Disease

Pancreatitis

About the Disease
Acute Pancreatitis, also known as pancreatitis, acute necrotizing, is related to pancreatitis, hereditary and igg4-related disease. An important gene associated with Acute Pancreatitis is CPB1 (Carboxypeptidase B1), and among its related pathways/superpathways are Sudden infant death syndrome (SIDS) susceptibility pathways and CCL18 signaling pathway. The drugs Cefoperazone and Acetylcysteine have been mentioned in the context of this disorder. Affiliated tissues include pancreas, bone marrow and liver, and related phenotypes are no effect and no effect

Common Targets
KLK7 | HSD17B2 | MAD1L1 | LPAR2 | ASNS | CCND2 | SFN | CCR6 | CELA3B | TMPRSS15 | HLA-B | G1029 | TYK2 | IGSF3 | ORAI1 | HLA-DRB1 | HLA-DQA1 | ALDH2 | TPMT | G7124 | Somatostatin receptor (nonspecified subtype) | T-Type Calcium Channel | TRPM8 | GH1 | Phospholipase A2 (nonspecified subtype) | PTPRE | Calcium release-activated channel (CRAC) | DHODH | HMGCR | Chymotrypsin (nonspecified subtype) | CTSL | CCKBR | Integrin alpha4beta7 (LPAM-1) receptor | NOTCH4 | TRPV1 | MORC4 | ZNF233 | TRPV2 | HLA-A | PRSS1 | DPP4 | RIPPLY1 | ACHE | Protein Kinase D (PKD) (nonspecified subtype) | IAPP | AKR1B1 | GLO1 | Amylin receptor | F2 | G5743 | ALKAL1 | CES1 | HLA-DPA1 | GCKR | ADH1B | CPB1 | Mitogen-Activated Protein Kinase (nonspecified subtype) | SERPINA9 | IL-6 receptor | QPCT | DHPS | RAF1 | KLK1 | Trypsin (nonspecified subtype) | CTRB2 | Caspase (nonspecified subtype) | Elastase (nonspecified subtype) | SST | CHIA | FASLG | PDE5A | CTSC | CELA1 | PTPRN2 | UCHL1 | TXNRD1 | Tryptase (nonspecified subtype) | RASSF10 | ITPA | NOS2 | TRPA1 | USP10 | CCKAR | IL1B | CFTR | TACR1 | HYDIN | SLC6A18 | APC | HLA-DPB1 | PLA2G2D | G3569 | SPINK1 | Phospholipase A2, Secretory (sPLA2) (nonspecified subtype) | CTRC | CTSB | KLKB1 | FTO | CADM1 | FUT2 | APOE | Nitric oxide synthase (NOS) (nonspecified subtype) | RIPK3 | KRR1 | CALCR | HLA-C | MADCAM1 | RIPK1 | HLA-DQB1 | GPR55 | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) (nonspecified subtype) | CX3CR1 | RASSF1 | ATF5 | IL23R | FOS | GPSM3 | TAP2 | PI3 | PTAFR | ONECUT1 | CDH4 | Phosphodiesterase (nonspecified subtype) | PLA2G2A | CPA2 | USP13 | CCK receptor (nonspecified subtype) | CDH13 | BDKRB2

