Disease

Colorectal Adenoma

About the Disease
Colorectal Adenoma, also known as adenoma of large intestine, is related to polyposis syndrome, hereditary mixed, 1 and adenoma. An important gene associated with Colorectal Adenoma is GREM1 (Gremlin 1, DAN Family BMP Antagonist), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Endometrial cancer. The drugs Celecoxib and Rofecoxib have been mentioned in the context of this disorder. Affiliated tissues include colon, rectum and liver, and related phenotypes are neoplasm and digestive/alimentary

Common Targets
GATA4 | SFRP2 | SLIT2 | ROCK1 | PPP2R5A | CCND2 | G999 | NGFR | CDKN2B | RUNX3 | G7124 | C12orf40 | LOC105370507 | G4609 | ADIPOQ | TAS2R38 | TAS2R16 | GNAL | WNT3A | G3845 | LINC00992 | PRKCA | IL1B | FZD2 | SEZ6 | VIM | CYP1A1 | MEGF10 | FRAT1 | RHOF | NFATC1 | FLNC | C9orf50 | NR2E1 | IL10 | CDKN2B-AS1 | CBLN2 | ALOX12 | PANTR1 | DAAM2 | PPP3CC | GSTT1 | POLD3 | SLC16A7 | GPNMB | SYNPR | LRP5 | MTRR | KCNH5 | ANO5 | PPP2R1A | SFMBT2 | FZD1 | LSM2 | ARID2 | CASC8 | STAC2 | TP73 | FZD3 | SALL1 | SMC1A | HPGD | SDC2 | G7015 | CAHM | LEP | PPP2R5C | CSNK2A1 | ERCC2 | ERICH1 | SENP2 | SORCS3 | G7157 | KY | GPX1 | IQGAP2 | VANGL1 | CDO1 | WIF1 | SEPTIN9 | DACH1 | SFRP4 | COLCA1 | BTRC | NRG3 | TRABD2B | SMAD7 | GRIN2A | TLE6 | PDGFRA | ACVR2A | MAL | TIAM1 | FZD7 | NDRG4 | APC | ATP8B2 | PTPRH | ITGA4 | CRHBP | UGT1A6 | LAMC1 | TBL1X | G673 | TBX3 | STK32B | CCND3 | FLI1 | PLXNA4 | ELMO1 | GSTM1 | G472 | GNAS | APBA2 | AXIN1 | LOC105369625 | CTNNB1 | ARHGEF4 | MGMT | SOX5 | GATA5 | GRIA4 | PPP2R1B | MTAP | FZD9 | APOE | G9734 | G7099 | PRKCB | G3576 | LONRF2 | RHPN2 | BCAT1 | RXRA | GLRA3 | RUVBL1 | LINC01798 | TGFB1 | TYMS | TLE2 | FCGR2A | VANGL2 | LRRC4 | KCNQ5 | TLE3 | MUC2 | CDIP1 | PRICKLE1 | CACYBP | TLE4 | IGSF5 | AXIN2 | CD59 | PDX1 | CYP26A1 | PPP3R1 | SYNE1 | CNTFR | SLC32A1 | MLH1 | CXXC4 | SCN3B | SMAD3 | PEBP1 | G3082 | CHD8 | SLC11A2 | CNTN1 | LOC105376400 | SFRP1 | MAPK10 | DAB2IP | LOC105369765 | KRBA1 | ZMIZ1-AS1 | G1029 | SNAP91 | POU2AF3 | MAOB | USP44 | FAM43B | MTR | NQO1 | LRP1B | PKNOX2 | TRIM9 | NFAT5 | CHL1 | LRRC38 | MKX | CRP | MDGA2 | SLCO2A1 | FUT2 | HEPHL1 | TAMALIN | FBXW7 | MSH6 | JAM2 | TCF7L2 | SLITRK5 | ABCC4 | IL23R | PRIMA1 | NFKB1 | FOXL1 | AMH | DKK4 | HOXC4 | NRAS | CABLES2 | CHORDC1 | PRKACA | AURKA | NTRK2 | APBA1 | RBX1 | G6714 | MIR9-3 | MUC5AC | EPHA7 | NXN | PLCB1 | TMBIM1 | IRX4 | ROR2 | PRKX | SLIT1 | ODC1 | MINDY4 | PITX1-AS1 | PPP2CA | DOCK7 | PPARG | PER3 | TFPI2 | ZFP90 | PLA2G1B | FMN1 | PIK3CA | G1956 | CDH13 | LINC00693 | PITX1 | RASSF2 | RNASEL | LRRC49 | IGFBP7 | CP | GALNT14 | GSC2 | Monoamine oxidase (MAO) (nonspecified subtype) | OPLAH | XPC | MYNN | RIMS4 | L1TD1 | LRP6 | G5599 | LAMA5 | G5743 | COL25A1 | FAM107A | WNT5A | GDNF | ESPNP | TCF7L1 | PRH1-PRR4 | PTGS1 | PLCB4 | G3569 | GLB1L3 | IKZF1 | PSEN1 | CLIP4

