|
831
|
|
|
TNF receptor superfamily member 18 |
AITR, CD357, ENERGEN, GITR, GITR-D |
|
|
832
|
|
|
TNF receptor superfamily member 11a |
CD265, FEO, LOH18CR1, ODFR, OFE, OPTB7, OSTS, PDB2, RANK, TRANCE-R, TRANCER |
Anemia, Asthma, Congenital pectus carinatum, Cranial nerve paralysis, Developmental delay, Dwarfism, Dysosteosclerosis, Eczema, Expansile osteolysis, Hearing loss, Hydrocephalus, Hyperphosphatasemia with bone disease, Hypertension, Hyperuricemia, Hypocalcemic seizures, Lymphocytic leukemia, Macrocephaly, Melanocytic nevus, Motor delay, Myasthenia gravis, Nystagmus, Optic atrophy, Osteopetrosis, Osteopetrosis-hypogammaglobulinemia syndrome, Osteoporosis, Osteosarcoma, Paget disease, Brain stem compression, Proptosis, VitiligoView all (15 more) |
|
833
|
|
|
TNF receptor superfamily member 10c |
CD263, DCR1, DCR1-TNFR, LIT, TRAIL-R3, TRAILR3, TRID |
|
|
834
|
|
|
TNF receptor superfamily member 10b |
CD262, DR5, KILLER, KILLER/DR5, TRAIL-R2, TRAILR2, TRICK2, TRICK2A, TRICK2B, TRICKB, ZTNFR9 |
Carcinoma, Carcinoma of the head and neck, Carcinoma of the nasal cavity and paranasal sinuses, Carcinoma of the oral cavity, Hypopharyngeal carcinoma, Laryngeal carcinoma, Lip carcinoma, Oropharyngeal carcinoma, Pancreatic neoplasm, Pancreatic cancer, Salivary gland carcinoma, Carcinoma of lip, Oral cavity carcinoma |
|
835
|
|
|
TNF receptor superfamily member 10a |
APO2, CD261, DR4, TRAILR-1, TRAILR1 |
Adenocarcinoma, Alopecia, Alopecia, male pattern, Androgenetic alopecia, Anemia, Anorexia, Benign neoplasm, Carcinoma, Colonic neoplasms, Esophagus neoplasm, Age-related macular degeneration, Malignant neoplasm, Neoplasms, Nervous system diseases, Neutropenia, Prostatic neoplasms, Prostate cancer, PseudopeladeView all (3 more) |
|
836
|
|
|
Tripartite motif containing 24 |
PTC6, RNF82, TF1A, TIF1, TIF1A, TIF1ALPHA, hTIF1 |
|
|
837
|
|
|
TSC22 domain family member 1 |
HUCEP-2, Ptg-2, TGFB1I4, TSC22 |
|
|
838
|
|
|
Tax1 binding protein 1 |
CALCOCO3, T6BP, TXBP151 |
|
|
839
|
|
|
Timeless circadian regulator |
FASPS4, TIM, TIM1, hTIM |
|
|
840
|
|
|
- |
- |
Addison`s disease, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Dementia, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired cognition, Intestinal obstruction, Left ventricular hypertrophy, Malabsorption syndrome, Malformation of cortical development, Melas syndrome, Mental depression, Merrf syndrome, Microcephaly, Migraine, Mitochondrial encephalopathy, Mitochondrial myopathy, Movement disorders, Multiple lipomata, Myoclonic seizures, Myopathy, Nephritis, Nephrotic syndrome, Nyctalopia, Optic atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Seizure, Sensorineural hearing loss, Thyroiditis, Wolff-parkinson-white syndromeView all (47 more) |
