281
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Transducin beta like 3 |
SAZD, UTP13 |
Curated: N/A
Unreviewed: Diabetes mellitus, type 2, Sepsis
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282
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TATA-box binding protein |
GTF2D, GTF2D1, HDL4, SCA17, TBP1, TFIID |
Curated: Parkinson disease, Diabetes mellitus type 1, Hereditary parkinson disease, Schizophrenia, Spinocerebellar ataxia
Unreviewed: Adenocarcinoma, Adenoma, Amyotrophic lateral sclerosis, Anodontia, Apraxia, Arthritis, Astrocytoma, Ataxia, Atherosclerosis, Autoimmune disease, Autoimmune Diseases, Benign Hereditary Chorea, beta Thalassemia, Bladder carcinoma, Bladder Neoplasm, Blepharospasm, Brainstem Atrophy, Breast Cancer, Breast neoplasm, Bulbospinal Atrophy, X-Linked, Carcinogenesis, Carcinoma Of The Head And Neck, Cardiovascular disease, Cerebellar Ataxia, Cerebellar atrophy, Cerebral Atrophy, Cerebral cortical atrophy, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Chordoma, Chorea, Cognition disorder, Colonic neoplasm, Colorectal neoplasm, Creutzfeldt-Jakob Disease, Dementia, Dementia Of Frontal Lobe, Dentatorubral Pallidoluysian Atrophy, Diabetes, Diabetes Mellitus, Dysarthria, Dysphagia, Dyssomnia, Dystonia, Endometrial Stromal Sarcoma, Frontotemporal dementia, Glioblastoma, Hallucinations, Heart disease, Hemophilia b, Hepatocellular carcinoma, Hereditary Spherocytosis, Hodgkin Disease, Huntington Disease, Huntington Disease-Like, Hypoxia, Inflammatory Bowel Disease, Kidney Neoplasm, Laryngeal neoplasm, Leukemia, Liposarcoma, Liver carcinoma, Liver neoplasm, Liver neoplasms, Lung carcinoma, Lung neoplasms, Machado-Joseph Disease, Major depressive disorder, Male breast neoplasms, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Mental Depression, Mental retardation, MOHR-TRANEBJAERG SYNDROME, Multiple system atrophy, Myeloid leukemia, Myocardial infarction, Nasopharyngeal Carcinoma, Neoplasms, Nervous System Disorder, Neuroblastoma, Neurodegenerative Disorders, Neuroferritinopathy, Nystagmus, Obesity, Open angle glaucoma, Osteoarthritis, Ovarian neoplasm, Paranoia, Periodontitis, Prostate cancer, Prostatic neoplasm, Renal Carcinoma, Renal cell carcinoma, Restless Legs Syndrome, Rhabdomyosarcoma, Rheumatoid arthritis, Rotator cuff syndrome, Senile Dementia, Sleep Disorders, Spherocytosis, Spinocerebellar Ataxia, Squamous cell carcinoma, Systemic lupus erythematosus, Systemic sclerosis, Thrombophlebitis, Triple negative breast cancer, Urinary bladder cancer, Urinary bladder neoplasms, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS, Writer`s Cramp
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283
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|
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TATA-box binding protein like 1 |
MGC:8389, MGC:9620, STUD, TLF, TLP, TRF2 |
Curated: Prostate cancer, Hypertension
Unreviewed: Age-related macular degeneration, Allergic rhinitis, Anemia, Arthritis, Asthma, Atrial Fibrillation, Beckwith-Wiedemann Syndrome, Benign Prostatic Hyperplasia, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Carcinoma, Cardiovascular Diseases, Cataract, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Cockayne Syndrome, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Common Migraine, Congenital Chromosomal Disease, Congestive Heart Failure, Corneal Diseases, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Crohn Disease, Cystic Fibrosis, Dermatitis, Dermatologic Disorders, Diabetes Mellitus, Diabetic Retinopathy, Dowling-Degos Disease, Ductal carcinoma, Dwarfism, Dyskeratosis Congenita, Dyslipidemias, Erectile Dysfunction, Erythema, Fanconi Anemia, Fibrosarcoma, Focal