疾病靶点研报
Colorectal Adenoma

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

Other Diseases

Ovarian Sex Cord-stromal Tumor | Evans Syndrome | Neuroectodermal Tumors, Primitive | Porokeratosis | Klippel-Feil Syndrome | Rickets | MIRAGE Syndrome | Usher Syndrome Type IIC | Recurrent Respiratory Papillomatosis | Waardenburg Syndrome Type 4A | Incontinentia Pigmenti | Batten Disease | Charcot-Marie-Tooth Disease, Type 6 | Spinocerebellar Ataxia Type 31 | Jaundice, Obstructive | Pyelonephritis | Renpenning Syndrome | Sick Sinus Syndrome | Autoimmune Autonomic Ganglionopathy | Adenoma, Pituitary | Cyst | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Dysthymia | Nicotine Dependence | Sweet Syndrome | Sleep Apnea | Papulopustular Rosacea | Hyperuricemia | Pseudomyxoma Peritonei | Nemaline Myopathy 8 | Lactose Intolerance | Amelanotic Melanoma | Non-bullous Congenital Ichthyosiform Erythroderma | Neutropenia | Dysequilibrium Syndrome | Multiple Sclerosis, Chronic Progressive | Nasodigitoacoustic Syndrome | Epilepsy, Generalized | Calcium Pyrophosphate Deposition Disease | Schwannoma | Microcephaly, Seizures, And Developmental Delay | Premature Ejaculation | Cheilitis | Pelizaeus-Merzbacher Disease | Miyoshi Myopathy | Angelman Syndrome | Delirium | Dystrophy, Cone-rod | GM2-gangliosidosis AB Variant | VACTERL Association | Alstrom Syndrome | Arteriosclerosis | Leber Congenital Amaurosis | Cancer, Breast | Eating Disorder | Tyrosinemia | Galactosialidosis | Cleidocranial Dysplasia | Dermatomyositis | Urethritis | Nanophthalmos | Keratosis, Seborrheic | Achromatopsia | Esophageal Motility Disorders | Episodic Ataxia Type 2 | Papilledema | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Poikiloderma With Neutropenia | Methylmalonic Acidemia | Congenital Aniridia | Pernicious Anemia | Pulmonary Vein Stenosis | Tonsillitis | Multiple Sclerosis | Palmoplantar Keratoderma | Coronary Restenosis | C3 Glomerulonephritis | Tietze Syndrome | Primary Hyperoxaluria Type 3 | Eclampsia | Language Disorders | Blue Nevus | Autism | Subacute Sclerosing Panencephalitis | Hairy Cell Leukemia | Combined Malonic And Methylmalonic Acidemia | Kidney Stones | Macular Corneal Dystrophy Type 1 | Hypercalcemia | Adenomyosis | Spondylocarpotarsal Synostosis Syndrome | Leukemia | Bullous Pemphigoid | Weill-Marchesani Syndrome | Sepiapterin Reductase Deficiency | Prune Belly Syndrome | Neurodegeneration With Brain Iron Accumulation | Inflammatory Joint Disease | Encephalitis, Tick-borne | Schizoaffective Disorder | Pulverulent Zonular Cataract | Spinal And Bulbar Muscular Atrophy | Nephrotic Syndrome Type 1 | Spinocerebellar Ataxia Type 6 | Kernicterus | Reye Syndrome | Harlequin Ichthyosis | B-cell Prolymphocytic Leukemia | Sporadic Inclusion Body Myositis | Chloridorrhea, Congenital | Amyloidosis | Craniofacial Dysostosis | Peritonitis | Glomerulonephritis | Hypertension, Portal | Woodhouse-Sakati Syndrome | Vascular Cognitive Impairment | Neuroblastoma | McCune-Albright Syndrome | Insulinoma | Uterine Leiomyoma | Asphyxia Neonatorum | Duodenal Atresia | Budd-Chiari Syndrome | Graves Disease | Congenital Stationary Night Blindness | Hypoplastic Left Heart Syndrome | Chanarin-Dorfman Syndrome | Stickler Syndrome | Barakat Syndrome | Primary Hyperoxaluria Type 1 | Anorexia Nervosa | Thyroid Hormone Resistance | Mitochondrial DNA Depletion Syndrome 13 | Gangliosidosis | Necrobiosis Lipoidica | Tetraplegia | Congenital Bile Acid