631
|
|
|
Transglutaminase 5 |
PSS2, TG(X), TGASE5, TGASEX, TGM6, TGMX, TGX |
Curated: Acral peeling skin syndrome, Major depressive disorder, Lung cancer, Peeling skin syndrome, Squamous cell carcinoma
Unreviewed: Acral Peeling Skin Syndrome, Acyl CoA Dehydrogenase Deficiency, Adrenogenital Syndrome, Alpha 1-Antitrypsin Deficiency, Attention Deficit Hyperactivity Disorder, Cholesteatoma, Cognitive disorder, Congenital adrenal hyperplasia, Congenital Ichthyosis, Darier disease, Dermatitis, Dermatologic Disorders, Development Disorder, Eczema, Epidermolysis Bullosa, Epidermolysis Bullosa Simplex, Glioblastoma, Hearing Loss, Ichthyosis, Ichthyosis Vulgaris, Impaired Cognition, Keratoconus, Keratosis Follicularis, Lung carcinoma, Lung neoplasms, Nasal polyp, Polyglucosan body myopathy, Psoriasis, Psychotic disorders, Schizophrenia, Skin disease, Skin Erosion, Uncombable Hair Syndrome, Von Willebrand Disorder
|
632
|
|
|
Transglutaminase 6 |
SCA35, TG6, TGM3L, TGY, dJ734P14.3 |
Curated: Alzheimer disease, Spinocerebellar ataxia, Parkinson disease, Polyneuropathy
Unreviewed: Amyotrophic Lateral Sclerosis, Ataxia, Autism Spectrum Disorder, Autoimmune disease, Autoimmune Diseases, Brain atrophy, Celiac disease, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar diseases, Cerebral Atrophy, Colorectal neoplasm, Dysarthria, Epilepsy, Gastrointestinal disease, Gluten intolerance, Leukemia, Mental retardation, Multiple Sclerosis, Myeloid Leukemia, Nervous System Disorder, Neuropathy, Progressive supranuclear palsy, Pseudobulbar Palsy, Secondary parkinson disease, Spinocerebellar Ataxia
|
633
|
|
|
Transglutaminase 7 |
TGMZ |
Curated: N/A
Unreviewed: Breast Cancer, Breast Carcinoma, Epithelial ovarian carcinoma, Lung neoplasms, Neoplasms, Ovarian cancer, Ovarian Epithelial carcinoma, Renal cell carcinoma, Rheumatoid arthritis, Urinary bladder neoplasms, Uterine neoplasm
|
634
|
|
|
Trans-golgi network protein 2 |
TGN38, TGN46, TGN48, TGN51, TTGN2, hTGN46, hTGN48, hTGN51 |
Curated: Myocardial ischemia, Thyroid disease
Unreviewed: Esophageal squamous cell carcinoma, Mood Disorder, Thyroid Diseases
|
635
|
|
|
Trimethylguanosine synthase 1 |
NCOA6IP, PIMT, PIPMT |
Curated: Basal cell carcinoma, Insomnia
Unreviewed: N/A
|
636
|
|
|
Tyrosine hydroxylase |
DYT14, DYT5b, TYH |
Curated: Bipolar disorder, Brain disease, Hepatocellular carcinoma, Catalepsy, Delirium, Major depressive disorder, Dyskinesia, drug-induced, Dystonia, Hypertension, Heart disease, Hyperkinesia, Intellectual developmental disorder, Learning disorders, Lewy body disease, Mood disorder, Neuroblastoma, Obesity, Parkinson disease, Periodontitis, Pheochromocytoma, Depression, Tyrosine hydroxylase–deficient dopa-responsive dystonia, Diabetes mellitus type 1, Diabetes mellitus type 2, Tyrosine hydroxylase deficiency
Unreviewed: 6-pyruvoyl-tetrahydropterin synthase deficiency, Adjustment Disorders, Adrenal Gland Pheochromocytoma, Akinesia, Alopecia, Alopecia Areata, alpha-Thalassemia Mental Retardation Syndrome, X-Linked, Alzheimer disease, Anemia, Anxiety Disorder, Arthritis, Asthma, Atrial Fibrillation, Atrophy, Attention Deficit Hyperactivity Disorder, Autism, Autoimmune Diseases, B-Cell Lymphoma, Bipolar Disorder, Borderline personality disorder, Breast neoplasm, Bronchopulmonary Dysplasia, Cardiac valvular disease, Cardiovascular Diseases, Colitis, Congenital Clubfoot, Congestive Heart Failure, Delusional Disorder, Dental Enamel Hypoplasia, Deuteranomaly, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diverticulitis, Dopamine Beta Hydroxylase Deficiency, Dwarfism, Dyskinesia, Dyskinetic Syndrome, Dystonia, dopa-responsive, with or without hyperphenylalaninemia, Embryonal Rhabdomyosarcoma, Epileptic encephalopathy, Erythroblastic Leukemia, Ewing sarcoma, Extra-Adrenal Pheochromocytoma, Fanconi Anemia, Focal dystonia, Ganglioneuroblastoma, Ganglioneuroma, Glaucoma, Guillain-Barre Syndrome, Heart