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condensed chromosome inner kinetochore Gene SetFrom 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 chromosome inner kinetochore Gene SetFrom 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 chromosome inner kinetochore Gene SetFrom 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 SetFrom 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 SetFrom 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 chromosome kinetochore Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
condensed chromosome outer kinetochore Gene SetFrom 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. |
condensed nuclear chromosome kinetochore Gene SetFrom 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 SetFrom 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. |
condensed chromosome kinetochore Gene SetFrom 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. |
condensed chromosome outer kinetochore Gene SetFrom 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. |
condensed nuclear chromosome kinetochore Gene SetFrom 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 SetFrom 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 chromosome kinetochore Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
condensed chromosome outer kinetochore Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome outer kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
protein localization to kinetochore involved in kinetochore assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein localization to kinetochore involved in kinetochore assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein localization to kinetochore involved in kinetochore assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein localization to kinetochore involved in kinetochore assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
condensed nuclear chromosome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
condensed chromosome, centromeric region Gene SetFrom 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. |
condensed chromosome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the condensed chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
condensed nuclear chromosome, centromeric region Gene SetFrom 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. |
condensed nuclear chromosome Gene SetFrom 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. |
condensed chromosome Gene SetFrom 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. |
condensed chromosome, centromeric region Gene SetFrom 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. |
condensed nuclear chromosome, centromeric region Gene SetFrom 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. |
condensed nuclear chromosome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the condensed nuclear chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
condensed chromosome, centromeric region Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
condensed chromosome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the condensed chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
condensed nuclear chromosome, centromeric region Gene SetFrom 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. |
protein localization to condensed chromosome Gene SetFrom 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. |
condensed chromosome, centromeric region Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
condensed nuclear chromosome Gene SetFrom 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 SetFrom GO Cellular Component Annotations 2023 proteins localized to the condensed chromosome cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
protein localization to condensed chromosome Gene SetFrom 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. |
condensed chromosome, centromeric region Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
condensed nuclear chromosome Gene SetFrom 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 SetFrom GO Cellular Component Annotations 2025 proteins localized to the condensed chromosome cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Condensed chromosome Gene SetFrom 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. |
Condensed chromosome, centromeric region Gene SetFrom 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 SetFrom 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. |
Condensed nuclear chromosome Gene SetFrom 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 SetFrom 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. |
Condensed chromosome Gene SetFrom 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. |
Inner kinetochore Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inner kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Inner kinetochore Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
chromosome passenger complex localization to kinetochore Gene SetFrom 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. |
histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore Gene SetFrom 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. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom 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. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom 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 SetFrom 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. |
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
condensed Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term condensed in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
kinetochore Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
kinetochore microtubule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the kinetochore microtubule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
kinetochore Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
kinetochore microtubule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the kinetochore microtubule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
NDC80 kinetochore complex Gene Setproteins in the NDC80 kinetochore complex protein complex from the CORUM Protein Complexes dataset. |
kinetochore Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term kinetochore in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of mitotic attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of mitotic attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
kinetochore organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the kinetochore organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of kinetochore assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of kinetochore assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset. |
kinetochore assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the kinetochore assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
kinetochore Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the kinetochore cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
kinetochore microtubule Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the kinetochore microtubule cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
kinetochore binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the kinetochore binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Kinetochore assembly subunit CENP-C, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore assembly subunit CENP-C, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore Mis14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore Mis14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore-associated protein Dsn1/Mis13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore-associated protein Dsn1/Mis13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore-Ndc80 subunit Spc24 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore-Ndc80 subunit Spc24 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore protein Ndc80 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Ndc80 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore component CENP-S Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore component CENP-S protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore protein Nuf2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Nuf2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spindle and kinetochore-associated protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle and kinetochore-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
kinetochore assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the kinetochore assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of kinetochore assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of kinetochore assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
lateral attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lateral attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lateral attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lateral attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
kinetochore organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the kinetochore organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
monopolar spindle attachment to meiosis I kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the monopolar spindle attachment to meiosis I kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lateral attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lateral attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2023 dataset. |
kinetochore microtubule Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the kinetochore microtubule cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
repair of mitotic kinetochore microtubule attachment defect Gene SetFrom GO Biological Process Annotations 2025 genes participating in the repair of mitotic kinetochore microtubule attachment defect biological process from the curated GO Biological Process Annotations 2025 dataset. |
kinetochore assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the kinetochore assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of kinetochore assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of kinetochore assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
lateral attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lateral attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lateral attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lateral attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
kinetochore organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the kinetochore organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
spindle attachment to meiosis I kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spindle attachment to meiosis I kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein localization to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein localization to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of attachment of spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of attachment of spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lateral attachment of mitotic spindle microtubules to kinetochore Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lateral attachment of mitotic spindle microtubules to kinetochore biological process from the curated GO Biological Process Annotations 2025 dataset. |