segmental glomerulosclerosis, Glaucoma, Glioblastoma, Glomerulosclerosis, Head and neck cancer, Head And Neck Carcinoma, Heart Failure, Hematological Disease, Hydrocephalus, Hypercalcemia, Hypercholesterolemia, Hypophosphatemic Rickets, Hypoxic-Ischemic Encephalopathy, Inflammatory Bowel Disease, Interstitial Cystitis, Intervertebral Disc Degeneration, Iron Overload, Isodicentric Chromosome 15 Syndrome, Isovaleryl-CoA dehydrogenase deficiency, Kidney Disease, Leigh Syndrome, Leukemia, Lip and Oral Cavity Carcinoma, Liver Cancer, Liver carcinoma, Lung carcinoma, Lupus Erythematosus, Lymphoblastic Leukemia, Lymphoma, Malignant Neoplasm, Malignant neoplasm of mouth, Mammary Neoplasms, Melanoma, Metabolic Diseases, Metaphyseal Chondrodysplasia, Migraine, Mitochondrial myopathy, Monoclonal Gammapathies, Mucolipidosis, Multiple myeloma, Myocardial Infarction, Neoplasms, Neuroblastoma, Nijmegen Breakage Syndrome, Obesity, Oropharyngeal Dysphagia, Pancreatitis, Pelizaeus-Merzbacher disease, Polycystic kidney disease, Premature aging, Prostatic Neoplasms, Pulmonary arterial hypertension, Pulmonary Emphysema, Pulmonary Fibrosis, Renal Carcinoma, Renal Glomerular Disease, Rheumatoid arthritis, Salivary gland neoplasms, Schizophrenia, Septicemia, Skin cancer, Skin Erosion, Skin Neoplasms, Stomach Carcinoma, Stomach Neoplasms, Stroke, Syndromic Mental Retardation, X-linked, T-cell leukemia, T-Cell Lymphoma/Leukemia, Ulcerative colitis, Urinary bladder cancer, Uterine neoplasm, Vascular Diseases, Vitamin D-Dependent Rickets
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284
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TBPL1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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285
|
|
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TATA-box binding protein like 2 |
TBP2, TRF3 |
Curated: Major depressive disorder
Unreviewed: Arteriosclerosis, Atherosclerosis, Cataract, Colonic neoplasm, Colonic Neoplasms, Diabetes, Diabetes Mellitus, Endometriosis, Female infertility, Hereditary breast and ovarian cancer syndrome, Hypoglycemia, Infertility, Leiomyoma, Malignant Neoplasm, Metabolic Diseases, Neoplasms, Osteosarcoma, Ovarian diseases, Ovarian Failure, Premature Menopause, Retinoblastoma, T-cell leukemia, T-Cell Lymphoma/Leukemia, Uterine Fibroids
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286
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|
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T-box brain transcription factor 1 |
AUTS5, IDDAS, TBR-1, TES-56 |
Curated: Attention deficit hyperactivity disorder, Autism, Neurodevelopmental disorder, Cortical dysplasia, Cortical occipital malformations, Developmental delay with language impairment and movement disorder, Focal cortical dysplasia, Intellectual developmental disorder autism speech, Intellectual developmental disorder speech autism dysmorphic, Intellectual developmental disorder, Non-specific syndromic intellectual disability, complex neurodevelopmental disorder
Unreviewed: 2q24 microdeletion syndrome, Antisocial personality disorder, Apraxia, Autism spectrum disorder, Cataract, Congenital abnormalities, Congenital ocular coloboma, Cortical Dysplasia, Cortical Occipital Malformations, Developmental Delay, Developmental disability, Frontotemporal dementia, Glioblastoma, Hypoplastic hippocampus, Hypotonia, Intellectual Developmental Disorder With Autism And Speech Delay, Language development disorders, Medulloblastoma, Mental retardation, Microcephaly, Microphthalmos, Multiple sclerosis, Neurodevelopmental Disorders, Occipital Pachygyria And Polymicrogyria, Pachygyria, Renal cell carcinoma, Schizophrenia, Sleep Apnea, Social Communication Disorder, Stereotyped Behavior, Syndactyly Of The Toes, Temporal lobe epilepsy
