Disease

Skin Cancer

About the Disease
Skin Carcinoma, also known as skin cancer, is related to xeroderma pigmentosum, complementation group f and rothmund-thomson syndrome, type 2. An important gene associated with Skin Carcinoma is TP53 (Tumor Protein P53), and among its related pathways/superpathways are Homology Directed Repair and Transcription-Coupled Nucleotide Excision Repair (TC-NER). The drugs Petrolatum and Etanercept have been mentioned in the context of this disorder. Affiliated tissues include skin, tissues of the skin and lymph node, and related phenotypes are Synthetic lethal with MLN4924 (a NAE inhibitor) and Synthetic lethal with MLN4924 (a NAE inhibitor)

Common Targets
Vascular endothelial growth factors (VEGF) (nonspecified subtype) | STPG1 | G6647 | ABL1 | TMC8 | CCR10 | ACTA2 | IL1B | Prostaglandin EP Receptor (nonspecified subtype) | CDC42BPB | G7015 | G3569 | MC1R | AKAP12 | G2335 | PRKACG | CSK | Tyrosine-Protein Kinases Src (nonspecified subtype) | HDAC2 | LRRK2 | Melanin | L-type voltage-dependent calcium channel complex | CCND2 | NR3C2 | HRAS | NRAS | NF-kappaB (NFkB) | G5133 | IL2RA | XRCC2 | SLC7A5 | AXL | KIT | PADI6 | G7099 | CSF1R | TMC6 | AQP3 | ACE | LOC102724428 | G5728 | MUTYH | TYR | KRT5 | KEAP1 | BCR | EVC | LOC101928135 | LOC102724520 | G23411 | IL-5 receptor | LINC-PINT | CDKN2B-AS1 | HDAC3 | G1029 | ABCA1 | PDGFRB | CD40 | IRF4 | ANGPT2 | PBK | HDAC1 | SMURF1 | Reverse transcriptase (Telomerase) | TGFBR1 | LILRB2 | PTGS1 | CSMD1 | TGM3 | PRF1 | XDH | Anandamide membrane transporter (AMT) | Interferon (nonspecified subtype) | G7157 | G3630 | NR1H4 | G836 | FAAH | RXRA | Leukotriene B4 receptor (LTB4-R) (nonspecified subtype) | Tubulin | ABCC8 | CLPTM1L | Transcriptional Enhancer Factor (TEAD) (nonspecified subype) | SIK2 | PRKCB | L-Type calcium channel (nonspecified subtype) | IL1A | SLC45A2 | CDC42BPA | CTLA4 | G5743 | SIK1 | LRP2 | VDR | LOC105374875 | NT5E | RXRG | PDGFRA | IL10 | MGMT | TOP2A | MTHFR | GRHL3-AS1 | TFPI2 | SIK3 | KDR | LOC101927668 | NCKAP5 | APC | XRCC1 | TNFRSF9 | G1956 | TLR7 | Monoamine oxidase (MAO) (nonspecified subtype) | G10413 | Superoxide dismutase (SOD) (nonspecified subtype) | RGS22 | IL2RB | G3845

