Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
851 to 860 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

851
Trafficking kinesin protein 1
DEE68, EIEE68, MILT1, OIP106
Attention deficit hyperactivity disorder, Autism, Developmental and epileptic encephalopathy, Developmental disability, Heart failure, Major depressive disorder, Metabolic syndrome, Sarcoidosis, Schizophrenia, Diabetes mellitus type 2

852
Trafficking kinesin protein 2
ALS2CR3, CALS-C, GRIF-1, GRIF1, MILT2, OIP98
Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma, Non-melanoma skin carcinoma, Ovarian cancer
View all (4 more)

853
Translocation associated membrane protein 1
PNAS8, TRAM, TRAMP
Multiple sclerosis, Osteoarthritis, Prostate cancer

854
Translocation associated membrane protein 1 like 1
-
Bronchopulmonary dysplasia, Obesity, Ulcerative colitis

855
Translocation associated membrane protein 2
-
Peripheral arterial disease, Scoliosis

856
Tetratricopeptide repeat and ankyrin repeat containing 1
LBA1
Alzheimer disease, Autism, Bilirubin metabolism disease, Bipolar disorder, Bipolar depression, Hypothyroidism, Kleine-levin syndrome, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2, Ulcerative colitis

857
TNF receptor associated protein 1
HSP 75, HSP75, HSP90L, TRAP-1
Asthma, Atrial fibrillation, Congenital anomalies of the kidney and urinary tract, Gout, Osteoarthritis, Sclerosing cholangitis, Stomach neoplasms, Diabetes mellitus type 2, Vacterl association

858
Trafficking protein particle complex subunit 10
EHOC-1, EHOC1, GT334, NEDMISS, TMEM1, TRS130, TRS30
Primary microcephaly, Crohn disease, Dermatologic disorder, Inflammatory bowel disease, Intellectual developmental disorder, Neurodevelopmental disorder, Skin disease, Ulcerative colitis

859
Trafficking protein particle complex subunit 11
C4orf41, FOIGR, GRY, LGMD2S, LGMDR18
Androgenetic alopecia, Limb girdle muscular dystrophy, Glucocorticoid deficiency with achalasia, Intellectual developmental disorder movement cerebellar, Limb-girdle muscular dystrophy, Muscular dystrophy, Myopathy, Obesity, Sarcoidosis, Systemic lupus erythematosus, Triple a syndrome

860
Trafficking protein particle complex subunit 12
CGI-87, PEBAS, TTC-15, TTC15
Cerebral amyloid angiopathy, Dementia, Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome, Obesity