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287
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|
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Transforming growth factor beta regulator 1 |
NIAM, TB-5 |
Curated: Intellectual developmental disorder
Unreviewed: Acromesomelic dysplasia, Adenoma, Alzheimer disease, B-Cell Lymphoma, Benign Neoplasm, Burkitt lymphoma, Gaucher disease, Growth disorder, Hemangioma, Marfan syndrome, Neoplasms, Ovarian neoplasm, Papillary Adenoma, Urinary bladder neoplasms
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288
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|
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Transforming growth factor beta regulator 4 |
CPR2, FASTKD4 |
Curated: Colorectal adenoma, Colorectal cancer, Duchenne muscular dystrophy
Unreviewed: Carcinogenesis, Glioblastoma, Malignant Neoplasm, Multiple myeloma, Sezary syndrome
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289
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|
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T-box transcription factor 1 |
CAFS, CATCH22, CTHM, DGCR, DGS, DORV, TBX1C, TGA, VCF, VCFS |
Curated: 22q11.2 deletion syndrome, Breast cancer, Basal cell carcinoma, Chromosome 22q11.2 microduplication syndrome, Obstructive pulmonary disease, Color vision deficiency, Combined immunodeficiency disease, Common arterial trunk with aortic dominance, Common arterial trunk with pulmonary dominance and interrupted aortic arch, Congenital heart disease, Conotruncal anomaly face syndrome, Conotruncal cardiac defect, Craniofacial abnormalities, Digeorge syndrome, Epilepsy, Congenital heart defects, Hypoplastic left heart syndrome, Mood disorder, Nasal polyp, Non-organic psychosis, Polycystic ovary syndrome, Prostate cancer, Psychotic disorders, Rheumatoid arthritis, Schizophrenia, Scoliosis, Hearing loss, Shprintzen-goldberg syndrome, Tetralogy of fallot, Velocardiofacial syndrome, Ventricular septal defect
Unreviewed: 22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 duplication syndrome, 3C syndrome, Acne, Acrocephaly, Adenocarcinoma, Adenoid cystic carcinoma, Adenoma, Agenesis Of Corpus Callosum, Alagille Syndrome, Anaplasia, Anemia, Anhedonia, Antithrombin Deficiency, Anxiety Disorder, Aortic Coarctation, Aphthous Ulcer, Aplasia Cutis Congenita, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial Septal Defect, Atrioventricular septal defect, Atrophy, Attention Deficit Hyperactivity Disorder, Autism, Autism spectrum disorder, Behavior Disorders, beta Thalassemia, Bipolar Disorder, Blepharophimosis, Bone neoplasm, Bone neoplasms, Bowel incontinence, Brachydactyly, Breast Cancer, Breast Carcinoma, Breast neoplasm, C9 Deficiency, Camptodactyly, Camptodactyly of fingers, Carcinoma, Cardiac Defects, Cardiovascular Abnormalities, Cat Eye Syndrome, Cataract, Caudal regression sequence, Celiac disease, Choanal Atresia, Cholelithiasis, Chondrosarcoma, Chordoma, Chronic Obstructive Pulmonary Disease, Cleft lip, Cleft palate, Cleidocranial Dysplasia, Colorectal Cancer, Colorectal neoplasm, Complete Atrioventricular Canal Defect, Congenital Chromosomal Disease, Congenital Clubfoot, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital Exomphalos, Congenital heart defect, Congenital Heart Disease, Congenital Hypoplasia Of Thymus, Congenital malrotation of intestine, Congenital microtia, Conotruncal Anomaly Face Syndrome, Conotruncal defect, Conotruncal heart defect, Contiguous gene syndrome, Corneal Neovascularization, Coronary Heart Disease, Cryptorchidism, Deafness, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, DiGeorge