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 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1151
Tumor suppressor candidate 3
D8S1992, M33, MRT22, MRT7, MagT2, N33, OST3A, SLC58A2
Alzheimer disease, Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Biliary atresia, Congenital disorder of glycosylation, Congenital neurologic anomalies, Corneal astigmatism, Intellectual developmental disorder, Liver cirrhosis, Metabolic syndrome, Neurodevelopmental disorder, Obsessive-compulsive disorder, Paraplegia, Hypertension, Diabetes mellitus type 2

1152
Terminal uridylyl transferase 1, U6 snRNA-specific
PAPD2, RBM21, STARPAP, TENT1, TUTase, URLC6
Obstructive pulmonary disease

1153
Terminal uridylyl transferase 4
PAPD3, TENT3A, ZCCHC11
Colorectal cancer

1154
Terminal uridylyl transferase 7
PAPD6, TENT3B, ZCCHC6
Asthma, Atrial fibrillation, Metabolic syndrome, Ocular hypertension, Diabetes mellitus type 2

1155
Trans-golgi network vesicle protein 23 homolog A
FAM18A, YDR084C
Oligodendroglioma

1156
Twinfilin actin binding protein 1
A6, PTK9
Crohn disease, Inflammatory bowel disease, Lymphoma, Oligodendroglioma, Ulcerative colitis

1157
Twinfilin actin binding protein 2
A6RP, A6r, MSTP011, PTK9L
Autism, Bipolar disorder, Colorectal cancer, Colonic neoplasms, Diverticular disease, Osteoarthritis, Schizophrenia

1158
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
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1159
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

1160
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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