疾病靶点研报
Skin Cancer

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

Other Diseases

Hyperinsulinemic Hypoglycemia | DICER1 Syndrome | Optic Neuritis | Meningococcal Infections | Spinocerebellar Ataxia Type 10 | Hemosiderosis | Aplastic Anemia | Central Retinal Artery Occlusion | Colon Adenoma | Nager Acrofacial Dysostosis | Hyperparathyroidism, Primary | Hyperglycemia | Raine Syndrome | Spinocerebellar Ataxia Type 1 | Renal Medullary Carcinoma | Tibial Muscular Dystrophy | Pure Autonomic Failure | Cutaneous T-cell Lymphoma | Spasticity | Nephronophthisis | Discoid Lupus Erythematosus | Congenital Heart Block | Distal Spinal Muscular Atrophy | Spinocerebellar Ataxia Type 5 | Acute Tubular Necrosis | Blepharitis | Trichothiodystrophy | Angioedema | Thyroid Hormone Resistance | Cancer, Bladder | Cardiomyopathy, Peripartum | Nemaline Myopathy | Gastroenteritis, Eosinophilic | Reye Syndrome | Parapsoriasis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Agammaglobulinemia | Arteriovenous Malformations | Borjeson-Forssman-Lehmann Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Kernicterus | Prader-Willi Syndrome | Waardenburg Syndrome Type 4A | Chronic Lymphocytic Leukemia | ADNP Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Intracerebral Hemorrhage | Inflammatory Bowel Disease | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hereditary Sensory Neuropathy Type 1 | Bone Giant Cell Tumor | Campomelic Dysplasia | Amyloidosis | Nevus | Pycnodysostosis | Wiedemann-Steiner Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Gingivitis | Epidermolysis Bullosa Simplex, Localized | Gardner Syndrome | Cryptococcal Meningitis | Blepharospasm | Carpenter Syndrome | Greig Cephalopolysyndactyly Syndrome | Lipid Storage Diseases | Familial Male-limited Precocious Puberty | Epidermolysis Bullosa Acquisita | Chronic Kidney Disease | Niemann-Pick Disease, Type A | Usher Syndrome Type II | Cardiac Sarcoidosis | Diabetes Mellitus, Transient Neonatal | Apert Syndrome | Premenstrual Syndrome | Asthma, Nocturnal | Ganglioglioma | Usher Syndrome Type I | Endometriosis | Presbyopia | Analgesia | Metachondromatosis | Hernia, Inguinal | Adrenoleukodystrophy, X-linked | Cartilage Disorders | Esophageal Motility Disorders | Schizophrenia | Cranioectodermal Dysplasia | Hemorrhoids | Down Syndrome | Sialidosis Type I | Androgen Insensitivity | Leiomyoma | Thyroiditis, Autoimmune | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Primary Torsion Dystonia | Shwachman-Bodian-Diamond Syndrome | Fibromuscular Dysplasia | Usher Syndrome Type III | Aceruloplasminemia | Hypertelorism | TARP Syndrome | Retinitis Pigmentosa | Paget's Disease Of The Breast | Geleophysic Dysplasia | Dystrophy, Cone-rod | Reflex Epilepsy | Thrombosis | Cardiomyopathy, Dilated, 1L | Angioimmunoblastic T-cell Lymphoma | Spinocerebellar Ataxia Type 20 | Restrictive Dermopathy | Intestinal Pseudo-obstruction | Viral Meningitis | Adenoma, Villous | Leukoplakia | Pseudoexfoliation Syndrome | HUPRA Syndrome | Myasthenia Gravis | Spinocerebellar Ataxia Type 16 | Astrocytoma, Anaplastic | Chediak-Higashi Syndrome | Macrodactyly | Anti-glomerular Basement Membrane Disease | Glutathione Synthetase Deficiency | Keratoconus | Rhizomelic Chondrodysplasia Punctata | Tonsillitis | Hemolytic Uremic Syndrome | Leigh Syndrome | Familial Glucocorticoid Deficiency | Hereditary