Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
13811 to 13820 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13811
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

13812
Transportin 1
IPO2, KPNB2, MIP, MIP1, TRN
Atrial fibrillation, Bladder calculus, Obstructive pulmonary disease, Tourette syndrome, Nephrolithiasis, Urolithiasis

13813
Transportin 2
IDDHISD, IPO3, KPNB2B, TRN2
Diffuse large b-cell lymphoma, Intellectual developmental disorder speech dysmorphic, Multiple sclerosis, Neurodevelopmental disorder, Polycystic ovary syndrome

13814
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

13815
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

13816
Trinucleotide repeat containing 18
CAGL79, TNRC18A
Crohn disease, Inflammatory bowel disease, Uveitis, Prostate cancer, Psoriasis, Seborrheic dermatitis, Ulcerative colitis

13817
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

13818
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)

13819
Trinucleotide repeat containing adaptor 6C
-
Alzheimer disease, Colorectal cancer, Intellectual developmental disorder, Metabolic syndrome, Diabetes mellitus type 2

13820
Tensin 1
MST091, MST122, MST127, MSTP091, MSTP122, MSTP127, MXRA6, PPP1R155, TNS
Asthma, Atrial fibrillation, Breast cancer, Obstructive pulmonary disease, Colorectal cancer, Coronary artery disease, Diverticular disease, Myocardial infarction, Open angle glaucoma, Psoriatic arthritis, Seasonal allergic rhinitis, Tetralogy of fallot, Diabetes mellitus type 2, Uterine fibroid