kinetochore microtubule Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the kinetochore microtubule cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Outer kinetochore Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Kinetochore Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Kinetochore microtubule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Kinetochore microtubule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Kinetochore Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Outer kinetochore Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Kinetochore microtubule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Kinetochore microtubule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
OB inner plexiform layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in OB inner plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Main olfactory bulb, inner plexiform layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Main olfactory bulb, inner plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
inner SZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in rostral perirhinal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in rostral perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in orbital frontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in orbital frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner portion of medial ganglionic eminence Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner portion of medial ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in dorsomedial frontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in dorsomedial frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in (rostral) midinferior temporal cortex (area 36) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in (rostral) midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in dorsolateral prefrontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in dorsolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in midinferior temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in posterosuperior (dorsal) parietal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in caudal cingulate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in ventrolateral prefrontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in ventrolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in granular insular cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in granular insular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in dorsomedial frontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in dorsomedial frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in ventromedial extrastriate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in ventromedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in posteroinferior (ventral) parietal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in caudal perirhinal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in ventromedial extrastriate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in ventromedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in midcingulate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in midcingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in posteroinferior (ventral) parietal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in dorsomedial parietal cortex (area 7m) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in midlateral extrastriate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in midlateral extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in posterosuperior (dorsal) parietal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in ventrolateral prefrontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in ventrolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in midlateral extrastriate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in midlateral extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in dorsomedial parietal cortex (area 7m) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in dorsomedial extrastriate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in dorsomedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in subgenual (subcallosal) cingulate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in subgenual (subcallosal) cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in frontal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in frontal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in dysgranular insular cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in dysgranular insular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in dorsomedial extrastriate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in dorsomedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in posteror frontal cortex (motor cortex) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in rostral cingulate cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in rostral cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in frontal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in frontal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in dorsolateral prefrontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in dorsolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner portion of lateral ganglionic eminence Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner portion of lateral ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in orbital frontal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in orbital frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in posteror frontal cortex (motor cortex) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom 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. |
mitochondrial inner membrane peptidase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
organelle inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the organelle inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
inner acrosomal membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the inner acrosomal membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
intrinsic component of nuclear inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the intrinsic component of nuclear inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
photoreceptor inner segment membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the photoreceptor inner segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial inner membrane presequence translocase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
intrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
integral component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the integral component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
extrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
photoreceptor inner segment Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the photoreceptor inner segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
integral component of nuclear inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the integral component of nuclear inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
inner mucus layer Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the inner mucus layer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nuclear inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
plastid inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plastid inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
inner dynein arm Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inner dynein arm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial inner membrane peptidase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial inner membrane peptidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
viral inner capsid Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the viral inner capsid cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female germline ring canal inner rim Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germline ring canal inner rim cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
inner acrosomal membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inner acrosomal membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
organelle inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the organelle inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
photoreceptor inner segment membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the photoreceptor inner segment membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial inner membrane presequence translocase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial inner membrane presequence translocase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
intrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the intrinsic component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
integral component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the integral component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
photoreceptor inner segment Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the photoreceptor inner segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
inner mucus layer Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inner mucus layer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
chloroplast inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chloroplast inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
inner membrane complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inner membrane complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial inner membrane protein insertion complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial inner membrane protein insertion complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
nuclear inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset. |
inner ear disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease inner ear disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
inner ear disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inner ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
inner Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term inner in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
inner ear morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner ear morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner ear receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
nuclear inner membrane organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nuclear inner membrane organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of inner ear receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
