Migraine
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

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.tech.
Other Diseases
T-cell Leukemia | Hyperlipidemia Type V | Walker-Warburg Syndrome | Best Macular Dystrophy | Headache | Retinitis Pigmentosa 3 | Gilbert Syndrome | Infectious Diarrhea | Hyperglycemia | Esophageal Carcinoma | Benign Recurrent Intrahepatic Cholestasis 1 | Cancer, Kidney | Skin Carcinoma | Parvovirus B19 Infection | Myasthenia Gravis | Hereditary Coproporphyria | Crohn's Disease | Glaucoma, Congenital | Pulmonary Vein Stenosis | Malonyl-CoA Decarboxylase Deficiency | Microcephaly | Diabetes Type 1 | Dwarfism | Calcium Pyrophosphate Deposition Disease | Charcot-Marie-Tooth Disease, Type 2C | Dengue Shock Syndrome | Strabismus | Smith-Lemli-Opitz Syndrome | Retinal Telangiectasia | Diffuse Palmoplantar Keratoderma | Giant Cell Glioblastoma | Niemann-Pick Disease, Type A | Astigmatism | Acne | Congenital Dyserythropoietic Anemia | Fragile X Syndrome | Keratitis | Neurodegeneration With Brain Iron Accumulation | High Molecular Weight Kininogen Deficiency | Meier-Gorlin Syndrome | Granular Corneal Dystrophy Type 1 | Chediak-Higashi Syndrome | Meckel-Gruber Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Craniofrontonasal Syndrome | Pathological Gambling | Hereditary Sensory And Autonomic Neuropathy | Alopecia Totalis | IMAGe Syndrome | Primary Carnitine Deficiency | Pulmonary Tuberculosis | Bursitis | Waardenburg Syndrome Type 2 | Trichotillomania | FG Syndrome | Pneumonia, Bacterial | Veno-occlusive Disease | Obesity, Morbid | Congenital Ichthyosiform Erythroderma | Shwachman-Bodian-Diamond Syndrome | Vitamin B12 Deficiency | Nanophthalmos | Hypermethioninemia | Unverricht-Lundborg Syndrome | Carcinoid Syndrome | Encephalopathy, Hepatic | Familial Digital Arthropathy-brachydactyly | Hemosiderosis | Alexander Disease | Aceruloplasminemia | Syndactyly | Bladder Exstrophy | Schizophrenia | Werner's Syndrome | Alagille Syndrome | Autoimmune Disease | Molybdenum Cofactor Deficiency | Polycystic Kidney, Autosomal Dominant | Myositis | Menkes Disease | Pheochromocytoma | Thrombophilia | Cryptosporidiosis | Intestinal Hypomagnesemia 1 | Cryopyrin-associated Periodic Syndromes | Chronic Neutrophilic Leukemia | Bare Lymphocyte Syndrome | Twin-to-twin Transfusion Syndrome | Cyst | Porphyria | Neural Tube Defect | Retinopathy, Diabetic | Familial Episodic Pain Syndrome | Aplasia Cutis Congenita | Meesmann Corneal Dystrophy | Macrophagic Myofasciitis | Clouston Hidrotic Ectodermal Dysplasia | Tyrosine Hydroxylase Deficiency | Renal Tubular Acidosis | Hereditary Pyropoikilocytosis | Congenital Adrenal Hyperplasia | Myotonia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Angina Pectoris | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Trigonocephaly | Phosphoglycerate Dehydrogenase Deficiency | Dysthymia | Pure Autonomic Failure | Overactive Bladder | Leishmaniasis, Visceral | Pseudohypoparathyroidism Type 1A | Woodhouse-Sakati Syndrome | TARP Syndrome | Schwannomatosis | Corneal Neovascularization | Nestor-Guillermo Progeria Syndrome | Myelomeningocele | Canavan Disease | Barakat Syndrome | Hemorrhage | Dystonia-parkinsonism, X-linked | Lipid Storage Diseases | Methemoglobinemia Type IV | Teratozoospermia | Chromosome 16p11.2 Deletion Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Open-angle