Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
301 to 310 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

301
Transmembrane protein 179
C14orf90, TMEM179A
Rheumatoid arthritis

302
Transmembrane protein 212
-
Hypertension

303
Tripartite motif containing 77
TRIM77P
Leukemia

304
Testis expressed 41
DKFZp686O1327, LINC00953
Alopecia, Ankylosing spondylitis, Atrial fibrillation, Cholangitis, Coronary artery disease, Crohn disease, Esophagus neoplasm, Inflammatory bowel disease, Leukemia, Paroxysmal atrial fibrillation, Psoriasis, Rheumatic aortic stenosis, Ulcerative colitis

305
Translocase of outer mitochondrial membrane 5
C9orf105, Tom5, bA613M10.3
Coronary heart disease, Coronary syndrome

306
Tripartite motif containing 26B, pseudogene
TRIM26P, TRIM26P1
Diabetes mellitus, Lung cancer, Lupus erythematosus, Rheumatoid arthritis

307
Tumor associated calcium signal transducer 2
EGP-1, EGP1, GA733-1, GA7331, GP50, M1S1, TROP2
Corneal dystrophy, Endometrioma, Endometriosis, Gelatinous droplike corneal dystrophy

308
TNFSF12-TNFSF13 readthrough
TWE-PRIL
Atrial fibrillation, Glomerulonephritis, Uterine fibroids, Plexiform leiomyoma

309
Transient receptor potential cation channel subfamily M member 1
CSNB1C, LTRPC1, MLSN1
Alzheimer disease, Congenital stationary night blindness, Diabetes mellitus, Disorder of eye, Eczema, Hypoplasia of optic disc, Age-related macular degeneration, Myopia, Night blindness, Nyctalopia, Nystagmus, Schizophrenia, Strabismus, Congenital stationary night blindness, x-linked

310
Transmembrane protein 151B
C6orf137, TMEM193, bA444E17.5
Combined oxidative phosphorylation deficiency, Pulmonary hypoplasia, Dysmorphic features, Hydrops fetalis, Leukoencephalopathy, with ovarian failure, Multiple congenital anomalies, Sclerocystic ovaries, Pericardial effusion, Pleural effusion, Polycystic ovary syndrome