Disease

Alveolar Soft Part Sarcoma

About the Disease
Alveolar Soft Part Sarcoma, also known as asps, is related to sarcoma and connective tissue benign neoplasm. An important gene associated with Alveolar Soft Part Sarcoma is ASPSCR1 (ASPSCR1 Tether For SLC2A4, UBX Domain Containing), and among its related pathways/superpathways are Mesenchymal Stem Cells and Lineage-specific Markers and Type 2 papillary renal cell carcinoma. The drugs Dacarbazine and Ifosfamide have been mentioned in the context of this disorder. Affiliated tissues include lung, liver and brain, and related phenotypes are alveolar soft part sarcoma and no effect

Common Targets
PDGFRB | FLT4 | CTLA4 | KDR | TOP2A | Fibroblast Growth Factor Receptor (FGFR) (nonspecified subtype) | G5133 | G29126

疾病靶点研报
Alveolar Soft Part Sarcoma

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

Other Diseases

Chondromyxoid Fibroma | Myosin Storage Myopathy | Migraine | Ectrodactyly | Gangliosidosis, GM1 | Niemann-Pick Disease, Type C | Papillorenal Syndrome | Bacterial Meningitis | Apert Syndrome | Diabetic Neuropathy | Pseudo-pseudohypoparathyroidism | Glycogen Storage Disease Type 1a | Saul-Wilson Syndrome | Micropenis | Lymphangioma | Relapsing Polychondritis | Ocular Surface Squamous Neoplasia | Necrotizing Autoimmune Myopathy | DEND Syndrome | Skin Fragility-woolly Hair Syndrome | Spinocerebellar Ataxia Type 10 | Pancreatitis | CEDNIK Syndrome | Papillon-Lefevre Syndrome | Sarcoidosis, Pulmonary | Netherton Syndrome | Huntington's Disease-like 2 | Tetraplegia | Polymyositis | Parkinsonism | Congenital Stationary Night Blindness | Fontaine Progeroid Syndrome | Hypertension, Renovascular | Hypokalemic Periodic Paralysis | Malaria, Cerebral | Mycosis Fungoides | Neurocutaneous Melanocytosis | Maple Syrup Urine Disease | Hepatic Adenomatosis | Babesiosis | KBG Syndrome | Stroke, Hemorrhagic | Low Tension Glaucoma | Lateral Meningocele Syndrome | Congenital Aniridia | AIDS Dementia Complex | Pulverulent Zonular Cataract | Xeroderma Pigmentosum Variant Type | Epidermolysis Bullosa | Hypotrichosis | Congenital Hypofibrinogenemia | Chronic Myeloid Leukemia | Persistent Hyperplastic Primary Vitreous | Panic Disorder | Erythromelalgia | Conn Syndrome | Usher Syndrome Type III | Menetrier Disease | Gyrate Atrophy Of The Choroid And Retina | Renal Hypouricemia | Hypohidrotic Ectodermal Dysplasia, X-linked | Erythema Multiforme | Facioscapulohumeral Muscular Dystrophy Type 1 | Ischemia | Inflammatory Linear Verrucous Epidermal Nevus | Hypobetalipoproteinemias | Angioedema | Lattice Corneal Dystrophy Type 1 | Porokeratosis | Early Infantile Epileptic Encephalopathy 1 | Autosomal Recessive Spastic Paraplegia Type 54 | Hepatitis, Autoimmune | Insulin Resistance | Lathosterolosis | Lymphoma, Mantle Cell | Neuromyelitis Optica | Cutis Laxa | Calcium Pyrophosphate Deposition Disease | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Multiple Sclerosis, Primary Progressive | Tuberculous Meningitis | Arthritis, Psoriatic | Charcot-Marie-Tooth Disease Axonal Type 2N | DRESS Syndrome | Spinocerebellar Ataxia Type 42 | Pouchitis | Autosomal Recessive Spastic Paraplegia Type 75 | Peyronie's Disease | Williams Syndrome | Robinow Syndrome | Hemorrhagic Disorders | Hepatitis B, Chronic | Systemic Mastocytosis | Hyperglycemia | Primary Erythromelalgia | Dysfibrinogenemia | Vasculitis | Extramammary Paget's Disease | Corneal Dystrophy | Walker-Warburg Syndrome | Arteriovenous Malformations | Tylosis With Esophageal Cancer | Stuttering | Proteus Syndrome | Hypoglycemia | Esophageal Motility Disorders | Central Retinal Artery Occlusion | Spasticity | Fabry's Disease | Nasodigitoacoustic Syndrome | Liebenberg Syndrome | Alopecia Areata | Cancer, Prostate | Cleidocranial Dysplasia | Myoclonic Atonic Epilepsy | Basan Syndrome | Gastritis | Sweet Syndrome | Nemaline Myopathy | Microtia | Peters-plus Syndrome | Aspergillosis | Lymphoma | Autoimmune Polyendocrine Syndrome | Melanoma | Retinal Coloboma | Riboflavin Transporter Deficiency Neuronopathy | Corneal Dystrophies, Hereditary | Beckwith-Wiedemann Syndrome | Infantile Liver Failure Syndrome 1 | Nevus | Bulimia Nervosa | Impetigo | X-linked Charcot-Marie-Tooth Disease | Hereditary Hemorrhagic Telangiectasia | Hernia, Inguinal | Hyperphenylalaninemia | Treacher Collins Syndrome | Cherubism | Cellulitis | Early Infantile Epileptic Encephalopathy | Nephrotic Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Renpenning Syndrome | Primary Carnitine Deficiency | Mucormycosis | Deafness, Dystonia, And Cerebral Hypomyelination | Acute Coronary Syndrome | ADNP Syndrome | Pheochromocytoma | Acrodermatitis Enteropathica | Occipital Neuralgia | Uveitis, Anterior | Mitochondrial Encephalomyopathy | Temtamy Preaxial Brachydactyly Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Thalassemia, Beta | Episodic Ataxia | Basal Ganglia Disease | Hyperinsulinism-hyperammonemia Syndrome | Liver Diseases | Cerebellofaciodental Syndrome | Addison Disease | Acute Lung Injury | Takayasu's Arteritis | Kaposi Sarcoma | Arrhythmogenic Right Ventricular Cardiomyopathy | Spinal Muscular Atrophy Type 2 | Still Disease | Tetanus | Angiodysplasia | Conduct Disorder | Hyperkalemic Periodic Paralysis | Angioedema, Acquired | Multisystemic Smooth Muscle Dysfunction Syndrome | Oculocutaneous Albinism Type 1 | Hypercalciuria | Macrodactyly | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Benign Recurrent Intrahepatic Cholestasis 1 | Hemochromatosis | Gastroschisis | Barakat Syndrome | Lichen Sclerosus | Axenfeld-Rieger Syndrome | Spinocerebellar Ataxia Type 40 | Peripheral T-cell Lymphoma | Scapuloperoneal Spinal Muscular Atrophy | Benign Familial Neonatal Convulsions | Hidradenitis Suppurativa | Iron Metabolism Disorders | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Thyroiditis, Autoimmune | Congenital Dyserythropoietic Anemia Type 1 | Holt-Oram Syndrome | B-cell Prolymphocytic Leukemia | Pierpont Syndrome | Klippel-Feil Syndrome | Myocardial Infarction | Vertebrobasilar Insufficiency | Spinocerebellar Ataxia Type 15 | Waardenburg Syndrome Type 2A | Myopia | HELLP Syndrome | Hemangioblastoma | Binge Eating Disorder | Glaucomatocyclitic Crisis | Batten Disease | Common Variable Immunodeficiency | Dubin-Johnson Syndrome | TARP Syndrome | Anemia | Rothmund-Thomson Syndrome | 3C Syndrome | Craniosynostosis | Localized Scleroderma | Lipodystrophy | Chronic Mucocutaneous Candidiasis | Benign Familial Infantile Seizures | Agnathia-Otocephaly Complex | Hepatoblastoma | Hyperparathyroidism | Lymphomatoid Granulomatosis | Colitis | Oligoastrocytoma | Peutz-Jeghers Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Endometritis | Lattice Corneal Dystrophy | Thanatophoric Dysplasia Type 1 | Myofibrillar Myopathy | Inflammatory Myofibroblastic Tumor | Microphthalmia | Neutrophilia | Sturge-Weber Syndrome | Hypothyroidism | Acute Lymphocytic Leukemia | Hypopigmentation | Rubinstein-Taybi Syndrome | Fanconi Anemia | Hyperuricemia | Neurofibroma, Plexiform | Nephroblastoma | Fragile X Syndrome | Diarrhea | Spinocerebellar Ataxia Type 5 | Milk Allergy | Pantothenate Kinase-associated Neurodegeneration | Ocular Albinism Type 1 | Alpha-thalassemia Myelodysplasia Syndrome | Heavy Chain Disease | Heterotaxy | Blepharoconjunctivitis | Spinocerebellar Ataxia Type 17 | Insulinoma | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Leri-Weill Dyschondrosteosis | Aromatic L-amino Acid Decarboxylase Deficiency | Usher Syndrome Type I | Asthma, Nocturnal | Vitiligo | Carney Triad | Hereditary Hemorrhagic Telangiectasia Type 2 | Mood Disorder | Retinopathy Of Prematurity | Primary Aldosteronism | Alpha-1 Antitrypsin Deficiency | Adenoid Cystic Carcinoma | Toxoplasmosis | Idiopathic Pulmonary Fibrosis | Charcot-Marie-Tooth Disease Type 4E | Waldenstrom Macroglobulinemia | Kindler Syndrome | Persistent Truncus Arteriosus | Myelitis | Mitochondrial DNA Depletion Syndrome | Sialidosis | Myasthenia | Dyslexia | Greig Cephalopolysyndactyly Syndrome | Follicular Dendritic Cell Sarcoma | Muckle-Wells Syndrome | Hepatitis D | Autoimmune Hemolytic Anemia | Aicardi-Goutieres Syndrome | Coenzyme Q10 Deficiency | Carpal Tunnel Syndrome | Adams-Oliver Syndrome | Adrenoleukodystrophy, X-linked | H Syndrome | Chediak-Higashi Syndrome | Eczema | Benign Hereditary Chorea | Primary Torsion Dystonia | Myopathy | Crimean-Congo Hemorrhagic Fever | Ichthyosis, X-linked | Astrocytoma, Anaplastic | Premenstrual Syndrome | Autism | Smith-Kingsmore Syndrome | Maternally Inherited Diabetes And Deafness | Uremia | Danon Disease | Intellectual Disability, Autosomal Dominant 5 | Microcephalic Primordial Dwarfism | Kaposiform Hemangioendothelioma | Heimler Syndrome | Ameloblastic Carcinoma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Vascular Cognitive Impairment | Parkinson Disease 6, Autosomal Recessive Early-onset | Autism Spectrum Disorders | Spitzoid Melanoma | Keratosis, Actinic | Myoclonus-dystonia Syndrome | Hyper IgE Syndrome | Micro Syndrome | Nicotine Addiction | Influenza | Hemochromatosis Type 2 | Large Granular Lymphocytic Leukemia | Cocaine-Related Disorders | Oculodentodigital Dysplasia | Bethlem Myopathy | Lamellar Ichthyosis | Hypermethioninemia | Essential Fructosuria | Adrenal Insufficiency | Acrodysostosis | Cardiofaciocutaneous Syndrome | Trismus-pseudocamptodactyly Syndrome | Polycystic Kidney, Autosomal Dominant | Hereditary Mixed Polyposis Syndrome | Medulloblastoma | Juvenile Myelomonocytic Leukemia | Crouzon Syndrome With Acanthosis Nigricans | Roberts Syndrome | Hereditary Neuropathy With Liability To Pressure Palsies | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Pyoderma Gangrenosum | Carcinoid Syndrome | Atrial Septal Defect | Gangliosidosis | Norrie Disease | Acute Generalized Exanthematous Pustulosis | Retinal Detachment | Brachydactyly | Amebiasis | Melanoma, Malignant | Renal Tubular Acidosis | Vitreoretinopathy, Proliferative | HUPRA Syndrome | Olmsted Syndrome | Osteogenesis Imperfecta Type I | Vitamin B12 Deficiency | Encephalopathy, Glycine | Hypopituitarism | Astigmatism | Phenylketonuria II | Hypotrichosis Simplex | Peripheral Neuropathy | Myelitis, Transverse | Lymphoma Lymphoblastic | Nail Disorder, Nonsyndromic Congenital | Gallstones | Primary Familial Brain Calcification | Communication Disorders | Giant Cell Arteritis | Filariasis | Encephalocele | Mastitis | Hashimoto Thyroiditis | Multiple Sclerosis | Polyradiculopathy | Congenital Primary Aphakia | Syncope | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Herpes Simplex Dermatitis | Brenner Tumor | Superficial Spreading Melanoma | Brugada Syndrome 1 | Iron Overload | Multiple Hamartoma Syndrome | Silver-Russell Syndrome | Geleophysic Dysplasia | Craniofacial Dysostosis | Pancytopenia | Pupil Disorders | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Postaxial Polydactyly | Hereditary Multiple Exostoses | Cystinosis | Epilepsy, Generalized | Multiple Sclerosis, Secondary Progressive | Hyperparathyroidism-jaw Tumor Syndrome | Preaxial Polydactyly | Asplenia | Frontotemporal Dementia | Epiphyseal Chondrodysplasia, Miura Type