1481
|
|
|
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
|
1482
|
|
|
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
|
1483
|
|
|
Torsin 1A interacting protein 2 |
IFRG15, LULL1, NET9 |
Curated: Limb girdle muscular dystrophy
Unreviewed: Dyskinesia, Dystonia, Neurodegenerative Disorders
|
1484
|
|
|
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
|
1485
|
|
|
TOR1B pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1486
|
|
|
Torsin family 2 member A |
TORP1 |
Curated: N/A
Unreviewed: Arteriosclerosis, Atherosclerosis, Blepharospasm, Cardiomyopathy, Cardiovascular Diseases, Congestive Heart Failure, Coronary artery disease, Diabetes Mellitus, Diabetic cardiomyopathy, Heart Failure, Hypertension, Iron overload, Kidney Failure, Multiple Sclerosis, Neuroblastoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Parkinson disease, Polycystic Ovary Syndrome, Stomach neoplasms
|
1487
|
|
|
Torsin family 3 member A |
ADIR, ADIR2 |
Curated: N/A
Unreviewed: Autism, Autism Spectrum Disorder, Mental retardation, Multiple myeloma, ST Segment Elevation Myocardial Infarction
|
1488
|
|
|
Torsin family 4 member A |
C9orf167 |
Curated: N/A
Unreviewed: Glioma, Moyamoya disease, Systemic lupus erythematosus
|
1489
|
|
|
Thymocyte selection associated high mobility group box |
TOX1 |
Curated: Attention deficit hyperactivity disorder, Cannabis abuse, Colorectal cancer, Essential tremor, Inflammatory bowel disease, Insomnia, Iron-refractory iron deficiency anemia, Major depressive disorder, Schizophrenia, Scoliosis, Substance abuse, Diabetes mellitus type 1, Diabetes mellitus type 2
Unreviewed: Adenoma, Anaplastic Lymphoma, Autoimmune disease, Autoimmune Diseases, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Central Nervous System Lymphoma, Colorectal Cancer, Colorectal neoplasm, Dermatitis, Dermatologic Disorders, Diabetes Mellitus, Diabetes mellitus, type 2, Eczema, Glioblastoma, Glioma, Hematologic neoplasm, Hereditary breast and ovarian cancer syndrome, Hodgkin disease, Hypertension, Intracranial Aneurysm, Juvenile arthritis, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lymphoblastic Leukemia, Lymphoma, Lymphomatoid Papulosis, Malignant Neoplasm, Mycosis fungoides, Myeloid leukemia, Neoplasms, Neuroblastoma, Ovarian neoplasm, Pharyngeal Neoplasms, Phyllodes Tumor, Renal cell carcinoma, Rheumatic fever, Sarcoma, Sezary Syndrome, Skin disease, Skin Lesion, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, T-Cell Lymphoma/Leukemia, Thrombosis, Vitiligo
|
1490
|
|
|
TOX divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|