|
451
|
|
|
Teashirt zinc finger homeobox 3 |
TSH3, ZNF537 |
|
|
452
|
|
|
Tribbles pseudokinase 3 |
C20orf97, NIPK, SINK, SKIP3, TRB3 |
|
|
453
|
|
|
Trafficking protein particle complex subunit 1 |
BET5, MUM2 |
|
|
454
|
|
|
Transient receptor potential cation channel subfamily V member 4 |
BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA, SSQTL1, TRP12, VRL2, VROAC |
Abducens palsy, Acquired kyphoscoliosis, Aplasia of muscle, Arthritis, Arthrogryposis multiplex congenita, Arthropathy, Aseptic necrosis, Avascular necrosis of femoral head, Avascular necrosis of the capital femoral epiphysis, Bone disease, Brachydactyly, Brachyolmia, Bulbospinal neuronopathy, Camptodactyly of fingers, Cataract, Charcot-marie-tooth disease, Chondrodystrophic myotonia, Chronic obstructive pulmonary disease, Clinodactyly, Distal spinal muscular atrophy, congenital nonprogressive, Congenital clubfoot, Congenital kyphoscoliosis, Congenital nonprogressive spinal muscular atrophy, Congenital pectus carinatum, Digital arthropathy-brachydactyly, Distal amyotrophy, Distal hereditary motor neuronopathy, Distal muscular atrophy, Distal spinal muscular atrophy, Dwarfism, Dysautonomia, Dyschondroplasias, Dysmorphic features, Elbow flexion contracture, Epiphyseal dysplasia, Facial paralysis, Femur head necrosis, Hearing loss, Hereditary motor and sensory neuropathy, Hip contracture, Hydrocephalus, Hyperopia, Hypersomnia, Legg-calve-perthes disease, Melnick-needles syndrome, Metatropic dwarfism, Metatropic dysplasia, Micromelia, Motor delay, Multiple congenital anomalies, Multiple epiphyseal dysplasia, Muscular atrophy, Myelopathic muscular atrophy, Neuromuscular diseases, Oculomotor nerve palsy, Oculopharyngeal spinal muscular atrophy, Osteoarthritis of hip, Osteoarthritis of the hand, Osteoarthrosis deformans, Osteochondrodysplasia, Derealization, Parastremmatic dwarfism, Partial paralysis vocal cords, Peroneal muscle atrophy, Polyneuropathy, Progressive muscular atrophy, Progressive proximal myelopathic muscular atrophy, Respiratory failure, Roussy-levy syndrome, Scapuloperoneal spinal muscular atrophy, Schwartz-jampel syndrome, Scoliosis, Sensory neuropathy, Short-trunk short stature, Skeletal dysplasia, Sleep apnea, Spinal cord compression, Spinal muscular atrophy, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia, Spondylometaphyseal dysplasia, Strudwick syndrome, Urination disorders, Van buchem disease, Vocal cord paralysisView all (70 more) |
|
455
|
|
|
Tripartite motif containing 27 |
RFP, RNF76 |
|
|
456
|
|
|
Testis specific serine kinase substrate |
PPP1R161, STK22S1, TSKS1, TSSKS |
|
|
457
|
|
|
TRNA methyltransferase 11 |
C6orf75, MDS024, TRM11, TRMT11-1 |
Alopecia, Breast cancer, Mammary neoplasms, Breast carcinoma, Colonic neoplasms, Esophagus neoplasm, Giant cell glioblastoma, Glioblastoma, Liver neoplasms, Liver cancer, Lung carcinoma, Lymphatic metastasis, Marfan syndrome, Ovarian neoplasm, Ovarian cancer |
|
458
|
|
|
Trafficking protein particle complex subunit 11 |
C4orf41, FOIGR, GRY, LGMD2S, LGMDR18 |
Achalasia, Apraxia, Cataract, Cerebral atrophy, Congenital coloboma of iris, Developmental delay, Developmental regression, Dwarfism, Dysarthria, Exophoria, Fatty liver, Glucocorticoid deficiency with achalasia, Hearing loss, Hypopituitarism, Intellectual disability-hyperkinetic movement-truncal ataxia syndrome, Limb-girdle muscular dystrophy, Lupus erythematosus, Mental retardation, Microcephaly, Myopathy, Myopia, Optic atrophy, Palmoplantar keratoderma, Scoliosis, Seizure, Strabismus, Triple a syndrome, Right ventricular dilatationView all (13 more) |
|
459
|
|
|
Tetraspanin 31 |
SAS |
|
|
460
|
|
|
THADA armadillo repeat containing |
ARMC13, GITA, Trm732 |
Alopecia, Alopecia, male pattern, Androgenetic alopecia, Ankylosing spondylitis, Cardiovascular diseases, Cholangitis, Coronary artery disease, Coronary heart disease, Crohn disease, Diabetes mellitus, Inflammatory bowel disease, Nasopharyngeal carcinoma, Polycystic ovary syndrome, Prostate cancer, Psoriasis, Ulcerative colitisView all (1 more) |
