Genes | GeDiPNet - Gene Disease Pathway & Associations

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13871 to 13880 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
13871	7139	TNNT2	Troponin T2, cardiac type	CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC, cTnT	Arrhythmogenic right ventricular cardiomyopathy, Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Cardiovascular disease, Obstructive airway disease, Congestive heart failure, Costello syndrome, Hypertrophic cardiomyopathy, Restrictive cardiomyopathy, Glycogen storage disease, Heart disease, Heart failure, Cardiac injury, Left ventricular disease View all (8 more)
13872	7140	TNNT3	Troponin T3, fast skeletal type	DA2B2, TNTF, beta-TnTF	Arthrogryposis multiplex congenita, Distal arthrogryposis, Breast cancer, Congenital myopathy, Digitotalar dysmorphism, Hypertension, Nemaline myopathy, Sheldon-hall syndrome
13873	3842	TNPO1	Transportin 1	IPO2, KPNB2, MIP, MIP1, TRN	Atrial fibrillation, Bladder calculus, Obstructive pulmonary disease, Tourette syndrome, Nephrolithiasis, Urolithiasis
13874	30000	TNPO2	Transportin 2	IDDHISD, IPO3, KPNB2B, TRN2	Diffuse large b-cell lymphoma, Intellectual developmental disorder speech dysmorphic, Multiple sclerosis, Neurodevelopmental disorder, Polycystic ovary syndrome
13875	23534	TNPO3	Transportin 3	IPO12, LGMD1F, LGMDD2, MTR10A, TRN-SR, TRN-SR2, TRNSR	Systemic scleroderma, Autoimmune musculoskeletal system disorder, Limb girdle muscular dystrophy, Biliary cirrhosis, Diffuse cutaneous systemic sclerosis, Hypothyroidism, Crest syndrome, Muscular dystrophy, Myositis, Biliary cholangitis, Rheumatoid arthritis, Sjogren syndrome, Systemic lupus erythematosus, Systemic sclerosis
13876	7143	TNR	Tenascin R	NEDSTO, TN-R	Attention deficit hyperactivity disorder, Corneal astigmatism, Dementia, Major depressive disorder, Neurodevelopmental disorder, Open angle glaucoma, Parkinson disease, Sarcoidosis, Schizophrenia, Age-related macular degeneration
13877	84629	TNRC18	Trinucleotide repeat containing 18	CAGL79, TNRC18A	Crohn disease, Inflammatory bowel disease, Uveitis, Prostate cancer, Psoriasis, Seborrheic dermatitis, Ulcerative colitis
13878	27327	TNRC6A	Trinucleotide repeat containing adaptor 6A	CAGH26, FAME6, GW1, GW182, TNRC6	Alzheimer disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Myoclonic epilepsy, Familial adult myoclonic epilepsy, Adult myoclonic epilepsy, Heart failure, Hypertension, Metabolic syndrome, Substance abuse, Diabetes mellitus type 2
13879	23112	TNRC6B	Trinucleotide repeat containing adaptor 6B	GDSBA	Autism, Breast cancer, Cholecystolithiasis, Colonic neoplasms, Neurodevelopmental disorder, Developmental disability, Diverticular disease, Estrogen-receptor negative breast cancer, Female infertility, Gallstones, Global developmental delay, Hypertrophic cardiomyopathy, Metabolic syndrome, Myocardial infarction, Non-specific syndromic intellectual disability View all (4 more)
13880	57690	TNRC6C	Trinucleotide repeat containing adaptor 6C	-	Alzheimer disease, Colorectal cancer, Intellectual developmental disorder, Metabolic syndrome, Diabetes mellitus type 2

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