187921
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TBX2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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187922
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T-box transcription factor 20 |
ASD4 |
Curated: Aortic valve disease, Atherosclerosis, Atrial fibrillation, Atrial septal defect, Brugada syndrome, Cardiomegaly, Dilated cardiomyopathy, Fatigue syndrome, Liver cirrhosis, Congenital heart disease, Congestive heart failure, Coronary artery disease, Dementia, Hypertension, Heart failure, Hypoplastic left heart syndrome, Left ventricular disease, Myocardial infarction, Nonalcoholic fatty liver disease, Obesity, Right hypoplastic heart syndrome, Tetralogy of fallot, Ventricular remodeling, Ventricular septal defect, Wolff-parkinson-white syndrome
Unreviewed: Aortic Aneurysm, Arteriosclerosis, Atrial Septal Defect, Bicuspid aortic valve, Blepharophimosis, ptosis, and epicanthus inversus syndrome, Carcinogenesis, Carcinoma, Cardiac arrhythmias, Cardiomyopathy, Cardiovascular disease, Cardiovascular Diseases, Colorectal neoplasm, Congenital abnormalities, Congenital heart defect, Congenital heart defects, Congenital Heart Disease, Congenital heart septal defect, Congestive Heart Failure, Coronary Heart Disease, Double Outlet Right Ventricle, Heart disease, Heart Diseases, Heart Failure, Hypoplastic Heart Syndrome, Hypoplastic Left Heart Syndrome, Intellectual developmental disorder, Long QT Syndrome, Microphthalmia, Myocardial Infarction, Patent ductus arteriosus, Pulmonary Venous Return Anomaly, Retinitis Pigmentosa, Secundum atrial septal defect, Squamous cell carcinoma, Tetralogy of Fallot, Thoracic aortic aneurysm, Wolff-Parkinson-White Syndrome
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187923
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T-box transcription factor 21 |
IMD88, T-PET, T-bet, TBET, TBLYM |
Curated: Asthma, Eczema, Autoimmune thyroid disease, Dementia, Diverticular disease, Hypothyroidism, Immunodeficiency, Kidney failure, Major depressive disorder, Metabolic syndrome, Myopathy, Respiratory system disease, Schizophrenia, Diabetes mellitus type 2, Depression, Asthma, aspirin-induced, susceptibility to
Unreviewed: Alzheimer disease, Amelogenesis Imperfecta, X-Linked, Androgen-Insensitivity Syndrome, Anemia, Angioimmunoblastic T-cell lymphoma, Ankylosing Spondylitis, Aplastic anemia, Arthritis, Ataxia telangiectasia, Atopic dermatitis, Autism, Autoimmune disease, Autoimmune Diseases, Autoimmune hepatitis, Behcet disease, Behcet Syndrome, Bile duct neoplasms, Biliary Cirrhosis, Breast neoplasm, Bronchial Hyperreactivity, Carcinogenesis, Carotid artery disease, Cognition disorder, Colorectal Cancer, Colorectal neoplasm, Complete Atrioventricular Block, Coronary artery disease, Coronary Syndrome, Critical illness, Crohn Disease, Dermatitis, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Diarrhea, Dilated cardiomyopathy, Ectodermal dysplasia, Endometriosis, Eosinophilia, Esophageal achalasia, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Gastroesophageal reflux disease, Gingival diseases, Glioma, Gout, Graft-versus-host disease, Graves Disease, Hairy Cell Leukemia, Hashimoto Disease, Hematologic disease, Hepatitis c, Hepatocellular carcinoma, Hodgkin Disease, Hyperglycemia, Hypersensitivity, Hyperthyroidism, Idiopathic pulmonary fibrosis, Immune system disease, Immune System Diseases, Immune Thrombocytopenic