Influenza

About the Disease
Influenza, also known as flu, is related to avian influenza and swine influenza, and has symptoms including chills, fever and sore throat. An important gene associated with Influenza is IVNS1ABP (Influenza Virus NS1A Binding Protein), and among its related pathways/superpathways are Innate Immune System and Disease. The drugs Hops and Coal tar have been mentioned in the context of this disorder. Affiliated tissues include heart, t cells and brain, and related phenotypes are no effect and no effect

Common Targets
NLRP3 Inflammasome | METTL3 | Importin alpha/beta-1 | MAGEA3 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | Prostanoid Receptor (nonspecified subtype) | TMPRSS13 | TLR7 | RAC1 | F2RL1 | G114548 | ST14 | Interleukin 17 (nonspecified subtype) | HLA-DQB1 | G3576 | TLR8 | TLR3 | G7124 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | VIM | HDAC6 | HMOX2 | T-Type Calcium Channel | IL10RA | Protein Kinase B (PKB/Akt) (nonspecified subtype) | IL1B | LTA | TMPRSS11D | G3569 | NOTCH4 | G5133 | Chloride channel (nonspecified subtype) | PDK4 | G29126 | TMPRSS2 | DHODH | NF-kappaB (NFkB) | NR1I2 | PIK3CD | XPO1 | EIF5A | IMPDH2 | CD55 | G7099 | MAP4K1 | HLA-DRB1 | CCL1 | NLRP1 Inflammasome | Trypsin (nonspecified subtype) | Toll-Like Receptor (nonspecified subtype) | Interferon (nonspecified subtype) | XDH | Interferon alpha/beta Receptor (nonspecified subtype) | PTGDR2 | Vacuolar H+ ATPase | PTGER4 | MBL2 | Serine protease (nonspecified subtype) | LANCL2 | S1PR5 | CD80 | CLK1 | Heat shock protein 70 (nonspecified subtype) | GSN | F2RL3 | TLR2 | IFITM3 | TEK | CXCR2 | Complement Complex | GAA | C3 | TLR6 | GPR182 | Collagenase (nonspecified subtype) | Protein phosphatase-1 | SERPING1 | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) (nonspecified subtype) | TLR4/MD-2 complex | LY96 | CAMKK2 | Tubulin | NOS2 | TLR9 | STING1 | S1PR1 | IFNG

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Other Diseases

Synovitis | Sitosterolemia | Palsy, Cerebral | Pelizaeus-Merzbacher Disease | Alopecia Areata | Hypoalbuminemia | Vasculitis | Amenorrhea | Lymphoma, Follicular | Neurodegeneration With Brain Iron Accumulation | Muir-Torre Syndrome | Porokeratosis | Pyruvate Kinase Deficiency | Cataract | Neonatal Progeroid Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Lymphoma | Charcot-Marie-Tooth Disease Type 2T | Frontometaphyseal Dysplasia | Ataxia-ocular Apraxia 2 | Postpoliomyelitis Syndrome | Myoclonus-dystonia Syndrome | Beckwith-Wiedemann Syndrome | Hemangioendothelioma | X-linked Creatine Transporter Deficiency | Weill-Marchesani Syndrome | Esophageal Motility Disorders | Ichthyosis Hystrix, Curth-Macklin Type | Chorioretinitis | Smoldering Myeloma | Compartment Syndrome | Okihiro Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Herpes Simplex Dermatitis | Usher Syndrome Type II | Hypertension, Pulmonary | Mountain Sickness | Saethre-Chotzen Syndrome | Tendinopathy | Erythematotelangiectatic Rosacea | Cirrhosis | Demyelinating Diseases | Meckel-Gruber Syndrome | Lymphangioleiomyomatosis | Giant Cell Glioblastoma | Hydrocephalus, Normal Pressure | Glycogen Storage Disease Type 1a | Choriocarcinoma | Myelomeningocele | Charcot-Marie-Tooth Disease, Type 2A | Deafness, Dystonia, And Cerebral Hypomyelination | Tyrosinemia Type 