Prolactinoma

About the Disease
Prolactinoma, also known as prolactin-producing pituitary gland adenoma, is related to prolactin producing pituitary tumor and pituitary adenoma 1, multiple types. An important gene associated with Prolactinoma is MEN1 (Menin 1), and among its related pathways/superpathways are Nanog in Mammalian ESC Pluripotency and Signal Transduction. The drugs Cabergoline and Dopamine have been mentioned in the context of this disorder. Affiliated tissues include pituitary, breast and bone marrow, and related phenotypes are impotence and galactorrhea

Common Targets
GNAI2 | OR5AN1 | PDHX | MRC2 | YARS1 | HSPA4L | G1026 | DYSF | G1029 | CARM1 | PAQR5 | DRD2 | KIF2B | ADRM1 | NUP54 | SREBF2 | RIPK4 | STIP1 | FAM177B | MPDZ | G6PC2 | MYO9A | ZYX | ZNF407 | MITF | ANKK1 | SF3B1 | PITHD1 | GMNC | ZNF804B | MCM3AP | G999 | TRIM35 | CCDC65 | YTHDC1 | PCNX2 | SH2D3C | ACAP3 | NOTCH2NLA | DNAH6 | MECOM | PZP | MEN1 | FAM162A | TRARG1 | UBR2 | UNC13C | RNF20 | ORAI2 | ACP3 | MTMR12 | PDPR | RBL1 | SACS | PDE4C | LRRC4 | CENPN | INCENP | CDKN1B | GJA1 | RYR3 | MDN1 | ZDBF2 | AGTR1 | ADAMTS4 | HYDIN | LOXL4 | PRLR | DMXL2 | SPAG9 | ECE1 | VCX | CFAP73 | DHX33 | WDFY3 | ALPK2 | SATB2 | HPSE2 | SND1 | AIP | ACTL6B | ETFB | PHLPP1 | GALNT9 | PRRC2C | DOP1A | ZNF695 | THBD | ZNF687 | R3HDM4 | CHI3L2 | EXOC8 | GRB2 | DHRS7C | MPC2 | TERF2

Note: If you'd like to get a target analysis report for Prolactinoma, 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 Prolactinoma at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

X-linked Charcot-Marie-Tooth Disease | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Stickler Syndrome | Familial Dysautonomia | Protein S Deficiency | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Myoclonic Epilepsy With Ragged Red Fibers | Acrodysostosis | Hepatic Veno-occlusive Disease | Porencephaly | Personality Disorders | Centronuclear Myopathy | Osteoporosis, Postmenopausal | Postpoliomyelitis Syndrome | Leukocyte Adhesion Deficiency | Osteopathia Striata With Cranial Sclerosis | Idiopathic Multicentric Castleman Disease | Glycogen Storage Disease Type 1b | Niemann-Pick Disease | PHARC Syndrome | Congenital Torticollis | B-cell Prolymphocytic Leukemia | Babesiosis | Sclerosteosis 2 | Acute Lymphocytic Leukemia | Blepharitis | Hennekam Lymphangiectasia-lymphedema Syndrome | Acne Vulgaris | Discoid Lupus Erythematosus | Hypotension, Orthostatic | Retinopathy, Diabetic | Weill-Marchesani Syndrome | Wieacker-Wolff Syndrome | Congenital Mirror Movements | Lissencephaly 2 | Von Willebrand Disease | Sensorineural Hearing Loss | Tumoral Calcinosis | LRBA Deficiency | Gestational Trophoblastic Disease | Hepatorenal Syndrome | Delirium | Spinocerebellar Ataxia Type 16 | Sick Sinus Syndrome | Facioscapulohumeral Muscular Dystrophy | Perivascular Epithelioid Cell Tumor | Dyslexia | Rosacea | Dyggve-Melchior-Clausen Disease | Pontocerebellar Hypoplasia Type 7 | Myelofibrosis | DiGeorge Syndrome | Myelitis | Cardiospondylocarpofacial Syndrome | Glycogen Storage Disease | Congenital Tufting Enteropathy | Wilson's Disease | Primary Biliary Cholangitis | Dysthymia | Gardner Syndrome | Sepiapterin Reductase Deficiency | Nephrotic Syndrome Type 1 | Hyperparathyroidism, Primary | Neurodegeneration With Brain Iron Accumulation | Spondyloperipheral Dysplasia | Lichen Sclerosus | Osteogenesis Imperfecta Type IV | Cholangitis | Chronic Lymphocytic Leukemia | Osteogenesis Imperfecta Type V | Thalassemia | Schindler Disease | Vitelliform Macular Dystrophy | Rheumatic Heart Disease | Hyperphenylalaninemia | Carcinoid Syndrome | Oligoastrocytoma | Holoprosencephaly | Dowling-Degos Disease | Glucagonoma | Kidney Stones | Atelosteogenesis Type 1 | Interstitial Lung Diseases | Ebstein Anomaly | Situs Inversus | Porokeratosis | Colon Adenoma | Nanophthalmos | Pyruvate Decarboxylase