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
13181 to 13190 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13181
Tafazzin, phospholipid-lysophospholipid transacylase
BTHS, CMD3A, EFE, EFE2, G4.5, LVNCX, TAZ, Taz1
Barth syndrome, Cardiomyopathy, Dilated cardiomyopathy, Coronary artery disease, Left ventricular disease, Left ventricular noncompaction cardiomyopathy

13182
T cell activation RhoGTPase activating protein
ARHGAP47, FKSG15, IDDM21, TAGAP1
Ankylosing spondylitis, Rheumatoid arthritis, Eczema, Autoimmune disease, Celiac disease, Crohn disease, Dermatitis, Hypothyroidism, Iga nephropathy, Inflammatory bowel disease, Multiple sclerosis, Psoriasis, Psoriasis vulgaris, Sclerosing cholangitis, Systemic lupus erythematosus
View all (3 more)

13183
Transgelin
SM22, SM22-alpha, SMCC, TAGLN1, TGLN, WS3-10
Breast cancer, Cardiovascular disease, Colonic neoplasms, Endometriosis, Esophageal squamous cell carcinoma, Hypothyroidism, Lipidoses, Lipoidosis, Metabolic syndrome, Diabetes mellitus type 2

13184
Transgelin 2
HA1756
Hepatocellular carcinoma, Renal cell carcinoma, Crohn disease, Ileocolitis, Liver cirrhosis

13185
TAL bHLH transcription factor 1, erythroid differentiation factor
SCL, TCL5, bHLHa17, tal-1
Insomnia, Lymphoblastic leukemia, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Open angle glaucoma, Diabetes mellitus type 2

13186
TAL bHLH transcription factor 2
-
Lymphoblastic leukemia, Schizophrenia

13187
Transaldolase 1
TAL, TAL-H, TALDOR, TALH
Carbohydrate metabolism disease, Hepatocellular carcinoma, Cataract, Kidney disease, Transaldolase deficiency, Disorder of carbohydrate metabolism, Parkinson disease

13188
Trafficking regulator and scaffold protein tamalin
GRASP
Major depressive disorder

13189
TAM41 mitochondrial translocator assembly and maintenance homolog
C3orf31, COXPD56, RAM41, TAM41
Ptosis, Combined oxidative phosphorylation deficiency, Deglutition disorder

13190
Tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1
ROLSB, TANC
Colorectal adenoma, Colorectal cancer, Intellectual developmental disorder