Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14231 to 14240 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14231
Twinkle mtDNA helicase
ATXN8, C10orf2, IOSCA, MTDPS7, PEO, PEO1, PEOA3, PRLTS5, SANDO, SCA8, TWINL
Auditory neuropathy, Progressive external ophthalmoplegia, Cerebellar ataxia, Ptosis, Atrioventricular block, Mitochondrial dna depletion syndrome, Major depressive disorder, Dysphonia, Gonadal dysgenesis, Mitochondrial disease, Mitochondrial hepatopathy, Perrault syndrome, Nonsyndromic hearing loss, Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis, Hereditary spastic paraplegia
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14232
Twisted gastrulation BMP signaling modulator 1
TSG
Esophageal squamous cell carcinoma, Holoprosencephaly

14233
TXK tyrosine kinase
BTKL, PSCTK5, PTK4, RLK, TKL
Breast cancer, Multiple sclerosis

14234
Taxilin beta
C6orf198, LST001, MDP77, dJ522B19.2
Obesity

14235
Thioredoxin
TRDX, TRX, TRX1, TXN1, Trx80
Breast neoplasms, Bronchopulmonary dysplasia, Cardiomyopathy, Congenital abnormalities, Contact dermatitis, Gout, Hydrocephalus, Alzheimer disease, Liver disease, Mesothelioma, Pelvic organ prolapse

14236
Thioredoxin 2
COXPD29, MT-TRX, MTRX, TRX2, TXN
Combined oxidative phosphorylation deficiency

14237
Thioredoxin domain containing 11
EFP1
Rheumatoid arthritis

14238
Thioredoxin domain containing 15
BUG, C5orf14, MKS14, TMX5, UNQ335
Ciliopathy, Congenital cystic kidney disease, Meckel-gruber syndrome, Parkinson disease, Severe combined immunodeficiency, Diabetes mellitus type 2

14239
Thioredoxin domain containing 16
ERp90, KIAA1344
Alzheimer disease, Central nervous system cancer, Gastroesophageal reflux disease, Glioblastoma, Glioma, Orofacial cleft, Peripheral arterial disease, Rheumatoid arthritis, Smooth surface dental caries

14240
Thioredoxin domain containing 17
TRP14, TXNL5
Esophageal squamous cell carcinoma