renal inner medulla development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the renal inner medulla development biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein import into mitochondrial inner membrane Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein import into mitochondrial inner membrane biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cellular morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cellular morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner ear receptor cell development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner ear receptor cell development biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of inner ear receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner ear development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner ear development biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner dynein arm assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner dynein arm assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of inner ear receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner ear receptor stereocilium organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner ear receptor stereocilium organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner cell mass cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner cell mass cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner mitochondrial membrane organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner mitochondrial membrane organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner ear receptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner ear receptor cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondrial inner membrane peptidase complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
organelle inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the organelle inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
inner acrosomal membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the inner acrosomal membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
intrinsic component of nuclear inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the intrinsic component of nuclear inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
photoreceptor inner segment membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the photoreceptor inner segment membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
integral component of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the integral component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
mitochondrial inner membrane presequence translocase complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
extrinsic component of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
photoreceptor inner segment Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the photoreceptor inner segment cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
intrinsic component of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
integral component of nuclear inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the integral component of nuclear inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
inner mucus layer Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the inner mucus layer cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
nuclear inner membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the nuclear inner membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
inner ear disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease inner ear disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
neoplasm of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the vestibule of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent inner and outer dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent inner and outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dilated vestibule of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the dilated vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
functional abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent inner dynein arms Gene SetFrom HPO Gene-Disease Associations genes associated with the absent inner dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Mitochondrial import inner membrane translocase subunit Tim21 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim21 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial import inner membrane translocase subunit Tim44 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim44 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial import inner membrane translocase subunit Tim10/Tim12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim10/Tim12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inner centromere protein, ARK-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inner centromere protein, ARK-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial inner membrane translocase complex, subunit Tim23 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim23 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inner nuclear membrane protein MAN1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inner nuclear membrane protein MAN1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial inner membrane protease subunit 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial inner membrane protease subunit 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial inner membrane protein Mitofilin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial inner membrane protein Mitofilin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial import inner membrane translocase subunit Tim16 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim16 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial import inner membrane translocase subunit Tim50 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim50 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial inner membrane translocase complex, subunit Tim17 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim17 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
organelle inner membrane Gene SetFrom LOCATE Curated Protein Localization Annotations proteins localized to the organelle inner membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset. |
mitochondrial inner membrane Gene SetFrom LOCATE Curated Protein Localization Annotations proteins localized to the mitochondrial inner membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset. |
abnormal retinal inner nuclear layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
disorganized photoreceptor inner segment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cochlear inner hair cell degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short photoreceptor inner segment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal cone cell inner segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair follicle inner root sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inner cell mass degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inner ear cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inner ear cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner cell mass proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent retinal inner plexiform layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal orientation of inner hair cell stereociliary bundles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner hair cell kinocilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased inner cell mass proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small inner medullary pyramid Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrial inner membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial inner membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed inner ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner cell mass proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
photoreceptor inner segment degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner ear vestibule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner ear vestibule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner cell mass apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner hair cell synaptic ribbon morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner hair cell kinocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood-inner ear barrier function Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood-inner ear barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent photoreceptor inner segment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner ear canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner ear canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cochlear inner hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner ear canal fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner ear canal fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin retinal inner nuclear layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fused inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased inner hair cell stereocilia number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner ear morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner ear morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
disorganized inner root sheath cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized inner root sheath cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney outer medulla inner stripe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney outer medulla inner stripe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin hair follicle inner rooth sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin hair follicle inner rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin retinal inner plexiform layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner cell mass morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner cell mass morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal rod cell inner segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney inner medulla morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney inner medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent active-zone-anchored inner hair cell synaptic ribbon Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner ear vestibule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner ear vestibule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal photoreceptor inner segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal photoreceptor inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner ear Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner ear phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inner ear hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inner ear hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retina inner limiting membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retina inner limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner plexiform layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner nuclear layer thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
