Disease

Spinocerebellar Ataxia Type 31

About the Disease
Spinocerebellar Ataxia 31, also known as spinocerebellar ataxia type 31, is related to spinocerebellar ataxia 1 and spinocerebellar ataxia 6, and has symptoms including gait ataxia An important gene associated with Spinocerebellar Ataxia 31 is BEAN1 (Brain Expressed Associated With NEDD4 1). Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are dysarthria and gait ataxia

Common Targets
NOP56 | BEAN1

疾病靶点研报
Spinocerebellar Ataxia Type 31

Note: If you'd like to get a target analysis report for Spinocerebellar Ataxia Type 31, 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 Spinocerebellar Ataxia Type 31 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Mast Cell Leukemia | Hereditary Coproporphyria | Leiomyoma | Meconium Ileus | Glycogen Storage Disease Type 3 | Mucolipidosis Type IV | Non-small Cell Lung Cancer | Juvenile Myoclonic Epilepsy | Salla Disease | Agoraphobia | Porphyria | Cardiomyopathy, Peripartum | Congenital Stromal Corneal Dystrophy | Acne | Corneal Neovascularization | Diverticulitis | Hypoalbuminemia | Toxoplasmosis | Anovulation | Multiple Sclerosis | Pericarditis | Microcephaly | Enterocolitis, Necrotizing | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Cutaneous Mastocytosis | Herpes Simplex Dermatitis | Cardiac Sarcoidosis | Pulmonary Capillary Hemangiomatosis | Hyperuricemic Nephropathy, Familial Juvenile | Epidermolysis Bullosa Dystrophica | Imerslund-Grasbeck Syndrome | Coffin-Lowry Syndrome | Binge Eating Disorder | Amish Infantile Epilepsy Syndrome | Myocarditis | Benign Familial Neonatal Convulsions | Epithelioid Hemangioma | Cenani-Lenz Syndactyly Syndrome | Adenomatoid Tumor | Pearson Syndrome | Lymphoma, AIDS-related | Prader-Willi Syndrome | Thrombophlebitis | Double Outlet Right Ventricle | Dominant Optic Atrophy | Coronary Artery Disease | Giant Cell Glioblastoma | Rash | Premature Ejaculation | Hyperprolactinemia | Congenital Heart Defects | Hypertension, Pulmonary | Hepatic Steatosis | Marinesco-Sjogren Syndrome | Carotid Artery Disease | Optic Neuropathy, Anterior Ischemic | Polycystic Ovary Syndrome | Nicotine Addiction | Cohen Syndrome | Bloom Syndrome | Cerebrovascular Disorders | Dysfibrinogenemia | Periventricular Nodular Heterotopia | Niemann-Pick Disease, Type A | Endometriosis | Thalassemia | T-cell Chronic Lymphocytic Leukemia | Congenital Dyserythropoietic Anemia | Sleep Disorder | Central Pain Syndrome | Muscular Dystrophy | Phenylketonuria II | Chronic Idiopathic Myelofibrosis | Partington Syndrome | T-cell Leukemia | Colitis, Collagenous | Stomatitis | Esthesioneuroblastoma | Congenital Sodium Diarrhea | Primary Hyperoxaluria Type 3 | Conduct Disorder | Osteochondroma | Cardiomyopathy, Restrictive | Hydrolethalus Syndrome | Hemorrhage | Chronic Enteropathy Associated With SLCO2A1 Gene | Fundus Albipunctatus | Heimler Syndrome | Cutis Laxa | Chromosome 8q21.11 Deletion Syndrome | Autosomal Recessive Bestrophinopathy | Multiple Sclerosis, Secondary Progressive | Sleep Apnea, Central | Tracheal Disorders | Hydrocephalus | AIDS | Neuromyelitis Optica | Esophagitis, Eosinophilic | Hyperinsulinemia | Chondrodysplasia Punctata | Glutaric Aciduria Type 2 | 3C Syndrome | Potocki-Shaffer Syndrome | Jaundice, Obstructive | Fatty Aldehyde Dehydrogenase Deficiency | Hepatitis C, Chronic | Glaucomatocyclitic Crisis | Hypermetropia | DICER1 Syndrome | Diastrophic Dysplasia | Cri-du-chat Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Sertoli Cell-only Syndrome | Cancer, Breast | Chitayat Syndrome | Spondyloperipheral Dysplasia | Common Variable Immunodeficiency | Erythromelalgia | Brenner Tumor | Prolymphocytic Leukemia | Granular Corneal Dystrophy Type 1 | Microtia | Tetanus | Hydrocephalus, Normal Pressure | Carpal Tunnel Syndrome | Keratosis, Actinic | Primary Progressive Aphasia | Spinocerebellar Ataxia Type 7 | Mitochondrial Cytopathy | Asthma, Nocturnal | Pitt-Hopkins Syndrome | Tendinopathy | Porphyria Cutanea Tarda | Progressive Familial Intrahepatic Cholestasis Type 1 | Epidermolysis Bullosa Simplex | Waardenburg Syndrome Type 2 | Purpura | Tangier Disease | Lesch-Nyhan Syndrome | Small Lymphocytic Lymphoma | Kleine-Levin Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Hemorrhoids | Biotinidase Deficiency | Netherton Syndrome | Bethlem Myopathy | Neurodevelopmental Disorders | Autoimmune Disease | Auriculocondylar Syndrome | Lissencephaly 2 | Spinocerebellar Ataxia Type 27 | Diabetes | Hemochromatosis Type 1 | Ichthyosis | Spinocerebellar Ataxia Type 17 | Coloboma | Congenital Lipoid Adrenal Hyperplasia | Clouston Hidrotic Ectodermal Dysplasia | Basal Cell Nevus Syndrome | Meningioma | Cornelia De Lange Syndrome | Congenital Torticollis | Kindler Syndrome | Sarcoma, Alveolar Soft Part | Sarcosinemia | Pheochromocytoma | Primary Biliary Cholangitis | Focal Cortical Dysplasia Type 2 | Arthritis, Reactive | Malnutrition | Thrombosis | Birk-Barel Syndrome | Schizophrenia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Tietze Syndrome | Narcolepsy | Histoplasmosis | Herpes Genitalis | Skin Fragility-woolly Hair Syndrome | Birt-Hogg-Dube Syndrome | Protein C Deficiency | Mucolipidosis Type III | 3-methylglutaconic Aciduria | Crimean-Congo Hemorrhagic Fever | Corneal Edema | Enlarged Vestibular Aqueduct | Congenital Absence Of Vas Deferens | Infantile Liver Failure Syndrome 1 | Fibrodysplasia Ossificans Progressiva | Vascular Cognitive Impairment | Raynaud Phenomenon | Diffuse Palmoplantar Keratoderma | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Atrial Septal Defect | Hernia, Inguinal | Malaria, Cerebral | Androgenic Alopecia | Charcot-Marie-Tooth Disease, Type 2A | Keratocystic Odontogenic Tumor | Anosmia, Congenital | Keratopathy | Pilomatrix Carcinoma | Compartment Syndrome | Trichorhinophalangeal Syndrome | Oculocutaneous Albinism Type 2 | Adenomyosis | Polymyositis | Hepatitis | Adrenoleukodystrophy, X-linked | Fahr Disease | Antisocial Personality Disorder | Scleroderma, Diffuse | Pure Autonomic Failure | Spitzoid Melanoma | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Neurofibromatosis Type 2 | Triphalangeal Thumb-polysyndactyly Syndrome | Acute Generalized Exanthematous Pustulosis | Iron Deficiency Anemia | Benign Familial Pemphigus | Nance-Horan Syndrome | Von Hippel-Lindau Disease | Mesothelioma, Malignant | Benign Hereditary Chorea | Glycogen Storage Disease Type 5 | Non-Hodgkin Lymphoma | Thrombophilia | Infertility | Restless Legs Syndrome | Schizencephaly | Hashimoto Thyroiditis | B-cell Chronic Lymphocytic Leukemia | Spinal And Bulbar Muscular Atrophy | Absence Epilepsy | Hepatitis B, Chronic | Rhabdomyosarcoma, Alveolar | Constipation | Hypohidrotic Ectodermal Dysplasia, X-linked | Reticular Dysgenesis | TARP Syndrome | Oculocutaneous Albinism Type 1 | Renal-hepatic-pancreatic Dysplasia | Aldosterone Deficiency | Muscle Wasting | Infantile Nephropathic Cystinosis | Cerebral Amyloid Angiopathy | Prolactinoma | Strabismus | Congenital Primary Aphakia | Infantile Neuroaxonal Dystrophy | Multiple Sclerosis, Relapsing-remitting | Nail-Patella Syndrome | Osteonecrosis | Giant Axonal Neuropathy | Rosacea | Arthropathy | Niemann-Pick Disease, Type C | Low Phospholipid Associated Cholelithiasis | Non-epidermolytic Palmoplantar Keratoderma | Primary Familial Brain Calcification | Gastritis, Atrophic | Still Disease | Pleomorphic Xanthoastrocytoma | Familial Hypertrophic Cardiomyopathy | Pompe Disease | Heterotopic Ossification | Follicular Dendritic Cell Sarcoma | Apraxia | Choriocarcinoma | Renal Hypouricemia | Renal Tubular Acidosis | Xeroderma Pigmentosum | Anemia | Jawad Syndrome | Lymphedema-distichiasis Syndrome | Pemphigus | Acrodysostosis | Myosin Storage Myopathy | Camptocormia | Intracranial Hypertension | Macrophagic Myofasciitis | Ichthyosis Bullosa Of Siemens | Superficial Spreading Melanoma | Autism | Thyroiditis, Autoimmune | Glioblastoma Multiforme | Bipolar Disorder | Macular Degeneration | Mastitis | Intracerebral Hemorrhage | Poretti-Boltshauser Syndrome | Hepatitis, Chronic | Focal Segmental Glomerulosclerosis | Atopy | WAGR Syndrome | Hypertension, Essential | Autosomal Recessive Congenital Ichthyosis | Sialidosis | Poirier-Bienvenu Neurodevelopmental Syndrome | Otosclerosis | Cholelithiasis | Glutaric Aciduria Type 1 | Urofacial Syndrome | Stroke, Ischemic | Congenital Dyserythropoietic Anemia Type 1 | Hyperinsulinemic Hypoglycemia | Early Infantile Epileptic Encephalopathy 13 | Hypoparathyroidism | Vici Syndrome | Tonsillitis | Diarrhea | Spondyloepiphyseal Dysplasia Tarda, X-linked | Congenital Myasthenic Syndrome | Chloridorrhea, Congenital | Mucormycosis | Charcot-Marie-Tooth Disease, Type 1A | Cholecystitis | Rett Syndrome | Paraganglioma, Carotid Body | Nicotine Dependence | Optic Atrophy 2 | Smith-Kingsmore Syndrome | Hereditary Elliptocytosis | Hereditary Multiple Exostoses | Retinitis | Usher Syndrome Type III | Retinitis Pigmentosa | Tardive Dyskinesia | Nephrotic Syndrome | Larsen Syndrome | Vitamin A Deficiency | McKusick Type Metaphyseal Chondrodysplasia | Cerebrotendinous Xanthomatosis | Cerebellofaciodental Syndrome | Chronic Mucocutaneous Candidiasis | Chanarin-Dorfman Syndrome | Ameloblastic Carcinoma | Neuronal Ceroid Lipofuscinosis | Facioscapulohumeral Muscular Dystrophy | Glycogen Storage Disease Type 9 | Ichthyosis Hystrix, Curth-Macklin Type | Down Syndrome | Ataxia-ocular Apraxia 2 | Renal Tubular Dysgenesis | Hypersensitivity Pneumonitis | Parvovirus B19 Infection | Spastic Paraplegia Type 7 | Diabetic Encephalopathy | Contact Dermatitis | Fetal Alcohol Syndrome | Primary Erythromelalgia | Frank-ter Haar Syndrome | Familial Pheochromocytoma-paraganglioma | Aphasia | Farber Disease | Cervicitis | Hypertriglyceridemia | Familial Hyperaldosteronism | Tinea | Acute Lymphocytic Leukemia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Addison Disease | Spinocerebellar Ataxia Type 8 | Paracoccidioidomycosis | Sjogren Syndrome | Creutzfeldt-Jakob Disease | Kohlschutter-Tonz Syndrome | Androgen Insensitivity | Fascioliasis | Myasthenia | Polyomavirus Nephropathy | Hypophosphatasia | Transient Bullous Dermolysis Of The Newborn | Aceruloplasminemia | Polymicrogyria | Meesmann Corneal Dystrophy | Rhabdoid Tumor | Dystonia | Progressive Encephalopathy-optic Atrophy Syndrome | Chylomicron Retention Disease | Anal Fissure | CREST Syndrome | Hypoplastic Left Heart Syndrome | Alcoholism | Gilbert Syndrome | Kashin-Beck Disease | Trigonocephaly | Disseminated Superficial Actinic Porokeratosis | Familial Cerebral Amyloid Angiopathy | Multiple Hamartoma Syndrome | Retinal Detachment | Necrotizing Autoimmune Myopathy | Nager Acrofacial Dysostosis | Rheumatoid Arthritis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Perivascular Epithelioid Cell Tumor | Sepiapterin Reductase Deficiency | Lactose Intolerance | Vogt-Koyanagi-Harada Syndrome