Purpura, Incontinentia Pigmenti Achromians, Inflammatory Bowel Disease, Irritable Bowel Syndrome, Juvenile arthritis, Kawasaki disease, Kidney disease, Leukemia, Liver carcinoma, Liver neoplasms, Lung adenocarcinoma, Lung carcinoma, Lung Neoplasms, Lupus Erythematosus, Lupus Vulgaris, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphoma, Lymphoproliferative syndrome, Malignant Neoplasm, Melanoma, Mental Depression, Multiple Sclerosis, Myocardial infarction, Myocarditis, Nasal polyp, Nasal polyposis, Neoplasms, Nephrotic syndrome, Neutrophilia, Obesity, Oropharyngeal neoplasm, Osteoporosis, Ovarian cancer, Ovarian Epithelial carcinoma, Pancytopenia, Parkinson disease, Periodontal disease, Periodontitis, Prostate cancer, Pseudohyperkalemia Cardiff, Psoriatic arthritis, Pulmonary Fibrosis, Renal cell carcinoma, Rheumatoid arthritis, Sarcoidosis, Scleroderma, Sclerosing cholangitis, Sezary Syndrome, Sjogren syndrome, Sleep deprivation, Spondyloarthritis, Squamous cell carcinoma, Status epilepticus, Stomach Carcinoma, Stomach Neoplasms, Stress Disorder, Systemic lupus erythematosus, Systemic sclerosis, T-Cell Lymphoma, Thrombocytopenia, Thyroid Diseases, Thyroiditis, Triple negative breast cancer, Triple Negative Breast Neoplasms, Tropical spastic paraparesis, Turcot syndrome, Ulcerative colitis, Urinary bladder neoplasms, Uveitis, Uveomeningoencephalitic syndrome, Vasculitis, Wiskott-Aldrich Syndrome
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187924
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T-box transcription factor 22 |
ABERS, CLPA, CPX, TBXX, dJ795G23.1 |
Curated: Abruzzo-erickson syndrome, Cleft palate, Cleft palate with ankyloglossia, Cleft palate x-linked, Orofacial cleft, Scoliosis, Uranostaphyloschisis, X-linked cleft palate and ankloglossia, Cleft lip
Unreviewed: Abruzzo-Erickson Syndrome, Acute Myeloid Leukemia, Ankyloglossia, Anodontia, Aortic Valve Sclerosis, Atrial Septal Defect, Brachydactyly, Cleft Palate And Ankyloglossia, X-Linked, Cleft Palate With Ankyloglossia, Cleft palate with coloboma of eye and deafness, Clinodactyly, Colorectal Cancer, Colorectal neoplasm, Congenital Coloboma Of Iris, Congenital Epicanthus, Congenital ocular coloboma, Coronal hypospadias, Cryptorchidism, Cystic Fibrosis, Dwarfism, Dysmorphism, Fundus Coloboma, Gastrointestinal Neoplasms, Growth disorder, Hearing Loss, Hematologic Neoplasms, Hypodontia, Hypospadias, Kidney disease, Leukemia, Macrotia, Mental retardation, Microcornea, Monocytic Leukemia, Myeloblastic Leukemia, Myeloid leukemia, Osteomyelitis, Otofaciocervical syndrome, Polydactyly, Radioulnar Synostosis, Renal Insufficiency, Retinal coloboma, Submucosal cleft palate, Syndactyly Of The Toes, Van der woude syndrome, Warburg micro syndrome
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187925
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T-box transcription factor 23, pseudogene |
TBX23 |
Curated: N/A
Unreviewed: N/A
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187926
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T-box transcription factor 3 |
TBX3-ISO, UMS, XHL |
