|
81
|
|
|
DNA topoisomerase II binding protein 1 |
Dpb11, TOP2BP1 |
|
|
82
|
|
|
Tripartite motif containing 31 |
C6orf13, HCG1, HCGI, RNF |
Ankylosing spondylitis, Autoimmune thyroiditis, Breast carcinoma, Dermatitis, Development disorder, Diabetes, Diabetes mellitus, Liver carcinoma, Lung adenocarcinoma, Lung cancer, Lupus erythematosus, Mental depression, Myasthenia gravis, Oral ulcer, Prostate cancer, Rheumatoid arthritis, Schizophrenia, VitiligoView all (3 more) |
|
83
|
|
|
Tubulin polymerization promoting protein |
TPPP/p25, TPPP1, p24, p25, p25alpha |
|
|
84
|
|
|
TRIO and F-actin binding protein |
DFNB28, HRIHFB2122, TAP68, TARA, dJ37E16.4 |
|
|
85
|
|
|
TBC1 domain family member 8 |
AD3, GRAMD8, HBLP1, TBC1D8A, VRP |
|
|
86
|
|
|
Trehalase |
TRE, TREA, TREHD |
|
|
87
|
|
|
TP53 target 1 |
LINC00096, NCRNA00096, P53TG1, P53TG1-D, TP53AP1, TP53LC12 |
|
|
88
|
|
|
Tubulin alpha 3e |
- |
|
|
89
|
|
|
Three prime repair exonuclease 1 |
AGS1, CRV, DRN3, HERNS, RVCLS |
Acquired porencephaly, Aicardi goutieres syndrome, Anemia, Aortic aneurysm, Apraxia, Arrhinencephaly, Arthritis, Autoinflammatory disease, Brain atrophy, Cerebellar hypoplasia, Cerebral atrophy, Cerebroretinal vasculopathy, Chilblain lupus erythematosus, Chilblain lesions, Cutis marmorata, Degeneration of the striatum, Dementia, Demyelinating neuropathy, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Enchondroma, Epileptic encephalopathy, Glaucoma, Glaucoma, congenital, Hemiplegia/hemiparesis, Hypertrophic cardiomyopathy, Hypoplasia of corpus callosum, Hypothyroidism, Kidney disease, Lymphocytic leukemia, Leukodystrophy, Leukoencephalopathy, Leukopenia, Lipoatrophy, Lipodystrophy, Lupus erythematosus, Macular edema, Mental retardation, Microcephaly, Micronodular cirrhosis, Migraine, Myositis, Alloimmune thrombocytopenia, Nephritis, Nonbacterial verrucal endocardiosis, Nystagmus, Panniculitis, Penis agenesis, Pericarditis, Plagiocephaly, Pleuritis, Gastric polyposis, Porencephalic cyst, Pseudo-torch syndrome, Psychosis, Ptosis, Raynaud phenomenon, Renal glomerular disease, Retinal diseases, Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Scoliosis, Spastic quadriplegia, Strabismus, Stroke, Systemic lupus erythematosus, Vasculitis, Vasculopathy, retinal, with cerebral leukodystrophyView all (55 more) |
|
90
|
|
|
TP53 regulating kinase |
BUD32, C20orf64, GAMOS4, Nori-2, Nori-2p, PRPK, TPRKB, dJ101A2 |
Aqueductal stenosis, Cerebellar hypoplasia, Cerebral atrophy, Developmental delay, Dwarfism, Galloway-mowat syndrome, Glomerulonephritis, Glomerulosclerosis, Hemiplegia/hemiparesis, Hiatal hernia, Impaired cognition, Kidney disease, Macrotia, Mesangial sclerosis, Microcephaly, Micrognathism, Nephrotic syndrome, Pachygyria, PolymicrogyriaView all (4 more) |
