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"
801 to 810 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
-
-
Combined oxidative phosphorylation deficiency

802
TPD52 like 1
D53, TPD53
Prostatic neoplasms

803
TPD52 like 2
D54, TPD54
Metabolic syndrome, Diabetes mellitus type 2

804
TPD52 like 3
D55, NYDSP25, TPD55, hD55
Asthma, Cystic kidney disease, Kidney disease

805
Tubulin polyglutamylase complex subunit 2
C18orf10, HMFN0601, L17, PGs2
Obesity

806
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

807
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

808
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

809
Thiamin pyrophosphokinase 1
HTPK1, PP20, THMD5
Breast cancer, Lymphocytic leukemia, Leigh syndrome, Metabolic syndrome, Thiamine metabolism dysfunction syndrome

810
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