Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
431 to 440 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

431
Transmembrane serine protease 4
CAP2, CAPH2, MT-SP2, TMPRSS3
Cerebral atrophy

432
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
View all (1 more)

433
Tripartite motif containing 39
RNF23, TFP, TRIM39B
Intestinal pseudo-obstruction, Cutaneous lupus erythematosus, Major depressive disorder, Rheumatoid arthritis

434
Transcription elongation factor A like 7
WEX5
Prostatic neoplasm

435
Transcriptional and immune response regulator
C8orf4, TC-1, TC1
Hepatocellular carcinoma

436
TUB like protein 4
TUSP
Alzheimer disease, Attention deficit hyperactivity disorder, Color vision deficiency, Colorectal cancer, Conotruncal cardiac defect, Hyperopia, Substance abuse, Systemic sclerosis

437
Twisted gastrulation BMP signaling modulator 1
TSG
Esophageal squamous cell carcinoma, Holoprosencephaly

438
T-box transcription factor 20
ASD4
Aortic valve disease, Atherosclerosis, Atrial fibrillation, Atrial septal defect, Brugada syndrome, Cardiomegaly, Cardiomyopathy, Fatigue syndrome, Liver cirrhosis, Congenital heart disease, Congenital hereditary endothelial dystrophy, Coronary artery disease, Dementia, Dilated cardiomyopathy, Dysentery
View all (10 more)

439
Transient receptor potential cation channel subfamily C member 7
TRP7
Bipolar disorder, Insomnia, Peripheral neuropathy, Severe acute respiratory syndrome

440
Tripartite motif containing 54
MURF, MURF-3, RNF30, muRF3
Charcot-marie-tooth disease, Navajo neurohepatopathy