Diseases, Heart Failure, High Altitude Pulmonary Edema, Homocystinuria, Huntington Disease, Hydatidiform Mole, Hyperphenylalaninemia, Hyperthyroidism, Hypertrophy, Hypotension, Irritable Bowel Syndrome, Isolated Somatotropin Deficiency, Learning Disorders, Lesch-Nyhan Syndrome, Lewy Body Disease, Liver carcinoma, Long qt syndrome, Lymphoma, Major Affective Disorder, Malabsorption Syndrome, Malignant Neoplasm, Malnutrition, Mental Depression, Mental Disorders, Mental retardation, Metabolic Syndrome, Migraine, Mitral Valve Stenosis, Mood Disorder, Motor delay, Movement Disorders, Mucopolysaccharidosis, Multiple Endocrine Neoplasia, Multiple Sclerosis, Myeloid leukemia, Myelomonocytic Leukemia, Myocardial Infarction, Myotonic dystrophy, Neoplasms, Nephroblastoma, Nervous System Disorder, Neurodegenerative disorder, Neuromuscular Diseases, Nonorganic Psychosis, Oculocutaneous albinism, Optic Nerve Glioma, Osteosarcoma, Ovarian Cysts, Paraganglioma, Paranoid Schizophrenia, Parkinsonian disease, Periodontal Diseases, Perry Syndrome, Phenylketonuria, Pituitary Diseases, Polycystic Ovary Syndrome, Polyglandular autoimmune syndrome, Polymicrogyria, Postnatal asphyxia, Premature aging, Progressive Supranuclear Palsy, Prolactinoma, Prostate cancer, Prostatic neoplasm, Psychosis, Ptosis, Pulmonary arterial hypertension, Ramsay Hunt Paralysis Syndrome, Restless Legs Syndrome, Rett Syndrome, Rhabdomyosarcoma, Schizophrenia, Sclerosing Cholangitis, Segawa Syndrome, Septicemia, Sexual Dysfunction, Sleep Apnea, Spastic Paraplegia, Spinocerebellar Ataxia, Stomach Carcinoma, Stomach disease, Stomach Neoplasms, Stress Disorder, Stroke, Subarachnoid hemorrhage, Tauopathies, Tendinopathy, Timothy Syndrome, Tourette Syndrome, Trichohepatoenteric Syndrome, Van Der Woude Syndrome, Ventricular arrhythmia, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS, Von Hippel-Lindau Syndrome, Vulval varices, Willis-ekbom disease, Wolfram Syndrome
|
637
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
638
|
|
|
T helper type 2 locus control region associated RNA |
TH2-LCR |
Curated: N/A
Unreviewed: Alopecia Areata, Asthma, Atopic dermatitis, Breast Carcinoma, Dermatitis, Diabetes mellitus, type 2, Eczema, Hepatocellular carcinoma, Hereditary Cancer Syndrome, Hodgkin Disease, Multiple Sclerosis, Nijmegen Breakage Syndrome-Like Disorder, Psoriasis, Psoriasis vulgaris, Respiratory Tract Diseases, Spinal muscular atrophy
|
639
|
|
|
Threonine aldolase 1, pseudogene |
GLY1 |
Curated: N/A
Unreviewed: Prostate cancer
|
640
|
|
|
THADA armadillo repeat containing |
ARMC13, GITA, Trm732 |
Curated: Androgenetic alopecia, Ankylosing spondylitis, Jeune syndrome, Atrial fibrillation, Behcet disease, Breast cancer, Cancer, Cardiovascular disease, Cholecystolithiasis, Colorectal cancer, Coronary artery disease, Crohn disease, Major depressive disorder, Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic retinopathy, Estrogen-receptor negative breast cancer, Hemorrhagic disease, Hypertension, Hypothyroidism, Inflammatory bowel disease, Latent autoimmune diabetes in adults, Lung cancer, Meniere disease, Metabolic syndrome, Migraine, Myocardial infarction, Obstructive sleep apnea syndrome, Orofacial cleft, Ovarian cancer, Ovarian serous carcinoma, Polycystic ovary syndrome, Prostate cancer, Psoriasis, Sclerosing cholangitis, Scoliosis, Squamous cell carcinoma, Thrombocytopenia, Ulcerative colitis, Uterine fibroid
Unreviewed: Adenoma, Alopecia, Alopecia, Male Pattern, Androgenetic Alopecia, Ankylosing Spondylitis, Breast neoplasm, Cardiovascular Diseases, Cholangitis, Colorectal neoplasm, Coronary Heart Disease, Crohn Disease, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Endometrial carcinoma, Gestational diabetes, Hyperandrogenism, Inflammatory Bowel Disease, Nasopharyngeal Carcinoma, Neoplasms, Obesity, Polycystic Ovary Syndrome, Prostatic neoplasm, Thyroid cancer, Thyroid Gland Follicular Adenoma
|