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"
341 to 350 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

341
Thrombospondin 3
TSP3
Bipolar disorder, Breast cancer, Carpal tunnel syndrome, Diffuse gastric adenocarcinoma, Gastric cancer, Tourette syndrome, Gout, Hypertension

342
Thrombospondin 4
TSP-4, TSP4
Attention deficit hyperactivity disorder, Substance abuse

343
Thioesterase superfamily member 4
CTMP
Atrial fibrillation, Hepatocellular carcinoma, Digestive system disease, Diverticular disease

344
Thymocyte selection associated
C6orf190, C6orf207, GASP, SPOT, THEMIS1, TSEPA
Ankylosing spondylitis, Asthma, Celiac disease, Lymphocytic leukemia, Colorectal cancer, Crohn disease, Hodgkin lymphoma, Inflammatory bowel disease, Multiple sclerosis, Narcolepsy, Psoriasis, Respiratory system disease, Sclerosing cholangitis, Ulcerative colitis, Uterine fibroid

345
Thymocyte selection associated family member 2
C1orf38, ICB-1, ICB1
Breast neoplasms

346
TRNA-histidine guanylyltransferase 1 like
ICF45, IHG-1, IHG1, SCAR28, THG1, hTHG1
Kidney disease, Neurodevelopmental disorder, Spinocerebellar ataxia

347
Threonine synthase like 2
SOFAT, THS2, TSH2
Autoimmune thrombocytopenic purpura, Basal cell carcinoma, Color vision deficiency, Keratinocyte carcinoma, Non-melanoma skin carcinoma, Obstructive sleep apnea syndrome, Skin cancer, Skin neoplasms, Uveal melanoma

348
THO complex subunit 1
DFNA86, HPR1, P84, P84N5
Alzheimer disease, Deafness, Hearing loss, Nonsyndromic hearing loss

349
THO complex subunit 2
AMC7, CXorf3, MRX12, MRX35, THO2, XLID12, dJ506G2.1, hTREX120
Arthrogryposis multiplex congenita, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability

350
THO complex subunit 5
C22orf19, Fmip, PK1.3, fSAP79
Uterine fibroid