterochromatin formation biological process from the curated GO Biological Process Annotations 2023 dataset.
homologous chromosome pairing at meiosis Gene Set From GO Biological Process Annotations 2023 genes participating in the homologous chromosome pairing at meiosis biological process from the curated GO Biological Process Annotations 2023 dataset.
protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2023 genes participating in the protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2023 dataset.
chromosome organization Gene Set From GO Biological Process Annotations 2023 genes participating in the chromosome organization biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of chromosome separation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of chromosome separation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of dosage compensation by inactivation of X chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of dosage compensation by inactivation of X chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2023 dataset.
apoptotic chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the apoptotic chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of chromosome organization Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2023 dataset.
protein localization to chromosome, centromeric region Gene Set From GO Biological Process Annotations 2023 genes participating in the protein localization to chromosome, centromeric region biological process from the curated GO Biological Process Annotations 2023 dataset.
protein localization to chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the protein localization to chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of chromosome separation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of chromosome separation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of chromosome organization Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2023 dataset.
mitotic chromosome movement towards spindle pole Gene Set From GO Biological Process Annotations 2023 genes participating in the mitotic chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations 2023 dataset.
microtubule plus-end directed mitotic chromosome migration Gene Set From GO Biological Process Annotations 2023 genes participating in the microtubule plus-end directed mitotic chromosome migration biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of establishment of protein localization to chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
inactivation of X chromosome by genomic imprinting Gene Set From GO Biological Process Annotations 2023 genes participating in the inactivation of X chromosome by genomic imprinting biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of chromosome organization Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of homologous chromosome segregation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2023 dataset.
nuclear chromosome segregation Gene Set From GO Biological Process Annotations 2023 genes participating in the nuclear chromosome segregation biological process from the curated GO Biological Process Annotations 2023 dataset.
male meiosis chromosome separation Gene Set From GO Biological Process Annotations 2023 genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2023 dataset.
random inactivation of X chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the random inactivation of X chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
establishment of chromosome localization Gene Set From GO Biological Process Annotations 2023 genes participating in the establishment of chromosome localization biological process from the curated GO Biological Process Annotations 2023 dataset.
homologous chromosome movement towards spindle pole in meiosis I anaphase Gene Set From GO Biological Process Annotations 2023 genes participating in the homologous chromosome movement towards spindle pole in meiosis I anaphase biological process from the curated GO Biological Process Annotations 2023 dataset.
meiotic chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the meiotic chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
establishment of protein localization to chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
protein localization to condensed chromosome Gene Set From GO Biological Process Annotations 2023 genes participating in the protein localization to condensed chromosome biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of meiotic chromosome separation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of meiotic chromosome separation biological process from the curated GO Biological Process Annotations 2023 dataset.
condensed chromosome, centromeric region Gene Set From GO Cellular Component Annotations 2023 proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2023 dataset.
chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
nuclear chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
condensed nuclear chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the condensed nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
condensed chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the condensed chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
chromosome, subtelomeric region Gene Set From GO Cellular Component Annotations 2023 proteins localized to the chromosome, subtelomeric region cellular component from the curated GO Cellular Component Annotations 2023 dataset.
inactive sex chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the inactive sex chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
X chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the X chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
chromosome, telomeric repeat region Gene Set From GO Cellular Component Annotations 2023 proteins localized to the chromosome, telomeric repeat region cellular component from the curated GO Cellular Component Annotations 2023 dataset.
sex chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the sex chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
polytene chromosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the polytene chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal chromosome number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal chromosome number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal chromosome morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal chromosome morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
chromosome breakage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the chromosome breakage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
induced chromosome breakage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the induced chromosome breakage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spontaneous chromosome breakage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spontaneous chromosome breakage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mitochondrial chromosome morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mitochondrial chromosome morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal dosage compensation, by inactivation of X chromosome Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dosage compensation, by inactivation of X chromosome phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal X-Y chromosome synapsis during male meiosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal X-Y chromosome synapsis during male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal X-Y chromosome synaptonemal complex assembly during male meiosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal X-Y chromosome synaptonemal complex assembly during male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Chromosome Maintenance Gene Set From Reactome Pathways 2024 proteins participating in the Chromosome Maintenance pathway from the Reactome Pathways 2024 dataset.
male meiosis chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the male meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
female meiosis chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the female meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
homologous chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
mitotic metaphase chromosome alignment Gene Set From GO Biological Process Annotations 2025 genes participating in the mitotic metaphase chromosome alignment biological process from the curated GO Biological Process Annotations 2025 dataset.
dosage compensation by inactivation of X chromosome Gene Set From GO Biological Process Annotations 2025 genes participating in the dosage compensation by inactivation of X chromosome biological process from the curated GO Biological Process Annotations 2025 dataset.
homologous chromosome pairing at meiosis Gene Set From GO Biological Process Annotations 2025 genes participating in the homologous chromosome pairing at meiosis biological process from the curated GO Biological Process Annotations 2025 dataset.
protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2025 genes participating in the protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2025 dataset.
metaphase chromosome alignment Gene Set From GO Biological Process Annotations 2025 genes participating in the metaphase chromosome alignment biological process from the curated GO Biological Process Annotations 2025 dataset.
chromosome organization Gene Set From GO Biological Process Annotations 2025 genes participating in the chromosome organization biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of chromosome separation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of chromosome separation biological process from the curated GO Biological Process Annotations 2025 dataset.
establishment of chromosome localization Gene Set From GO Biological Process Annotations 2025 genes participating in the establishment of chromosome localization biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
sex-chromosome dosage compensation Gene Set From GO Biological Process Annotations 2025 genes participating in the sex-chromosome dosage compensation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2025 dataset.
