188101
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TENT5C divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
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188102
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Terminal nucleotidyltransferase 5D |
CT1.26, CT112, FAM46D |
Curated: Congenital heart disease
Unreviewed: Melanoma, Multiple myeloma, Testicular neoplasm
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188103
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Telomerase associated protein 1 |
TLP1, TP1, TROVE1, VAULT2, p240 |
Curated: Cerebral palsy, Cervical cancer, Lung neoplasms
Unreviewed: Age-related macular degeneration, Alternating hemiplegia of childhood, Behcet Syndrome, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cardiovascular disease, Diabetes Mellitus, Diabetes mellitus, type 2, Esophageal squamous cell carcinoma, Glioblastoma, Glioma, Hamartoma, Hepatoblastoma, Hepatocellular carcinoma, Hydatidiform Mole, Intrahepatic Cholangiocarcinoma, Ischemic stroke, Leber hereditary optic neuropathy, Liver carcinoma, Liver Cirrhosis, Lung Cancer, Lung carcinoma, Lung Neoplasms, Malignant Neoplasm, Mental Depression, Mesothelioma, Neoplasms, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pachyonychia Congenita, Prostate cancer, Prostatic hyperplasia, Prostatic neoplasm, Renal Carcinoma, Rheumatoid arthritis, Schizophrenia, Seborrheic keratosis, Stomach Carcinoma, Stomach Neoplasms, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Urinary bladder neoplasms
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188104
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TEPSIN adaptor related protein complex 4 accessory protein |
C17orf56, ENTHD2 |
Curated: N/A
Unreviewed: Frontotemporal dementia, Psoriasis
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188105
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TEPSIN antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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188106
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Telomere repeat binding bouquet formation protein 1 |
CCDC79, SPGF60 |
Curated: Azoospermia, Male infertility single gene azoospermia, Spermatogenic failure, Testicular azoospermia
Unreviewed: Infertility, Male infertility
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188107
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Telomere repeat binding bouquet formation protein 2 |
C15orf43, SPGF59 |
Curated: Male infertility single gene azoospermia, Spermatogenic failure, Testicular azoospermia
Unreviewed: Azoospermia
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188108
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Telomerase RNA component |
DKCA1, PFBMFT2, SCARNA19, TER, TR, TRC3, hTR |
Curated: Dyskeratosis congenita, autosomal dominant 1, Dyskeratosis congenita, Aplastic anemia, Hoyeraal hreidarsson syndrome, Bone marrow failure, Mds, aml
Unreviewed: 22q13 monosomy syndrome, Adenocarcinoma, Adrenal Gland Pheochromocytoma, Alopecia, alpha Thalassemia, alpha-Thalassemia Mental Retardation Syndrome, X-Linked, Alternating hemiplegia of childhood, Alzheimer disease, Anemia, Aneuploidy, Astrocytoma, Ataxia Telangiectasia, Attention Deficit Hyperactivity Disorder, Autoimmune Polyendocrinopathy, Bladder carcinoma, Bladder Neoplasm, Bone marrow failure syndromes, Borderline personality disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchiectasis, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cardiac arrhythmias, Cardiovascular Diseases, Cataract, Cerebellar Hypoplasia, Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Cholestasis of pregnancy, Choriocarcinoma, Cirrhosis, Colitis, Colon Carcinoma, Colonic Aganglionosis, Colorectal Cancer, Colorectal neoplasm, Congenital Contractural Arachnodactyly, Congenital thrombocytopenia, Connective Tissue Disease, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Coronary Syndrome, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Diffuse interstitial pulmonary fibrosis, Down Syndrome, Dwarfism, Dyskeratosis Congenita, Dyskeratosis Congenita, X-Linked, Dystonia, Eclampsia, Endometrial Cancer, Endometrial carcinoma, Endometrial hyperplasia, Esophageal Carcinoma, Esophageal Stenosis, Esophagus Neoplasm, Extrinsic