Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13271 to 13280 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13271
Transforming growth factor beta regulator 4
CPR2, FASTKD4
Colorectal adenoma, Colorectal cancer, Duchenne muscular dystrophy

13272
T-box transcription factor 1
CAFS, CATCH22, CTHM, DGCR, DGS, DORV, TBX1C, TGA, VCF, VCFS
22q11.2 deletion syndrome, Breast cancer, Basal cell carcinoma, Chromosome 22q11.2 microduplication syndrome, Obstructive pulmonary disease, Color vision deficiency, Combined immunodeficiency disease, Common arterial trunk with aortic dominance, Common arterial trunk with pulmonary dominance and interrupted aortic arch, Congenital heart disease, Conotruncal anomaly face syndrome, Conotruncal cardiac defect, Craniofacial abnormalities, Digeorge syndrome, Epilepsy
View all (16 more)

13273
T-box transcription factor 10
TBX13, TBX7
Metabolic syndrome, Orofacial cleft, Diabetes mellitus type 2

13274
T-box transcription factor 15
TBX14
Androgenetic alopecia, Breast cancer, Chagas cardiomyopathy, Cousin syndrome, Craniofacial abnormalities, Desbuquois syndrome, Growth disorder, Obstructive sleep apnea syndrome, Osteoarthritis, Pelviscapular dysplasia

13275
T-box transcription factor 18
CAKUT2, PUJO
Androgenetic alopecia, Anophthalmia, Breast cancer, Congenital anomalies of the kidney and urinary tract, Cardiac embolism, Cardioembolic stroke, Carpal tunnel syndrome, Central nervous system cancer, Kidney disease, Renal agenesis, Congenital anomalies of kidney and urinary tract, Glioblastoma, Glioma, Hypertension, Immune system disease
View all (3 more)

13276
T-box transcription factor 19
TBS19, TPIT, dJ747L4.1
Congenital isolated acth deficiency, Major depressive disorder, Duodenitis, Gastroenteritis, Pituitary stalk interruption syndrome

13277
T-box transcription factor 2
VETD
Atrial septal defect, Ischemic heart disease, Congenital septal defect of heart, Coronary artery disease, Hypertension, Metabolic syndrome, Myocardial ischemia, Nephrolithiasis, Neuroblastoma, Osteoarthritis, Vertebral anomalies with endocrine and t-cell dysfunction

13278
T-box transcription factor 20
ASD4
Aortic valve disease, Atherosclerosis, Atrial fibrillation, Atrial septal defect, Brugada syndrome, Cardiomegaly, Dilated cardiomyopathy, Fatigue syndrome, Liver cirrhosis, Congenital heart disease, Congestive heart failure, Coronary artery disease, Dementia, Dysentery, Hypertension
View all (11 more)

13279
T-box transcription factor 21
IMD88, T-PET, T-bet, TBET, TBLYM
Asthma, Eczema, Autoimmune thyroid disease, Dementia, Diverticular disease, Hypothyroidism, Immunodeficiency, Kidney failure, Major depressive disorder, Metabolic syndrome, Myopathy, Respiratory system disease, Schizophrenia, Diabetes mellitus type 2, Depression

13280
T-box transcription factor 22
ABERS, CLPA, CPX, TBXX, dJ795G23.1
Abruzzo-erickson syndrome, Cleft palate, Cleft palate with ankyloglossia, Cleft palate x-linked, Orofacial cleft, Scoliosis, Uranostaphyloschisis, X-linked cleft palate and ankloglossia