Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13291 to 13300 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13291
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

13292
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

13293
Tec protein tyrosine kinase
PSCTK4
Myositis, Psoriasis, Rheumatoid arthritis, Uterine fibroid

13294
Tectonin beta-propeller repeat containing 1
-
Gout, Moyamoya angiopathy

13295
Tectonin beta-propeller repeat containing 2
HSAN9, KIAA0329, SPG49
Autism, Birdshot chorioretinopathy, Hereditary sensory and autonomic neuropathy, Intellectual developmental disorder, Paraparesis, Hereditary spastic paraplegia

13296
Trans-2,3-enoyl-CoA reductase
GPSN2, MRT14, SC2, TER
Nonsyndromic intellectual disability, Intellectual developmental disorder

13297
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

13298
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

13299
Tectorin beta
-
Biliary atresia, Liver disease, Metabolic syndrome, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

13300
Tubulin epsilon and delta complex 1
C14orf80
Primary microcephaly, Color vision deficiency, Microcephaly, Psoriasis