Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
731 to 740 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

731
Troponin I1, slow skeletal type
SSTNI, TNN1
Arthrogryposis

732
Troponin I2, fast skeletal type
AMCD2B, DA2B, DA2B1, FSSV, fsTnI
Arthrogryposis multiplex congenita, Distal arthrogryposis, Congenital finger flexion contractures, Digitotalar dysmorphism, Myopathy, Sheldon-hall syndrome

733
Troponin I3, cardiac type
CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Ciliary dyskinesia, Hypertrophic cardiomyopathy, Restrictive cardiomyopathy, Heart disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Myocardial infarction

734
TNNI3 interacting kinase
CARK, CCDD
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Attention deficit hyperactivity disorder, Bronchial disease, Cardiac conduction disease, Dilated cardiomyopathy, Central nervous system cancer, Atrial tachyarrhythmia, infra-hisian cardiac conduction disease, Glioblastoma, Glioma, Insomnia, Meniere disease, Metabolic syndrome, Obesity, Substance abuse
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735
Troponin T1, slow skeletal type
ANM, NEM5, STNT, TNT, TNTS
Amish nemaline myopathy, Cardiomyopathy, Nemaline myopathy, Myopathy

736
Troponin T2, cardiac type
CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC, cTnT
Arrhythmogenic right ventricular cardiomyopathy, Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Cardiovascular disease, Obstructive airway disease, Congestive heart failure, Costello syndrome, Hypertrophic cardiomyopathy, Restrictive cardiomyopathy, Glycogen storage disease, Heart disease, Heart failure, Cardiac injury, Left ventricular disease
View all (7 more)

737
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

738
Transportin 1
IPO2, KPNB2, MIP, MIP1, TRN
Atrial fibrillation, Bladder calculus, Obstructive pulmonary disease, Tourette syndrome, Nephrolithiasis, Urolithiasis

739
Transportin 2
IDDHISD, IPO3, KPNB2B, TRN2
Diffuse large b-cell lymphoma, Intellectual developmental disorder speech dysmorphic, Multiple sclerosis, Neurodevelopmental disorder, Polycystic ovary syndrome

740
Transportin 3
IPO12, LGMD1F, LGMDD2, MTR10A, TRN-SR, TRN-SR2, TRNSR
Systemic scleroderma, Autoimmune musculoskeletal system disorder, Limb girdle muscular dystrophy, Biliary cirrhosis, Diffuse cutaneous systemic sclerosis, Hypothyroidism, Crest syndrome, Muscular dystrophy, Myositis, Biliary cholangitis, Rheumatoid arthritis, Sjogren syndrome, Systemic lupus erythematosus, Systemic sclerosis