Deficiency | Myhre Syndrome | Renal Tubular Dysgenesis | Danon Disease | Plasma Cell Dyscrasia | Evans Syndrome | Adenylosuccinate Lyase Deficiency | Primary Aldosteronism | Learning Disability | Cheilitis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Deafness, Dystonia, And Cerebral Hypomyelination | Corneal Dystrophy | Diffuse Intrinsic Pontine Glioma | Glycogen Storage Disease Type 0, Muscle | Adrenal Insufficiency | Non-Hodgkin Lymphoma | Optic Neuritis | Narcolepsy | Coma | Progressive Encephalopathy-optic Atrophy Syndrome | Chitayat Syndrome | Nijmegen Breakage Syndrome | Macrophage Activation Syndrome | Norrie Disease | Ectopia Lentis, Isolated, Autosomal Recessive | Hemorrhagic Disorders | Infectious Diarrhea | Syphilis | Vaginitis | Silver-Russell Syndrome | Blepharophimosis Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Osteoglophonic Dysplasia | Pulmonary Stenosis | Hypereosinophilic Syndrome | Synpolydactyly | Low Tension Glaucoma | Charcot-Marie-Tooth Disease, Type 6 | Rhizomelic Chondrodysplasia Punctata | Platelet Disorders | Bacterial Meningitis | Congenital Central Hypoventilation Syndrome | Arthritis, Reactive | Chronic Mucocutaneous Candidiasis | Keratosis | Crouzon Syndrome With Acanthosis Nigricans | Paraganglioma | Amebiasis | Asperger Syndrome | Urofacial Syndrome | Biotinidase Deficiency | Headache | Congenital Stromal Corneal Dystrophy | Malonyl-CoA Decarboxylase Deficiency | Varices | Metatropic Dysplasia | Atopy | Hypospadias | Otopalatodigital Syndrome Type 2 | Alopecia Totalis | VEXAS Syndrome | Birk-Barel Syndrome | Familial Digital Arthropathy-brachydactyly | Pyruvate Kinase Deficiency | Atelosteogenesis Type 2 | Lymphoma, Follicular | Sialidosis Type I | Myotonia | Pemphigoid | Early Infantile Epileptic Encephalopathy 4 | Hypoparathyroidism | Chediak-Higashi Syndrome | Intermittent Claudication | Asplenia | Dystonia-parkinsonism, X-linked | Renal Oncocytoma | Acromesomelic Dysplasia | Pycnodysostosis | Metabolic Diseases | Antisocial Personality Disorder | Congenital Sodium Diarrhea | Combined Malonic And Methylmalonic Acidemia | Temtamy Preaxial Brachydactyly Syndrome | Cornelia De Lange Syndrome | Tendinopathy | Epidermolysis Bullosa Simplex, Generalized | GLUT1 Deficiency Syndrome | Niemann-Pick Disease, Type A | Currarino Syndrome | Williams Syndrome | Transthyretin-related Amyloidosis | Aplasia Cutis Congenita | Thrombophilia | Neurofibromatosis | Parapsoriasis | Hemophagocytic Lymphohistiocytosis | Bladder Exstrophy | Fahr Disease | Li-Fraumeni Syndrome | Roberts Syndrome | Hereditary Elliptocytosis | Spina Bifida | Papulopustular Rosacea | Van Der Knaap Disease | Osteomalacia | Adrenomyeloneuropathy | Ischemia | Osteogenesis Imperfecta | Stuttering | Primary Hyperoxaluria | Metabolic Syndrome | Thyrotoxic Periodic Paralysis | Mitochondrial Encephalomyopathy | Budd-Chiari Syndrome | Duchenne Muscular Dystrophy | Spinal Cord Diseases | Neuroleptic Malignant Syndrome | Epidermodysplasia Verruciformis | Frank-ter Haar Syndrome | Robinow Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Ollier Disease | Distal Myopathy | Postpartum Depression | Bicuspid Aortic Valve | Pendred Syndrome | Histoplasmosis | Clouston Hidrotic Ectodermal Dysplasia | Encephalitis | Syncope | Alzheimer Disease, Late Onset | Uveitis | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Stuve-Wiedemann Syndrome | Acne | Brooke-Spiegler Syndrome | Tietze Syndrome | Epidermolysis Bullosa | Aspartylglycosaminuria | Aceruloplasminemia | Gerodermia Osteodysplastica | Preaxial Polydactyly | Heart Failure | Hereditary Hemorrhagic Telangiectasia | Chromosome 5q Deletion Syndrome | Ventricular Septal Defect | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Demyelinating Diseases | Emery-Dreifuss Muscular Dystrophy | Fuchs Dystrophy | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Pulmonary