|
561
|
|
|
Telomerase RNA component |
DKCA1, PFBMFT2, SCARNA19, TER, TR, TRC3, hTR |
Alopecia, Anemia, Aplastic anemia, Bronchiectasis, Carcinoma, Cataract, Cerebellar hypoplasia, Cirrhosis, Developmental delay, Diabetes mellitus, Diffuse interstitial pulmonary fibrosis, Dwarfism, Dyskeratosis congenita, Dyskeratosis congenita, x-linked, Esophageal stenosis, Gastroesophageal reflux disease, Honeycomb lung, Hoyeraal-hreidarsson syndrome, Hypodontia, Hypoplasia of the maxilla, Leukemia, Leukoplakia, Liver failure, Lung carcinoma, Lung adenocarcinoma, Lymphoma, Lymphopenia, Malabsorption syndrome, Malignant neoplasm of tongue, Myelodysplasia, Myelodysplastic syndrome, Myeloid leukemia, Nail dystrophy, Neutropenia, Osteoporosis, Palmoplantar keratoderma, Pancreatic neoplasm, Pancytopenia, Periodontitis, Prostatic neoplasms, Prostate cancer, Pulmonary fibrosis, Hamman-rich syndrome, Pulmonary fibrosis and/or bone marrow failure, Scoliosis, Skin carcinoma, Specific learning disorder, Taurodontism, Tongue neoplasmsView all (34 more) |
|
562
|
|
|
Telomeric repeat binding factor 2 |
TRBF2, TRF2 |
|
|
563
|
|
|
Telomerase reverse transcriptase |
CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT |
5p partial monosomy syndrome, Acral lentiginous malignant melanoma, Adrenocortical carcinoma, Alopecia, Anemia, Aplastic anemia, Atypical mole melanoma syndrome, Benign neoplasm, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Bronchiectasis, Carcinoma, Cardiomyopathy, Cataract, Cerebellar hypoplasia, Cerebral cortical atrophy, Uterine cervix neoplasm, Cervical cancer, Cirrhosis, Coronary arteriosclerosis, Coronary artery disease, Developmental delay, Diabetes mellitus, Diffuse interstitial pulmonary fibrosis, Dwarfism, Dyskeratosis congenita, Dyskeratosis congenita, x-linked, Esophageal stenosis, Esophageal stricture, Gastroesophageal reflux disease, Glioblastoma, Glioma, Honeycomb lung, Hoyeraal-hreidarsson syndrome, Hypodontia, Hypoplasia of the maxilla, Hypoplastic anemia, Immunologic deficiency syndromes, Kidney disease, Leukemia, Leukopenia, Leukoplakia, Liver neoplasms, Liver cancer, Liver carcinoma, Liver failure, Lung adenocarcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Lung diseases, Lupus erythematosus, Lymphoid leukemia, Lymphoma, Lymphopenia, Malabsorption syndrome, Malignant neoplasm, Marfan syndrome, Melanoma, Meningioma, Mental depression, Mental retardation, Microcephaly, Myelodysplasia, Myelodysplastic syndrome, Myeloid leukemia, Myeloproliferative disorder, Nail diseases, Nail dysplasia, Nail dystrophy, Neoplasms, Neuroblastoma, Neutropenia, Nevus, Nonbacterial verrucal endocardiosis, Osteoporosis, Ovarian neoplasm, Ovarian cancer, Palmoplantar keratoderma, Palmoplantar keratosis, Pancreatic neoplasm, Pancreatic cancer, Pancytopenia, Periodontitis, Prostatic neoplasms, Prostate cancer, Pulmonary arterial hypertension, Pulmonary fibrosis, Hamman-rich syndrome, Pulmonary fibrosis and/or bone marrow failure, Retinal diseases, Sarcoma of kidney, Scoliosis, Skin carcinoma, Specific learning disorder, Stomach neoplasms, Taurodontism, Thyroid neoplasm, Thyroid carcinoma, Thyroid gland follicular adenomaView all (88 more) |