disorganized retinal inner nuclear layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle inner root sheath morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased inner cell mass apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
deafness, congenital with inner ear agenesis, microtia, and microdontia Gene SetFrom OMIM Gene-Disease Associations genes associated with the deafness, congenital with inner ear agenesis, microtia, and microdontia phenotype from the curated OMIM Gene-Disease Associations dataset. |
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset. |
inner ear Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue inner ear from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
renal inner medulla Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal inner medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner nuclear layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner nuclear layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner ear Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair follicle inner root sheath Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner ear vestibulum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner ear vestibulum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner dental epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner dental epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner plexiform layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner chondrogenic layer of perichondrium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner chondrogenic layer of perichondrium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Punctate Inner Choroidopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Punctate Inner Choroidopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autoimmune Inner Ear Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Inner Ear Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dilated Vestibule Of The Inner Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dilated Vestibule Of The Inner Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Aplasia Of Inner Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Aplasia Of Inner Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Abnormal Shape Of Inner Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Abnormal Shape Of Inner Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Inner And Outer Dynein Arms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Inner And Outer Dynein Arms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Inner Dynein Arms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Inner Dynein Arms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Inner Ear Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inner Ear Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Morphological Abnormality Of The Inner Ear Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Morphological Abnormality Of The Inner Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
inner mitochondrial membrane organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner mitochondrial membrane organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner dynein arm assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner dynein arm assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner ear receptor cell development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner ear receptor cell development biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner ear receptor cell stereocilium organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner ear receptor cell stereocilium organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner ear morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner ear morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein insertion into mitochondrial inner membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein insertion into mitochondrial inner membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner ear receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
nuclear inner membrane organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nuclear inner membrane organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of inner ear auditory receptor cell fate specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of inner ear auditory receptor cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein insertion into mitochondrial inner membrane from matrix Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein insertion into mitochondrial inner membrane from matrix biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner cell mass cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein localization to nuclear inner membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein localization to nuclear inner membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner ear auditory receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of inner ear auditory receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein insertion into membrane from inner side Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein insertion into membrane from inner side biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner ear receptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner ear receptor cell fate commitment biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
nuclear inner membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the nuclear inner membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
TIM23 mitochondrial import inner membrane translocase complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the TIM23 mitochondrial import inner membrane translocase complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
TIM22 mitochondrial import inner membrane insertion complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the TIM22 mitochondrial import inner membrane insertion complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
matrix side of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the matrix side of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
extrinsic component of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
organelle inner membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the organelle inner membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
inner dynein arm Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the inner dynein arm cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
inner acrosomal membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the inner acrosomal membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal inner ear morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner ear morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
inner ear cyst Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the inner ear cyst phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner ear vestibule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner ear vestibule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cochlear inner hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner ear canal fusion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner ear canal fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear inner hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inner cell mass proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cochlear inner hair cell degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal photoreceptor inner segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal photoreceptor inner segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear inner hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney inner medulla morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney inner medulla morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short photoreceptor inner segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small inner medullary pyramid Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina inner nuclear layer morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner nuclear layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner cell mass proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner cell mass proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner cell mass proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner cell mass proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased inner cell mass apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased inner cell mass apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner cell mass morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner cell mass morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle inner root sheath morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin retina inner nuclear layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina inner nuclear layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
inner cell mass degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina inner plexiform layer morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner plexiform layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner ear vestibule Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner ear vestibule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell stereociliary bundle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin retina inner plexiform layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina rod cell inner segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina rod cell inner segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell synaptic ribbon morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent active-zone-anchored inner hair cell synaptic ribbon Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized retina inner nuclear layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized retina inner nuclear layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner cell mass apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner cell mass apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner ear canal morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner ear canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent photoreceptor inner segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent photoreceptor inner segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal orientation of inner hair cell stereociliary bundles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed inner ear development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear inner hair cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear inner hair cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner cell mass Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner cell mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner ear Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner ear phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inner hair cell stereocilia number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood-inner ear barrier function Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood-inner ear barrier function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney outer medulla inner stripe morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney outer medulla inner stripe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair follicle inner root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized photoreceptor inner segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized photoreceptor inner segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell kinocilium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
