Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13351 to 13360 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13351
TEA domain transcription factor 3
DTEF-1, ETFR-1, TEAD-3, TEAD5, TEF-5, TEF5
Insomnia, Leber congenital amaurosis, Metabolic syndrome, Retinitis pigmentosa, Diabetes mellitus type 2

13352
TEA domain transcription factor 4
EFTR-2, RTEF1, TCF13L1, TEF-3, TEF3, TEFR-1, hRTEF-1B
Atrial fibrillation, Cancer, Coronary artery disease, Diabetes mellitus, Heart failure, Narcolepsy, Stroke

13353
Tec protein tyrosine kinase
PSCTK4
Myositis, Psoriasis, Rheumatoid arthritis, Uterine fibroid

13354
Tectonin beta-propeller repeat containing 1
-
Gout, Moyamoya angiopathy

13355
Tectonin beta-propeller repeat containing 2
HSAN9, KIAA0329, SPG49
Autism, Birdshot chorioretinopathy, Hereditary sensory and autonomic neuropathy, Intellectual developmental disorder, Paraparesis, Hereditary spastic paraplegia

13356
Trans-2,3-enoyl-CoA reductase
GPSN2, MRT14, SC2, TER
Nonsyndromic intellectual disability, Intellectual developmental disorder

13357
Trans-2,3-enoyl-CoA reductase like
CPVT3, GPSN2L, SRD5A2L2, TERL
Aortic valve disease, Catecholaminergic polymorphic ventricular tachycardia, Follicular lymphoma, Long qt syndrome, Kawasaki disease, Obesity, Polymorphic catecholaminergic ventricular tachycardia, Psoriasis

13358
Tectorin alpha
DFNA12, DFNA8, DFNB21
Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Congenital sensorineural hearing loss, Deafness, Esophageal disease, Esophageal ulcer, Hearing impairment, Hearing loss, Hereditary hearing loss, Alzheimer disease, Meniere disease

13359
Tectorin beta
-
Biliary atresia, Liver disease, Metabolic syndrome, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

13360
Tubulin epsilon and delta complex 1
C14orf80
Primary microcephaly, Color vision deficiency, Microcephaly, Psoriasis