Glaucoma | Amyotrophic Lateral Sclerosis | Vestibular Disease | Glioblastoma | Beare-Stevenson Syndrome | Spinocerebellar Ataxia Type 3 | Trimethylaminuria | Swine Influenza | Cluster Headache | Relapsing Polychondritis | Hemangioendothelioma | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Small Lymphocytic Lymphoma | Congenital Fiber-type Disproportion Myopathy | Hydronephrosis | Familial Glucocorticoid Deficiency | Gitelman Syndrome | Subcortical Band Heterotopia | Myopathy | Epiphyseal Chondrodysplasia, Miura Type | Vaginitis | Renal Hypouricemia | Dysfibrinogenemia | Seasonal Mood Disorder | Acral Lentiginous Melanoma | Sclerosteosis | Mucolipidosis Type II | Hepatitis C, Chronic | Venous Insufficiency | Inflammatory Myopathy | PASLI Disease | Heroin Dependence | Chloridorrhea, Congenital | Sialidosis | Hypertensive Nephropathy | Birt-Hogg-Dube Syndrome | Osteopetrosis | Pierson Syndrome | Lymphoproliferative Disorders | Donnai-Barrow Syndrome | Klippel-Feil Syndrome | Bartsocas-Papas Syndrome | Epithelioid Hemangioma | Acanthosis Nigricans | Pouchitis | Cryoglobulinemia | Hartsfield Syndrome | Neurocutaneous Melanocytosis | C3 Glomerulonephritis | Mucormycosis | Leukoplakia, Oral | Congenital Mirror Movements | Gangliosidosis | Retinoblastoma | Peritonitis | Central Retinal Artery Occlusion | Diabetes Insipidus | Disseminated Intravascular Coagulation | Spondylosis | Protein C Deficiency | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Porphyria, Acute Intermittent | Hidradenitis | Hypogammaglobulinemia | Hypodontia | Binge Eating Disorder | Insulinoma | Basal Cell Nevus Syndrome | Greig Cephalopolysyndactyly Syndrome | Charcot-Marie-Tooth Disease Type 2E | Spinocerebellar Ataxia Type 20 | Schwannoma | Interstitial Lung Diseases | Hyperthyroidism | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Deafness, Dystonia, And Cerebral Hypomyelination | Carney Triad | Narcolepsy | Primary Cutaneous Amyloidosis | Hypothyroidism | Panuveitis | Bardet-Biedl Syndrome | Hypercholesterolemia, Familial | Absence Epilepsy | Panic Disorder | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Parkinson's Disease | Proopiomelanocortin Deficiency | Persistent Hyperplastic Primary Vitreous | Vitreoretinopathy, Proliferative | Hydrocephalus | Schizencephaly | Enlarged Vestibular Aqueduct | Osteonecrosis Of The Jaw | Posterior Polar Cataract | Periodontitis | Hemolytic Anemia | Multiple Hamartoma Syndrome | Acute Tubular Necrosis | Skin Fragility-woolly Hair Syndrome | Coma | Insulin Resistance | Premature Ejaculation | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Parkinsonism | Juvenile Xanthogranuloma | Heterotopic Ossification | Cramp Fasciculation Syndrome | Retinal Diseases | Hypokalemic Periodic Paralysis | LRBA Deficiency | Endocarditis | Cousin Syndrome | Alopecia | Rickets | Poretti-Boltshauser Syndrome | Oligodendroglioma | Anorectal Fistula | Autosomal Recessive Bestrophinopathy | Syncope | IgA Deficiency | Otitis Media | Ependymoma | Lymphangioma | Cutaneous Lupus Erythematosus | Chorioretinitis | Congenital Stromal Corneal Dystrophy | Botulism | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Tylosis With Esophageal Cancer | Paracoccidioidomycosis | Immunoproliferative Disorders | Myofibrillar Myopathy | 3-methylglutaconic Aciduria | Tracheal Disorders | Encephalocele | Hepatitis D | Proteus Syndrome | Spondylo-ocular Syndrome | Pterygium | Specific Granule Deficiency | Blue Nevus | Osmotic Demyelination Syndrome | Castleman Disease | Ectodermal Dysplasia | Hereditary Spherocytosis | Choroideremia | Vitamin D Deficiency | Keloid | Trichuriasis | Zollinger-Ellison Syndrome | Gardner Syndrome | Exocrine Pancreatic Insufficiency | Spastic Paraplegia Type 7 | Gaucher Disease | Congenital Sodium Diarrhea | Congenital Bile Acid Synthesis Defect | Costello Syndrome | T-cell Prolymphocytic Leukemia | Plasma Cell Leukemia | Cholestasis, Intrahepatic | Cryptococcal Meningitis | Thyroiditis, Autoimmune | Cataplexy | Encephalopathy, Ethylmalonic | Obsessive-compulsive Disorder | Adenomyosis | Nicolaides-Baraitser Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Urofacial Syndrome | Hypotonia-cystinuria Syndrome | Sarcoidosis | Spinocerebellar Ataxia Type 17 | Progressive Myoclonic Epilepsy | Shprintzen-Goldberg Syndrome | Farber Disease | Glutaric Aciduria Type 2 | Alzheimer Disease, Late Onset | Congenital Myopathy | Esotropia | Porokeratosis | Megalencephaly | Kaposiform Hemangioendothelioma | Osteoporosis-pseudoglioma Syndrome | Sweet Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Glycogen Storage Disease Type 9 | Patent Ductus Arteriosus | Constipation | Coronary Restenosis | HANAC Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Pfeiffer Syndrome | Arthritis | Ollier Disease | Combined Deficiency Of Factor V And Factor VIII | Neurodermatitis | Familial Hemiplegic Migraine | Chondrodysplasia Punctata | Methemoglobinemia | Prostatitis | Colon Adenoma | Hypotrichosis | Charcot-Marie-Tooth Disease | Esophageal Motility Disorders | Acrodermatitis | Hepatitis, Chronic | Autosomal Recessive Spastic Paraplegia Type 54 | Blastoma, Pleuropulmonary | Hyperbilirubinemia, Neonatal | Harlequin Ichthyosis | Hepatic Veno-occlusive Disease | Nephrotic Syndrome | Rheumatic Heart Disease | Hemorrhoids | Congenital Generalized Lipodystrophy | Antithrombin III Deficiency | Li-Fraumeni Syndrome | Tonsillitis | Dubin-Johnson Syndrome | Phenylketonuria | Spinocerebellar Ataxia Type 23 | Spinocerebellar Ataxia Type 15 | Stiff-man Syndrome | Encephalitis, Tick-borne | Mucolipidosis | Larsen Syndrome | Congenital Heart Defects | Schaaf-Yang Syndrome | LEOPARD Syndrome | Kearns-Sayre Syndrome | Hemochromatosis Type 1 | Phenylketonuria II | Pemphigus | Progressive Encephalopathy-optic Atrophy Syndrome | Birk-Barel Syndrome | Cystitis, Interstitial | Corneal Ulcer | Camptocormia | Diabetes Type 2 | Spinocerebellar Ataxia Type 42 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Spitz Nevus | Sleep Apnea | Retinitis Pigmentosa | Pontocerebellar Hypoplasia Type 7 | Paroxysmal Nocturnal Hemoglobinuria | Erectile Dysfunction | Cholestasis | Primary Aldosteronism | Sjogren Syndrome | Fascioliasis | Cherubism | Primary Ovarian Insufficiency | Nijmegen Breakage Syndrome | Astrocytoma | Familial Hypobetalipoproteinemia | Progressive External Ophthalmoplegia | Acute Chest Syndrome | Stuttering | Temporal Lobe Epilepsy | Oculocutaneous Albinism Type 2 | Methylmalonic Acidemia | Coronary Artery Disease | Hyperacusis | CREST Syndrome | Renal Hypomagnesemia 3 | Fanconi Anemia | Spasticity | Polycythemia Vera | Spinal Muscular Atrophy Type 2 | Herpes Genitalis