Curated: Benign prostatic hyperplasia, Breast cancer, Breast neoplasms, Cerebrovascular disorder, Colorectal adenoma, Colorectal cancer, Desbuquois syndrome, Heart disease, Congenital anomaly of limb, Periprosthetic osteolysis, Prostatic neoplasms, Stomach neoplasms, Stroke, Thyroid disease, Tooth abnormalities, Ulnar-mammary syndrome, Squamous cell carcinoma, Adenoid cystic carcinoma, Thyroid carcinoma, Osteosarcoma, Anaplastic oligodendroglioma, Lobular carcinoma, Carcinoma, Small cell carcinoma, Lymphoblastic leukemia, Diffuse large b-cell lymphoma, Leiomyosarcoma, Glioblastoma, Pancreatic ductal carcinoma, Ductal carcinoma of breast, Gastrointestinal stromal tumor, Ovarian mucinous adenocarcinoma, B-cell acute lymphoblastic leukemia, Lung cancer, Uveal melanoma, Esophageal adenocarcinoma, Non-small cell lung carcinoma, Large cell carcinoma, Hepatocellular carcinoma, Oral cavity carcinoma, Renal cell carcinoma, Endometrial hyperplasia, Skin cancer, Melanoma, Gastric cancer, Small cell lung carcinoma, Testicular carcinoma, Anaplastic astrocytoma, Oligodendroglioma, Hodgkin lymphoma, Basal cell carcinoma, Prostate cancer, Esophageal squamous cell carcinoma, Transitional cell carcinoma, Childhood kidney wilms tumor, Neuroblastoma, Clear cell renal cell carcinoma, Parathyroid carcinoma, Bile duct cancer, Gallbladder neoplasms, Nodular malignant melanoma, Metaplastic breast carcinoma, Brain stem glioblastoma, Eccrine porocarcinoma, T-cell large granular lymphocyte leukemia, Small intestine adenocarcinoma, Adrenal cortex carcinoma, Breast phyllodes tumor, Thyroid gland oncocytic adenoma, B-cell non-hodgkin lymphoma, Conjunctival intraepithelial neoplasm, Mantle cell lymphoma, Ovarian clear cell adenocarcinoma, Rectum adenocarcinoma, Cecum adenocarcinoma, T-cell prolymphocytic leukemia, Duodenal adenocarcinoma, Gallbladder adenoma, Breast carcinoma by gene expression profile, Acral lentiginous melanoma, Gastric neuroendocrine tumor g1, Extramammary paget disease, Gastresophageal junction adenocarcinoma, Endometrium adenocarcinoma, Superficial spreading melanoma, Melanocytic skin neoplasm, Her2 positive breast carcinoma, Lentigo maligna melanoma, Adenosquamous lung carcinoma, Prostatic adenoma, Gastric adenoma, Extranodal nasal nk/t cell lymphoma, Gallbladder biliary intraepithelial neoplasia, Adnexal spiradenoma/cylindroma of a sweat gland, Spindle cell melanoma, Ovarian steroid cell tumor, Astrocytoma (excluding glioblastoma), Endometrial endometrioid adenocarcinoma, Gastric intestinal type adenocarcinoma, Thyroid gland undifferentiated (anaplastic) carcinoma, Endometrial serous adenocarcinoma, Undifferentiated gallbladder carcinoma, Mixed lobular and ductal breast carcinoma, Plasma cell myeloma, Peripheral t-cell lymphoma, not otherwise specified, Colon adenocarcinoma, Fibroadenoma, Endometrial mixed adenocarcinoma, Spindle cell intraocular melanoma
Unreviewed: Arthritis, Astrocytoma, Ataxia telangiectasia, Atrial fibrillation, Atrioventricular block, Benign Prostatic Hyperplasia, Bladder carcinoma, Bladder Neoplasm, Breast Adenocarcinoma, Breast aplasia, Breast Cancer, Breast Carcinoma, Breast hypoplasia, Breast neoplasm, Carcinoma Of The Head And Neck, Cardiac Defects, Chondrosarcoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Conduction Disorder Of The Heart, Congenital heart defect, Congenital heart defects, Congenital Hypoplasia Of Penis, Congenital Hypoplasia Of Radius, Congenital Pectus Carinatum, Conotruncal cardiac defect, Conotruncal defect, Coronary Heart Disease, Cryptorchidism, Development Disorder, Diabetes mellitus, DiGeorge Syndrome, Disorder Of Eye, Ductal carcinoma, Dwarfism, Ectopic anus, Fibrosarcoma, Gastric Cancer, Glaucoma, Glomerulosclerosis, Gonadotropin Deficiency, Heart failure, Hepatitis c, Hepatoblastoma, Hernia Of Abdominal Wall, Hodgkin disease, Holt-Oram