Syndrome, Dolichocephaly, Double Outlet Right Ventricle, Down Syndrome, Dwarfism, Dysmorphic Features, Dysphasia, Ear Diseases, Ehlers-Danlos Syndrome, Embryonal carcinoma, Epidermolysa Bullosa Simplex And Limb Girdle Muscular Dystrophy, Esophoria, Esotropia, Exotropia, Facial dysmorphism, Fanconi Anemia, Folic Acid Deficiency, Friedreich Ataxia, Gastroesophageal Reflux Disease, Glaucoma, Glioblastoma, Glioma, Glomerulosclerosis, Goldenhar syndrome, Graves disease, Hashimoto Disease, Hearing Loss, Hernia, Femoral, High palate, Hirschsprung Disease, Hodgkin disease, Holt-Oram Syndrome, Hydrocephalus, Hydronephrosis, Hyperglycemia, Hyperlipoproteinemia, Hypertension, Hyperthyroidism, Hypocalcemia, Hypoparathyroidism, Hypophosphatemic Rickets, Hypoplastic Left Heart Syndrome, Hypospadias, Hypothyroidism, Immunologic Deficiency Syndromes, Imperforate anus, Inguinal Hernia, Interrupted aortic arch, Kenny-Caffey Syndrome, Kidney Failure, Knee osteoarthritis, Laryngeal neoplasm, Laryngomalacia, Larynx cancer, Learning Disorders, LEPTIN DEFICIENCY OR DYSFUNCTION, Lesch-Nyhan Syndrome, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lymphatic metastasis, Major Affective Disorder, Malignant Neoplasm, Mammary Neoplasms, Meckel Syndrome, Melanoma, Mental Depression, Mental Disorders, Mental retardation, Microcephaly, Microdontia, Microglossia, Micrognathism, Microphthalmos, Microstomia, Mood Disorder, Mood swings, Motor delay, Mouth neoplasm, Multiple renal cysts, Myeloid leukemia, Myelomeningocele, Neoplasms, Neural Tube Defect, Neuroblastoma, Neurofibromatosis, Nonorganic Psychosis, Obesity, Obsessive-Compulsive Disorder, Optic Atrophy, Orofacial cleft, Otitis media, Papillary thyroid carcinoma, Paranoia, Parathyroid agenesis, Parathyroid hypoplasia, Parathyroid neoplasm, Parathyroid Neoplasms, Patent ductus arteriosus, Periodontitis, Persistent truncus arteriosus, Pfaundler-Hurler Syndrome, Phenylketonuria, Pierre-Robin Syndrome, Platybasia, Polycystic kidney disease, Polycystic Ovary Syndrome, Polydactyly, Polydactyly Of Toes, Polyglandular autoimmune syndrome, Posterior embryotoxon, Precocious Pubarche, Proptosis, Prostatic neoplasm, Protein C Deficiency, Psychosis, Ptosis, Pulmonary arterial hypertension, Pulmonary dysgenesis, Renal aplasia, Renal cell carcinoma, Renal dysplasia, Renal fibrosis, Renal hypoplasia, Retinoblastoma, Sacral Agenesis, Schizoaffective Disorder, Sclerocornea, Sclerocystic Ovaries, Scleroderma, Seborrheic dermatitis, Seminoma, Severe combined immunodeficiency disease, Shprintzen Syndrome, Shprintzen-Goldberg Syndrome, Situs ambiguus, Situs Inversus, Skin Neoplasms, Small cell carcinoma, Small cell lung carcinoma, Specific Learning Disorder, Speech Disorders, Spondylocostal dysostosis, Squamous cell carcinoma, Stereotyped Behavior, Strabismus, Stroke, Teratoid Rhabdoid Tumor, Testicular Germ Cell Tumor, Tetralogy of Fallot, Thrombasthenia, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Transposition Of Great Vessels, Trichohepatoenteric Syndrome, Tricuspid Atresia, Triple negative breast cancer, Triple Negative Breast Neoplasms, Tumor, Ulnar-Mammary Syndrome, Uranostaphyloschisis, Urinary bladder neoplasms, Uterine Anomalies, Uterine neoplasm, Velopharyngeal Insufficiency, Vesicoureteral Reflux, Vitamin D-Dependent Rickets, von Willebrand disorder, Vulval varices, Zellweger Syndrome
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290
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T-box transcription factor 10 |
TBX13, TBX7 |
Curated: Metabolic syndrome, Orofacial cleft, Diabetes mellitus type 2
Unreviewed: Cleft lip, Cleft palate, Hodgkin disease
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