inner ear hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the inner ear hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin hair follicle inner root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin hair follicle inner root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent retina inner plexiform layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell kinocilium location or orientation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell kinocilium location or orientation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina inner limiting membrane morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner limiting membrane morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased inner canthal distance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased inner canthal distance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina cone cell inner segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina cone cell inner segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner hair cell kinocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
photoreceptor inner segment degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized inner root sheath cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized inner root sheath cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick retina inner plexiform layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina inner nuclear layer thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner nuclear layer thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inner canthal distance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inner canthal distance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mitochondrial inner membrane morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mitochondrial inner membrane morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner ear development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner ear development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retina inner nuclear layer morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal retina inner nuclear layer morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Kidney - L2 - Inner Medullary Collecting Duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Inner Medullary Collecting Duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Inner radial glial cell_Cortex_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner radial glial cell_Cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner hair cell_Cochlea_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner hair cell_Cochlea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner phalangeal cell_Inner Ear_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner phalangeal cell_Inner Ear_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner Cell_Embryo_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner Cell_Embryo_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner cell mass cell_Embryo_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner cell mass cell_Embryo_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner cell mass_Embryo_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner cell mass_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner cell mass cell_Inner cell mass_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner cell mass cell_Inner cell mass_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner Medullary Collecting Ductal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner Medullary Collecting Ductal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner Medullary Collecting Ductal cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner Medullary Collecting Ductal cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner root sheath cell_Skin_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner root sheath cell_Skin_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Sensory processing of sound by inner hair cells of the cochlea Gene Setproteins participating in the Sensory processing of sound by inner hair cells of the cochlea pathway from the Reactome Pathways 2024 dataset. |
inner mitochondrial membrane organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner mitochondrial membrane organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner dynein arm assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner dynein arm assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner ear receptor cell development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner ear receptor cell development biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner ear receptor cell stereocilium organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner ear receptor cell stereocilium organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner cell mass cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner ear morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner ear morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein insertion into mitochondrial inner membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein insertion into mitochondrial inner membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondrial inner membrane fusion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondrial inner membrane fusion biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner ear receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
nuclear inner membrane organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nuclear inner membrane organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein insertion into mitochondrial inner membrane from matrix Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein insertion into mitochondrial inner membrane from matrix biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of inner ear auditory receptor cell fate specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of inner ear auditory receptor cell fate specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein localization to nuclear inner membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein localization to nuclear inner membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner ear auditory receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein insertion into membrane from inner side Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein insertion into membrane from inner side biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of inner ear auditory receptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner ear receptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner ear receptor cell fate commitment biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
nuclear inner membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the nuclear inner membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
TIM23 mitochondrial import inner membrane translocase complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the TIM23 mitochondrial import inner membrane translocase complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
matrix side of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the matrix side of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
TIM22 mitochondrial import inner membrane insertion complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the TIM22 mitochondrial import inner membrane insertion complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
inner acrosomal membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the inner acrosomal membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
inner dynein arm Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the inner dynein arm cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
extrinsic component of mitochondrial inner membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
mitochondrial inner membrane peptidase complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Inner ear disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Inner ear disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inner ear disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inner ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inner ear cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inner ear cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inner ear Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Inner ear from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner ear Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner nuclear layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner nuclear layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle inner root sheath Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner ear vestibulum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner ear vestibulum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner plexiform layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner chondrogenic layer of perichondrium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner chondrogenic layer of perichondrium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner dental epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner dental epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Renal inner medulla Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal inner medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner mantle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner mantle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Organelle inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Organelle inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Nuclear inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor inner segment Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Photoreceptor inner segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
TIM22 mitochondrial import inner membrane insertion complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the TIM22 mitochondrial import inner membrane insertion complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Inner mitochondrial membrane protein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inner mitochondrial membrane protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor inner segment membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Photoreceptor inner segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Matrix side of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Matrix side of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
