Disease

Migraine

About the Disease
Migraine with or Without Aura 1, also known as migraine, is related to familial hemiplegic migraine and migraine without aura, and has symptoms including back pain, headache and hemiplegia. An important gene associated with Migraine with or Without Aura 1 is NOTCH3 (Notch Receptor 3), and among its related pathways/superpathways are Type II diabetes mellitus and Cellular roles of Anthrax toxin. The drugs Mineral oil and Betamethasone have been mentioned in the context of this disorder. Affiliated tissues include brain, pituitary and cortex, and related phenotypes are photophobia and vomiting

Common Targets
CACNA2D1 | BIVM-ERCC5 | Prostanoid Receptor (nonspecified subtype) | PHACTR1 | GRM5 | CYSLTR1 | ADCYAP1 | HTR1F | L-type voltage-dependent calcium channel complex | ADRA1A | Calcium channel (nonspecified subtype) | TRPM8 | Kainate Receptor (GluR) (nonspecified subtype) | CACNA2D2 | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | HCN4 | ESR2 | NOS1 | BPIFC | CHRM4 | Interleukin-1 (nonspecified subtype) | NPTX2 | COMT | DRD4 | MAOA | GRIK1 | HTR1A | CNR1 | MTNR1A | Tachykinin Receptor (nonspecified subtype) | KCNQ4 | TRMT9B | Alpha-2 Adrenergic receptors (nonspecified subtype) | SLC6A2 | LTA | PHF20 | CAMK1 | CDH12 | GRIN2C | TRPV1 | Lipoxygenase (nonspecified subtype) | MIR452 | GH1 | NR3C1 | SIGMAR1 | PRDM16 | MGLL | SYNE2 | CHRM1 | SRR | Estrogen receptor (nonspecified subtype) | HDAC1 | T-Type Calcium Channel | NPY1R | PTGS1 | KCNK18 | KCNQ3 | GABRG2 | ACSF3 | G2099 | PGR | ADORA1 | GABA(A) receptor | GABRB2 | ADARB2 | ARPC4-TTLL3 | ACHE | HLA-A | HTR2B | HTR4 | POMC | ADORA2B | P2RX3 | G5743 | Voltage-Gated Sodium Channel Complex | CA12 | CRH | ANKK1 | LOC105375655 | OGG1 | SLC22A3 | SSTR3 | Small Conductance Calcium-Activated Potassium Channel (SK) (nonspecified subtype) | MTHFR | Glutamate Transporter (nonspecified subtype) | SCN8A | alpha-Adrenoceptor (nonspecified subtype) | G5243 | CCR2 | ADORA2A | G3630 | KCNK2 | DBH | SLC17A8 | GRIK2 | GRIN2D | GRM2 | PRRT2 | CHRNA7 | Opioid receptor (nonspecified subtype) | Sodium channel (nonspecified subtype) | LOC101927995 | TNFSF10 | GRIA2 | NAPEPLD | KCNS1 | Gap junction Connexin ( (nonspecified subtype) | ADRA2A | OXT | SLC6A9 | CFDP1 | PIEZO1 | SERPINE1 | MTNR1B | PLCE1 | GRM7 | NOS3 | RNF213 | RAMP1 | IL10 | XRCC3 | ANO3 | HEY2-AS1 | OPRD1 | OPRL1 | KCNK10 | GRIA3 | HTR5A | ERCC2 | NSD1 | SSTR4 | GRIN2A | ADAMTSL1 | PTGER4 | ADORA3 | Prolactin receptor (isoform 1) | MEF2D | KDM2A | SLC6A4 | KCNQ Channels (K(v) 7) (nonspecified subtype) | P2RX4 | GABRA1 | IL-6 receptor | KLC1 | DRD1 | GABRB3 | KLC3 | PDE5A | ZNF555 | POMT2 | ADRB1 | MME | FAAH | NRP1 | HCRTR2 | Glycogen synthase kinase 3 (GSK-3) (nonspecified subtype) | WFS1 | HTR2A | beta-Adrenoceptor (nonspecified subtype) | ABCC8 | CALCA | SUGCT | GRIK3 | HCN2 | CHIA | CALCRL | NBEA | sigma Receptor (nonspecified subtype) | NOS2 | TRPA1 | NMDA receptor | LRP1 | LOC101927066 | TRPV3 | HRH1 | RMI1 | GHR | CHRNA3 | PDE2A | LOC105378316 | ADRA1D | Dopamine receptor (nonspecified subtype) | NF1 | AOC1 | TACR1 | AGTR1 | NOX3 | ASTN1 | L-Type calcium