Spinocerebellar Ataxia Type 42

About the Disease
Spinocerebellar Ataxia 42, also known as spinocerebellar ataxia type 42, is related to spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits and hereditary ataxia. An important gene associated with Spinocerebellar Ataxia 42 is CACNA1G (Calcium Voltage-Gated Channel Subunit Alpha1 G). Affiliated tissues include spinal cord, cerebellum and eye, and related phenotypes are dysarthria and unsteady gait

Common Targets
CACNA1G

Note: If you'd like to get a target analysis report for Spinocerebellar Ataxia Type 42, 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 42 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Schnyder Crystalline Corneal Dystrophy | Cervical Dystonia | Proximal Symphalangism | Schizotypal Personality Disorder | Diabetic Encephalopathy | Spinocerebellar Ataxia Type 27 | Urea Cycle Disorder | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Gout | Oculocutaneous Albinism Type 1 | Encephalocele | Hydrocephalus | Meckel-Gruber Syndrome | Lymphedema | Neuromuscular Disorders | Keratoacanthoma | Echinococcosis | Oculopharyngeal Muscular Dystrophy | Trigonocephaly | Retinal Telangiectasia | Synpolydactyly | Pre-eclampsia | Ichthyosis Hystrix, Curth-Macklin Type | Demyelinating Diseases | Osteochondroma | Tyrosinemia Type 2 | Thalassemia, Beta | HANAC Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Pachyonychia Congenita | Malaria | Cardiomyopathy, Dilated, 1L | Left Ventricular Noncompaction | Sarcoidosis, Pulmonary | AIDS Dementia Complex | Charcot-Marie-Tooth Disease Type 4D | Graves Disease | Vitamin D Deficiency | Proctitis | Liver Failure | Transthyretin-related Amyloidosis | Cancer, Skin | Pituitary Dwarfism | Polyarteritis Nodosa | Niemann-Pick Disease, Type A | Neuroleptic Malignant Syndrome | Chorea | Tricho-hepato-enteric Syndrome | Small Lymphocytic Lymphoma | Retinal Degeneration | Trichuriasis | Juvenile Myoclonic Epilepsy | Cranial Nerve Disease | Pathological Gambling | Pleomorphic Xanthoastrocytoma | Dominant Optic Atrophy | Epilepsy, Generalized | Wieacker-Wolff Syndrome | Motor Neuron Diseases | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Precocious Puberty | Omenn Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Familial Episodic Pain Syndrome | Glycogen Storage Disease Type 5 | Pemphigus | Cutis Laxa | Vestibular Disease | Acute Coronary Syndrome | Leber Congenital Amaurosis | Tyrosinemia Type 1 | Spinocerebellar Ataxia Type 16 | Meier-Gorlin Syndrome | Obesity | Hyperuricemia | Panniculitis | Sporadic Hemiplegic Migraine | Agoraphobia | Ischemia | Alkaptonuria | Keratopathy | Myoclonus-dystonia Syndrome | Cryptococcal Meningitis | Lipid Storage Diseases | MIRAGE Syndrome | Osteosclerosis | Micro Syndrome | Acromicric Dysplasia | Primary Aldosteronism | Lesch-Nyhan Syndrome | Thrombosis | Maternally Inherited Diabetes And Deafness | Rhinitis | Farber Disease | Bethlem Myopathy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Aplasia Cutis Congenita | Ocular Albinism Type 1 | Tangier Disease | Woodhouse-Sakati Syndrome | Botulism | Choroiditis | Fraser Syndrome | Lattice Corneal Dystrophy | Paroxysmal Nocturnal Hemoglobinuria | Melanoma | Renal Hypomagnesemia 3 | Achromatopsia | Torticollis | Autoimmune Polyendocrine Syndrome | Tumoral Calcinosis | Norrie Disease | Mandibuloacral Dysplasia With Type A Lipodystrophy | Esophageal Motility Disorders | Lymphomatoid Granulomatosis | 3-methylglutaconic Aciduria Type IV | Aspartylglycosaminuria | Scabies | Cellulitis | Spondylosis | Atopic Dermatitis | Bladder Exstrophy | Uterine Leiomyoma | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Dental Caries | Chondrodysplasia Punctata 1, X-linked Recessive | Ovarian Hyperstimulation Syndrome | Congenital Nystagmus | Acute Lung Injury | Nephrosclerosis | Arthritis, Gouty | Emery-Dreifuss Muscular Dystrophy | GNE Myopathy | Nicolaides-Baraitser Syndrome | Ectodermal Dysplasia | Osteoporosis-pseudoglioma Syndrome | Stickler Syndrome | Diarrhea | Duodenal Atresia | Leukoplakia | Lymphangioma | Hereditary Folate Malabsorption | Amyloidosis | 5-oxoprolinase Deficiency | Bare Lymphocyte Syndrome | Polymyositis | Lymphedema-distichiasis Syndrome | Keratoconjunctivitis | Crouzon Syndrome With Acanthosis Nigricans | Prediabetes | Hepatorenal Syndrome | Pneumonia, Viral | Teratozoospermia | Asphyxia Neonatorum | Smoldering Myeloma | Glycogen Storage Disease Type 4 | Purpura | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Relapsing Polychondritis | Hydrolethalus Syndrome | COACH Syndrome | Myoclonic Atonic Epilepsy | Schwartz-Jampel-Aberfeld Syndrome | Otosclerosis | Cancer, Lung | Adams-Oliver Syndrome | Achondrogenesis | Ileitis | Mabry Syndrome | Pituitary Disorders | Diabetes Type 1 | Hepatitis D | Familial Partial Lipodystrophy | Spermatocele | Dysfibrinogenemia | Branchiootorenal Syndrome | 3-M Syndrome | Whipple's Disease | Hypercholesterolemia, Familial | Aneurysm, Abdominal Aortic | Asplenia | Spinocerebellar Ataxia | Mitochondrial Encephalomyopathy | Coffin-Siris Syndrome | Mucolipidosis Type III | IgA Deficiency | Analgesia | Renpenning Syndrome | Mucolipidosis Type IV | Centronuclear Myopathy | Motion Sickness | Situs Inversus | Trichorhinophalangeal Syndrome | Angioimmunoblastic T-cell Lymphoma | Cyst | Stromal Corneal Dystrophy | Retinoschisis | Parkinsonism | Platelet Disorders | Rothmund-Thomson Syndrome | Pulmonary Sclerosing Hemangioma | Waldenstrom Macroglobulinemia | Usher Syndrome | Epidermolysis Bullosa Simplex | Proteasome-associated Autoinflammatory Syndrome 2 | Combined Deficiency Of Factor V And Factor VIII | X-linked Acrogigantism | Charcot-Marie-Tooth Disease Type 3 | Bartsocas-Papas Syndrome | Myositis | Anti-glomerular Basement Membrane Disease | Pontocerebellar Hypoplasia | Goiter, Nodular | Roberts Syndrome | Glucagonoma | Aldosterone Deficiency | Protein C Deficiency | Lichen Planus | Exostoses | Hypopituitarism | Esophageal Adenocarcinoma | Cabezas Syndrome | Sclerosing Cholangitis | Progressive External Ophthalmoplegia | Autoimmune Polyendocrinopathy Syndrome Type I | Spinocerebellar Ataxia Type 13 | Spinal And Bulbar Muscular Atrophy | Dysferlinopathy | Spondylolisthesis | Sarcoma | Discoid Lupus Erythematosus | Tonsillitis | Asperger Syndrome | Primary Progressive Aphasia | Spinocerebellar Ataxia Type 1 | Empyema | Charcot-Marie-Tooth Disease Type 2T | Basal Cell Nevus Syndrome | Walker-Warburg Syndrome | Sulfite Oxidase Deficiency | Hyperbilirubinemia, Neonatal | Nemaline Myopathy 10 | Chronic Leukemia | Chorea-acanthocytosis | Medulloblastoma | Anorectal Fistula | Distal Myopathy 2 | Gardner Syndrome | Hyperkalemic Periodic Paralysis | Mitochondrial DNA Depletion Syndrome | Diabetic Nephropathy | Myotonia | Diffuse Intrinsic Pontine Glioma | Charcot-Marie-Tooth Disease, Type 1A | Autism | Congenital Hemolytic Anemia | Sleep Apnea, Obstructive | Cardiomyopathy, Hypertrophic | Primary Torsion Dystonia | Paraganglioma | Pleural Tuberculosis | Blepharophimosis Syndrome | Genee-Wiedemann Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Tyrosine