Hemorrhagic Telangiectasia | Stevens-Johnson Syndrome | Bethlem Myopathy | Spinocerebellar Ataxia Type 15 | Charcot-Marie-Tooth Disease, Type 2C | Chronic Neutrophilic Leukemia | Metanephric Adenoma | Neutropenia | Alstrom Syndrome | Multicystic Renal Dysplasia | Charcot-Marie-Tooth Disease Axonal Type 2N | Pierpont Syndrome | Oculocutaneous Albinism Type 1 | Usher Syndrome | Chudley-McCullough Syndrome | Adrenal Insufficiency | Priapism | Primary Aldosteronism | Wolman Disease | Nephrotic Syndrome | Raynaud Phenomenon | Generalized Epilepsy With Febrile Seizures Plus | Hepatoblastoma | Adenylosuccinate Lyase Deficiency | Alopecia | Autosomal Recessive Spastic Paraplegia Type 75 | Deafness, Dystonia, And Cerebral Hypomyelination | Veno-occlusive Disease | Pneumothorax | Malaria, Cerebral | Pouchitis | Bare Lymphocyte Syndrome | Chylomicron Retention Disease | Angiosarcoma Of The Breast | Sporadic Hemiplegic Migraine | Anovulation | Fuchs Heterochromic Iridocyclitis | Carey-Fineman-Ziter Syndrome | Acrodermatitis Enteropathica | Alopecia Areata | Still Disease | Long QT Syndrome Type 1 | Prediabetes | Infantile Spasm | Steel Syndrome | Haim-Munk Syndrome | Sarcomatoid Carcinoma Of The Lung | Chronic Idiopathic Myelofibrosis | Sclerosteosis | Sulfite Oxidase Deficiency | Absence Epilepsy | Keratocystic Odontogenic Tumor | Hyperkalemic Periodic Paralysis | Autonomic Nervous System Disorders | Progressive Osseous Heteroplasia | PASLI Disease | Autism Spectrum Disorders | Pachyonychia Congenita | Primrose Syndrome | Loeys-Dietz Syndrome | Postpoliomyelitis Syndrome | Nail Disorder, Nonsyndromic Congenital | Paternal Uniparental Disomy Of Chromosome 14 | Spondylocarpotarsal Synostosis Syndrome | Nasodigitoacoustic Syndrome | Pseudohypoparathyroidism Type 1B | Gallstones | Seizures | Waardenburg Syndrome Type 2E | Focal Segmental Glomerulosclerosis | Uveitis | Erythema Multiforme | Wieacker-Wolff Syndrome | Personality Disorders | Vitiligo | Pfeiffer Syndrome | Congenital Adrenal Hyperplasia | Epilepsy Of Infancy With Migrating Focal Seizures | Mabry Syndrome | Myopia | Rolandic Epilepsy | Scleroderma | Cannabis Abuse | Hypobetalipoproteinemias | Opisthorchiasis | Hyperuricemia | Usher Syndrome Type IIC | Acute Kidney Injury | Weill-Marchesani Syndrome | Filariasis | Hyperphenylalaninemia | Triphalangeal Thumb-polysyndactyly Syndrome | Bone Marrow Necrosis | Dystonia Musculorum Deformans | Auriculocondylar Syndrome | Knobloch Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Spinocerebellar Ataxia Type 17 | Hoyeraal-Hreidarsson Syndrome | Encephalopathy, Ethylmalonic | Emery-Dreifuss Muscular Dystrophy | Galloway-Mowat Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Primary Carnitine Deficiency | Cancer, Skin | Relapsing Polychondritis | Corneal Dystrophy And Perceptive Deafness | Heterotopic Ossification | Scoliosis | DEND Syndrome | Bartsocas-Papas Syndrome | Lentigo | X-linked Myotubular Myopathy | Congenital Fiber-type Disproportion Myopathy | Diabetes Insipidus, Nephrogenic | Histiocytosis | Polycystic Liver | Pulmonary Tuberculosis | Spinocerebellar Ataxia Type 3 | Dermatitis Herpetiformis | Lymphedema | Neurofibroma, Plexiform | Unverricht-Lundborg Syndrome | Amebiasis | Adenomatoid Tumor | Hyperinsulinemia | Allergic Contact Dermatitis | Alveolar Capillary Dysplasia | Renal Tubular Acidosis | Craniopharyngioma | Cheilitis | Obesity | Myofibrillar Myopathy | Blood Protein Disorders | Maple Syrup Urine Disease | Desmosterolosis | Urethritis | Nutrition Disorders | Genitopatellar Syndrome | Pilomatrix Carcinoma | Teratozoospermia | Episodic Ataxia Type 1 | Pigment Dispersion Syndrome | Infantile Neuroaxonal Dystrophy | Enlarged Vestibular Aqueduct | Nephroblastoma | Dent Disease | Encephalopathy, Glycine | Xeroderma Pigmentosum Variant Type | X-linked Acrogigantism | Nicotine Addiction | Asplenia | Fibronectin Glomerulopathy | Acute Motor Axonal Neuropathy | Acromicric Dysplasia | Blomstrand Osteochondrodysplasia | Methylmalonic Aciduria And Homocystinuria, CblC Type | DiGeorge Syndrome | Ophthalmoplegia | Erdheim-Chester Disease | Short-chain Acyl-CoA Dehydrogenase Deficiency | Bruck Syndrome | Becker Muscular Dystrophy | Epidermolysis Bullosa Simplex With Mottled Pigmentation | McLeod Syndrome | Non-Hodgkin Lymphoma | Epidermolysis Bullosa | Farber Disease | Exostoses | Glanzmann Thrombasthenia | Infantile Refsum Disease | Rickets | Brugada Syndrome 1 | Autism | Iron Metabolism Disorders | Colitis | Kallmann Syndrome | Bloom Syndrome | Acromegaly | Carney-Stratakis Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Purpura, Thrombotic Thrombocytopenic | Endocarditis | SAPHO Syndrome | Scabies | Cystinuria | Carbohydrate Metabolism Disorders | Stargardt Disease | Myoclonic Epilepsy With Ragged Red Fibers | Tylosis With Esophageal Cancer | Nephritis, Interstitial | Autonomic Neuropathy | Ichthyosis | Lymphoma, AIDS-related | Progressive Encephalopathy-optic Atrophy Syndrome | Batten Disease | Polymyalgia Rheumatica | VEXAS Syndrome | Hereditary Mixed Polyposis Syndrome | Renal Dysplasia | Cyst | Mucolipidosis Type II | Synpolydactyly | Conjunctivitis, Allergic | Mastitis | Non-small Cell Lung Cancer | Rhabdomyosarcoma | Myosin Storage Myopathy | Cornelia De Lange Syndrome | Takenouchi-Kosaki Syndrome | Gitelman Syndrome | Burn-McKeown Syndrome | Hypoalbuminemia | Carpal Tunnel Syndrome | Necrobiosis Lipoidica | Scapuloperoneal Spinal Muscular Atrophy | Hereditary Sensory And Autonomic Neuropathy | Feingold Syndrome | Hereditary Spastic Paraplegia | Cancer, Lung | Hyperparathyroidism-jaw Tumor Syndrome | Stuve-Wiedemann Syndrome | Ligneous Conjunctivitis | Coma | Uveitis, Anterior | Choroideremia | Varices | Binge Eating Disorder | Carcinoma, Transitional Cell | Dwarfism | Succinic Semialdehyde Dehydrogenase Deficiency | Creutzfeldt-Jakob Disease | Constipation | Charcot-Marie-Tooth Disease Type 2T | IgA Nephropathy | Pneumonia, Bacterial | Hemophilia | Herpes Simplex Dermatitis | Basal Cell Nevus Syndrome | Thalassemia, Beta | Myoclonus | Leiomyosarcoma | Hereditary Hemorrhagic Telangiectasia Type 2 | Nail-Patella Syndrome | Hypotonia-cystinuria Syndrome | Intermittent Claudication | Familial Partial Lipodystrophy | Huntington's Disease | DRESS Syndrome | Esotropia | Poikiloderma With Neutropenia | Panic Disorder | Dominant Optic Atrophy | Hyperparathyroidism | Keloid | Glycogen Storage Disease Type 0 | Focal Facial Dermal Dysplasia | Rubinstein-Taybi Syndrome | Meningeal Melanocytoma | Gastritis, Atrophic | Schnitzler Syndrome | Dysfibrinogenemia | Gnathodiaphyseal Dysplasia | Myocarditis | Aplasia Cutis Congenita | Lassa Fever | Stomatitis | X-linked Charcot-Marie-Tooth Disease | Precocious Puberty | Thrombophilia