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
13221 to 13230 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13221
T-box transcription factor 3
TBX3-ISO, UMS, XHL
Benign prostatic hyperplasia, Breast cancer, Breast neoplasms, Cerebrovascular disorder, Colorectal adenoma, Colorectal cancer, Desbuquois syndrome, Heart disease, Congenital anomaly of limb, Periprosthetic osteolysis, Prostatic neoplasms, Stomach neoplasms, Stroke, Thyroid disease, Tooth abnormalities
View all (1 more)

13222
T-box transcription factor 4
ICPPS, PAPPAS, SPS
17q23.1q23.2 microdeletion syndrome, Amelia, Arthropathy, Chromosome 17q23.1-q23.2 duplication syndrome, Congenital hypoplasia of lung, Coxopodopatellar syndrome, Desbuquois syndrome, Clubfoot, Pulmonary hypertension, Pulmonary arterial hypertension, Hydronephrosis, Hypertension, Hypoplastic left heart syndrome, Ischiocoxopodopatellar syndrome with pulmonary arterial hypertension, Osteoarthritis
View all (3 more)

13223
T-box transcription factor 5
HOS
Alzheimer disease, Aortic valve disease, Atrial fibrillation, Atrial flutter, Atrial septal defect, Atrioventricular block, Atrioventricular septal defect, Brugada syndrome, Cardiac arrhythmia, Cardioembolic stroke, Dilated cardiomyopathy, Obstructive pulmonary disease, Congenital heart disease, Desbuquois syndrome, Diverticular disease
View all (11 more)

13224
T-box transcription factor 6
SCDO5
Asthma, Spondylocostal dysostosis, Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Desbuquois syndrome, Jarcho-levin syndrome, Mayer-rokitansky-kuster-hauser syndrome, Multiple sclerosis, Scoliosis

13225
Thromboxane A2 receptor
BDPLT13, TXA2-R
Asthma, Platelet-type bleeding disorder, Platelet disorder, Hemorrhagic disease, Necrosis, Rhinitis, Schizophrenia

13226
Thromboxane A synthase 1
BDPLT14, CYP5, CYP5A1, GHOSAL, THAS, TS, TXAS, TXS
Alzheimer disease, Imperforate anus, Ischemic stroke, Cervical cancer, Lymphoblastic leukemia, Coronary artery disease, Desbuquois syndrome, Diabetic neuropathy, Ghosal hematodiaphyseal dysplasia, Migraine, Myocardial infarction, Obesity, Penile hypospadia, Prostatic neoplasms, Schizophrenia
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13227
T-box transcription factor T
SAVA, T, TFT
Asthma, Breast cancer, Chordoma, Neural tube defect, Neural tube defects, x-linked, Neural tube defects, susceptibility to, Sacral agenesis

13228
Tandem C2 domains, nuclear
C14orf47, C2CD1, MTAC2D1, TAC2N, Tac2-N
Alzheimer disease, Coronary artery disease, Crohn disease, Gastroesophageal reflux disease, Inflammatory bowel disease, Ulcerative colitis, Venous thromboembolism

13229
TRPM8 channel associated factor 1
FAM115A, GATD9A
Colorectal cancer, Dilated cardiomyopathy

13230
TRPM8 channel associated factor 2
FAM115C, FAM139A, GATD9, GATD9B
Diabetes mellitus type 2