apoptotic chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the apoptotic chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
homologous chromosome orientation in meiotic metaphase I Gene Set From GO Biological Process Annotations 2025 genes participating in the homologous chromosome orientation in meiotic metaphase I biological process from the curated GO Biological Process Annotations 2025 dataset.
mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of chromosome organization Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2025 dataset.
protein localization to chromosome, centromeric region Gene Set From GO Biological Process Annotations 2025 genes participating in the protein localization to chromosome, centromeric region biological process from the curated GO Biological Process Annotations 2025 dataset.
protein localization to chromosome Gene Set From GO Biological Process Annotations 2025 genes participating in the protein localization to chromosome biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of chromosome separation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of chromosome separation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of chromosome organization Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2025 dataset.
random inactivation of X chromosome Gene Set From GO Biological Process Annotations 2025 genes participating in the random inactivation of X chromosome biological process from the curated GO Biological Process Annotations 2025 dataset.
mitotic chromosome movement towards spindle pole Gene Set From GO Biological Process Annotations 2025 genes participating in the mitotic chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations 2025 dataset.
microtubule plus-end directed mitotic chromosome migration Gene Set From GO Biological Process Annotations 2025 genes participating in the microtubule plus-end directed mitotic chromosome migration biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of establishment of protein localization to chromosome Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of chromosome organization Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of chromosome organization biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of homologous chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of homologous chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
nuclear chromosome segregation Gene Set From GO Biological Process Annotations 2025 genes participating in the nuclear chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset.
male meiosis chromosome separation Gene Set From GO Biological Process Annotations 2025 genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations 2025 dataset.
broken chromosome clustering Gene Set From GO Biological Process Annotations 2025 genes participating in the broken chromosome clustering biological process from the curated GO Biological Process Annotations 2025 dataset.
homologous chromosome movement towards spindle pole in meiosis I anaphase Gene Set From GO Biological Process Annotations 2025 genes participating in the homologous chromosome movement towards spindle pole in meiosis I anaphase biological process from the curated GO Biological Process Annotations 2025 dataset.
chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
meiotic chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the meiotic chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
establishment of protein localization to chromosome Gene Set From GO Biological Process Annotations 2025 genes participating in the establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations 2025 dataset.
protein localization to condensed chromosome Gene Set From GO Biological Process Annotations 2025 genes participating in the protein localization to condensed chromosome biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of mitotic chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of mitotic chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of protein localization to chromosome, telomeric region Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations 2025 dataset.
meiotic metaphase I homologous chromosome alignment Gene Set From GO Biological Process Annotations 2025 genes participating in the meiotic metaphase I homologous chromosome alignment biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of chromosome condensation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of chromosome condensation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of meiotic chromosome separation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of meiotic chromosome separation biological process from the curated GO Biological Process Annotations 2025 dataset.
condensed chromosome, centromeric region Gene Set From GO Cellular Component Annotations 2025 proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2025 dataset.
chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
nuclear chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
condensed nuclear chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the condensed nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
condensed chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the condensed chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
chromosome, subtelomeric region Gene Set From GO Cellular Component Annotations 2025 proteins localized to the chromosome, subtelomeric region cellular component from the curated GO Cellular Component Annotations 2025 dataset.
mitochondrial chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the mitochondrial chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
inactive sex chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the inactive sex chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
X chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the X chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
chromosome, telomeric repeat region Gene Set From GO Cellular Component Annotations 2025 proteins localized to the chromosome, telomeric repeat region cellular component from the curated GO Cellular Component Annotations 2025 dataset.
sex chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the sex chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
polytene chromosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the polytene chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Chromosome 15q24 deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 15q24 deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 15q13.3 microdeletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 15q13.3 microdeletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 19p13.13 deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 19p13.13 deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 1q21.1 deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 1q21.1 deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 18q deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 18q deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 5q deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 5q deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 22q11.2 microduplication syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 22q11.2 microduplication syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 17q12 deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 17q12 deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 1p36 deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 1p36 deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 2q37 deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosome 2q37 deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosome 4q21 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 4q21 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 13q14 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 13q14 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 9p deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 9p deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 15q13.3 microdeletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 15q13.3 microdeletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 5q deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 5q deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 1q21.1 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 1q21.1 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q12 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q12 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q11.2 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q11.2 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 19q13.11 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 19q13.11 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 1p36 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 1p36 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 3q29 microdeletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 3q29 microdeletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 3q29 microduplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 3q29 microduplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17p13.3 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17p13.3 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome Xp11.22 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome Xp11.22 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 2q37 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 2q37 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 15q24 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 15q24 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 18q deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 18q deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 22q11.2 microduplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q11.2 microduplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q23.1-q23.2 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q23.1-q23.2 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 6q24-q25 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 6q24-q25 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p11.2 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p11.2 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 