疾病靶点研报
Pancreatitis

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

Other Diseases

Meningioma, Benign | Thyrotoxic Periodic Paralysis | GLUT1 Deficiency Syndrome | Primary Biliary Cholangitis | Sepiapterin Reductase Deficiency | Retinitis | Thyroid Hormone Resistance | Epidermolytic Hyperkeratosis | Otosclerosis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Leprosy | Nicotine Addiction | Dupuytren Disease | Paternal Uniparental Disomy Of Chromosome 14 | Chondrodysplasia Punctata 2, X-linked Dominant | Auriculocondylar Syndrome | Autism | Bipolar Disorder | Leukemia-lymphoma, Adult T-cell | Speech Disorders | Hypertensive Nephropathy | Sturge-Weber Syndrome | Oligospermia | Bullous Pemphigoid | Axenfeld-Rieger Syndrome | AIDS Dementia Complex | Distal Spinal Muscular Atrophy | Azoospermia | Tremor | Malnutrition | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Cohen Syndrome | Stroke, Hemorrhagic | Optic Neuritis | Renal Hypouricemia | Otitis Media | Epidermolytic Ichthyosis, Annular | Pouchitis | Inflammatory Myofibroblastic Tumor | Farber Disease | Craniofrontonasal Syndrome | Lymphangiomatosis | Familial Hyperaldosteronism | 3-methylcrotonyl-CoA Carboxylase Deficiency | Adrenal Insufficiency | Anxiety Disorders | Hypersensitivity Pneumonitis | Obsessive-compulsive Disorder | Lamellar Ichthyosis | Hepatopulmonary Syndrome | Thyroid Dyshormonogenesis | Smith-Magenis Syndrome | Tendinitis | Dubin-Johnson Syndrome | Periodontitis | Leukoplakia | Crisponi Syndrome | Central Retinal Artery Occlusion | Carbonic Anhydrase VA Deficiency | Combined Malonic And Methylmalonic Acidemia | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Hypertension, Renovascular | Osteoarthritis | Glutaric Aciduria Type 1 | Leishmaniasis, Cutaneous | Antley-Bixler Syndrome | Down Syndrome | Primary Progressive Nonfluent Aphasia | Juvenile Polyposis | Neutropenia | Norrie Disease | Toxic Epidermal Necrolysis | Glaucoma, Congenital | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Ocular Surface Squamous Neoplasia | Benign Recurrent Intrahepatic Cholestasis 1 | Takotsubo Cardiomyopathy | Retinal Coloboma | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | IMAGe Syndrome | Nicotine Dependence | Epithelioid Hemangioma | Fragile X Syndrome | Cirrhosis | Cardiac Sarcoidosis | Colitis, Collagenous | Sertoli Cell-only Syndrome | Cardiofaciocutaneous Syndrome | Antisocial Personality Disorder | Dwarfism | Angioimmunoblastic T-cell Lymphoma | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Pemphigoid | Alstrom Syndrome | Optic Nerve Hypoplasia, Bilateral | Pure Red Cell Aplasia | Spastic Paraplegia Type 7 | Erythropoietic Protoporphyria | Hereditary Inclusion Body Myopathy | Impetigo | Narcolepsy | Encephalitis | Atopy | Desmosterolosis | DNA Ligase IV Deficiency | Major Depression | Dystrophy, Cone-rod | Non-proliferative Diabetic Retinopathy | Progressive Familial Intrahepatic Cholestasis | Episodic Ataxia Type 2 | Hereditary Elliptocytosis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Huntington's Disease | Palsy, Cerebral | Primary Ovarian Insufficiency | Sengers Syndrome | Spondylo-ocular Syndrome | Waldenstrom Macroglobulinemia | Gastroschisis | Sclerosing Cholangitis | Skin Carcinoma | Aphasia | Papilloma | Intestinal Obstruction | Pneumonia, Mycoplasma | Esophagitis | Melanoma, Malignant | Agnathia-Otocephaly Complex | Heart Block | Spina Bifida | Keratoconus | Hereditary Sensory Neuropathy Type 1 | Diabetes | Fabry's Disease | Rotor Syndrome | Colon Adenoma | Cholestasis, Intrahepatic | Peutz-Jeghers Syndrome | Botulism | Keratoacanthoma | Empyema | Constipation | Keratosis, Seborrheic | Dysplastic Nevus | Episodic Ataxia Type 1 | Ocular Albinism Type 1 | Chylothorax, Congenital | HELLP Syndrome | Osteosclerosis | Lyme Disease | Bone Giant Cell Tumor | Menkes Disease | Paronychia | Herpes Simplex Dermatitis | Twin-to-twin Transfusion Syndrome | Lymphoproliferative Disease, X-linked | Glycogen Storage Disease Type 5 | Thyroiditis | Pulmonary Alveolar Microlithiasis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Pyruvate Carboxylase Deficiency Disease | Gestational Trophoblastic Disease | Pelizaeus-Merzbacher Disease | Bulimia Nervosa | Progressive Osseous Heteroplasia | Cavitary Optic Disc Anomalies | Glaucoma | Ventricular Septal Defect | Fibromyalgia | Hereditary Mixed Polyposis Syndrome | Acute