Capillary Hemangiomatosis | Thrombocythemia, Essential | Asthma | Pyelonephritis | Hepatitis, Chronic | Wiedemann-Steiner Syndrome | Optic Neuropathy, Anterior Ischemic | Neurofibromatosis Type 1 | Lymphoma, Mantle Cell | Silicosis | Hereditary Spastic Paraplegia | Leiomyoma | Neovascular Glaucoma | Spinocerebellar Ataxia Type 21 | Pupil Disorders | Uremia | Neuronal Ceroid Lipofuscinosis | Spinocerebellar Ataxia Type 5 | Episodic Ataxia | COACH Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Papillon-Lefevre Syndrome | Fascioliasis | MIRAGE Syndrome | Hashimoto Thyroiditis | Liver Failure, Acute Infantile | Central Pain Syndrome | Hamartoma | Neurodevelopmental Disorders | Onchocerciasis | Thyroid Dyshormonogenesis | Schwannomatosis | SAPHO Syndrome | Sorsby Fundus Dystrophy | Multicystic Renal Dysplasia | Aneurysm, Thoracic Aortic | VACTERL Association | Polymyalgia Rheumatica | Pemphigus Foliaceus | Periodic Limb Movement Disorder | Citrullinemia | Bruck Syndrome | Lymphoma Lymphoblastic | Primary Sclerosing Cholangitis | Castleman Disease | Waardenburg Syndrome Type 2 | Ellis-Van Creveld Syndrome | Major Depression | Gastric Atrophy | Meconium Ileus | Agammaglobulinemia | Delayed Sleep Phase Syndrome | Common Cold | Wagner Disease | Niemann-Pick Disease, Type C | Chondrodysplasia Punctata 2, X-linked Dominant | Choroiditis | Adenocarcinoma | Neurofibroma | Vasculitis | Fundus Albipunctatus | Long QT Syndrome Type 2 | Esophageal Carcinoma | Adenomatoid Tumor | Christianson Syndrome | Sengers Syndrome | Pseudohypoparathyroidism Type 1A | Pyruvate Carboxylase Deficiency Disease | Cancer, Lung | Metanephric Adenoma | Proteasome-associated Autoinflammatory Syndrome 2 | Enlarged Vestibular Aqueduct | Azoospermia | Apparent Mineralocorticoid Excess Syndrome | Frontometaphyseal Dysplasia | Long QT Syndrome Type 1 | Pain | Vertigo | Dubin-Johnson Syndrome | Gitelman Syndrome | Smith-Lemli-Opitz Syndrome | Withdrawal Syndrome | Lupus Erythematosus | Milk Allergy | Antenatal Bartter Syndrome Type 1 | Odonto-onycho-dermal Dysplasia | Primary Carnitine Deficiency | Iron Deficiency Anemia | Behcet's Disease | Tricho-hepato-enteric Syndrome | Autoimmune Hemolytic Anemia | Inflammatory Linear Verrucous Epidermal Nevus | Acromegaly | Microtia | Hyperparathyroidism | Vitiligo | Acral Lentiginous Melanoma | Pancreatitis, Chronic | Hypercalcemia | Dyskeratosis Congenita | Progressive External Ophthalmoplegia | Hypopigmentation | Opisthorchiasis | Mucolipidosis Type IV | Alstrom Syndrome | Compartment Syndrome | Peripheral Neuropathy | Infantile Spasm | Adenoma, Pituitary | Congenital Nephrotic Syndrome | Hyperinsulinemic Hypoglycemia | Progressive Familial Intrahepatic Cholestasis Type 3 | Androgen Insensitivity | Cancer, Prostate | Beckwith-Wiedemann Syndrome | Renpenning Syndrome | Angioedema, Acquired | Primary Hyperoxaluria Type 3 | Primrose Syndrome | Myocardial Infarction | Arthritis, Gouty | Obesity | Leiomyosarcoma | Vascular Calcification | Retinitis Pigmentosa | Shock, Cardiogenic | Sarcoma, Ewing | Bartter Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Polyomavirus Nephropathy | Neurotoxicity | Eccrine Porocarcinoma | Hyperbilirubinemia, Neonatal | Okihiro Syndrome | Pulmonary Veno-occlusive Disease | Coenzyme Q10 Deficiency | Salla Disease | Xeroderma Pigmentosum | Hypertensive Retinopathy | Adenomyosis | Auriculocondylar Syndrome | Hidradenitis | Cystitis, Interstitial | FG Syndrome | Speech Disorders | Hepatitis D | Pituitary Dwarfism | Pleurisy | Bainbridge-Ropers Syndrome | Alpha-1 Antitrypsin Deficiency | 3-methylglutaconic Aciduria Type I | Cabezas Syndrome | Smith-Kingsmore Syndrome | Lipid Storage Myopathy | Brachial Plexus Neuropathy | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Zollinger-Ellison Syndrome | Exocrine Pancreatic Insufficiency | Restless Legs Syndrome