|
721
|
|
|
Transmembrane immune signaling adaptor TYROBP |
DAP12, KARAP, PLOSL, PLOSL1 |
Agnosia, Apraxia, Cerebral atrophy, Cerebral cortical atrophy, Dementia, Dementia of frontal lobe, Developmental regression, Hydrocephalus, Hypoplasia of corpus callosum, Leukemia, Leukoencephalopathy, Nasu-hakola disease, Oculomotor apraxia, Oculovestibuloauditory syndrome, Osteochondrodysplasia, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, Skeletal dysplasia, Speech disordersView all (3 more) |
|
722
|
|
|
Tyrosinase related protein 1 |
CAS2, CATB, GP75, OCA3, TRP, TRP1, TYRP, b-PROTEIN |
Adenocarcinoma, Albinism, Carcinoma, Disorder of eye, Lung neoplasms, Lung cancer, Melanoma, Nystagmus, Ocular albinism, Oculocutaneous albinism, Piebaldism, Strabismus |
|
723
|
|
|
Transient receptor potential cation channel subfamily V member 1 |
VR1 |
Atherosclerosis, Benign neoplasm, Urinary bladder cancer, Bladder neoplasm, Epilepsy, Esophageal diseases, Eosinophilia, Malignant neoplasm, Neoplasms, Obesity, Pancreatitis |
|
724
|
|
|
Transmembrane protein 258 |
C11orf10, Kud, Kuduk |
Ankylosing spondylitis, Asthma, Atrial septal defect, Cardiac-urogenital syndrome, Cholangitis, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Pulmonary hypoplasia, Congenital total pulmonary venous return anomaly, Crohn disease, Cryptorchidism, Dextrocardia, Encephalitis/encephalopathy with reversible myelin vacuolization, High palate, Hypoplastic left heart syndrome, Kidney disease, Kidney failure, Lung cancer, Metabolic syndrome, Muscular ventricular septal defect, Nasal polyposis, Patent ductus arteriosus, Penile hypospadias, Polycythemia, Psoriasis, Respiratory tract diseases, Scimitar syndrome, Ulcerative colitisView all (15 more) |
|
725
|
|
|
Tripartite motif containing 25 |
EFP, RNF147, Z147, ZNF147 |
|
|
726
|
|
|
Tripartite motif containing 26 |
AFP, RNF95, ZNF173 |
|
|
727
|
|
|
Trans-golgi network vesicle protein 23 homolog A |
FAM18A, YDR084C |
|
|
728
|
|
|
Tubulin alpha 1a |
B-ALPHA-1, LIS3, TUBA3 |
Agenesis of corpus callosum, Agyria, Limb-girdle muscular dystrophy, Cerebellar agenesis, Cryptorchidism, Developmental delay, Dysmorphic features, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Mental retardation, Lissencephaly, Malformation of cortical development, Microcephaly, Motor delay, Movement disorders, Multiple congenital anomalies, Myocardial ischemia, Neuronal heterotopia, Pachygyria, Polymicrogyria, Spastic quadriplegia, Tubulinopathy-associated dysgyria, UranostaphyloschisisView all (8 more) |
|
729
|
|
|
TRNA splicing endonuclease subunit 34 |
LENG5, PCH2C, SEN34, SEN34L |
Congenital microcephaly, Dysphagia, Esophageal dysphagia, Hemeralopia, Mental retardation, Microcephaly, Microlissencephaly, Movement disorders, Oropharyngeal dysphagia, Pontoneocerebellar hypoplasia, Status marmoratus, Vision disability |
|
730
|
|
|
Transient receptor potential cation channel subfamily M member 8 |
LTRPC6, LTrpC-6, TRPP8, trp-p8 |
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