Disease

Osteoarthritis

About the Disease
Osteoarthritis, also known as osteoarthrosis, is related to cartilage disease and exostosis, and has symptoms including arthralgia, back pain and metatarsalgia. An important gene associated with Osteoarthritis is HOTAIR (HOX Transcript Antisense RNA), and among its related pathways/superpathways are ECM proteoglycans and Extracellular matrix organization. The drugs Fentanyl and Benzocaine have been mentioned in the context of this disorder. Affiliated tissues include Cartilage and Bone, and related phenotype is limbs/digits/tail.

Common Targets
GPR55 | GCGR | Inositol Monophosphatase (nonspecified subtype) | G10413 | PIM2 | G5243 | Phosphodiesterase (nonspecified subtype) | G7422 | IL23R | SCN5A | BDKRB2 | TIMP3 | Fibroblast Growth Factor Receptor (FGFR) (nonspecified subtype) | HRH3 | YES1 | ENPP2 | PIK3CG | G114548 | JAK3 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | TNKS | MST1R | TNFRSF11B | P2RY1 | JAK1 | CCDC91 | NFKB1 | CDC42BPB | MAP2K4 | CACNA1B | ADAMTS7 | CYP3A4 | G6714 | ALPL | G596 | IL6ST | RUNX2 | Prostanoid Receptor (nonspecified subtype) | G3576 | KDR | COL18A1 | SNCA | PDGFB | RORC | DIO2 | TTR | CRBN | LCORL | ADAMTS6 | EPHB2 | EIF4A1 | Carbonic Anhydrase (nonspecified subtype) | ALDH1A2 | PTGES | MC1R | RAC1 | DIO3 | IL7 | ST14 | TLR3 | FAP | GBA1 | SPR | JAK2 | MEG3 | gamma-Secretase | IL1B | HFE | ITGA10 | Tachykinin Receptor (nonspecified subtype) | CLSTN2 | I-kappa-B-kinase (IKK) complex | ORAI1 | G6774 | EIF4F translation-initiation complex | MIR23A | IL1RN | Interleukin-1 (nonspecified subtype) | OPRK1 | SOST | CILP | SMO | PDE4B | COL6A4P1 | IKBKB | AKR1C2 | PLA2G4A | Phosphodiesterase IV (PDE4) (nonspecified subtype) | FGFR2 | TRPV4 | COL1A1 | G3569 | SLC17A3 | Acid-Sensing Ion Channel (ASIC) (nonspecified subtype) | LPAR1 | OPRM1 | ROCK1 | GNG5 | Heat shock protein 90 (nonspecified subtype) | KCNQ3 | MIR155 | BTK | C5 | CTSS | CNR2 | BMP2 | ELANE | IL17RA | IMPA1 | ASAH1 | Hedgehog Protein (nonspecified subtype) | Mucin (nonspecified subtype) | MIR140 | MAPK11 | Folate Receptor (nonspecified subtype) | HRH2 | MMP3 | LTB4R2 | Casein kinase I (nonspecified subtype) | SGK1 | ADAMTS5 | ACE | MAP3K5 | ADP-Ribosyl Cyclase/cyclic ADP-Ribose Hydrolase (ADPRC) (nonspecified subtype) | CTSL | Matrix Metalloproteinase (MMP) (nonspecified subtype) | IL-1 Receptor (nonspecified subtype) | Calcium channel (nonspecified subtype) | LRP5 | TUFT1 | AURKB | CHEK1 | G1432 | TGFB1 | AXL | LCK | MUTYH | RAMP2 | LOC102724428 | BGLAP | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | G842 | Protein kinase C (nonspecified subtype) | G1950 | G598 | CLK4 | Fibroblast growth factor (FGF) (nonspecified subtype) | MAOA | MMP12 | PIM3 | G7099 | MCF2L | NF-kappaB (NFkB) | TYK2 | CSF1R | G7295 | SGK2 | Nicotinic alpha3beta4 Receptor | ADAM17 | TRPM8 | Neurotrophic Factor (nonspecified subtype) | EIF4E | CHRNA9 | TNFSF11 | RAMP1 | SLC6A2 | DLG2 | P2RY11 | IKZF1 | Opioid receptor (nonspecified subtype) | Oxysterols receptor LXR (nonspecified subtype) | IAPP | CDK9/Cyclin T1 | PIK3CB | EPHB4 | WSB1 | DDR2 | G23411 | MAP2K1 | Nicotinic alpha4beta2 receptor | Amylin receptor | ABCA1 | EIF4G1 | RAMP3 | CNR1 | DKK1 | Estrogen receptor (nonspecified subtype) | TGM2 | EIF4G2 | BRD4 | CCN2 | EIF2AK4 | Inhibitory kappaB Kinase (IKK) (nonspecified subtype) | DYRK1A | PIK3CD | GIPR | CCR2 | GNL3 | Casein kinase II (CKII) | DNA Topoisomerase II (nonspecified subtype) | TMSB4X | CDK9 | MC3R | TNKS2 | CD38 | KIF1C | IRAK4 | G142 | MAPKAPK2 | IHH | GLT8D1 | IL-6 receptor | SYK | HEXB | TRPV1 | PTCH1 | IL1R1 | TGFBR1 | Phospholipase A2, Cytosolic (nonspecified subtype) | Ectonucleotide pyrophosphatase/phosphodiesterase (E-NPP) (nonspecified subtype) | F2 | G3605 | Voltage-Gated Sodium Channel Complex | G4170 | XDH | CAV1 | CCNT1 | ADORA3 | OPRD1 | PTGS1 | COL10A1 | CXCR3 | CLEC3B | ACHE | CASP8 | PRG4 | CALCA | PPARG | CSNK1A1 | Triacylglycerol Lipase (TG Lipase) (nonspecified subtype) | PTGDR2 | SOD3 | NTRK1 | GSK3B | Retinoid acid receptor (nonspecified subtype) | LIPC | FDPS | ANAPC13 | TBX5 | EPHA4 | Glycogen synthase kinase 3 (GSK-3) (nonspecified subtype) | MERTK | PTGER4 | CDH2 | TNFRSF11A | CALCRL | OGA | TRPV3 | CTH | Aggrecanase (nonspecified subtype) | ADAM12 | FAAH | G3480 | CCR1 | GHR | G3630 | IL17F | CSF2 | SOX9 | Caspase (nonspecified subtype) | MMP13 | Sodium channel (nonspecified subtype) | LEPR | ABCC8 | G2099 | TYRO3 | PTPN4 | DACH2 | BDKRB1 | PDE2A | ADAMTS4 | TGFB2 | COL6A2 | Nicotinic alpha4beta4 receptor | EIF4G3 | Mitogen-Activated Protein Kinase (nonspecified subtype) | FGFR1 | G836 | GRM1 | CLK1 | ENPP1 | DOT1L | GJA1 | TPSB2 | Ikzf1 | EPHA2 | G4318 | AP-1 Transcription Factor Complex | SIK2 | CYSLTR2 | DYRK1B | APOA1 | Janus Kinase (nonspecified subtype) | NR3C1 | PTH1R | CTSK | ROCK2 | IL1A | MSR1 | DDR1 | PIM1 | P2RY14 | FLNB | AKR1B10 | SCN9A | ASIC1 | Gastric H+/K+-ATPase | SLC6A4 | Cyclooxygenase (COX) (nonspecified subtype) | MMP8 | Nicotinic alpha9alpha10 Receptor | NAAA | TIMP2 | C5AR1 | IL2 | GAA | NOX3 | LIPE | NMDA receptor | LYN | SMAD3 | UTRN | LTC4S | CTSB | MRGPRX2 | SIK1 | CASP1 | MIR1288 | 5-Hydroxytryptamine Receptor (nonspecified subtype) | SULF1 | RUNX1 | MMP2 | ASTN2 | CALCR | Nicotinic alpha3beta2 receptor | MIR146A | MAPK7 | cGMP-inhibited 3',5'-cyclic phosphodiesterase 3 (PDE3) (nonspecified subtype) | USP33 | FAS | Neuronal acetylcholine receptor alpha2beta2 receptor | Collagenase (nonspecified subtype) | G367 | NOS2 | G4233 | VDR | P2RX7 | TRPA1 | G5743 | COL2A1 | Rho kinase (ROCK) (nonspecified subtype) | MMP14 | GSPT1 | CCL2 | PDE1A | TBK1 | NADPH Oxidase Complex | PITX1 | CHRNB2 | MIF | ABCC1 | DPP9 | TGFB3 | THRA | PIK3CA | FYN | GDF5 | CLK2 | TXK | S1PR1 | ABCC3 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | COL11A2 | IL-23 receptor complex | ALOX5 | ENOX2 | NLRP3 Inflammasome | CTSD | DHFR | SIK3 | GLP1R | HEXD | EN1 | AOC3 | LIPG | MTHFR | FLT3 | PTGER2 | ZNF678 | G7124 | H19 | HSD17B3 | IL10 | NGF | KCNQ2 | OSCAR | CDK1 | NADPH Oxidase (nonspecified subtype) | Nicotinic alpha1beta1deltagamma Receptor | NKAIN2 | CHST11

疾病靶点研报
Osteoarthritis

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

Other Diseases

Methemoglobinemia Type IV | Hepatitis B, Chronic | Pneumonia, Bacterial | Atopic Dermatitis | Micropenis | Polymyositis | LEOPARD Syndrome | Idiopathic Pulmonary Fibrosis | Renal-hepatic-pancreatic Dysplasia | VACTERL Association | Urea Cycle Disorder | Fahr Disease | Congenital Hereditary Endothelial Dystrophy Type II | Microphthalmia, Syndromic 7 | Progressive Osseous Heteroplasia | Chondromyxoid Fibroma | Congenital Hypofibrinogenemia | Prader-Willi Syndrome | Dyslipidemia | Charcot-Marie-Tooth Disease Type 4D | Empyema | Persistent Fetal Circulation | Diabetes Type 1 | Zygomycosis | Stiff-man Syndrome | Schwannoma | Pearson Syndrome | Sialidosis | Chromosome 17q21.31 Deletion Syndrome | Conduct Disorder | Autosomal Recessive Spastic Paraplegia Type 35 | Mitochondrial Encephalomyopathy | Gigantism | Juvenile Polyposis | Hereditary Elliptocytosis | Mitochondrial DNA Depletion Syndrome 13 | Fuchs Dystrophy | Brachydactyly | Osteoporosis, Postmenopausal | Blau Syndrome | Lymphedema-distichiasis Syndrome | Bainbridge-Ropers Syndrome | Placenta Previa | Oculopharyngeal Muscular Dystrophy | Rheumatoid Arthritis | Myofibromatosis | Viral Meningitis | Rhizomelic Chondrodysplasia Punctata | Carbonic Anhydrase VA Deficiency | Adrenomyeloneuropathy | Giant Axonal Neuropathy | Membranous Nephropathy | Congenital Myasthenic Syndrome | Mevalonate Kinase Deficiency | Hypophosphatasia | Familial Hypobetalipoproteinemia | Infertility, Male | Spinocerebellar Ataxia Type 6 | Proopiomelanocortin Deficiency | Craniolenticulosutural Dysplasia | Spinocerebellar Ataxia Type 27 | Chronic Mucocutaneous Candidiasis | Mumps | Frank-ter Haar Syndrome | Becker Muscular Dystrophy | Fibromuscular Dysplasia | Still Disease | Goiter | Meier-Gorlin Syndrome | Phenylketonuria II | IgA Nephropathy | Lymphoma, Mantle Cell | Vertebrobasilar Insufficiency | Inflammatory Myofibroblastic Tumor | Imerslund-Grasbeck Syndrome | Retinal Dystrophy | Renal Tubular Dysgenesis | Rhabdomyosarcoma, Alveolar | Sotos Syndrome | Familial Hemiplegic Migraine | Alpha-thalassemia Myelodysplasia Syndrome | Tangier Disease | Osteomyelitis | Hereditary Hemorrhagic Telangiectasia Type 2 | Chondrosarcoma | Juvenile Myelomonocytic Leukemia | Esotropia | Norrie Disease | Schistosomiasis | Specific Granule Deficiency | Cantu Syndrome | Neuroblastoma | Canavan Disease | Lattice Corneal Dystrophy Type 1 | Urticaria | Mucolipidosis | Motor Neuron Diseases | Binge Eating Disorder | Diabetes Insipidus | Pityriasis Rubra Pilaris | Neuroendocrine Cancer | Pulmonary Alveolar Microlithiasis | Li-Fraumeni Syndrome | Carbohydrate Metabolism Disorders | Gallstones | Rett Syndrome | Intracranial Hypertension | Huntington's Disease | Sarcoidosis, Pulmonary | Currarino Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Schizophrenia | Myoclonic Epilepsy With Ragged Red Fibers | Pseudohypoaldosteronism | Epidermolytic Ichthyosis, Annular | Hyperparathyroidism-jaw Tumor Syndrome | Waardenburg Syndrome Type 2 | Vascular Cognitive Impairment | Pleurisy | Leber Congenital Amaurosis | Gardner Syndrome | Schistosomiasis Mansoni | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Bicuspid Aortic Valve | Porphyria, Variegate | Gastritis, Atrophic | Anosmia, Congenital | Supravalvular Aortic Stenosis | Cholangiocarcinoma | Polycystic Kidney, Autosomal Dominant | Chronic Inflammatory Demyelinating Polyneuropathy | Rosacea | GATA2 Deficiency | Bardet-Biedl Syndrome | Situs Inversus | Von Willebrand Disease | Autoimmune Polyendocrine Syndrome | Lymphomatoid Granulomatosis | Central Pain Syndrome | Thin Basement Membrane Disease | Kashin-Beck Disease | Dysfibrinogenemia | Hereditary Neuropathy With Liability To Pressure Palsies | Schindler Disease | Pemphigus | Antisocial Personality Disorder | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Multiple