Synthesis Defect | Zimmermann-Laband Syndrome | Vogt-Koyanagi-Harada Syndrome | Hyperkeratosis | Congenital Heart Block | Porencephaly | Wilson's Disease | Lipid Metabolism Disorders | Angiodysplasia | Sleep Apnea, Central | Alopecia Areata | Wolman Disease | Acne Vulgaris | Chronic Granulomatous Disease, X-linked | ADNP Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Gynecomastia | Bainbridge-Ropers Syndrome | Porphyria, Acute Intermittent | Systemic Lupus Erythematosus | Jawad Syndrome | Ataxia-ocular Apraxia 2 | Progressive Osseous Heteroplasia | Gout | Aromatic L-amino Acid Decarboxylase Deficiency | Vestibular Disease | Camptocormia | Non-epidermolytic Palmoplantar Keratoderma | Hepatic Steatosis | CDKL5 Deficiency Disorder | Superficial Spreading Melanoma | Craniofrontonasal Syndrome | Hemorrhage | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | DICER1 Syndrome | Treacher Collins Syndrome | Brachial Plexus Neuropathy | Blue Rubber Bleb Nevus Syndrome | X-linked Acrogigantism | Infertility, Male | Thalassemia, Beta | Facioscapulohumeral Muscular Dystrophy Type 1 | Lathosterolosis | Arts Syndrome | Intracerebral Hemorrhage | Fahr Disease | Hartsfield Syndrome | Li-Fraumeni Syndrome | Histiocytosis | Bronchiectasis | Glycogen Storage Disease Type 0 | Overactive Bladder | Guanidinoacetate Methyltransferase Deficiency | Antisynthetase Syndrome | Niemann-Pick Disease, Type A | Carpal Tunnel Syndrome | Keratoconus | Primary Hyperoxaluria | Osteoarthritis | Esophageal Carcinoma | Cornelia De Lange Syndrome | Fibrillation, Atrial | Congenital Adrenal Hyperplasia | Centronuclear Myopathy | Goiter, Nodular | Cranial Nerve Disease | Lymphoproliferative Disease, X-linked | Gastric Atrophy | Cryptococcal Meningitis | Renal Hypomagnesemia 3 | Hyperostosis | Arthritis, Reactive | Fukuyama Congenital Muscular Dystrophy | Methemoglobinemia | Cancer, Lung | Pompe Disease | Coronary Heart Disease | Apparent Mineralocorticoid Excess Syndrome | Alopecia Totalis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Peripheral Neuropathy | Episodic Ataxia Type 1 | Congenital Central Hypoventilation Syndrome | Anosmia, Congenital | Pathological Gambling | Addison Disease | Malignant Fibrous Histiocytoma | Polydactyly | IgA Nephropathy | Acrodermatitis Enteropathica | Corneal Dystrophy And Perceptive Deafness | Adrenal Insufficiency | Duchenne Muscular Dystrophy | Oligospermia | Pheochromocytoma | Multisystemic Smooth Muscle Dysfunction Syndrome | Hypocalcemia | Dystonia-parkinsonism, X-linked | Reticular Dysgenesis | Cerebrotendinous Xanthomatosis | Seminoma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Tyrosinemia Type 2 | Metatropic Dysplasia | Currarino Syndrome | Multiple Myeloma | Thin Basement Membrane Disease | Polycystic Kidney, Autosomal Dominant | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hemochromatosis Type 1 | TARP Syndrome | Postpoliomyelitis Syndrome | Multiple Sclerosis, Primary Progressive | Acute Lymphocytic Leukemia | Transthyretin-related Amyloidosis | Takenouchi-Kosaki Syndrome | Hepatic Adenomatosis | Oligoasthenoteratozoospermia | Hypertrophy | Tendinopathy | Hemophagocytic Lymphohistiocytosis | Pierson Syndrome | Conjunctivitis, Allergic | Carcinoma, Signet Ring Cell | Disseminated Intravascular Coagulation | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Hypoglycemia | Influenza | Klinefelter Syndrome | Carey-Fineman-Ziter Syndrome | Hyperoxaluria | Familial Exudative