|
351
|
|
|
Tubulin delta 1 |
TUBD |
|
|
352
|
|
|
Translational activator of cytochrome c oxidase I |
CCDC44, MC4DN8 |
Anemia, Cerebellar ataxia, Cytochrome-c oxidase deficiency, Developmental delay, Dysarthria, Encephalopathy, Fanconi syndrome, Hearing loss, High palate, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Leukoencephalopathy, Mitochondrial diseases, Mood swings, Motor delay, Necrotizing encephalomyelopathy, Nervous system diseases, Nystagmus, Optic atrophy, Phosphate diabetes, Ptosis, Renal tubular disorder, Retinitis pigmentosa, Strabismus, Ventricular septal defectView all (14 more) |
|
353
|
|
|
TBC1 domain family member 7 |
MGCPH, PIG51, TBC7 |
|
|
354
|
|
|
Transmembrane protein 216 |
HSPC244, RP98 |
Anencephaly, Arima syndrome, Autism, Brachydactyly, Cataract, Cerebellar vermis agenesis, Ciliopathies, Clinodactyly, Coloboma of optic disc, Asplenia, Congenital cerebral hernia, Congenital coloboma of iris, Congenital epicanthus, Congenital heart defects, Congenital hepatic fibrosis, Congenital meningocele, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Developmental delay, Disorder of eye, Dolichocephaly, Double ureter, Dwarfism, Dysmorphic features, Esotropia, Fibrosis of pancreas, Foot polydactyly, Frontal bossing, Fundus coloboma, Hearing loss, High palate, Hirschsprung disease, Hydrocephalus, Hypothalamic hamartomas, Joubert syndrome, Joubert syndrome with oculorenal defect, Kidney disease, Lobar holoprosencephaly, Macrocephaly, Male pseudohermaphroditism, Malformation of cortical development, Meckel syndrome, Meckel-gruber syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Multiple congenital anomalies, Nephronophthisis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Orofaciodigital syndrome, Pancreatic cyst, Polycystic liver disease, Polydactyly, Polydactyly of toes, Ptosis, Radial polydactyly, Renal agenesis, Renal cyst, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Sclerocornea, Scoliosis, Situs inversus, Sleep apnea, Strabismus, Syndactyly, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (64 more) |
|
355
|
|
|
Toll like receptor 7 |
IMD74, SLEB17, TLR7-like |
|
|
356
|
|
|
Translocase of inner mitochondrial membrane domain containing 1 |
C3orf1, MC1DN31 |
Arthritis, Biliary cirrhosis, Developmental delay, Diabetes mellitus, Epileptic encephalopathy, Hearing loss, Hypertrophic cardiomyopathy, Hypoglycemia, Hypothyroidism, Isolated complex i deficiency, Leukodystrophy, Leukoencephalopathy, Lupus erythematosus, Microcephaly, Mitochondrial complex deficiency, Mitochondrial myopathy, Multiple sclerosis, Nervous system diseases, Nystagmus, Oligoarticular arthritis, Pauciarticular chronic arthritis, Seronegative polyarthritis, Ptosis, Rheumatoid arthritis, Still disease, StrabismusView all (11 more) |
|
357
|
|
|
Toll like receptor 8 |
CD288, IMD98, TLR-8, hTLR8 |
|
|
358
|
|
|
TNF receptor superfamily member 12A |
CD266, FN14, TWEAKR |
|
|
359
|
|
|
TAO kinase 3 |
DPK, JIK, MAP3K18, hKFC-A |
|
|
360
|
|
|
Trafficking protein particle complex subunit 4 |
CGI-104, HSPC172, NEDESBA, PTD009, SBDN, SYNBINDIN, TRS23 |
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