channel (nonspecified subtype) | ADRB2 | GABRQ | HTR6 | CA2 | ADCYAP1R1 | SCN1A | TPH1 | GAA | APEX1 | HTR1B | Glycine receptor | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | USH2A | 5-Hydroxytryptamine Receptor 2 (5-HT2) (nonspecified subtype) | BDKRB1 | NF-kappaB (NFkB) | Histone deacetylase (nonspecified subtype) | OPN4 | TMEM97 | alpha1-Adrenoceptor (nonspecified subtype) | Gastric H+/K+-ATPase | GJA1 | CA9 | GRM1 | NLRP3 Inflammasome | Cyclooxygenase (COX) (nonspecified subtype) | TH | G3576 | CACNA1A | ARPC4 | LOC105378525 | SSTR5 | HTR2C | CYP19A1 | G114548 | MAPK10 | PTGER1 | DRD3 | NADPH Oxidase Complex | G472 | ASIC1 | HLA-C | KLKB1 | KCNK5 | Nitric oxide synthase (NOS) (nonspecified subtype) | P2RX7 | Large Conductance BK(Ca) Potassium Channel (Maxi K+ Channel) (nonspecified subtype) | DAGLA | Gap Junction Protein (nonspecified subtype) | 5-Hydroxytryptamine Receptor (nonspecified subtype) | Histamine Receptor (HR) (nonspecified subtype) | MPPED2 | G7124 | GLP1R | SLC6A3 | Potassium Channels (nonspecified subtype) | XRCC1 | STX1A | GPR55 | SSTR1 | OXTR | KCNA1 | TGFB1 | GRM4 | MRGPRX2 | Endothelin receptor (nonspecified subtype) | MAOB | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | PCDHB8 | Tryptophan 5-Monooxygenase (nonspecified subtype) | NADPH Oxidase (nonspecified subtype) | SLC24A3 | ATR | ITGAL | alpha-Amylase (nonspecified subtype) | Soluble guanylyl cyclase | HPSE2 | CSNK1D | ASTN2 | GABRE | G7099 | GRIN2B | CHRM2 | G7157 | TRNL1 | ANPEP | PCDHB6 | ABAT | GABRA6 | TAAR1 | MRGPRX4 | HCG20 | Glutamate Receptor Ionotropic (nonspecified subtype) | SLC1A2 | FHL5 | HTR1D | AMP-activated protein kinase (AMPK) | GPR17 | KCNQ2 | ADRA2C | HTR7 | LOC105377013 | SVEP1 | IRAG1 | G10413 | GABRA3 | G5728 | Glutamate Receptor Ionotropic AMPA Receptor | OPRM1 | HRH3 | BDNF | TBXAS1 | SLC6A5 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | MIR4761 | SCN2A | Monoamine oxidase (MAO) (nonspecified subtype) | ERCC5 | CHRNA1 | APEH | CSF1R | 5-Hydroxytryptamine Receptor 3 (5-HT3 receptor) (nonspecified subtype) | ACE | TACR3 | OPRK1 | CNR2 | CARF | HLA-B | SV2A | CACNA1B | SSTR2 | TACR2 | HTR1E | SH2D5 | DRD2 | F2RL1

疾病靶点研报
Migraine

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

Other Diseases

Spinocerebellar Ataxia Type 15 | Superficial Spreading Melanoma | Myasthenia | Lymphangioleiomyomatosis | Progressive Familial Intrahepatic Cholestasis Type 2 | Behavioral Variant Of Frontotemporal Dementia | Encephalopathy, Hepatic | Diabetes Type 2 | Renal Tubular Acidosis | Spinocerebellar Ataxia Type 3 | Prolymphocytic Leukemia | Hypoglycemia | Thrombasthenia | Hypobetalipoproteinemias | Cerebral Cavernous Malformations | Hepatitis D | Congenital Nephrotic Syndrome | Walker-Warburg Syndrome | Cutaneous T-cell Lymphoma | Pseudohypoparathyroidism Type 1B | Malonyl-CoA Decarboxylase Deficiency | Hepatitis, Chronic | Compartment Syndrome | Large Granular Lymphocytic Leukemia | Oligoastrocytoma | Osteosarcoma | Metabolic Diseases | Treacher Collins Syndrome | Osteopathia Striata With Cranial Sclerosis | Retinal Degeneration | Hemorrhagic Disorders | Hereditary