TIM23 mitochondrial import inner membrane translocase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the TIM23 mitochondrial import inner membrane translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Integral component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Integral component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Intrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Inner acrosomal membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inner acrosomal membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner membrane peptidase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Mitochondrial inner membrane peptidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Inner dynein arm Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inner dynein arm cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Extrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Extrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Inner mucus layer Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inner mucus layer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Nuclear pore inner ring Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear pore inner ring cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Inner dense plaque of desmosome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Inner dense plaque of desmosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner membrane peptidase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial inner membrane peptidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Organelle inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Organelle inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Inner mitochondrial membrane protein complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner mitochondrial membrane protein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Nuclear inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
TIM23 mitochondrial import inner membrane translocase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the TIM23 mitochondrial import inner membrane translocase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Inner dynein arm Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner dynein arm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Integral component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Integral component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
TIM22 mitochondrial import inner membrane insertion complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the TIM22 mitochondrial import inner membrane insertion complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Inner mucus layer Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner mucus layer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Chloroplast inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Chloroplast inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Plastid inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Plastid inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor inner segment Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor inner segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Inner acrosomal membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner acrosomal membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Nuclear pore inner ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear pore inner ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Inner dense plaque of desmosome Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner dense plaque of desmosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor inner segment membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor inner segment membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner membrane assembly complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial inner membrane assembly complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner boundary membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial inner boundary membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Integral component of chloroplast inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Integral component of chloroplast inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of plastid inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of plastid inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Integral component of plastid inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Integral component of plastid inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of chloroplast inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of chloroplast inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cyanelle inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cyanelle inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Extrinsic component of mitochondrial inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Extrinsic component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Spore inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Spore inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Chromoplast inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Chromoplast inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Integral component of nuclear inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Integral component of nuclear inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Inner membrane pellicle complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Inner membrane pellicle complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of nuclear inner membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of nuclear inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial inner-outer membrane contact site Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial inner-outer membrane contact site cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Absent inner and outer dynein arms Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Absent inner and outer dynein arms phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
akap95 role in mitosis and chromosome dynamics Gene SetFrom Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset. |
Chromosome 2q32-q33 deletion syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chromosome 9q deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
cytoplasmic chromosome Gene SetFrom 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 SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the sex chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nuclear chromosome Gene SetFrom 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 SetFrom 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. |
nuclear chromosome part Gene SetFrom 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 SetFrom 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 SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial chromosome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nuclear chromosome, telomeric region Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome passenger complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
chromosome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytoplasmic chromosome Gene SetFrom 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 SetFrom 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. |
polytene chromosome chromocenter Gene SetFrom 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. |
polytene chromosome puff Gene SetFrom 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 SetFrom 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 SetFrom 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. |
y chromosome Gene SetFrom 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. |
nuclear chromosome part Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
z chromosome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
chromosome Gene SetFrom 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. |
Chromosome 17 deletion Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
increased chromosome aberrations and higher lung cancer risk Gene SetFrom 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. |
adenocarcinoma; chromosome deletion; lung neoplasms; neoplasm of lung Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma Gene SetFrom 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. |
acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
carcinoma, squamous cell; chromosome breakage; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene SetFrom 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. |
chromosome aberrations; dna damage Gene SetFrom 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. |
carcinoma, squamous cell; chromosome breakage; head and neck neoplasms Gene SetFrom 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. |
breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 spindle midzone Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GO Biological Process Annotations 2015 genes participating in the chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein localization to chromosome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GO Cellular Component Annotations 2015 proteins localized to the sex chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
nuclear chromosome Gene SetFrom 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 SetFrom GO Cellular Component Annotations 2015 proteins localized to the chromosome, centromeric core domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
nuclear chromosome part Gene SetFrom 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 SetFrom 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 SetFrom GO Cellular Component Annotations 2015 proteins localized to the chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
mitochondrial chromosome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
nuclear chromosome, telomeric region Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GO Cellular Component Annotations 2015 proteins localized to the chromosome passenger complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
chromosome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the chromosome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
abnormality of chromosome condensation Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dosage compensation, by inactivation of x chromosome phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrial chromosome morphology Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 5q14.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
chromosome Gene SetFrom 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 Setproteins participating in the Chromosome Maintenance pathway from the Reactome Pathways dataset. |
Philadelphia Chromosome Positive Chronic Myelogenous Leukemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome Gene SetFrom 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 2Q37 Deletion Syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |