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"
1151 to 1160 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1151
Terminal uridylyl transferase 7
PAPD6, TENT3B, ZCCHC6
Asthma, Atrial fibrillation, Metabolic syndrome, Ocular hypertension, Diabetes mellitus type 2

1152
Trans-golgi network vesicle protein 23 homolog A
FAM18A, YDR084C
Oligodendroglioma

1153
Twinfilin actin binding protein 1
A6, PTK9
Crohn disease, Inflammatory bowel disease, Lymphoma, Oligodendroglioma, Ulcerative colitis

1154
Twinfilin actin binding protein 2
A6RP, A6r, MSTP011, PTK9L
Autism, Bipolar disorder, Colorectal cancer, Colonic neoplasms, Diverticular disease, Osteoarthritis, Schizophrenia

1155
Twist family bHLH transcription factor 1
ACS3, BPES2, BPES3, CRS, CRS1, CSO, SCS, SWCOS, TWIST, bHLHa38
Androgenetic alopecia, Asthma, Atherosclerosis, Atrial fibrillation, Brachycephaly, Cardiovascular disease, Central nervous system cancer, Cerebrovascular disorder, Ischemic heart disease, Obstructive pulmonary disease, Colorectal cancer, Coronal craniosynostosis, Coronary artery disease, Craniosynostosis, Desbuquois syndrome
View all (16 more)

1156
Twist family bHLH transcription factor 2
AMS, BBRSAY, DERMO1, FFDD3, SETLSS, bHLHa39
Ablepharon macrostomia syndrome, Alzheimer disease, Androgenetic alopecia, Barber-say syndrome, Congenital ectodermal dysplasia of face, Dry eye syndrome, Focal facial dermal dysplasia, Peptic ulcer disease, Sjogren syndrome

1157
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)

1158
Twisted gastrulation BMP signaling modulator 1
TSG
Esophageal squamous cell carcinoma, Holoprosencephaly

1159
TXK tyrosine kinase
BTKL, PSCTK5, PTK4, RLK, TKL
Breast cancer, Multiple sclerosis

1160
Taxilin beta
C6orf198, LST001, MDP77, dJ522B19.2
Obesity