Spherocytosis | Fibrodysplasia Ossificans Progressiva | Cutaneous Lupus Erythematosus | Osteogenesis Imperfecta Type V | Urethritis | Coffin-Lowry Syndrome | Prader-Willi Syndrome | Retinal Detachment | Proximal Symphalangism | Obesity | Immunoproliferative Disorders | Erythematotelangiectatic Rosacea | Glycogen Storage Disease Type 4 | Osmotic Demyelination Syndrome | Azoospermia | GAPO Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Dystonia-parkinsonism, X-linked | Pelizaeus-Merzbacher Disease | Waardenburg Syndrome Type 4A | Hyperostosis | Incontinentia Pigmenti | Vitreoretinopathy, Proliferative | Metaphyseal Chondrodysplasia, Schmid Type | Encephalopathy, Glycine | Microcephaly | Epidermolysis Bullosa | Adenoma, Pituitary | Still Disease | Lymphoproliferative Disorders | Basal Ganglia Disease | Photosensitivity | Carey-Fineman-Ziter Syndrome | Diabetes Insipidus, Nephrogenic | Neurodermatitis | HELLP Syndrome | Progressive Myoclonic Epilepsy | Lafora Disease | Obesity, Morbid | Retinal Dystrophy, Early-onset Severe | Hypercholesterolemia | Retinopathy, Diabetic | Pyloric Stenosis, Infantile Hypertrophic | Oligoasthenoteratozoospermia | Anodontia | Inflammatory Myofibroblastic Tumor | Uveitis | Arthritis, Reactive | Bullous Pemphigoid | Tangier Disease | Creatine Deficiency Syndrome Due To AGAT Deficiency | Proopiomelanocortin Deficiency | Coronary Artery Disease | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Nicotine Dependence | Barrett Esophagus | Primary Hyperoxaluria | Colitis, Microscopic | Polycystic Liver | Gynecomastia | Preaxial Polydactyly | Hypoparathyroidism | Distal Myopathy | Glycogen Storage Disease Type 3 | Trachoma | Follicular Dendritic Cell Sarcoma | Evans Syndrome | Malignant Peripheral Nerve Sheath Tumor | Non-small Cell Lung Cancer | Encephalopathy | Mannosidase Deficiency Diseases | H Syndrome | Congenital Tufting Enteropathy | Hyperparathyroidism-jaw Tumor Syndrome | Hidradenitis | Autoimmune Disease | Wieacker-Wolff Syndrome | Atherosclerosis | Seizures-scoliosis-macrocephaly Syndrome | Antley-Bixler Syndrome | Oguchi Disease-2 | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Martsolf Syndrome | Hemorrhage | Acne Vulgaris | Silicosis | Glycogen Storage Disease Type 1a | Hartnup Disease | Dysfibrinogenemia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | LEOPARD Syndrome | Stiff-man Syndrome | Panic Disorder | Coma | Lymphedema-distichiasis Syndrome | Congenital Bile Acid Synthesis Defect | Dubin-Johnson Syndrome | Tetanus | Adenosine Deaminase Deficiency | Mabry Syndrome | Spinocerebellar Ataxia Type 5 | Withdrawal Syndrome | Retinoblastoma | Malignant Fibrous Histiocytoma | Arthrogryposis | Hyperthyroidism | Fetal Akinesia Deformation Sequence | Hyperekplexia | Malaria | Basal Cell Nevus Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Epilepsy, Generalized | Systemic Lupus Erythematosus | Polymicrogyria | Chronic Granulomatous Disease | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Exotropia | Sickle Cell Anemia | Trigonocephaly | WAGR Syndrome | Farber Disease | Osteoporosis-pseudoglioma Syndrome | Localized Scleroderma | Hyperparathyroidism | Pierre Robin Syndrome | Plasmacytoma | Liver Diseases | Tinea Versicolor | Hydrocephalus, Normal Pressure | Erythromelalgia | Short-chain Acyl-CoA Dehydrogenase Deficiency | Coronary Heart Disease | Polyomavirus Nephropathy | Hamartoma | PHARC Syndrome | Glaucoma, Congenital | Spinal Cord Diseases | Astrocytoma, Anaplastic | Thrombotic Microangiopathy | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Papilledema | Temporal Lobe Epilepsy | Erysipelas | Familial Digital Arthropathy-brachydactyly | Cryopyrin-associated Periodic Syndromes | Anuria | Leprosy | Leri-Weill Dyschondrosteosis | Leukemia | Congenital Dyserythropoietic Anemia Type 4 | Cutaneous Mastocytosis | Brugada Syndrome 1 | Congenital Stromal Corneal Dystrophy | Epidermolysis Bullosa Simplex, Localized | Carcinoma, Merkel Cell | Tay-Sachs Disease | Feingold Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Language Disorders | Cavitary Optic Disc Anomalies | Congenital Primary Aphakia | Sclerocornea | Neural Tube Defect | Clouston Hidrotic Ectodermal Dysplasia | Axenfeld-Rieger Syndrome | Dent Disease | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Coffin-Siris Syndrome | Congenital Adrenal Hyperplasia | Knobloch Syndrome | Isovaleric Acidemia | Prolidase Deficiency | Sarcosinemia | Craniopharyngioma | Adenomyosis | Familial Isolated Hyperparathyroidism | Wagner Disease | Hypoalbuminemia | Fundus Albipunctatus | Focal Cortical Dysplasia Type 2 | Usher Syndrome Type II | Juvenile Xanthogranuloma | Kabuki Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Neutrophilia | Trismus-pseudocamptodactyly Syndrome | Rett Syndrome | Japanese Encephalitis | Ameloblastic Carcinoma | LRBA Deficiency | Congenital Disorders Of Glycosylation | Hypodontia | Epiphyseal Chondrodysplasia, Miura Type | Spinocerebellar Ataxia Type 14 | Esophageal Motility Disorders | Acromegaly | Rhabdomyosarcoma, Alveolar | Open-angle Glaucoma | Fibrosis | Guillain-Barre Syndrome | Sulfite Oxidase Deficiency | Exfoliative Dermatitis | Primary Lateral Sclerosis | Acromicric Dysplasia | Neurodegeneration With Brain Iron Accumulation | Common Cold | Amyloidosis | Myopia | Pontocerebellar Hypoplasia Type 7 | Spinocerebellar Ataxia Type 12 | Glutaric Aciduria Type 3 | Heart Block | Hereditary Pyropoikilocytosis | Smith-Lemli-Opitz Syndrome | Tonsillitis | Schwannomatosis | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Rubeosis Iridis | Asthma, Exercise-induced | Dermatitis Herpetiformis | Thalassemia, Beta | Coronary Restenosis | Brenner Tumor | Sick Sinus Syndrome 1 | Speech Disorders | Lung Diseases | Actinomycetoma | Toxic Epidermal Necrolysis | Tremor | Anorchia | Myosin Storage Myopathy | Malaria, Cerebral | Endometriosis | Bethlem Myopathy | Idiopathic Multicentric Castleman Disease | Diabetic Neuropathy | Hemochromatosis | Rotor Syndrome | 3C Syndrome | Hemimegalencephaly | Kidney Stones | Influenza | Purpura, Thrombotic Thrombocytopenic | Camurati-Engelmann Disease | Pulverulent Zonular Cataract | Adrenoleukodystrophy, X-linked | Pancreatitis, Chronic | Blepharo-cheilo-odontic Syndrome | Behcet's Disease | Papulopustular Rosacea | Stromal Corneal Dystrophy | Paget's Disease Of The Breast | Panuveitis | Waardenburg Syndrome Type 1 | Corneal Dystrophy | Primary Ovarian Insufficiency | Carney-Stratakis Syndrome | Peroxisomal Disorder | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Ornithine Transcarbamylase Deficiency | Fucosidosis | Specific Granule Deficiency | Adrenal Insufficiency | Salla Disease | Hemolytic Uremic Syndrome, Atypical | Cancer, Bladder | Lichen Sclerosus | Infantile Liver Failure Syndrome 1 | Heavy Chain Disease | Adenylosuccinate Lyase Deficiency | Spondyloperipheral Dysplasia | Echinococcosis | Gastric Atrophy | Chronic Inflammatory Demyelinating Polyneuropathy | Meleda Disease | Rift Valley Fever | Esthesioneuroblastoma | Neuroleptic Malignant Syndrome | Congestive Heart Failure | Omenn Syndrome | Acute Motor Axonal Neuropathy | Chronic Thromboembolic Pulmonary Hypertension | Combined Malonic And Methylmalonic Acidemia | Glaucomatocyclitic Crisis | Hyperlipidemia, Familial Combined | Cole-Carpenter Syndrome | Aldosteronism | Congenital Dyserythropoietic Anemia Type 1 | Neurofibromatosis-Noonan Syndrome | Pneumothorax | Chromosome 5q Deletion Syndrome | Familial Partial Lipodystrophy | Werner's Syndrome | Apert Syndrome | Hemosiderosis | Leishmaniasis, Cutaneous | Fukuyama Congenital Muscular Dystrophy | Hyperinsulinism-hyperammonemia Syndrome | Waardenburg Syndrome Type 2E | Neovascular Glaucoma | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Diabetes Mellitus, Transient Neonatal | Encephalocele | Cerebellar Ataxia, Cayman Type | Crouzon Syndrome With Acanthosis Nigricans | Alpha-mannosidosis | Poikiloderma With Neutropenia | Stargardt Disease | Renal Dysplasia | B-cell Chronic Lymphocytic Leukemia | Benign Hereditary Chorea | Duodenal Atresia | Inflammatory Linear Verrucous Epidermal Nevus | Erythropoietic Protoporphyria | Waldenstrom Macroglobulinemia | Skin Fragility-woolly Hair Syndrome | Necrobiosis Lipoidica | Hypocalcemia | Lipodystrophy | Agoraphobia | Dystonia Musculorum Deformans | Multiple Sclerosis, Relapsing-remitting | Pulmonary Veno-occlusive Disease | Hepatitis B, Chronic | Dengue Shock Syndrome | Restrictive Dermopathy | VEXAS Syndrome | Chromosome 8q21.11 Deletion Syndrome | 3-methylglutaconic Aciduria | Campomelic Dysplasia | Neurogenic Bladder | Myopathy | Corneal Dystrophies, Hereditary | Li-Fraumeni Syndrome | Thyroiditis | Fowler's Syndrome | Jacobsen Syndrome | Duchenne Muscular Dystrophy | Congenital Ichthyosiform Erythroderma | Pleural Tuberculosis | Rhinitis | Smoldering Myeloma | Vitamin D Deficiency | Carcinoma, Signet Ring Cell | Cri-du-chat Syndrome | Hepatic Veno-occlusive Disease | Gardner Syndrome | Wolfram Syndrome 2 | Amebiasis | Fontaine Progeroid Syndrome | Cleidocranial Dysplasia | Fibrosarcoma | Dystonia | Goldenhar Syndrome | Bone Marrow Necrosis | Myocardial Infarction | Occipital Neuralgia | Nephrotic Syndrome Type 1 | Moyamoya Disease | Generalized Epilepsy And Paroxysmal Dyskinesia | Vogt-Koyanagi-Harada Syndrome | Hyperphenylalaninemia | Pernicious Anemia | Nephrocalcinosis | Exostoses | Rhabdoid Tumor | IMAGe Syndrome | Postpartum Depression