Brenner Tumor
Brenner Tumor
About the Disease
Ovarian Brenner Tumor, also known as benign ovarian brenner tumor, is related to cystic teratoma and struma ovarii. An important gene associated with Ovarian Brenner Tumor is UPK3A (Uroplakin 3A), and among its related pathways/superpathways are Keratinization and Cytoskeletal Signaling. The drugs Paclitaxel and Bevacizumab have been mentioned in the context of this disorder. Affiliated tissues include ovary, breast and endothelial, and related phenotype is renal/urinary system.
Common Targets
G4609 | G595
Note: If you'd like to get a target analysis report for Brenner Tumor, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Brenner Tumor at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Encephalitis, Tick-borne | CREST Syndrome | Cholangiocarcinoma | Asplenia | Hypermetropia | Silicosis | Left Ventricular Noncompaction | Achondrogenesis | Adrenoleukodystrophy, X-linked | Lichen Planus | Carcinoma, Small Cell | Globozoospermia | MELAS Syndrome | Glutaric Aciduria Type 2 | Hemangioblastoma | Spinocerebellar Ataxia Type 40 | Takayasu's Arteritis | Oligodendroglioma | Otitis Externa | Compartment Syndrome | Tietze Syndrome | Sweet Syndrome | Cutaneous T-cell Lymphoma | Senior-Loken Syndrome | Ophthalmoplegia | Precocious Puberty | Optic Nerve Hypoplasia, Bilateral | Hepatopulmonary Syndrome | Arthritis | Generalized Epilepsy With Febrile Seizures Plus | Influenza | Harlequin Ichthyosis | Teratozoospermia | Congestive Heart Failure | Treacher Collins Syndrome | Amelogenesis Imperfecta | Incontinentia Pigmenti | Primary Biliary Cholangitis | Richter's Syndrome | Bronchiectasis | Brachydactyly | Extramammary Paget's Disease | Glycogen Storage Disease Type 4 | Charcot-Marie-Tooth Disease Type 4 | Skin Carcinoma | Myelodysplasia | Pathological Gambling | Hypertension, Renovascular | Peters-plus Syndrome | Empyema | Congenital Lipoid Adrenal Hyperplasia | Autosomal Recessive Spastic Paraplegia Type 35 | Anal Fissure | Thanatophoric Dysplasia | Membranous Nephropathy | Hemosiderosis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hypokalemic Periodic Paralysis | Echinococcosis | Pure Autonomic Failure | Open-angle Glaucoma | Osteogenesis Imperfecta | Potocki-Shaffer Syndrome | Congenital Bile Acid Synthesis Defect | Purpura, Thrombotic Thrombocytopenic | Werner's Syndrome | Kearns-Sayre Syndrome | Porokeratosis | Cerebrotendinous Xanthomatosis | Delayed Sleep Phase Syndrome | Pituitary Disorders | Sezary Syndrome | Disseminated Intravascular Coagulation | Patent Foramen Ovale | Bartter Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Acne Vulgaris | Peeling Skin Syndrome, Acral Type | Carcinoma, Merkel Cell | Sotos Syndrome | Nasodigitoacoustic Syndrome | Alpers Syndrome | Systemic Lupus Erythematosus | Dysferlinopathy | ICF Syndrome | Aceruloplasminemia | Familial Advanced Sleep Phase Syndrome | Myasthenia Gravis | Retinoblastoma | Warsaw Breakage Syndrome | Blepharophimosis Syndrome | Goiter, Nodular | Majeed Syndrome | Genee-Wiedemann Syndrome | Pycnodysostosis | Thyroiditis | Schizoaffective Disorder | Spinocerebellar Ataxia Type 17 | Osteogenesis Imperfecta Type I | Renal Medullary Carcinoma | Hepatitis, Chronic | Subcortical Band Heterotopia | Placenta Previa | Cardiomyopathy, Restrictive | Hypophosphatasia | Pheochromocytoma | Malignant Peripheral Nerve Sheath Tumor | Proopiomelanocortin Deficiency | Coloboma | Alpha-mannosidosis | Erdheim-Chester Disease | Chronic Thromboembolic Pulmonary Hypertension | Alpha-thalassemia Myelodysplasia Syndrome | Odonto-onycho-dermal Dysplasia | Vitamin K Deficiency | Scoliosis | Acute Leukemia | Transthyretin-related Amyloidosis | Nemaline Myopathy 10 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Schwartz-Jampel-Aberfeld Syndrome | Bernard-Soulier Syndrome | Corneal Ulcer | Chronic Lymphocytic Leukemia | Ventricular Septal Defect | Myopathy | VACTERL Association | Intermittent Explosive Disorder | Low Phospholipid Associated Cholelithiasis | IgA Deficiency | Pituitary Dwarfism | Periodic Limb Movement Disorder | Rotor Syndrome | Pseudoexfoliation Syndrome | Beare-Stevenson Syndrome | DICER1 Syndrome | HIBCH Deficiency | Lysosomal Acid Lipase Deficiency | Anthrax | Lipoma | Hyperparathyroidism, Primary | Prolymphocytic Leukemia | Colon Adenoma | Trigonocephaly | Danon Disease | Nephronophthisis | Acrodermatitis Enteropathica | Lymphangioleiomyomatosis | Varices | Achromatopsia | Kabuki Syndrome 2 | Chronic Myelomonocytic Leukemia | Blepharoconjunctivitis | Diabetic Macular Edema | Ichthyosis Bullosa Of Siemens | Pseudohypoaldosteronism | X-linked Sideroblastic Anemia | Myopia | Glucagonoma | Sengers Syndrome | Bullous Pemphigoid | Ocular Albinism Type 1 | Anxiety Disorders | Mitochondrial DNA Depletion Syndrome 13 | Kernicterus | Mohr-Tranebjaerg Syndrome | Congenital Primary Aphakia | Dyslipidemia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Sitosterolemia | Craniosynostosis | Restless Legs Syndrome | Vascular Cognitive Impairment | Loeys-Dietz Syndrome | Stargardt Disease | Lissencephaly 2 | Thrombophilia | Early Infantile Epileptic Encephalopathy 28 | Plasma Cell Dyscrasia | Charcot-Marie-Tooth Disease, Type 2C | Chondrodysplasia Punctata 2, X-linked Dominant | Epidermolytic Hyperkeratosis | Tangier Disease | KBG Syndrome | Acute Generalized Exanthematous Pustulosis | Obesity | Angiomyolipoma | Hyperbilirubinemia | Osteosarcoma | Toxic Epidermal Necrolysis | Diabetes Insipidus, Nephrogenic | Pregnancy, Ectopic | Congenital Mirror Movements | Hereditary Mixed Polyposis Syndrome | Recurrent Respiratory Papillomatosis | Migraine | Restrictive Dermopathy | Facioscapulohumeral Muscular Dystrophy Type 1 | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Aphasia | X-linked Acrogigantism | Acute Motor Axonal Neuropathy | Crimean-Congo Hemorrhagic Fever | Angelman Syndrome | Autism | Lymphedema | McLeod Syndrome | Leber Congenital Amaurosis | Schizotypal Personality Disorder | Ameloblastic Carcinoma | Microcephaly, Seizures, And Developmental Delay | Acne | Cellulitis | Focal Facial Dermal Dysplasia | Kohlschutter-Tonz Syndrome | Hepatic Veno-occlusive Disease | Familial Pheochromocytoma-paraganglioma | Cystitis, Interstitial | Shock, Cardiogenic | Takotsubo Cardiomyopathy | Depression | Osteopathia Striata With Cranial Sclerosis | Wiedemann-Steiner Syndrome | Pure Red Cell Aplasia | Niemann-Pick Disease, Type A | Pompe Disease | Ocular Hypertension | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Microcephaly | Ectodermal Dysplasia | Colitis, Lymphocytic | Wagner Disease | Acute Tubular Necrosis | Presbyopia | Lymphopenia | Beta-Propeller Protein-associated Neurodegeneration | Hidradenitis Suppurativa | Hereditary Hemorrhagic Telangiectasia Type 2 | Spondyloepiphyseal Dysplasia Tarda, X-linked | Spitzoid Melanoma | Spina Bifida | Thrombophlebitis | Melanoma, Malignant | Gerodermia Osteodysplastica | Okihiro Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Craniometaphyseal Dysplasia | Retinal Dystrophy | Wolfram Syndrome | Mitochondrial Cytopathy | Uremia | Polyomavirus Nephropathy | Pain | Citrullinemia | Agranulocytosis | Lung Diseases | Eczema | Hepatic Steatosis | Rubeosis Iridis | Zimmermann-Laband Syndrome | Cardiofaciocutaneous Syndrome | Common Variable Immunodeficiency | Epiphyseal Chondrodysplasia, Miura Type | Pericarditis | Ellis-Van Creveld Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Rothmund-Thomson Syndrome | Endophthalmitis | Cornelia De Lange Syndrome | Acrodermatitis | Acral Lentiginous Melanoma | Persistent Mullerian Duct Syndrome | Acrocallosal Syndrome | Conduct Disorder | Sponastrime Dysplasia | Macrophage Activation Syndrome | Nail Disorder, Nonsyndromic Congenital | Myoclonus | Gastritis, Atrophic | Keratopathy | GM2-gangliosidosis AB Variant | Proctitis | Bardet-Biedl Syndrome | Van Der Knaap Disease | Pierson Syndrome | Canavan Disease | Retinopathy, Diabetic | Thrombasthenia | Bethlem Myopathy | Nijmegen Breakage Syndrome | Multiple Myeloma | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Hypoparathyroidism | Keratoconus | Feingold Syndrome | Inflammatory Myofibroblastic Tumor | Alzheimer Disease, Late Onset | Congenital Tufting Enteropathy | Hemimegalencephaly | Diabetes | Pemphigus Foliaceus | Klinefelter Syndrome | Jawad Syndrome | Multiple Sulfatase Deficiency | Dubin-Johnson Syndrome | Strabismus | Autosomal Recessive Bestrophinopathy | Congenital Central Hypoventilation Syndrome | Thyrotoxic Periodic Paralysis | Fetal And Neonatal Alloimmune Thrombocytopenia | LRBA Deficiency | Anencephaly | Lymphangiomatosis | Erythropoietic Protoporphyria | Vogt-Koyanagi-Harada Syndrome | Thyroid Hormone Resistance | Pulmonary Sclerosing Hemangioma | Eating Disorder | Pulmonary Alveolar Microlithiasis | Uremic Pruritus | Choroiditis | Nemaline Myopathy | Intestinal Obstruction | Agoraphobia | Vitiligo | Periodontitis | Analgesia | Panuveitis | Neurodegeneration With Brain Iron Accumulation | Paraplegia | Renal-hepatic-pancreatic Dysplasia | Osteitis | Behcet's Disease | Renal Tubular Acidosis | Renal Hypouricemia | Acute Chest Syndrome | Sclerocornea | Enterocolitis, Necrotizing | Von Hippel-Lindau Disease | Fibrosis | Spondylo-ocular Syndrome | Arteriovenous Malformations | Leukoplakia, Oral | Generalized Epilepsy And Paroxysmal Dyskinesia | Cramp Fasciculation Syndrome | Familial Glucocorticoid Deficiency | Stroke, Ischemic | Cat Eye Syndrome | Spinocerebellar Ataxia Type 13 | Heavy Chain Disease | Melanocytic Nevus | Early Infantile Epileptic Encephalopathy | Renal Dysplasia | LEOPARD Syndrome | Hypotrichosis | Iron Deficiency Anemia | Polymyalgia Rheumatica | Brugada Syndrome 1 | Ophthalmia, Sympathetic | Rubinstein-Taybi Syndrome | Osteogenesis Imperfecta Type IV | Inflammatory Bowel Disease | Proteasome-associated Autoinflammatory Syndrome 2 | Dementia | Mucolipidosis Type IV | Constipation | Lymphoma | Cirrhosis | Keratoacanthoma | Benign Hereditary Chorea | Hypersensitivity Pneumonitis | Gingivitis | Spondylolisthesis | Wilson's Disease | Lactose Intolerance | Platelet Disorders | Barakat Syndrome | Jalili Syndrome | Arthrogryposis | Dystonia | Prurigo Nodularis | Follicular Dendritic Cell Sarcoma | Fanconi Syndrome | Spinocerebellar Ataxia Type 20 | Congenital Sodium Diarrhea | Zellweger Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Hermansky-Pudlak Syndrome | Syncope | Spinal Muscular Atrophy Type 2 | Leri-Weill Dyschondrosteosis | Leukocyte Adhesion Deficiency | Chronic Leukemia | Glomerulonephritis, Membranoproliferative | Pneumococcal Meningitis | Spinocerebellar Ataxia Type 38 | Early Infantile Epileptic Encephalopathy 4 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Epidermal Nevus Syndrome | Neuroendocrine Cancer