Sclerosis, Secondary Progressive | 3-methylcrotonyl-CoA Carboxylase Deficiency | Congenital Muscular Dystrophy | Hepatitis, Autoimmune | Retinal Degeneration | Corneal Dystrophy | Duane Retraction Syndrome | Leukoplakia, Oral | Metachondromatosis | Hepatitis A | Uveitis, Anterior | Guanidinoacetate Methyltransferase Deficiency | Tremor | Osteomalacia | Paternal Uniparental Disomy Of Chromosome 14 | Hyperlipidemia, Familial Combined | Arthrogryposis | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Generalized Epilepsy With Febrile Seizures Plus | Congestive Heart Failure | Hypocalcemia | Aplasia Cutis Congenita | Osteochondroma | Vaginitis | McLeod Syndrome | Hepatitis E | Giant Cell Arteritis | Atrial Septal Defect | Wolfram Syndrome | Angioedema, Hereditary | Basal Ganglia Disease, Biotin-responsive | Chronic Thromboembolic Pulmonary Hypertension | Oligoastrocytoma | B-cell Chronic Lymphocytic Leukemia | Inflammatory Myopathy | Spinocerebellar Ataxia Type 42 | Cri-du-chat Syndrome | Hereditary Multiple Exostoses | Ichthyosis Hystrix, Curth-Macklin Type | Retinal Diseases | Oculocutaneous Albinism Type 2 | Neuronal Ceroid Lipofuscinosis | Hypokalemic Periodic Paralysis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Choriocarcinoma | Reye Syndrome | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Scapuloperoneal Spinal Muscular Atrophy | Neurofibromatosis-Noonan Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Lateral Meningocele Syndrome | Hereditary Coproporphyria | Heart Block | Contact Dermatitis | Osteogenesis Imperfecta Type II | Gaucher Disease | Pure Autonomic Failure | Hartnup Disease | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Spondylometaphyseal Dysplasia | Congenital Hereditary Endothelial Dystrophy Type I | Blomstrand Osteochondrodysplasia | Mucormycosis | Benign Hereditary Chorea | Chanarin-Dorfman Syndrome | Hemangioblastoma | Microcephaly, Seizures, And Developmental Delay | Enterocolitis, Necrotizing | Alopecia Totalis | Allan-Herndon-Dudley Syndrome | 3-methylglutaconic Aciduria Type IV | Multisystemic Smooth Muscle Dysfunction Syndrome | Periventricular Leukomalacia | Macular Corneal Dystrophy | Myopia | Gerstmann-Straussler-Scheinker Syndrome | Acute Coronary Syndrome | Nestor-Guillermo Progeria Syndrome | Adenosine Deaminase 2 Deficiency | Cerebellar Ataxia, Cayman Type | Esthesioneuroblastoma | Cocaine-Related Disorders | Syphilis | Irritable Bowel Syndrome | Conjunctivitis | Peeling Skin Syndrome, Acral Type | Delayed Sleep Phase Syndrome | Nevus | Warsaw Breakage Syndrome | T-cell Chronic Lymphocytic Leukemia | Non-bullous Congenital Ichthyosiform Erythroderma | Congenital Adrenal Hyperplasia 1 | Open-angle Glaucoma | Alpers Syndrome | Hypertensive Nephropathy | Scleritis | Burn-McKeown Syndrome | Angiomyolipoma | Renpenning Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Hereditary Xerocytosis | Paget's Disease Of The Breast | Familial Pheochromocytoma-paraganglioma | Erythema Multiforme | Micro Syndrome | Treacher Collins Syndrome | Spinocerebellar Ataxia Type 20 | Spinal Muscular Atrophy Type 3 | Relapsing Polychondritis | Retinitis Pigmentosa 3 | X-linked Charcot-Marie-Tooth Disease | Isovaleric Acidemia | Hypereosinophilic Syndrome | Primary Biliary Cholangitis | Acromesomelic Dysplasia | Richter's Syndrome | Glycogen Storage Disease Type 1 | Ocular Surface Squamous Neoplasia | Peripheral T-cell Lymphoma | Amelanotic Melanoma | Cryptorchidism | Headache | Budd-Chiari Syndrome | Pheochromocytoma | Stroke, Ischemic | Esophageal Adenocarcinoma | Porphyria Cutanea Tarda | Spinocerebellar Ataxia Type 7 | C3 Glomerulopathy | Silicosis | Endometrial Hyperplasia | Schizoaffective Disorder | Non-epidermolytic Palmoplantar Keratoderma | Blepharoconjunctivitis | Systemic Mastocytosis | Spinocerebellar Ataxia Type 15 | Cutaneous Mastocytosis | Congenital Heart Defects | Glycogen Storage Disease Type 1b | Multiple Epiphyseal Dysplasia | Myelitis | Muckle-Wells Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Measles | Pulmonary Veno-occlusive Disease | Tyrosinemia Type 2 | Trigonocephaly | Orotic Aciduria | Episodic Ataxia Type 2 | DRESS Syndrome | Optic Nerve Diseases | Encephalopathy, Glycine | Pelizaeus-Merzbacher Disease | AIDS Dementia Complex | Aplastic Anemia | Metaphyseal Chondrodysplasia, Schmid Type | Marinesco-Sjogren Syndrome | Enlarged Vestibular Aqueduct | Gliosarcoma | VACTERL/VATER Association | Polycystic Liver | Distal Myopathy 2 | Scabies | Keratoacanthoma | Speech Disorders | Synovitis | Cryoglobulinemia | Nijmegen Breakage Syndrome | Moyamoya Disease | Carcinoma, Small Cell | Sorsby Fundus Dystrophy | Mohr-Tranebjaerg Syndrome | Ameloblastic Carcinoma | Renal Tubular Acidosis | Corneal Dystrophies, Hereditary | Extramammary Paget's Disease | Desbuquois Syndrome | Coronary Restenosis | Infantile Refsum Disease | Ulcerative Colitis | Neuroma | Hyperphenylalaninemia | Peyronie's Disease | MELAS Syndrome | Pancytopenia | Platelet Disorders | Antisynthetase Syndrome | Cornelia De Lange Syndrome | Dysferlinopathy | Pierpont Syndrome | Spinocerebellar Ataxia Type 1 | Nephritis, Interstitial | Myoclonic Atonic Epilepsy | Diabetic Macular Edema | Ophthalmia, Sympathetic | Congenital Dysfibrinogenemia | Sialoadenitis | Neurofibrosarcoma | AIDS | Branchiootorenal Syndrome | Postpartum Depression | Ventricular Septal Defect | Congenital Primary Aphakia | Spondylocarpotarsal Synostosis Syndrome | Hereditary Hemorrhagic Telangiectasia | Heroin Dependence | McKusick Type Metaphyseal Chondrodysplasia | Acute Myeloid Leukemia | Biotinidase Deficiency | Lipid Storage Diseases | Dentinogenesis Imperfecta | Connective Tissue Disorders | Syncope | Mast Cell Leukemia | Cerebrotendinous Xanthomatosis | Epidermolytic Hyperkeratosis | Cutaneous Lupus Erythematosus | Japanese Encephalitis | Pseudoachondroplasia | Peeling Skin Syndrome Type B | Primrose Syndrome | Cerebrovascular Disorders | Cancer, Skin | Ectopia Lentis, Isolated, Autosomal Recessive | Corticobasal Syndrome | Oculocutaneous Albinism Type 1 | Porencephaly | Dental Caries | Erythematotelangiectatic Rosacea | Anencephaly | Cavitary Optic Disc Anomalies | Dystonia Musculorum Deformans | Schuurs-Hoeijmakers Syndrome | Syndactyly | Paraganglioma | Pemphigoid | Hereditary Sensory Neuropathy Type 1 | Pure Red Cell Aplasia | Hemolytic Uremic Syndrome | GNE Myopathy | Nephrocalcinosis | GLUT1 Deficiency Syndrome | Dent Disease | Blepharo-cheilo-odontic Syndrome | Hypertension, Portal | Retinopathy, Diabetic | Chromosome 8q21.11 Deletion Syndrome | Acute Motor Axonal Neuropathy | Autoimmune Hemolytic Anemia | Hypotrichosis | Achromatopsia | Hyperferritinemia-cataract Syndrome | Endophthalmitis