Syndrome, Hypertension, Hypodontia, Hypogonadism, Hypoplasia Of Nipple, Imperforate anus, Inguinal Hernia, Intraductal noninfiltrating carcinoma, Intrahepatic Cholangiocarcinoma, Ischemic stroke, Isolated Somatotropin Deficiency, Kidney Disease, Kidney Failure, Laryngeal neoplasm, Laryngomalacia, Liver Cancer, Liver carcinoma, Liver neoplasms, Lung carcinoma, Lung disease, Malignant Neoplasm, Mammary Neoplasms, Marfan Syndrome, Mental retardation, Neoplasms, Obesity, Odontome, Orofacial cleft, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Papillary thyroid carcinoma, Paroxysmal atrial fibrillation, Penis Agenesis, Persistent truncus arteriosus, Polydactyly, Postaxial hand polydactyly, Prostatic Neoplasms, Renal Carcinoma, Renal hypoplasia, Rhabdomyosarcoma, Rheumatoid arthritis, Short clavicles, Shprintzen Syndrome, Shprintzen-Goldberg Syndrome, Sinus Node Dysfunction, Somatotropin Deficiency, Sprengel Deformity, Stomach Carcinoma, Stomach Neoplasms, Thyroid cancer, Thyroid Diseases, Ulnar-Mammary Syndrome, Uranostaphyloschisis, Urinary bladder cancer, Urinary bladder diseases, Urinary bladder neoplasms, Uterine Anomalies, Uterine neoplasm, Vascular disease, Ventricular preexcitation, Ventricular septal defect
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187927
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TBX3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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187928
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T-box transcription factor 4 |
ICPPS, PAPPAS, SPS |
Curated: 17q23.1q23.2 microdeletion syndrome, Amelia, Arthropathy, Chromosome 17q23.1-q23.2 duplication syndrome, Congenital hypoplasia of lung, Coxopodopatellar syndrome, Desbuquois syndrome, Clubfoot, Pulmonary hypertension, Pulmonary arterial hypertension, Hydronephrosis, Hypertension, Hypoplastic left heart syndrome, Ischiocoxopodopatellar syndrome with pulmonary arterial hypertension, Osteoarthritis, Patellar aplasia, Sacral agenesis, Tetra-amelia syndrome, Posterior amelia with pelvic and pulmonary hypoplasia, Small patella syndrome, Amelia, posterior, with pelvic and pulmonary hypoplasia syndrome
Unreviewed: 17q23.1-Q23.2 Deletion Syndrome, 17q23.1-Q23.2 Duplication Syndrome, Adenoid cystic carcinoma, Alveolar capillary dysplasia, Anxiety Disorder, Apraxia, Ataxia telangiectasia, Atrial Septal Defect, Blindness, Breast neoplasm, Bronchiolitis obliterans, Camptodactyly of fingers, Chronic Obstructive Pulmonary Disease, Colorectal Cancer, Congenital Clubfoot, Congenital contracture, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital hemidysplasia with ichthyosiform erythroderma and limb defects, Congenital Microcephaly, Coxa Magna, Development Disorder, Developmental dysplasia of the hip, Dwarfism, Dysmorphism, Frontal bossing, Gastroesophageal Reflux Disease, Genitopatellar Syndrome, Growth disorder, Heart disease, Heritable Pulmonary Arterial Hypertension, High palate, Hydrops fetalis, Hyperparathyroidism, Learning disorders, Lung Cancer, Lung carcinoma, Lung disease, Lung Diseases, Malignant Neoplasm, Mental Depression, Microcephaly, Micrognathism, Microstomia, Neoplasms, Nonorganic Psychosis, Otitis media, Pancreatic adenocarcinoma, Pancreatic ductal carcinoma, Parkinson disease, Patent ductus arteriosus, Psychosis, Pulmonary Arterial Hypertension Associated With Congenital Heart Disease, Pulmonary Hypertension, Pulmonary hypoplasia, Pulmonary venoocclusive disease, Respiratory Failure, Sacral defect, Schizophrenia, Scoliosis, Short femur, Skin-picking, SMALL PATELLA SYNDROME, Stiff-Person Syndrome, Strabismus, Stress Disorder, Syndromic microphthalmia, Tracheal Stenosis, Tremor, Vascular disease, Vertical Talus
