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"
1171 to 1180 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1171
Thioredoxin domain containing 8
SPTRX-3, SPTRX3, TRX6, bA427L11.2
Gout, Pelvic organ prolapse

1172
Thioredoxin domain containing 9
APACD, PHLP3
Uterine fibroid

1173
Thioredoxin interacting protein
ARRDC6, EST01027, HHCPA78, THIF, VDUP1
Rheumatoid arthritis, Diabetic neuropathy, Endometriosis, Diffuse large b-cell lymphoma, Stomach neoplasms

1174
Thioredoxin like 1
HEL-S-114, TRP32, TXL-1, TXNL, Txl
Androgenetic alopecia

1175
Thioredoxin like 4A
BMKS, DIB1, DIM1, SNRNP15, TXNL4, U5-15kD
Burn-mckeown syndrome, Choanal atresia syndrome

1176
Thioredoxin reductase 1
GRIM-12, TR, TR1, TRXR1, TXNR, TXNR1
Amyotrophic lateral sclerosis, Autism, Lewis lung carcinoma, Colorectal neoplasms, Congestive heart failure, Contact dermatitis, Dementia, Epilepsy, Heart failure, Hypertrophic cardiomyopathy, Major depressive disorder, Mesothelioma, Myocardial ischemia, Obesity, Osteoarthritis
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1177
Thioredoxin reductase 2
GCCD5, SELZ, TR, TR-BETA, TR3, TRXR2, TXNR2
Autism, Cardiomyopathy, Dilated cardiomyopathy, Color vision deficiency, Glucocorticoid deficiency, Glaucoma, Open angle glaucoma, Primary angle closure glaucoma, Prostatic neoplasms, Depression

1178
Thioredoxin reductase 3
TGR, TR2, TR2IT1, TRXR3, TXNR3, TXNRD3IT1, TXNRD3NB, TXNRD3NT1
Cardiomyopathy

1179
Tyrosine kinase 2
IMD35, JTK1
Ankylosing spondylitis, Rheumatoid arthritis, Autism, Autoimmune disease, Autoimmune thyroid disease, Biliary cirrhosis, Crohn disease, Depression, Diabetes mellitus type 1, Erythematosquamous dermatosis, Hypothyroidism, Immunodeficiency, Inflammatory bowel disease, Liver cirrhosis, Major depressive disorder
View all (20 more)

1180
Thymidine phosphorylase
ECGF, ECGF1, MEDPS1, MNGIE, MTDPS1, PDECGF, TP, hPD-ECGF
Experimental arthritis, Carcinoma, Colonic neoplasms, Colorectal neoplasms, Esophageal squamous cell carcinoma, Intestinal obstruction, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial dna depletion syndrome, Mitochondrial encephalomyopathy, Pancreatic neoplasms, Stomach neoplasms, Urinary bladder neoplasms, Visceral neuropathy