Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13861 to 13870 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13861
Tankyrase 1 binding protein 1
CNOT12, TAB182
Alzheimer disease, Color vision deficiency, Gout, Hypertrophic cardiomyopathy, Insomnia, Metabolic syndrome, Squamous cell carcinoma, Diabetes mellitus type 2

13862
Tankyrase 2
ARTD6, PARP-5b, PARP-5c, PARP5B, PARP5C, TANK2, TNKL, pART6
Diabetic ketoacidosis, Diabetes mellitus type 1, Diabetes mellitus type 2

13863
Tenascin N
TN-W, TNW
Atrial fibrillation, Gout, Obsessive-compulsive disorder

13864
Troponin C1, slow skeletal and cardiac type
CMD1Z, CMH13, TN-C, TNC, TNNC
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy

13865
Troponin C2, fast skeletal type
CFAP85, CMYO15, CMYP15, FAP85, MYONRI
Congenital myopathy, Hypertrophic cardiomyopathy

13866
Troponin I1, slow skeletal type
SSTNI, TNN1
Arthrogryposis

13867
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

13868
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, Myocarditis

13869
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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13870
Troponin T1, slow skeletal type
ANM, NEM5, STNT, TNT, TNTS
Amish nemaline myopathy, Cardiomyopathy, Nemaline myopathy, Myopathy