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187929
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T-box transcription factor 5 |
HOS |
Curated: Alzheimer disease, Aortic valve disease, Atrial fibrillation, Atrial flutter, Atrial septal defect, Atrioventricular block, Atrioventricular septal defect, Brugada syndrome, Cardiac arrhythmia, Cardioembolic stroke, Dilated cardiomyopathy, Obstructive pulmonary disease, Congenital heart disease, Desbuquois syndrome, Diverticular disease, Heart disease, Hemorrhoid, Mitral valve prolapse, Obesity, Osteoarthritis, Prostate cancer, Long qt syndrome, Schizophrenia, Tetralogy of fallot, Ventricular septal defect, Wolff-parkinson-white syndrome, Holt-oram syndrome, Polydactyly
Unreviewed: Acheiropodia, Adrenocortical carcinoma, Anemia, Aortic Coarctation, Aortic Valve Disease, Arthritis, Ataxia, Atrial Fibrillation, Atrial Septal Defect, Atrial standstill, Autism, Barrett esophagus, Bladder carcinoma, Breast Cancer, Breast Carcinoma, Brugada Syndrome, Cardiac arrhythmias, Cardiac Defects, Cardiomegaly, Cardiomyopathy, Cardiovascular abnormalities, Cardiovascular disease, Choroid Plexus Carcinoma, Chronic obstructive pulmonary disease, Cleft palate, Clinodactyly, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Congenital anomaly of limb, Congenital anomaly of the hand, Congenital diaphragmatic hernia, Congenital heart defect, Congenital heart defects, Congenital Heart Disease, Congenital heart septal defect, Congenital Pectus Excavatum, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Development Disorder, Developmental Delay, Developmental disability, Diabetes mellitus, type 2, DiGeorge Syndrome, Double outlet right ventricle, Ectrodactyly, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Epithelioma, Esophageal Cancer, Esophageal Carcinoma, Ewing sarcoma, Fibrosarcoma, Heart Diseases, Heart Septal Defects, Hereditary Hemochromatosis, Heterotaxy syndrome, Holt-Oram Syndrome, Hypertension, Hypoplastic Left Heart Syndrome, Isolated Somatotropin Deficiency, Liver carcinoma, Lung adenocarcinoma, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Melanoma, Mental Depression, Metabolic Syndrome, Multiple Trichoepithelioma, Myeloid Leukemia, Myocardial Infarction, Neoplasms, Neuroblastoma, Oculocutaneous albinism, Osteosarcoma, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Pelvic organ prolapse, Persistent Ostium Primum, Phocomelia, Pulmonary hypoplasia, Pulmonary Venous Return Anomaly, Radioulnar Synostosis, Retinoblastoma, Retinopathy, Retinopathy of prematurity, Rheumatoid arthritis, Scoliosis, Secundum atrial septal defect, Short clavicles, Shprintzen Syndrome, Shprintzen-Goldberg Syndrome, Sprengel Deformity, Squamous cell carcinoma, Syndactyly of fingers, Teratoid Rhabdoid Tumor, Tetralogy of Fallot, Thumb Aplasia, Townes Syndrome, Tracheal Stenosis, Trichohepatoenteric Syndrome, Tricuspid Atresia, Ulnar-Mammary Syndrome, Upper extremity deformity, congenital, Wildervanck`s Syndrome
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187930
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TBX5 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Lung carcinoma
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