allergic alveolitis, Exudative retinopathy, Fanconi Anemia, Gastroesophageal Reflux Disease, Genetic predisposition to disease, Glioma, Graft-Vs-Host Disease, Hairy Cell Leukemia, Hamman-Rich syndrome, Head and neck cancer, Head And Neck Carcinoma, Heart failure, Hematologic neoplasm, Hematological Disease, Hemoglobinuria paroxysmal, Hepatocellular carcinoma, Honeycomb lung, Hoyeraal-Hreidarsson Syndrome, Hydatidiform Mole, Hypertension, Hypodontia, Hypoplasia of the maxilla, Idiopathic pulmonary fibrosis, Inherited Bone Marrow Failure Syndrome, Intestinal disease, Intracranial Neoplasm, Ischemic Stroke, Kidney neoplasm, Laryngeal carcinoma, Laryngeal neoplasm, Leber hereditary optic neuropathy, Leukemia, Leukocyte disorders, Leukoplakia, Li-Fraumeni Syndrome, Liposarcoma, Lissencephaly, Liver carcinoma, Liver Cirrhosis, Liver failure, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung Diseases, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Lymphopenia, Malabsorption Syndrome, Malignant Neoplasm, Malignant Neoplasm Of Tongue, Mammary Neoplasms, Melanoma, Meningomyelocele, Mental Depression, Mental retardation, Mouth disease, Multiple myeloma, Multiple Sclerosis, Myelodysplasia, Myelodysplastic Syndrome, Myeloid Leukemia, Nail dystrophy, Nasopharyngeal Carcinoma, Neoplasms, Neural Tube Defect, Neuroendocrine Tumors, Neutropenia, Non-Hodgkin lymphoma, Osteogenesis imperfecta, Osteoporosis, Ovarian neoplasm, Palmoplantar keratoderma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Pancytopenia, Papillary thyroid carcinoma, Paroxysmal Hemoglobinuria, Periodontitis, Pheochromocytoma, Premature aging, Promyelocytic Leukemia, Prostate adenocarcinoma, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Pulmonary Fibrosis, Pulmonary fibrosis and/or bone marrow failure, Pulmonary Hypertension, Renal Carcinoma, Rufous oculocutaneous albinism, Schizophrenia, Scleroderma, Sclerosing Cholangitis, Scoliosis, Skin carcinoma, Sleep Apnea, Specific Learning Disorder, Squamous cell carcinoma, Stomach neoplasms, Stress Disorder, Syndromic microphthalmia, Taurodontism, Thyroid cancer, Thyroid Hormone Resistance, Tongue Neoplasms, Urinary bladder cancer, Urinary bladder neoplasms, Uterine disease, Uterine neoplasm, Ventricular arrhythmia
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188109
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Telomeric repeat binding factor 1 |
PIN2, TRBF1, TRF, TRF1, hTRF1-AS, t-TRF1 |
Curated: Gastresophageal reflux disease, Insomnia, Major depressive disorder, Peptic ulcer disease, Post-traumatic stress disorder
Unreviewed: 22q13 monosomy syndrome, Acute Myeloid Leukemia, Alternating hemiplegia of childhood, Anaplasia, Aplastic anemia, Arthritis, Astrocytoma, Ataxia Telangiectasia, Attention Deficit Hyperactivity Disorder, Autism, Autism Spectrum Disorder, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Cardiovascular Diseases, Chromosomal instability, Cockayne Syndrome, Colorectal Cancer, Colorectal neoplasm, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Duchenne Muscular Dystrophy, Dyskeratosis Congenita, Endometriosis, Esophageal Carcinoma, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Glioblastoma, Glioma, Hepatocellular carcinoma, Hyperglycemia, Idiopathic pulmonary fibrosis, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung Neoplasms, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Macular degeneration, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Metabolic Diseases, Monoclonal Gammapathies, Moyamoya disease, Multiple myeloma, Muscular dystrophy, Myelodysplastic syndrome, Myeloid Leukemia, Neoplasms, Nephroblastoma, Neuroblastoma, Nicolaides Baraitser Syndrome, Nijmegen Breakage Syndrome, Obesity, Osteoarthritis, Osteosarcoma, Pancytopenia, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Renal Carcinoma, Renal cell carcinoma, Rheumatoid arthritis, Sarcoidosis, Skin cancer, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Systemic lupus erythematosus, Systemic sclerosis, T-cell leukemia, T-Cell Lymphoma/Leukemia, Werner syndrome
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188110
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TERF1 pseudogene 1 |
TERF1P |
Curated: N/A
Unreviewed: N/A
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