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Dataset:
Curated
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Showing genes starting with "T"
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21 to 30 of 913 Genes
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Entrez ID
Gene Symbol
Gene Name
Synonyms
Diseases
21
100506866
TTN-AS1
TTN antisense RNA 1
-
Acne
,
Atrial fibrillation
,
Atrial septal defect
,
Av nodal reentry tachycardia
,
Biventricular hypertrophy
,
Cardiomyopathy
,
Centronuclear myopathy
,
Complete atrioventricular block
,
Congenital muscular dystrophy
,
Congenital torticollis
,
Congestive heart failure
,
Developmental delay
,
Heart failure
,
Hereditary myopathy with early respiratory failure
,
Left ventricular noncompaction
,
Leukemia
,
Limb-girdle muscular dystrophy
,
Multiple congenital anomalies
,
Muscular dystrophy
,
Myopathy
,
Myopathy with fatal cardiomyopathy
,
Myopia
,
Neck webbing
,
Neuromuscular diseases
,
Noncompaction cardiomyopathy
,
Paroxysmal atrial fibrillation
,
Pulmonary arterial hypertension
,
Pulmonary stenosis
,
Scoliosis
,
Thoracolumbar scoliosis
,
Tibial muscular dystrophy
,
Ventricular arrhythmia
,
Wolff-parkinson-white syndrome
View all (18 more)
22
100507308
TARID
TCF21 antisense RNA inducing promoter demethylation
EYA4-AS1
Cardiomyopathy
,
Cardiovascular diseases
,
Coronary artery disease
,
Coronary heart disease
,
Deafness
,
Hypertension
,
Congenital hypertrophic pyloric stenosis
23
100507404
TMLHE-AS1
TMLHE antisense RNA 1
-
Agenesis of corpus callosum
,
Autism, x-linked
24
100527978
TLCD4-RWDD3
TLCD4-RWDD3 readthrough
TMEM56-RWDD3
Bipolar disorder
25
100529211
TMEM256-PLSCR3
TMEM256-PLSCR3 readthrough (NMD candidate)
C17orf61-PLSCR3, PLSCR3
Asphyxiating thoracic dystrophy
,
Brachydactyly
,
Syndactyly of fingers
26
10098
TSPAN5
Tetraspanin 5
NET-4, NET4, TM4SF9, TSPAN-5
Rheumatoid arthritis
27
10099
TSPAN3
Tetraspanin 3
TM4-A, TM4SF8, TSPAN-3
Diabetes mellitus
28
10100
TSPAN2
Tetraspanin 2
NET3, TSN2, TSPAN-2
Stroke
29
10102
TSFM
Ts translation elongation factor, mitochondrial
EFTS, EFTSMT
Cardiomyopathy
,
Combined oxidative phosphorylation deficiency
,
Concentric hypertrophic cardiomyopathy
,
Developmental delay
,
Epileptic encephalopathy
,
Fatal mitochondrial disease
,
Impaired cognition
,
Multiple sclerosis
,
Hypotonia
,
Optic atrophy
,
Patent ductus arteriosus
,
Patent foramen ovale
,
Respiratory failure
30
10107
TRIM10
Tripartite motif containing 10
HERF1, RFB30, RNF9
Dermatitis
,
Development disorder
,
Lung cancer
,
Rheumatoid arthritis
,
Schizophrenia
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