291
|
|
|
T-box transcription factor 15 |
TBX14 |
Curated: Androgenetic alopecia, Breast cancer, Chagas cardiomyopathy, Cousin syndrome, Craniofacial abnormalities, Desbuquois syndrome, Growth disorder, Obstructive sleep apnea syndrome, Osteoarthritis, Pelviscapular dysplasia
Unreviewed: Alopecia, Alopecia, Male Pattern, Ambiguous Genitalia, Androgenetic Alopecia, Blepharophimosis, Brachydactyly, Breast neoplasm, Camptodactyly of fingers, Carcinogenesis, Colorectal neoplasm, Congenital Camptodactyly, Congenital Clubfoot, Cystic fibrosis, Developmental dysplasia of the hip, Dislocated radial head, Dwarfism, Elbow flexion contracture, Esophageal neoplasm, Flexion Contracture Of Wrist, Frontal bossing, Glioma, Hydranencephaly, Hydrocephalus, Hydronephrosis, Lung neoplasms, Macrocephaly, Malignant Neoplasm, Mesomelia, Microcornea, Microglossia, Micrognathism, Microphthalmos, Neoplasms, Obesity, Osteoporosis, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic neoplasm, Pelviscapular Dysplasia, Pituitary neoplasm, Prostate cancer, Prostatic neoplasm, Ramer Ladda Syndrome, Renal cell carcinoma, Rhizomelia, Short femur, Stenosis Of External Auditory Canal, Strabismus, Syndactyly Of The Toes, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm
|
292
|
|
|
T-box transcription factor 18 |
CAKUT2, PUJO |
Curated: Androgenetic alopecia, Anophthalmia, Breast cancer, Congenital anomalies of the kidney and urinary tract, Cardiac embolism, Cardioembolic stroke, Carpal tunnel syndrome, Central nervous system cancer, Kidney disease, Renal agenesis, Congenital anomalies of kidney and urinary tract, Glioblastoma, Glioma, Hypertension, Immune system disease, Myasthenia gravis, Osteoarthritis, Scoliosis
Unreviewed: Arteriosclerosis, Atherosclerosis, Complete Atrioventricular Block, Congenital heart defect, Congenital heart defects, Congenital megaureter, Coronary Heart Disease, Hydronephrosis, Kidney Disease, Multicystic renal dysplasia, Neoplasms, Nephrolithiasis, Nephrotic Syndrome, Osteosarcoma, Renal dysplasia, Renal hypoplasia, Sarcoma Of Kidney, Sick Sinus Syndrome, Urolithiasis, Ventricular Fibrillation, Ventricular septal defect
|
293
|
|
|
TBX18 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
294
|
|
|
T-box transcription factor 19 |
TBS19, TPIT, dJ747L4.1 |
Curated: Congenital isolated acth deficiency, Major depressive disorder, Duodenitis, Pituitary stalk interruption syndrome
Unreviewed: Acromegaly, ACTH Deficiency, Adenoma, Adrenal Cortical Hypofunction, Adrenal Insufficiency, Adrenocorticotropic Hormone Deficiency, Adrenocorticotropin deficient adrenal insufficiency, Carcinogenesis, Cleft Palate With Ankyloglossia, Colonic disease, Colorectal neoplasm, Common Variable Immunodeficiency, Congenital Isolated ACTH Deficiency, Cushing syndrome, Hodgkin disease, Hypoglycemia, Hypoglycemic seizures, Lymphatic metastasis, Mental Depression, Pituitary adenoma, Pituitary neoplasm
|
295
|
|
|
T-box transcription factor 2 |
VETD |
Curated: Atrial septal defect, Ischemic heart disease, Congenital septal defect of heart, Coronary artery disease, Hypertension, Metabolic syndrome, Myocardial ischemia, Nephrolithiasis, Neuroblastoma, Osteoarthritis, Vertebral anomalies with endocrine and t-cell dysfunction
Unreviewed: Adrenocortical carcinoma, Alveolar capillary dysplasia, Alzheimer disease, Aplasia of the thymus, Astrocytoma, Atrial Septal Defect, Atrioventricular septal defect, Autism, Bladder carcinoma, Bladder Neoplasm, Brachycephaly, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cleft palate, Colorectal Cancer, Colorectal neoplasm, Congenital anomaly of eye, Congenital Camptodactyly, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital heart defects, Congenital Heart Disease, Congenital ocular coloboma, Congenital Pectus Carinatum, Conotruncal cardiac defect, Conotruncal defect, Coronary Heart Disease, Development Disorder, Developmental Delay, Double Outlet Right Ventricle, Dwarfism, Ectopic Pupil, Endocrine system disease, Endometrial neoplasm, Esophageal squamous cell carcinoma, Glabellar hemangioma, Glioblastoma, Hashimoto Disease, Hepatocellular carcinoma, Hodgkin disease, Hypoparathyroidism, Immune system disease, Inguinal Hernia, Isolated Somatotropin Deficiency, Kidney Failure, Klippel Feil syndrome, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Metastatic Prostate Carcinoma, Nasopharyngeal Cancer, Nasopharyngeal carcinoma, Neck Webbing, Neoplasms, Osteochondrodysplasias, Osteosarcoma, Ovarian serous adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Patent ductus arteriosus, Persistent truncus arteriosus, Prostate cancer, Prostatic neoplasm, Pulmonary arterial hypertension, Pulmonary hypoplasia, Pulmonary Stenosis, Renal cell carcinoma, Rhabdomyosarcoma, Rib fusion, Scoliosis, Somatotropin Deficiency, Spondylocostal dysostosis, Sprengel Deformity, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Thyroiditis, Urinary bladder cancer, Urinary bladder neoplasms, Uterine disease, Ventricular preexcitation, Ventricular septal defect, Vertebral anomalies and variable endocrine and T-cell dysfunction, Wolff-Parkinson-White Syndrome
|
296
|
|
|
TBX2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
297
|
|
|
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
|
298
|
|
|
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
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
|
299
|
|
|
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
Unreviewed: Abruzzo-Erickson Syndrome, Acute Myeloid Leukemia, Ankyloglossia, Anodontia, Aortic Valve Sclerosis, Atrial Septal Defect, Brachydactyly, Cleft lip, 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
|
300
|
|
|
T-box transcription factor 23, pseudogene |
TBX23 |
Curated: N/A
Unreviewed: N/A
|