18p deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 18p deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 22q11.2 deletion syndrome, distal Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q11.2 deletion syndrome, distal in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 1q21.1 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 1q21.1 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 3q13.31 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 3q13.31 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome Xp21 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome Xp21 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 2p16.1-p15 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 2p16.1-p15 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 10q23 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 10q23 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q21.31 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q21.31 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q12 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q12 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 6pter-p24 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 6pter-p24 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p13.3 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p13.3 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 22q13 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q13 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 15q11.2 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 15q11.2 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 14q11-q22 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 14q11-q22 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 1q41-q42 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 1q41-q42 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p12.2-p11.2 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p12.2-p11.2 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 8q21.11 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 8q21.11 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 5p13 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 5p13 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p11.2 deletion syndrome, 593-kb Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p11.2 deletion syndrome, 593-kb in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 15q26-qter deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 15q26-qter deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 2q31.2 deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 2q31.2 deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p11.2 deletion syndrome, 220-kb Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p11.2 deletion syndrome, 220-kb in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nuclear chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Condensed chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Condensed chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
chromosome, telomeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
chromosome, centromeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Condensed chromosome, centromeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Condensed chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Condensed nuclear chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Condensed nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Inactive sex chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inactive sex chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Mitochondrial chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Mitochondrial chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
chromosome, centromeric core domain Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the chromosome, centromeric core domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
chromosome, telomeric repeat region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the chromosome, telomeric repeat region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Chromosome passenger complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Chromosome passenger complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
chromosome, subtelomeric region Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the chromosome, subtelomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Polytene chromosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Polytene chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
chromosome, telomeric repeat region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the chromosome, telomeric repeat region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
chromosome, centromeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
chromosome, telomeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Mitochondrial chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Condensed nuclear chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Condensed nuclear chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Condensed chromosome, centromeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Condensed chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Chromosome passenger complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Chromosome passenger complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
chromosome, centromeric core domain Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the chromosome, centromeric core domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Condensed chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Condensed chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Nuclear chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Z chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Z chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
W chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the W chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Polytene chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Polytene chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
chromosome, subtelomeric region Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the chromosome, subtelomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Inactive sex chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inactive sex chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Plastid chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Plastid chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Polytene chromosome interband Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Polytene chromosome interband cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Active sex chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Active sex chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Polytene chromosome band Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Polytene chromosome band cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Polytene chromosome chromocenter Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Polytene chromosome chromocenter cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Chloroplast chromosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Chloroplast chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Polytene chromosome puff Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Polytene chromosome puff cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Chromosome 2q32-q33 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 17q23.1-q23.2 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 17q23.1-q23.2 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 2p16.3 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 2p16.3 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 17q11.2 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 17q11.2 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 1q21.1 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 1q21.1 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 5Q14.3 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 5Q14.3 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 2q37 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 2q37 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 1p32-p31 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 1p32-p31 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 1p36 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 1p36 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chromosome 22q11.2 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chromosome 22q11.2 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mosaic loss of chromosome Y Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosaic loss of chromosome Y phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
B cell acute lymphoblastic leukaemia (Philadelphia chromosome negative) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the B cell acute lymphoblastic leukaemia (Philadelphia chromosome negative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chromosomal aberration frequency (chromosome type) in genotoxic compound exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chromosomal aberration frequency (chromosome type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
High chromosomal aberration frequency (chromosome type) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromosome type) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chromosomal aberration frequency (chromosome type) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chromosomal aberration frequency (chromosome type) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multicentric osteolysis, nodulosis and arthropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy dilated with woolly hair and keratoderma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone fragility with contractures, arterial rupture, and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor v and factor viii, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary Paragangliomas and Pheochromocytomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Band-like calcification with simplified gyration and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

