Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13881 to 13890 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13881
Tryptophan hydroxylase 2
ADHD7, NTPH
Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Color vision deficiency, Bipolar depression, Major depressive disorder, Mood disorder, Panic disorder, Schizophrenia, Psychotic disorders, Hypertension, Depression

13882
Triosephosphate isomerase 1
HEL-S-49, TIM, TPI, TPID
Alzheimer disease, Hemolytic anemia, Carbohydrate metabolism disease, Squamous cell carcinoma, Carbohydrate metabolism disorder, Esophageal squamous cell carcinoma, Mouth neoplasms, Neuromuscular disease, Osteoporosis, Schizophrenia, Triose phosphate isomerase deficiency

13883
Thiamin pyrophosphokinase 1
HTPK1, PP20, THMD5
Breast cancer, Lymphocytic leukemia, Leigh syndrome, Metabolic syndrome, Thiamine metabolism dysfunction syndrome

13884
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, Metabolic syndrome, Neutropenia, Parkinson disease, Tetralogy of fallot, Diabetes mellitus type 2

13885
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

13886
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

13887
Tropomyosin 4
BDPLT25, HEL-S-108
Asbestosis, Macrothrombocytopenia, Platelet-type bleeding disorder, Platelet disorder, Esophageal neoplasms, Hemorrhagic disease, Oligodendroglioma, Osteoporosis, Thrombocytopenia

13888
Thiopurine S-methyltransferase
TPMTD
Autism, Neutropenia, Psoriasis, Thiopurine s-methyltransferase deficiency

13889
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)

13890
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