Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13941 to 13950 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13941
Tubulin polyglutamylase complex subunit 2
C18orf10, HMFN0601, L17, PGs2
Obesity

13942
Tryptophan hydroxylase 1
TPRH, TRPH
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Borderline personality disorder, Major depressive disorder, Pulmonary hypertension, Insomnia, Kidney neoplasms, Mood disorder, Schizophrenia, Scoliosis, Depression

13943
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

13944
Triosephosphate isomerase 1
HEL-S-49, TIM, TPI, TPID
Alzheimer disease, Hemolytic anemia, Carbohydrate metabolism disease, Squamous cell carcinoma, Disorder of carbohydrate metabolism, Esophageal squamous cell carcinoma, Mouth neoplasms, Neuromuscular disease, Osteoporosis, Schizophrenia, Triose phosphate isomerase deficiency

13945
Thiamin pyrophosphokinase 1
HTPK1, PP20, THMD5
Breast cancer, Lymphocytic leukemia, Leigh syndrome, Metabolic syndrome, Thiamine metabolism dysfunction syndrome

13946
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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13947
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

13948
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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13949
Tropomyosin 4
BDPLT25, HEL-S-108
Asbestosis, Macrothrombocytopenia, Platelet-type bleeding disorder, Platelet disorder, Esophageal neoplasms, Hemorrhagic disease, Liver cirrhosis, Oligodendroglioma, Osteoporosis, Thrombocytopenia

13950
Thiopurine S-methyltransferase
TPMTD
Autism, Neutropenia, Psoriasis, Thiopurine s-methyltransferase deficiency