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"
221 to 230 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

221
Tectonin beta-propeller repeat containing 2
HSAN9, KIAA0329, SPG49
Autism, Birdshot chorioretinopathy, Hereditary sensory and autonomic neuropathy, Intellectual developmental disorder, Paraparesis, Hereditary spastic paraplegia

222
Trans-2,3-enoyl-CoA reductase
GPSN2, MRT14, SC2, TER
Nonsyndromic intellectual disability, Intellectual developmental disorder

223
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

224
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

225
Tectorin beta
-
Biliary atresia, Liver disease, Metabolic syndrome, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

226
Tubulin epsilon and delta complex 1
C14orf80
Primary microcephaly, Color vision deficiency, Microcephaly, Psoriasis

227
Tubulin epsilon and delta complex 2
C16orf59
Hepatocellular carcinoma

228
TEF transcription factor, PAR bZIP family member
-
Asthma, Hypothyroidism, Insomnia, Irritable bowel syndrome, Major depressive disorder, Multiple sclerosis, Depression, Vitiligo

229
Transcription elongation factor, mitochondrial
C17orf42, COXPD58
Breast cancer, Combined oxidative phosphorylation deficiency, Lung cancer

230
TEK receptor tyrosine kinase
CD202B, GLC3E, TIE-2, TIE2, VMCM, VMCM1
Arteriovenous hemangioma, Blue rubber bleb nevus syndrome, Bockenheimer syndrome, Cardiac embolism, Cardioembolic stroke, Congenital venous anomaly, Congenital arteriovenous malformation, Congenital glaucoma, Coronary artery disease, Temporal lobe epilepsy, Glaucoma, Hemangiosarcoma, Hydrophthalmos, Liver neoplasms, Mucocutaneous venous malformations
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