Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
641 to 650 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
TNF alpha induced protein 6
TSG-6, TSG6
Juvenile arthritis, Allergic contact dermatitis, Dermatologic disorder, Diabetic maculopathy, Juvenile idiopathic arthritis, Lung cancer, Oligoarticular juvenile idiopathic arthritis, Prostate cancer, Skin disease, Squamous cell carcinoma, Diabetes mellitus, type 2

642
TNF receptor superfamily member 1A
CD120a, FPF, TBP1, TNF-R, TNF-R-I, TNF-R55, TNFAR, TNFR1, TNFR55, TNFR60, p55, p55-R, p60
Ankylosing spondylitis, Anorexia, Autoimmune disease, Autoinflammatory syndrome, Behcet disease, Biliary cirrhosis, Brain injuries, Brain ischemia, Cachexia, Charge syndrome, Crohn disease, Cystic fibrosis, Major depressive disorder, Experimental diabetes, Diabetes mellitus type 2
View all (16 more)

643
TNF receptor superfamily member 1B
CD120b, TBPII, TNF-R-II, TNF-R75, TNFBR, TNFR1B, TNFR2, TNFR80, p75, p75TNFR
Ankylosing spondylitis, Autism, Brain ischemia, Major depressive disorder, Diabetes mellitus type 2, Endometriosis, Heart failure, Hypersensitivity, Hypothyroidism, Iga nephropathy, Liver cirrhosis, Lupus nephritis, Depression, Nonalcoholic fatty liver disease, Obesity
View all (5 more)

644
Troponin C1, slow skeletal and cardiac type
CMD1Z, CMH13, TN-C, TNC, TNNC
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy

645
Troponin I2, fast skeletal type
AMCD2B, DA2B, DA2B1, FSSV, fsTnI
Arthrogryposis multiplex congenita, Distal arthrogryposis, Digitotalar dysmorphism, Myopathy, Sheldon-hall syndrome

646
Troponin I3, cardiac type
CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Ciliary dyskinesia, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Restrictive cardiomyopathy, Heart disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Myocardial infarction, Myocarditis

647
Troponin T1, slow skeletal type
ANM, NEM5, STNT, TNT, TNTS
Amish nemaline myopathy, Cardiomyopathy, Nemaline myopathy, Myopathy

648
Troponin T2, cardiac type
CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC, cTnT
Arrhythmogenic right ventricular cardiomyopathy, Cardiomegaly, Cardiomyopathy, Cardiovascular disease, Obstructive airway disease, Costello syndrome, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Restrictive cardiomyopathy, Glycogen storage disease, Heart disease, Heart failure, Cardiac injury, Left ventricular disease, Left ventricular noncompaction cardiomyopathy
View all (7 more)

649
Troponin T3, fast skeletal type
DA2B2, TNTF, beta-TnTF
Arthrogryposis multiplex congenita, Distal arthrogryposis, Breast cancer, Congenital myopathy, Digitotalar dysmorphism, Hypertension, Nemaline myopathy, Sheldon-hall syndrome

650
Tenascin R
NEDSTO, TN-R
Attention deficit hyperactivity disorder, Corneal astigmatism, Dementia, Major depressive disorder, Neurodevelopmental disorder, Open angle glaucoma, Parkinson disease, Sarcoidosis, Schizophrenia, Severe acute respiratory syndrome, Tuberculosis, Age-related macular degeneration