akap95 role in mitosis and chromosome dynamics Gene Set

akap95 Gene Set

A-kinase anchoring protein 95 (AKAP95) Gene Set

Intracellular signaling and cytoskeletal dynamics Gene Set

Cytoskeletal dynamics and intracellular transport Gene Set

Cytoskeletal organization and cell adhesion dynamics Gene Set

Mitochondrial dynamics and metabolism Gene Set

Regulation of Cytoskeletal Dynamics and Cell Morphology Gene Set

Regulation of Cytoskeletal Dynamics and Gene Expression Gene Set

GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene Set

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

dynamics Gene Set

Regulation of actin dynamics for phagocytic cup formation Gene Set

Regulation of actin dynamics for phagocytic cup formation Gene Set

APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set

APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set

FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set

chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

proximal chromosome 9p to q and distal chromosome 9q Gene Set

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

role of erbb2 in signal transduction and oncology Gene Set

role of ß-arrestins in the activation and targeting of map kinases Gene Set

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

endocytotic role of ndk phosphins and dynamin Gene Set

ion channels and their functional role in vascular endothelium Gene Set

role of brca1 brca2 and atr in cancer susceptibility Gene Set

The role of Nef in HIV-1 replication and disease pathogenesis Gene Set

Model for regulation of MSMP expression in cancer cells and its proangiogenic role in ovarian tumors Gene Set

MAP3K1 role in promoting and blocking gonadal determination Gene Set

The role of Nef in HIV-1 replication and disease pathogenesis Gene Set

NEVER IN MITOSIS GENE A-RELATED KINASE 1 Gene Set

mitosis Gene Set

positive regulation of transcription from rna polymerase ii promoter during mitosis Gene Set

negative regulation of transcription from rna polymerase ii promoter during mitosis Gene Set

positive regulation of exit from mitosis Gene Set

negative regulation of transcription during mitosis Gene Set

positive regulation of transcription on exit from mitosis Gene Set

negative regulation of exit from mitosis Gene Set

microtubule cytoskeleton organization involved in mitosis Gene Set

exit from mitosis Gene Set

regulation of transcription during mitosis Gene Set

cell cycle comprising mitosis without cytokinesis Gene Set

regulation of exit from mitosis Gene Set

positive regulation of transcription during mitosis Gene Set

abnormal mitosis Gene Set

mitosis Gene Set

cell cycle comprising mitosis without cytokinesis Gene Set

exit from mitosis Gene Set

positive regulation of exit from mitosis Gene Set

regulation of exit from mitosis Gene Set

microtubule cytoskeleton organization involved in mitosis Gene Set

negative regulation of exit from mitosis Gene Set

positive regulation of transcription involved in exit from mitosis Gene Set

abnormal mitosis Gene Set

cell cycle comprising mitosis without cytokinesis Gene Set

microtubule cytoskeleton organization involved in mitosis Gene Set

exit from mitosis Gene Set

positive regulation of exit from mitosis Gene Set

regulation of exit from mitosis Gene Set

negative regulation of exit from mitosis Gene Set

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene Set

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome Gene Set

chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set

chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set

chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set