Vitreoretinopathy | Glutathione Synthetase Deficiency | Melanoma, Uveal | Frontotemporal Dementia | Primary Aldosteronism | McKusick Type Metaphyseal Chondrodysplasia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Beckwith-Wiedemann Syndrome | Amebiasis | Uremia | Aldosterone Synthase Deficiency | Smith-Magenis Syndrome | Hypogammaglobulinemia | Hypersomnia | Behavioral Variant Of Frontotemporal Dementia | Pendred Syndrome | Bladder Exstrophy | Acrodysostosis | Crisponi Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Spinocerebellar Ataxia Type 17 | Agranulocytosis | Oculocutaneous Albinism Type 2 | Lennox-Gastaut Syndrome | Antenatal Bartter Syndrome Type 1 | Dwarfism | Basal Cell Nevus Syndrome | T-cell Chronic Lymphocytic Leukemia | Peters-plus Syndrome | Myoclonus-dystonia Syndrome | Dysferlinopathy | Progressive External Ophthalmoplegia | Pseudoachondroplasia | Osteogenesis Imperfecta Type IV | Spinal Muscular Atrophy Type 3 | Long QT Syndrome Type 3 | Jacobsen Syndrome | Panniculitis | Branchiootorenal Syndrome | AIDS | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Guillain-Barre Syndrome | Hepatitis E | Spondylometaphyseal Dysplasia | Congenital Myasthenic Syndrome | Chromosome 17q21.31 Deletion Syndrome | Choroiditis | Erythema Nodosum | Myelitis, Transverse | Johanson-Blizzard Syndrome | Congenital Myopathy | Hypersensitivity Pneumonitis | Teratozoospermia | Vasculitis | Diverticulitis | Hoyeraal-Hreidarsson Syndrome | Peutz-Jeghers Syndrome | Leiomyoma | Intestinal Tuberculosis | Cancer, Colon | Focal Segmental Glomerulosclerosis | Obesity | Raynaud Phenomenon | Myelomeningocele | Spinocerebellar Ataxia Type 27 | Shprintzen-Goldberg Syndrome | Kleine-Levin Syndrome | Stroke, Hemorrhagic | Abetalipoproteinemia | Sclerosing Cholangitis | Wolfram Syndrome 2 | Prolidase Deficiency | DEND Syndrome | Adenoma, Villous | Pouchitis | Chromosome 16p11.2 Deletion Syndrome | Kawasaki Disease | Persistent Hyperplastic Primary Vitreous | Congenital Disorders Of Glycosylation | Cocaine-Related Disorders | Succinic Semialdehyde Dehydrogenase Deficiency | Reflex Epilepsy | Erythropoietic Protoporphyria | Arthrogryposis | Cabezas Syndrome | Granular Corneal Dystrophy Type 1 | Hyperekplexia | Dentinogenesis Imperfecta | Walker-Warburg Syndrome | Charcot-Marie-Tooth Disease Type 2E | Crouzon Syndrome With Acanthosis Nigricans | Familial Cerebral Amyloid Angiopathy | Meier-Gorlin Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Liddle Syndrome | Presbyopia | Strabismus | Adenoma, Pleomorphic | Poirier-Bienvenu Neurodevelopmental Syndrome | Ischemia | Loeys-Dietz Syndrome | Familial Pheochromocytoma-paraganglioma | Stomatitis | Neuromuscular Disorders | Hypokalemic Periodic Paralysis | Christianson Syndrome | Paronychia | Pseudohypoaldosteronism | Generalized Epilepsy With Febrile Seizures Plus | Gyrate Atrophy Of The Choroid And Retina | Congenital Nystagmus | Chronic Kidney Disease | Amelogenesis Imperfecta | Synpolydactyly | Cystinosis | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Hypoalbuminemia | Chorioretinitis | Congenital Primary Aphakia | ICF Syndrome | Lattice Corneal Dystrophy | Hyperthyroidism | Pemphigus Vulgaris | Pseudohermaphroditism | Perivascular Epithelioid Cell Tumor | Shwachman-Bodian-Diamond Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Spondyloperipheral Dysplasia | Bulimia Nervosa | Congenital Fiber-type Disproportion Myopathy | Chondroma | Hypothyroidism