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 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
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

812
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, Myopathy, Stomach neoplasms, Thyroid neoplasms

813
Tropomyosin 4
BDPLT25, HEL-S-108
Asbestosis, Macrothrombocytopenia, Platelet-type bleeding disorder, Platelet disorder, Esophageal neoplasms, Hemorrhagic disease, Oligodendroglioma, Osteoporosis, Thrombocytopenia

814
Thiopurine S-methyltransferase
TPMTD
Autism, Neutropenia, Psoriasis, Thiopurine s-methyltransferase deficiency

815
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
View all (5 more)

816
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

817
Tripeptidyl peptidase 2
IMD78, TPP-2, TPP-II, TPPII
Autoimmune hemolytic anemia, Color vision deficiency, Cutis marmorata, Global developmental delay, Immunodeficiency, Thrombocytopenia

818
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

819
Tubulin polymerization promoting protein family member 2
C14orf8, CT152, P18, p25beta
Exostoses

820
Translocated promoter region, nuclear basket protein
MRT79
Nonsyndromic intellectual disability, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Differentiated thyroid carcinoma, Intellectual developmental disorder, Thyroid neoplasms