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"
721 to 730 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

721
TNFAIP3 interacting protein 2
ABIN2, FLIP1, KLIP
Multiple sclerosis, Systemic lupus erythematosus

722
TNFAIP3 interacting protein 3
ABIN-3, LIND
Multiple sclerosis, Psoriasis

723
Tyrosine kinase non receptor 1
KOS1
Uterine fibroid, Vascular dementia

724
Tyrosine kinase non receptor 2
ACK, ACK-1, ACK1, p21cdc42Hs
Bronchopulmonary dysplasia, Developmental and epileptic encephalopathy, Genetic generalized epilepsy, Liver neoplasms, Parkinson disease

725
Tankyrase
ARTD5, PARP-5a, PARP5A, PARPL, TIN1, TINF1, TNKS1, pART5
Asthma, Bipolar disorder, Cataract, Cervical cancer, Coronary artery disease, Endometriosis, Epilepsy, Generalized epilepsy, Hearing loss, Hypertension, Multiple myeloma, Neurotic disorder, Obesity, Partial epilepsy, Post-traumatic stress disorder
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726
Tankyrase 1 binding protein 1
CNOT12, TAB182
Alzheimer disease, Color vision deficiency, Gout, Hypertrophic cardiomyopathy, Insomnia, Metabolic syndrome, Squamous cell carcinoma, Diabetes mellitus type 2

727
Tankyrase 2
ARTD6, PARP-5b, PARP-5c, PARP5B, PARP5C, TANK2, TNKL, pART6
Diabetic ketoacidosis, Diabetes mellitus type 1, Diabetes mellitus type 2

728
Tenascin N
TN-W, TNW
Atrial fibrillation, Gout, Obsessive-compulsive disorder

729
Troponin C1, slow skeletal and cardiac type
CMD1Z, CMH13, TN-C, TNC, TNNC
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy

730
Troponin C2, fast skeletal type
CFAP85, CMYO15, CMYP15, FAP85, MYONRI
Congenital myopathy, Hypertrophic cardiomyopathy