Hydroxylase Deficiency | Congenital Heart Defects | Coronary Restenosis | C3 Glomerulonephritis | Colitis | Osteochondrosis | Acne | Multiple Hamartoma Syndrome | Corneal Neovascularization | Erythematotelangiectatic Rosacea | Thyroid Hormone Resistance | Hypertension, Pulmonary | Ebstein Anomaly | Greenberg Dysplasia | Colon Adenoma | Short-chain Acyl-CoA Dehydrogenase Deficiency | Reye Syndrome | McCune-Albright Syndrome | Kleine-Levin Syndrome | Argininosuccinic Aciduria | Granular Corneal Dystrophy Type 1 | Venous Insufficiency | Spinocerebellar Ataxia Type 17 | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Adenoma, Pituitary | Retinitis Pigmentosa 3 | Anterior Segment Dysgenesis | Dent Disease | Hemochromatosis Type 2 | Cancer, Brain | Bruck Syndrome | Schnitzler Syndrome | Impulse Control Disorder | Perry Syndrome | Acute Tubular Necrosis | Dystonia Musculorum Deformans | Facioscapulohumeral Muscular Dystrophy | Thrombasthenia | Cryptorchidism | Acne Vulgaris | Cri-du-chat Syndrome | Stuttering | Hepatic Veno-occlusive Disease | Infantile Nephropathic Cystinosis | Subacute Sclerosing Panencephalitis | Cancer, Bladder | Adrenomyeloneuropathy | Hennekam Lymphangiectasia-lymphedema Syndrome | Sitosterolemia | Tuberculous Meningitis | Barrett Esophagus | Hereditary Elliptocytosis | Vasculitis | Sturge-Weber Syndrome | Hypotrichosis | Generalized Epilepsy And Paroxysmal Dyskinesia | Hypersomnia | Restless Legs Syndrome | Congenital Hereditary Endothelial Dystrophy Type I | Conduct Disorder | Raynaud Phenomenon | Microcephaly, Seizures, And Developmental Delay | IgA Nephropathy | Hemophilia | Arteriovenous Malformations | Osteonecrosis | Diabetes Insipidus, Neurogenic | Phenylketonuria | Wiskott-Aldrich Syndrome | Hyperinsulinemic Hypoglycemia | Nicotine Addiction | Cataplexy | Progressive Myoclonic Epilepsy | Myhre Syndrome | Sepiapterin Reductase Deficiency | Chronic Thromboembolic Pulmonary Hypertension | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Neurodegeneration With Brain Iron Accumulation | Renal Tubular Acidosis | Charcot-Marie-Tooth Disease Type 4 | Cold-induced Sweating Syndrome | Megaloblastic Anemia | Renal Dysplasia | Pyloric Stenosis, Infantile Hypertrophic | Leukemia-lymphoma, Adult T-cell | Hereditary Multiple Exostoses | Campomelic Dysplasia | Diabetes Mellitus, Transient Neonatal | Aicardi-Goutieres Syndrome | Gastritis | Hyperlipidemia | Chondrodysplasia Punctata | Abetalipoproteinemia | Trichomegaly | Disseminated Superficial Actinic Porokeratosis | Peutz-Jeghers Syndrome | Phenylketonuria II | Cocaine-Related Disorders | Waardenburg Syndrome Type 2A | Glutathione Synthetase Deficiency | Blood Protein Disorders | Avian Influenza | Dysmorphophobia | Familial Male-limited Precocious Puberty | Rheumatic Heart Disease | Metatropic Dysplasia | Takenouchi-Kosaki Syndrome | Dermatomyositis | Progressive Familial Intrahepatic Cholestasis | Spinocerebellar Ataxia Type 42 | Depression | Silver-Russell Syndrome | Schuurs-Hoeijmakers Syndrome | Pseudohermaphroditism | Hypophosphatasia | Congenital Adrenal Hyperplasia 1 | Myasthenia | High Molecular Weight Kininogen Deficiency | Keratosis, Actinic | Yellow Fever | Pure Autonomic Failure | Hemochromatosis | Epidermolysis Bullosa Acquisita | Polycythemia Vera | Acrodermatitis | Vitamin K Deficiency | Alpers Syndrome | Multiple Sclerosis, Chronic Progressive | Cervicitis | Angiomyolipoma | Periodontitis | Eiken Syndrome | Insulin Resistance | Cirrhosis | Familial Digital Arthropathy-brachydactyly