Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
231 to 240 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

231
Transmembrane protein 98
TADA1
Nanophthalmos, Oligodendroglioma

232
TBC1 domain family member 29, pseudogene
TBC1D29

233
Torsin 1A interacting protein 1
LAP1, LAP1B, LAP1C, LGMD2Y
Limb girdle muscular dystrophy, Centronuclear myopathy, Muscular dystrophy, Prostate cancer

234
Tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2
IDDALDS, ROLSA, rols
Autism, Developmental delay, Dyslexia, Epilepsy, Insomnia, Intellectual developmental disorder autism speech, Intellectual developmental disorder, Alzheimer disease, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Peripheral arterial disease, Prostate cancer, Schizophrenia

235
Tectonic family member 3
C10orf61, JBTS18, OFD4, TECT3
Ciliopathies, Desbuquois syndrome, Diverticular disease, Aplasia of the vermis, Joubert syndrome, Meckel syndrome, Meckel-gruber syndrome, Orofaciodigital syndrome

236
Transient receptor potential cation channel subfamily C member 4 associated protein
C20orf188, PPP1R158, TRRP4AP, TRUSS
Angioedema, Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Coronary artery disease, Cutaneous squamous cell carcinoma, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Hypothyroidism
View all (11 more)

237
Testin LIM domain protein
TESS, TESS-2
Atrial fibrillation, Colitis, Glaucoma, Glioblastoma, Liver cirrhosis, Open angle glaucoma, Tuberculosis

238
Tubulin tyrosine ligase like 3
HOTTL
Ocular hypertension

239
TRAF3 interacting protein 1
CFAP116, FAP116, IFT54, MIP-T3, MIPT3, SLSN9
Ciliopathies, Desbuquois syndrome, Ellis-van creveld syndrome, Insomnia, Jeune thoracic dystrophy, Majewski syndrome, Open angle glaucoma, Psoriasis, Retinitis pigmentosa, Senior-loken syndrome, Short rib dysplasia-polydactyly syndrome

240
TERF1 interacting nuclear factor 2
DKCA3, DKCA5, TIN2
Bone marrow diseases, Cerebellar diseases, Dyskeratosis congenita, Growth disorder, Hoyeraal hreidarsson syndrome, Pulmonary fibrosis, Revesz debuse syndrome, Revesz syndrome