|
564
|
|
|
Testis associated actin remodelling kinase 1 |
- |
|
|
565
|
|
|
Transferrin |
HEL-S-71p, PRO1557, PRO2086, TFQTL1 |
Alzheimer disease, Anaplastic carcinoma, Anemia, Arthritis, Autism, Carcinoma, Cardiovascular abnormalities, Congenital atransferrinemia, Congestive heart failure, Fatty liver, Hemochromatosis, Hereditary hemochromatosis, Hypochromic anemia, Hypothyroidism, Iron metabolism disorders, Iron overload, Kidney failure, Leukemia, Lung adenocarcinoma, Malignant mesothelioma, Narcolepsy, Nephrotic syndrome, Obesity, Paratuberculosis, Acute kidney insufficiency, Restless legs syndrome, Schizophrenia, Senile dementiaView all (13 more) |
|
566
|
|
|
Transcription factor A, mitochondrial |
MTDPS15, MTTF1, MTTFA, TCF6, TCF6L1, TCF6L2, TCF6L3 |
Alzheimer disease, Atherosclerotic parkinsonism, Blood coagulation disorders, Bowen`s disease, Cardiomyopathic mitochondrial dna depletion syndrome, Cholestasis, Cirrhosis, Conjugated hyperbilirubinemia, Deoxyguanosine kinase deficiency, Hypoalbuminemia, Hypoglycemia, Liver cirrhosis, Liver failure, Neuronal ceroid lipofuscinosis, Parkinson disease, Senile dementiaView all (1 more) |
|
567
|
|
|
Transcription factor AP-2 alpha |
AP-2, AP-2alpha, AP2TF, BOFS, TFAP2 |
Accessory nipple, Aplasia cutis congenita, Branchial anomaly, Branchiooculofacial syndrome, Branchiootorenal syndrome, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Cataract, Cerebellar vermis agenesis, Clinodactyly, Coloboma of optic disc, Congenital coloboma of iris, Congenital epicanthus, Cryptorchidism, Dermoid cyst, Dolichocephaly, Dwarfism, Dysmorphic features, Elbow flexion contracture, Esotropia, Fingernail dysplasia, Gastroesophageal reflux disease, Hamartoma, Hearing loss, Hemangioma, High palate, Hydronephrosis, Hypoplasia of thumb, Hypospadias, Kidney disease, Lens subluxation, Malrotation of colon, Marfan syndrome, Melnick-fraser syndrome, Mental retardation, Microcephaly, Microcornea, Microdontia, Micrognathism, Micropenis, Microphthalmos, Microtia, Multicystic renal dysplasia, Multiple congenital anomalies, Myopia, Nystagmus, Penile hypospadias, Phakomatosis pigmentovascularis, Polydactyly, Postauricular fistula, Posteriorly rotated ear, Ptosis, Renal agenesis, Renal cyst, Retinal coloboma, Speech disorders, Strabismus, Syndactyly, Syndromic microphthalmiaView all (46 more) |
|
568
|
|
|
Transcription factor AP-2 beta |
AP-2B, AP-2beta, AP2-B, PDA2 |
Accessory nipple, Camptodactyly of fingers, Char syndrome, Clinodactyly, Congenital anomaly of the hand, Developmental delay, Diabetes mellitus, Dyssomnia, Mental retardation, Metabolic syndrome, Myopia, Obesity, Parasomnia, Patent ductus arteriosus, Polydactyly, Ptosis, Sleep disorders, Strabismus, Syndactyly of the toes, Urolithiasis, Ventricular septal defectView all (6 more) |
|
569
|
|
|
Transcription factor AP-2 gamma |
AP2-GAMMA, ERF1, TFAP2G, hAP-2g |
|
|
570
|
|
|
Transcription factor CP2 |
LBP1C, LSF, LSF1D, SEF, TFCP2C |
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