189101
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TOP6B like initiator of meiotic double strand breaks |
C11orf80, HYDM4, TOPOVIBL |
Curated: Bipolar disorder, Breast cancer, Hydatidiform mole, Gout
Unreviewed: Bipolar Disorder, Complete Hydatidiform Mole, Uterine neoplasm
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189102
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Testis and ovary specific TOPAZ 1 |
C3orf77 |
Curated: Oligodendroglioma, Schizophrenia
Unreviewed: Neoplasms, Uterine neoplasm
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189103
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DNA topoisomerase II binding protein 1 |
Dpb11, TOP2BP1 |
Curated: Lymphocytic b-cell leukemia, Oligodendroglioma, Pulmonary arterial hypertension
Unreviewed: Ataxia telangiectasia, Beta-ketothiolase deficiency, Bloom Syndrome, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Colorectal Cancer, Colorectal neoplasm, Congenital Chromosomal Disease, Ductal Carcinoma, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Epileptic Encephalopathy, Glycogen storage disease, Hereditary cancer, Laryngeal carcinoma, Laryngeal neoplasm, Larynx cancer, Leiomyosarcoma, Lobular carcinoma, Lung Cancer, Lung carcinoma, Lymphocytic Leukemia, Malignant Neoplasm, Mammary Neoplasms, Necrosis, Neoplasms, Opitz GBBB Syndrome, X-Linked, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Polycystic kidney disease, Prostatic neoplasm, Pulmonary Hypertension, Retinoblastoma, Sarcoma, Sick sinus syndrome, Stomach neoplasms, Vascular disease
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189104
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TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase |
LUN, P53BP3, RP31, TP53BPL |
Curated: Choroideremia, Ciliopathy, Hyperopia, Macular degeneration, Macular dystrophy, Metabolic syndrome, Optic atrophy, Orofaciodigital syndrome, Osteosarcoma, Retinitis pigmentosa, Diabetes mellitus type 2, TOPORS-related retinopathy
Unreviewed: Atrioventricular block, Cataract, Ciliopathies, Colorectal neoplasm, Congenital Hypoplasia Of Penis, Diabetes Mellitus, Disorder Of Eye, Glaucoma, Glioblastoma, Hearing Loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leukemia, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphoblastic Leukemia, Malnutrition, Mental retardation, Neoplasms, Nystagmus, Obesity, Optic Atrophy, Patterned macular dystrophy, Polydactyly, Promyelocytic leukemia, Prostate cancer, Prostatic Neoplasms, Retinal Dystrophy, Retinitis Pigmentosa, Rod-cone dystrophy, Small cell lung carcinoma
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189105
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Topoisomerase I binding, arginine and serine rich like, pseudogene |
TOPORSLP1 |
Curated: N/A
Unreviewed: N/A
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189106
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Torsin family 1 member A |
AMC5, DQ2, DYT1 |
Curated: Arthrogryposis multiplex congenita, Dystonia, Dystonia musculorum deformans, Torsion dystonia, Early-onset generalized limb-onset dystonia, Genetic torsion dystonia, Prostate cancer, Depression
Unreviewed: Anxiety Disorder, Arachnoid cysts, Arthrogryposis, Atherosclerosis, Autism, Autoimmune disease, Autoimmune hepatitis, Benign Essential Blepharospasm, Blepharospasm, Calcium metabolism disorders, Celiac disease, Choreoathetosis, CNS Disorder, Cognition disorder, Cognitive disorder, Colitis, Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects, Contracture, Coronary artery disease, Cortical development malformation, Crohn disease, Dementia, Dermatitis herpetiformis, Developmental Delay, Developmental disability, Diabetes Mellitus, Diabetes mellitus, type 1, Dysarthria, Dyskinesia, Dyskinetic Syndrome, Epilepsy, Extrapyramidal disease, Facial dysmorphism syndrome, Focal dystonia, Gastrointestinal disease, Hamartoma, Hereditary spastic paraplegia, Impaired Cognition, Intellectual developmental disorder, Irritable bowel syndrome, Laryngeal dystonia, Learning disorders, Lewy body disease, Limb-Onset Dystonia, Lymphoid leukemia, Machado-Joseph Disease, Major depressive disorder, Mental Depression, Miller Dieker Syndrome, Movement disorder, Movement Disorders, Multiple Sclerosis, Muscular dystrophy, Myelodysplastic Syndrome, Myoclonic Dystonia, Myoclonus-Dystonia Syndrome, Myotonic dystrophy, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Obsessive-Compulsive Disorder, Panic Disorder, Parkinson disease, Personality Disorders, Pili Torti-Deafness Syndrome, Prostate Cancer, Hereditary, Pycnodysostosis, Scoliosis, Selective immunoglobulin a deficiency, Skin disease, Spinal Cord Myoclonus, Strabismus, Symmetrical Dyschromatosis Of Extremities, Systemic lupus erythematosus, Tourette Syndrome, Trichohepatoenteric Syndrome, Trifunctional protein deficiency, Vascular disease, Writer`s Cramp
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189107
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Torsin 1A interacting protein 1 |
LAP1, LAP1B, LAP1C, LGMD2Y |
Curated: Limb girdle muscular dystrophy, Centronuclear myopathy, Muscular dystrophy, Prostate cancer, Multisystem disorder, Myopathy, TOR1AIP1-related myopathy
Unreviewed: Breast Cancer, Cardiomyopathy, Cataract, Cerebellar diseases, Congenital abnormalities, Congenital cataract, Congenital heart septal defect, Congestive Heart Failure, Contracture, Developmental disability, Dilated cardiomyopathy, Dysferlinopathy, Dysphagia, Dystonia, Emery-Dreifuss Muscular Dystrophy, X-Linked, Fatty Liver, Glaucoma, Growth disorder, Heart Failure, Limb-Girdle Muscular Dystrophy, Liver carcinoma, Melanoma, Microcephaly, MYOPATHY, WITH RIGID SPINE AND DISTAL JOINT CONTRACTURES, Nervous system disease, Non-Alcoholic Fatty Liver Disease
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189108
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Torsin 1A interacting protein 2 |
IFRG15, LULL1, NET9 |
Curated: Limb girdle muscular dystrophy
Unreviewed: Dyskinesia, Dystonia, Neurodegenerative Disorders
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189109
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Torsin family 1 member B |
DQ1 |
Curated: Nonalcoholic fatty liver disease, Prostate cancer
Unreviewed: Breast neoplasm, Crohn disease, Dystonia, Leprosy, Myotonic dystrophy, Narcolepsy, Renal cell carcinoma
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189110
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TOR1B pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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