Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
701 to 710 of 913 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

701
Titin
CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrial flutter, Centronuclear myopathy, Limb girdle muscular dystrophy, Brugada syndrome, Cardiac arrhythmia, Cardioembolic stroke, Cardiomyopathy, Cerebral palsy, Atrioventricular block, Congenital myopathy, Dilated cardiomyopathy, Distal muscular dystrophy, Distal myopathy
View all (25 more)

702
Alpha tocopherol transfer protein
ATTP, AVED, TTP1, alphaTTP
Ataxia with vitamin e deficiency, Atherosclerosis, Headache, Nervous system disease, Optic atrophy, Retinitis pigmentosa, Visual impairment, Combined vitamin k-dependent clotting factor deficiency

703
TUB bipartite transcription factor
RDOB, rd5
Autism, Coronary artery disease, Essential tremor, Hearing loss, Lung cancer, Retinitis pigmentosa

704
Transthyretin
ATTR, CTS, CTS1, HEL111, HsT2651, PALB, TBPA, TTN
Alzheimer disease, Amyloid neuropathy, Amyloid polyneuropathy, Amyloidosis, Brugada syndrome, Cardiomyopathy, Carpal tunnel syndrome, Charcot-marie-tooth disease, Major depressive disorder, Dystransthyretinemic euthyroidal hyperthyroxinemia, Heart disease, Hyperthyroxinemia, Kidney failure, Lung neoplasms, Depression
View all (3 more)

705
Tubulin alpha 4a
ALS22, CMYO26, FTDALS9, H2-ALPHA, OZEMA23, SPAX11, TUBA1
Amyotrophic lateral sclerosis, Macrothrombocytopenia, Blepharoptosis, Congenital myopathy, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Oocyte maturation defect, Spastic ataxia, Diabetes mellitus, type 2

706
Tubulin beta 2A class IIa
CDCBM5, TUBB, TUBB2
Juvenile arthritis, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Creutzfeldt-jakob disease, Vascular dementia, Developmental disability, Juvenile idiopathic arthritis, Myeloid leukemia, Neurodevelopmental disorders, Oligoarticular juvenile idiopathic arthritis, Tubulinopathy

707
Tubulin gamma 1
CDCBM4, GCP-1, TUBG, TUBGCP1
15q11.2 microdeletion syndrome, Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Lissencephaly, Cortical development malformation, Microcephaly, Myopathy, Myositis, Diabetes mellitus, type 2

708
Tu translation elongation factor, mitochondrial
COXPD4, EF-TuMT, EFTU, P43
Combined oxidative phosphorylation deficiency, Esophageal neoplasm, Hypogonadism, Inflammatory bowel disease, Metabolic syndrome, Mitochondrial disease, Diabetes mellitus, type 2

709
Tuftelin 1
WHSF
Myocardial infarction, Seborrheic keratosis, Woolly hair-skin fragility syndrome

710
TUB like protein 1
LCA15, RP14, TUBL1
Leber congenital amaurosis , Retinitis pigmentosa, Brachydactyly, Leber congenital amaurosis, Nonalcoholic fatty liver disease, Polydactyly, Stargardt disease, Syndactyly, Diabetes mellitus, type 2