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"
131 to 140 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

131
Transducin beta like 2
WBSCR13, WS-betaTRP
Gout, Hearing loss, Hypertriglyceridemia, Insomnia, Metabolic syndrome, Obesity, Diabetes mellitus type 2, Williams syndrome

132
TATA-box binding protein
GTF2D, GTF2D1, HDL4, SCA17, TBP1, TFIID
Parkinson disease, Diabetes mellitus type 1, Hereditary parkinson disease, Schizophrenia, Spinocerebellar ataxia

133
TATA-box binding protein like 1
MGC:8389, MGC:9620, STUD, TLF, TLP, TRF2
Prostate cancer, Hypertension

134
TATA-box binding protein like 2
TBP2, TRF3
Major depressive disorder

135
T-box brain transcription factor 1
AUTS5, IDDAS, TBR-1, TES-56
Attention deficit hyperactivity disorder, Autism, Neurodevelopmental disorder, Cortical dysplasia, Cortical occipital malformations, Developmental delay with language impairment and movement disorder, Focal cortical dysplasia, Intellectual developmental disorder autism speech, Intellectual developmental disorder speech autism dysmorphic, Intellectual developmental disorder, Non-specific syndromic intellectual disability

136
Transforming growth factor beta regulator 1
NIAM, TB-5
Intellectual developmental disorder

137
Transforming growth factor beta regulator 4
CPR2, FASTKD4
Colorectal adenoma, Colorectal cancer, Duchenne muscular dystrophy

138
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)

139
T-box transcription factor 10
TBX13, TBX7
Metabolic syndrome, Orofacial cleft, Diabetes mellitus type 2

140
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