|
721
|
|
|
Transmembrane immune signaling adaptor TYROBP |
DAP12, KARAP, PLOSL, PLOSL1 |
Caudate atrophy, Cerebellar atrophy, Cerebral cortical atrophy, Dementia, Desbuquois syndrome, Liver cirrhosis, Liver disease, Memory disorders, Nasu-hakola disease, Parkinson disease, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy |
|
722
|
|
|
Tyrosinase related protein 1 |
CAS2, CATB, GP75, OCA3, TRP, TRP1, TYRP, b-PROTEIN |
|
|
723
|
|
|
Transient receptor potential cation channel subfamily V member 1 |
VR1 |
Atherosclerosis, Endometrial neoplasm, Temporal lobe epilepsy, Esophageal disease, Esotropia, Hyperalgesia, Liver cirrhosis, Migraine, Obesity, Pancreatitis, Urinary bladder cancer |
|
724
|
|
|
Transmembrane protein 258 |
C11orf10, Kud, Kuduk |
Ankylosing spondylitis, Aortic stenosis, Asthma, Eczema, Benign neoplasm, Bipolar disorder, Colorectal adenoma, Colorectal cancer, Coronary artery disease, Crohn disease, Lipoprotein lipase deficiency, Inflammatory bowel disease, Major depressive disorder, Metabolic syndrome, Nasal polyp, Peptic ulcer disease, Psoriasis, Respiratory system disease, Rheumatoid arthritis, Sclerosing cholangitis, Seborrheic dermatitis, Diabetes mellitus, type 2, Ulcerative colitis, Venous thromboembolismView all (9 more) |
|
725
|
|
|
Tripartite motif containing 25 |
EFP, RNF147, Z147, ZNF147 |
|
|
726
|
|
|
Tripartite motif containing 26 |
AFP, RNF95, ZNF173 |
Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Obstructive pulmonary disease, Hypothyroidism, Lung cancer, Major depressive disorder, Psoriatic arthritis, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Squamous cell carcinoma, Ulcerative colitis, Upper aerodigestive tract neoplasm |
|
727
|
|
|
Trans-golgi network vesicle protein 23 homolog A |
FAM18A, YDR084C |
|
|
728
|
|
|
Tubulin alpha 1a |
B-ALPHA-1, LIS3, TUBA3 |
Basal cell carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cerebral palsy, Congenital neurologic anomalies , Cryptorchidism, Dandy-walker syndrome, Myoclonic encephalopathy, Fetal akinesia deformation sequence, Global developmental delay, Lissencephaly, Macrogyria, Cortical development malformation, Microcephaly, Movement disorder, Myocardial ischemia, Neurodevelopmental disorders, Pena-shokeir syndrome type i, Perisylvian syndrome, Tubulinopathy, West syndromeView all (5 more) |
|
729
|
|
|
TRNA splicing endonuclease subunit 34 |
LENG5, PCH2C, SEN34, SEN34L |
|
|
730
|
|
|
Transient receptor potential cation channel subfamily M member 8 |
LTRPC6, LTrpC-6, TRPP8, trp-p8 |
|
