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"
291 to 300 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

291
Transcription factor Dp-1
DILC, DP1, DRTF1, Dp-1
Alzheimer disease, Juvenile arthritis, Constitutional mismatch repair deficiency syndrome, Juvenile idiopathic arthritis, Constitutional mismatch repair deficiency, Oligoarticular juvenile idiopathic arthritis, Diabetes mellitus type 2

292
Transcription factor Dp-2
DP2
Attention deficit hyperactivity disorder, Autism, Kidney disease, Congenital left-sided heart lesions, Diverticular disease, Gout, Hearing loss, Kidney cancer, Mesothelioma, Metabolic syndrome, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2

293
Transcription factor binding to IGHM enhancer 3
MRXSPF, RCCP2, RCCX1, TFEA, bHLHe33
Renal cell carcinoma, Neurodevelopmental disorder, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Non-specific syndromic intellectual disability, X-linked complex neurodevelopmental disorder

294
Transcription factor EB
ALPHATFEB, BHLHE35, TCFEB
Attention deficit hyperactivity disorder, Colorectal cancer, Dupuytren contracture, Alzheimer disease, Diabetes mellitus type 2

295
Transcription factor EC
TCFEC, TFE-C, TFEC-L, TFECL, bHLHe34, hTFEC-L
Atrial fibrillation, Bipolar disorder, Glaucoma, Liver cirrhosis, Major depressive disorder, Open angle glaucoma, Schizophrenia

296
Trefoil factor 1
BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2
Celiac disease, Pancreatic cancer, Urinary bladder cancer

297
Trefoil factor 2
SML1, SP
Color vision deficiency, Pancreatic cancer

298
Trefoil factor 3
ITF, P1B, TFI
Color vision deficiency, Hepatitis animal, Kidney disease, Kidney failure, Mucositis

299
Trafficking from ER to golgi regulator
HMSNP, SPG57, TF6, TRKT3
Charcot-marie-tooth disease, Spastic paraplegia, Differentiated thyroid carcinoma, Extraskeletal myxoid chondrosarcoma, Hereditary motor and sensory neuropathies, Hereditary motor and sensory neuropathy, Hereditary spastic paraplegia

300
Tuftelin interacting protein 11
NTR1, STIP, STIP-1, Spp382, TIP39, bK445C9.6
Hypertension