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"
811 to 820 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
Thiamin pyrophosphokinase 1
HTPK1, PP20, THMD5
Breast cancer, Lymphocytic leukemia, Leigh syndrome, Metabolic syndrome, Thiamine metabolism dysfunction syndrome

812
Tropomyosin 1
C15orf13, CMD1Y, CMH3, HEL-S-265, HTM-alpha, LVNC9, TMSA
Arrhythmogenic right ventricular cardiomyopathy, Atrial septal defect, Cardiomyopathy, Dilated cardiomyopathy, Esophageal neoplasms, Esophageal squamous cell carcinoma, Hypertension, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Liver cirrhosis, Metabolic syndrome, Neutropenia, Parkinson disease, Tetralogy of fallot
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813
Tropomyosin 2
AMCD1, CMYO23, CMYP23, DA1, DA2B, DA2B4, HEL-S-273, NEM4, TMSB
Arthrogryposis, Arthrogryposis multiplex congenita, Distal arthrogryposis, Cap myopathy, Nemaline myopathy, Congenital fiber type disproportion myopathy, Congenital myopathy, Digitotalar dysmorphism, Esophageal squamous cell carcinoma, Gout, Sheldon-hall syndrome

814
Tropomyosin 3
CAPM1, CFTD, CMYO4A, CMYO4B, CMYP4A, CMYP4B, HEL-189, HEL-S-82p, NEM1, OK/SW-cl.5, TM-5, TM3, TM30, TM30nm, TM5, TPM3nu, TPMsk3, TRK, hscp30
Asthma, Cannabis abuse, Cap myopathy, Carcinoma, Centronuclear myopathy, Nemaline myopathy, Colonic neoplasms, Congenital fiber type disproportion myopathy, Congenital generalized hypercontractile muscle stiffness syndrome, Congenital myopathy, Congenital structural myopathy, Irritable bowel syndrome, Liver cirrhosis, Myopathy, Stomach neoplasms
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815
Tropomyosin 4
BDPLT25, HEL-S-108
Asbestosis, Macrothrombocytopenia, Platelet-type bleeding disorder, Platelet disorder, Esophageal neoplasms, Hemorrhagic disease, Liver cirrhosis, Oligodendroglioma, Osteoporosis, Thrombocytopenia

816
Thiopurine S-methyltransferase
TPMTD
Autism, Neutropenia, Psoriasis, Thiopurine s-methyltransferase deficiency

817
Thyroid peroxidase
MSA, TDH2A, TPX
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Bipolar disorder, Central nervous system cancer, Congenital hypothyroidism, Iodide peroxidase deficiency, Thyroid dyshormonogenesis, Glioma, Global developmental delay, Glomerulonephritis, Graves disease, Gross motor development delay, Hypothyroidism, Myocardial infarction
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818
Tripeptidyl peptidase 1
CLN2, GIG1, LPIC, SCAR7, TPP-1
Alzheimer disease, Angelman syndrome, Spinocerebellar ataxia, Neuronal ceroid lipofuscinosis, Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia, Congenital neurologic anomalies, Intellectual developmental disorder, Prostatic neoplasms

819
Tripeptidyl peptidase 2
IMD78, TPP-2, TPP-II, TPPII
Autoimmune hemolytic anemia, Color vision deficiency, Cutis marmorata, Global developmental delay, Immunodeficiency, Thrombocytopenia

820
Tubulin polymerization promoting protein
TPPP/p25, TPPP1, p24, p25, p25alpha
Barrett esophagus, Brugada syndrome, Kidney disease, Depression, Esophageal adenocarcinoma, Hemorrhoid, Hypothyroidism, Kidney failure, Osteoarthritis, Peptic ulcer disease