Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
13411 to 13420 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13411
THAP domain containing 9
hTh9
Cardiovascular disease

13412
Thrombomodulin
AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM, TM
Asthma, Hemolytic uremic syndrome, Carotid artery thrombosis, Ischemic stroke, Disseminated intravascular coagulation, Hyperalgesia, Kidney disease, Kidney failure, Promyelocytic leukemia, Liver disease, Myocardial infarction, Rheumatoid arthritis, Stomach neoplasms, Thrombocytopenia, Thrombomodulin-related bleeding disorder
View all (2 more)

13413
Thrombospondin 1
THBS, THBS-1, TSP, TSP-1, TSP1
Juvenile arthritis, Autism, Breast neoplasms, Congenital glaucoma, Diabetic angiopathies, Diabetic peripheral angiopathy, Diabetic retinopathy, Gout, Hearing impairment, Hepatic veno occlusive disease, Hypertension, Juvenile idiopathic arthritis, Liver cirrhosis, Premature ovarian failure, Oligoarticular juvenile idiopathic arthritis
View all (4 more)

13414
Thrombospondin 2
EDSCLL3, TSP2
Anorectal malformation, Brain infarction, Diabetes mellitus, Diabetic angiopathies, Diabetic peripheral angiopathy, Ehlers-danlos syndrome, Hemorrhoid, Intervertebral disc disease, Intervertebral disc displacement, Liver disease

13415
Thrombospondin 3
TSP3
Bipolar disorder, Breast cancer, Carpal tunnel syndrome, Diffuse gastric adenocarcinoma, Gastric cancer, Tourette syndrome, Gout, Hypertension

13416
Thrombospondin 4
TSP-4, TSP4
Attention deficit hyperactivity disorder, Substance abuse

13417
Thioesterase superfamily member 4
CTMP
Atrial fibrillation, Hepatocellular carcinoma, Digestive system disease, Diverticular disease

13418
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

13419
Thymocyte selection associated family member 2
C1orf38, ICB-1, ICB1
Breast neoplasms

13420
TRNA-histidine guanylyltransferase 1 like
ICF45, IHG-1, IHG1, SCAR28, THG1, hTHG1
Kidney disease, Neurodevelopmental disorder, Spinocerebellar ataxia