2 | Hyperlipidemia | Acute Anterior Uveitis | Binge Eating Disorder | Cholestasis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Wieacker-Wolff Syndrome | Camurati-Engelmann Disease | Huntington's Disease-like 2 | Patent Ductus Arteriosus | Duodenal Atresia | Hypothyroidism | Prolymphocytic Leukemia | Pneumonia, Bacterial | Rift Valley Fever | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Stomatitis | Barrett Esophagus | Focal Segmental Glomerulosclerosis | Dystonia Musculorum Deformans | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Ebstein Anomaly | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Esotropia | Abetalipoproteinemia | 3-M Syndrome | Myofibrillar Myopathy | Pleurisy | CHARGE Syndrome | Acromegaly | Thrombasthenia | Enterocolitis, Necrotizing | Osteogenesis Imperfecta Type I | Tuberculosis | Vulvovaginitis | Tardive Dyskinesia | Hodgkin Lymphoma | C3 Glomerulopathy | Spinal And Bulbar Muscular Atrophy | Pouchitis | Eczema | Cerebrotendinous Xanthomatosis | Proctitis | Joubert Syndrome 2 | Hypercholesterolemia, Familial | Diabetic Nephropathy | Gerstmann-Straussler-Scheinker Syndrome | Retinal Coloboma | Myopia | Rheumatic Heart Disease | Craniolenticulosutural Dysplasia | Congenital Absence Of Vas Deferens | DRESS Syndrome | Angioimmunoblastic T-cell Lymphoma | Oculocutaneous Albinism Type 2 | Tetraplegia | Thyroiditis, Autoimmune | Giant Cell Arteritis | Papilloma | Sclerosteosis 2 | Omenn Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Iron Deficiency Anemia | Frank-ter Haar Syndrome | Limb Girdle Muscular Dystrophy | Agoraphobia | Gastroschisis | Endometritis | Glutathione Synthetase Deficiency | Persistent Hyperplastic Primary Vitreous | Pericarditis | Chondrodysplasia Punctata 1, X-linked Recessive | Long QT Syndrome Type 2 | Hyperinsulinemic Hypoglycemia | Gastritis, Atrophic | Aarskog-Scott Syndrome | Cold Agglutinin Disease | Antenatal Bartter Syndrome Type 1 | Donnai-Barrow Syndrome | Periodontitis | Optic Neuropathy, Anterior Ischemic | Thalassemia | Glaucoma | Rosacea | Malaria | Hereditary Sensory Neuropathy Type 1 | Tetanus | Keratopathy | Hashimoto Thyroiditis | Distal Spinal Muscular Atrophy | Alopecia | Premature Ejaculation | Ocular Surface Squamous Neoplasia | Anuria | Diabetic Macular Edema | Bronchitis | Coenzyme Q10 Deficiency | Rhabdomyosarcoma | Spinocerebellar Ataxia Type 15 | Corneal Ulcer | Acute Chest Syndrome | Osteoarthritis | Cystitis | Polymyalgia Rheumatica | Asthma, Exercise-induced | Retinal Diseases | Chromosome 5q Deletion Syndrome | Asphyxia Neonatorum | Axenfeld-Rieger Syndrome | Blood Protein Disorders | Kawasaki Disease | Renal Oncocytoma | Encephalitis | Osteopetrosis | Whipple's Disease | Tatton-Brown-Rahman Syndrome | N-acetylglutamate Synthase Deficiency | Phosphoglycerate Dehydrogenase Deficiency | Inflammatory Myopathy | Postaxial Polydactyly | Hemochromatosis | Hereditary Spastic Paraplegia | Mannosidase Deficiency Diseases | Vogt-Koyanagi-Harada Syndrome | Blepharo-cheilo-odontic Syndrome | Osteopathia Striata With Cranial Sclerosis | Creatine Deficiency Syndrome | Antiphospholipid Syndrome | Spondylocostal Dysostosis | Methemoglobinemia | Graves Disease | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Cardiomyopathy, Peripartum | Pneumoconiosis | Arthropathy | Osteitis | Agranulocytosis | Barakat Syndrome | Porphyria, Acute Intermittent | Dyskeratosis Congenita | Primary Aldosteronism | Phenylketonuria | Blue Rubber Bleb Nevus Syndrome | Persistent Mullerian Duct Syndrome | Veno-occlusive Disease | Gastrointestinal Disorders | Lymphangioma | Neutropenia | Epidermolytic Palmoplantar Keratoderma | Lung Diseases | Hemimegalencephaly | Guttate Psoriasis | Brenner Tumor | Absence Epilepsy | Sandhoff Disease | Kaposi Sarcoma | Angioedema, Hereditary | Pain | Hydrolethalus Syndrome | Mevalonate Kinase Deficiency | Peeling Skin Syndrome Type B | Spinocerebellar Ataxia Type 1 | Esophageal Carcinoma | Familial Retinal Arterial Macroaneurysm | Schuurs-Hoeijmakers Syndrome | Dengue Shock Syndrome | Temporal Lobe Epilepsy | Bietti Crystalline Dystrophy | Spinal Muscular Atrophy Type 3 | Celiac Disease | Erythema Nodosum | Fragile X Syndrome | Benign Familial Infantile Seizures | Alagille Syndrome | Multiple Sclerosis, Primary Progressive | Osteochondroma | Cavitary Optic Disc Anomalies | Panuveitis | Strabismus | Hyperthyroidism | Dent Disease | Spinocerebellar Ataxia Type 40 | Aicardi-Goutieres Syndrome | Uremia | Protein S Deficiency | Bernard-Soulier Syndrome | Wiskott-Aldrich Syndrome | Milk Allergy | Angioedema | Leishmaniasis, Cutaneous | Epicondylitis | Infantile Refsum Disease | Wolfram Syndrome 2 | Epithelial-myoepithelial Carcinoma | Tuberculous Meningitis | REM Sleep Behavior Disorder | Bullous Pemphigoid | Varicocele | Spinocerebellar Ataxia Type 3 | Congenital Tufting Enteropathy | Sturge-Weber Syndrome | Intermittent Explosive Disorder | Emery-Dreifuss Muscular Dystrophy | Otosclerosis | Central Retinal Artery Occlusion | Congenital Disorders Of Glycosylation | Autoimmune Disease | Pleomorphic Xanthoastrocytoma | Ichthyosis | Alexander Disease | Familial Dysautonomia | Macrophagic Myofasciitis | Osteosarcoma | Congenital Adrenal Hyperplasia 1 | Hidradenitis Suppurativa | Cancer, Colon | Cholesteryl Ester Storage Disease | Hypersensitivity Pneumonitis | Charcot-Marie-Tooth Disease Axonal Type 2N | Osteoporosis | Focal Facial Dermal Dysplasia | Hemolytic Uremic Syndrome, Atypical | Charcot-Marie-Tooth Disease Type 4B1 | Hyperinsulinism-hyperammonemia Syndrome 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Dysostosis | Chromosome 9q34.3 Deletion Syndrome | Peeling Skin Syndrome, Acral Type | Cranial Nerve Disease | Lentigo | Stuve-Wiedemann Syndrome | Budd-Chiari Syndrome | Hermansky-Pudlak Syndrome | Cystinosis | Presbycusis | Cryptorchidism | Martsolf Syndrome | Mucolipidosis Type II | Aceruloplasminemia | Potocki-Shaffer Syndrome | Kaposiform Hemangioendothelioma | Rubeosis Iridis | Hyperuricemic Nephropathy, Familial Juvenile | Left Ventricular Noncompaction | Infantile Neuroaxonal Dystrophy | Esthesioneuroblastoma | Tay-Sachs Disease | Rett Syndrome | Astigmatism | Nephronophthisis | Cramp Fasciculation Syndrome | Kernicterus | Salla Disease | Usher Syndrome Type I | Nanophthalmos | Adrenoleukodystrophy, X-linked | COACH Syndrome | Endocarditis | Erectile Dysfunction | Anorchia | Bare Lymphocyte Syndrome | Lipid Storage Myopathy | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Glomerulonephritis, Membranous | Pneumothorax | Traboulsi Syndrome | Gastric Atrophy | Arts 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Hypofibrinogenemia