|
531
|
|
|
Transcription factor 7 |
TCF-1 |
Asthma, Autoimmune thyroid disease, Cancer, Crohn disease, Hypothyroidism, Iga nephropathy, Systemic lupus erythematosus, Multiple sclerosis, Open angle glaucoma, Respiratory system disease, Rheumatoid arthritis |
|
532
|
|
|
Transcription factor 7 like 2 |
TCF-4, TCF4 |
Alzheimer disease, Anemia, Juvenile arthritis, Atherosclerosis, Atrial fibrillation, Autism, Bipolar disorder, Bone disease, Breast cancer, Cancer, Cardiomyopathy, Cataract, Kidney disease, Obstructive pulmonary disease, Colonic neoplasm, Color vision deficiency, Colorectal adenoma, Colorectal cancer, Colorectal neoplasm, Neurodevelopmental disorder, Coronary artery disease, Dental caries, Dermatophytosis, Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic neuropathy, Diabetic polyneuropathy, Diabetic retinopathy, Estrogen-receptor negative breast cancer, Eye disease, Gestational diabetes, Glaucoma, Gout, Hearing loss, Heart failure, Primary congenital glaucoma, Hyperalgesia, Hyperlipidemia, Hyperplasia, Hypertensive heart disease, Hypertensive nephropathy, Insomnia, Intellectual developmental disorder, Juvenile idiopathic arthritis, Kidney failure, Major depressive disorder, Metabolic syndrome, Migraine, Obesity, Myocardial ischemia, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Obstructive sleep apnea syndrome, Open angle glaucoma, Osteoarthritis, Osteomyelitis, Oligoarticular juvenile idiopathic arthritis, Periodontitis, Peripheral arterial disease, Peripheral vascular disease, Prostate cancer, Psoriasis, Retinopathy, Schizoaffective disorder, Schizophrenia, Senile cataract, Stroke, Hypertension, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Type 2 diabetes nephropathy, Vascular diseaseView all (58 more) |
|
533
|
|
|
Transcription factor 12 |
CRS3, HEB, HH26, HTF4, HsT17266, TCF-12, bHLHb20, p64 |
Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Coronal craniosynostosis, Craniosynostosis, Desbuquois syndrome, Developmental delay, Developmental disability, Diabetes mellitus, Glaucoma, Global developmental delay, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Insomnia, Kallmann syndrome, Male infertility single gene azoospermia, Open angle glaucoma, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Sheehan syndrome, Diabetes mellitus, type 2View all (9 more) |
|
534
|
|
|
Transcription factor 15 |
EC2, PARAXIS, bHLHa40 |
|
|
535
|
|
|
Transcription factor 19 |
SC1, TCF-19 |
Hepatocellular carcinoma, Hepatitis b virus infection, Obstructive pulmonary disease, Colonic neoplasm, Hepatitis b, Membranous nephropathy, Schizophrenia, Hearing loss, Stevens-johnson syndrome, Toxic epidermal necrolysis, Diabetes mellitus, type 2 |
|
536
|
|
|
Transcription factor 20 |
AR1, DDVIBA, SPBP, TCF-20 |
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Blepharoptosis, Cannabis abuse, Craniosynostosis, Developmental delay with variable intellectual disability, Global developmental delay, Intellectual developmental disorder, Liver cirrhosis, Major depressive disorder, Metabolic syndrome, Intellectual disability, Enterocolitis, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Schizophrenia, Substance abuse, Tourette syndrome, Diabetes mellitus, type 2View all (7 more) |
|
537
|
|
|
Transcription factor 21 |
POD1, bHLHa23 |
Ischemic heart disease, Congenital hereditary endothelial dystrophy, Coronary artery disease, Gallstones, Heart disease, Hypertension, Large artery stroke, Myocardial infarction, Myocardial ischemia, Stroke, Ventricular septal defect |
|
538
|
|
|
Transcobalamin 1 |
HC, TC-1, TC1, TCI |
|
|
539
|
|
|
Transcobalamin 2 |
D22S676, D22S750, II, TC, TC II, TC-2, TC2, TCII |
Alzheimer disease, Megaloblastic anemia, Autism, Colorectal neoplasm, Deficiency anemia, Esophageal squamous cell carcinoma, Moyamoya disease, Pancytopenia, Parkinson disease, Prostatic neoplasm, Diabetes mellitus, type 2, Vitamin b12 deficiency, Vitamin b12-responsive methylmalonic acidemia, Combined vitamin k-dependent clotting factor deficiency |
|
540
|
|
|
Treacle ribosome biogenesis factor 1 |
MFD1, TCS, TCS1, treacle |
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