Motor Axonal Neuropathy | Spinocerebellar Ataxia Type 27 | Autonomic Neuropathy | Pontocerebellar Hypoplasia Type 2 | Hemolytic Anemia | Analgesia | Mumps | Cheilitis | Glycogen Storage Disease Type 1a | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Best Macular Dystrophy | Addison Disease | Autosomal Recessive Spastic Paraplegia Type 54 | Beta-Propeller Protein-associated Neurodegeneration | Hereditary Sensory And Autonomic Neuropathy | Occipital Neuralgia | MELAS Syndrome | Nephropathy | Enterocolitis, Necrotizing | Early Infantile Epileptic Encephalopathy | Metabolic Syndrome | Hypertelorism | Glycogen Storage Disease Type 9 | Primary Carnitine Deficiency | Encephalocele | Hypoalbuminemia | Familial Hemiplegic Migraine | D-2-Hydroxyglutaric Aciduria | Uremic Pruritus | Hereditary Coproporphyria | Meniere's Disease | HIBCH Deficiency | Abetalipoproteinemia | Pseudohypoparathyroidism Type 1B | Infantile Spasm | Adenomatoid Tumor | Achromatopsia | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Wiedemann-Steiner Syndrome | Subcortical Band Heterotopia | Sickle Cell Anemia | Crohn's Disease | Nephronophthisis | Epidermolysis Bullosa Dystrophica | Costello Syndrome | Chromosome 8q21.11 Deletion Syndrome | Diabetes Insipidus | Mitochondrial Disease | Multisystemic Smooth Muscle Dysfunction Syndrome | Retinal Telangiectasia | Chronic Lymphocytic Leukemia | Hamartoma | Carney-Stratakis Syndrome | Esotropia | Fahr Disease | Neuroblastoma | Usher Syndrome Type III | Neurofibromatosis Type 1 | Pseudohypoparathyroidism Type 1A | Hemosiderosis | Seizures | Cellulitis | Amelogenesis Imperfecta | Blue Nevus | Rolandic Epilepsy | Osteitis | Fetal And Neonatal Alloimmune Thrombocytopenia | Renal Medullary Carcinoma | Stuve-Wiedemann Syndrome | Pneumonia, Viral | Diabetic Nephropathy | Charcot-Marie-Tooth Disease Axonal Type 2N | Ganglioglioma | Dysmorphophobia | Walker-Warburg Syndrome | B-cell Chronic Lymphocytic Leukemia | Niemann-Pick Disease, Type A | Obesity | Fowler's Syndrome | Charcot-Marie-Tooth Disease Type 4E | Epidermal Nevus Syndrome | Usher Syndrome Type IIC | Holoprosencephaly | Sleep Apnea, Obstructive | Epiphyseal Chondrodysplasia, Miura Type | Arthritis, Gouty | Hereditary Xerocytosis | Inborn Errors Of Metabolism | Exostoses | Biotinidase Deficiency | Melnick-Needles Syndrome | Spondylosis | Gardner Syndrome | Angina Pectoris | Corneal Edema | Chronic Myelomonocytic Leukemia | Bietti Crystalline Dystrophy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Cocaine-Related Disorders | Sjogren Syndrome | Schuurs-Hoeijmakers Syndrome | Chylomicron Retention Disease | Myoclonus | Tricho-hepato-enteric Syndrome | Liebenberg Syndrome | Sensorineural Hearing Loss | Leukocyte Adhesion Deficiency Type 1 | Schwannoma | Stiff-man Syndrome | Bartter Syndrome | Schizophrenia, Paranoid | Hypercalcemia | Familial Episodic Pain Syndrome | Benign Familial Pemphigus | Alpha-1 Antitrypsin Deficiency | 3-M Syndrome | Asthma, Exercise-induced | Familial Hypertrophic Cardiomyopathy | Encephalopathy, Glycine | Schwartz-Jampel-Aberfeld Syndrome | Contact Dermatitis | T-cell Chronic Lymphocytic Leukemia | Malignant Peripheral Nerve Sheath Tumor | Erythematotelangiectatic Rosacea | Meconium Ileus | Thanatophoric Dysplasia | Mast Cell Leukemia | Glycogen Storage Disease Type 4 | Pseudoexfoliation Syndrome | Mycosis Fungoides | Adenylosuccinate Lyase Deficiency | Congenital Stationary Night Blindness | Polycystic Kidney, Autosomal Recessive | Erectile Dysfunction | Fukuyama Congenital Muscular Dystrophy | Lymphangioleiomyomatosis | Craniometaphyseal Dysplasia | Osteogenesis Imperfecta Type II | Congenital Afibrinogenemia | Neurofibromatosis-Noonan Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Leigh Syndrome | Optic Nerve Diseases | Glycogen Storage Disease Type 0 | Ebstein Anomaly | Birk-Barel Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Warsaw Breakage Syndrome | Hydrops Fetalis | Raynaud Phenomenon | Sporadic Inclusion Body Myositis | Spinal And Bulbar Muscular Atrophy | Purpura | DEND Syndrome | Autoimmune Polyendocrine Syndrome | Zimmermann-Laband Syndrome | Hepatic Steatosis | Cutaneous T-cell Lymphoma | Nestor-Guillermo Progeria Syndrome | Gnathodiaphyseal Dysplasia | Dentinogenesis Imperfecta | Tylosis With Esophageal Cancer | Heart Septal Defects | Sialoadenitis | Neuroleptic Malignant Syndrome | Endophthalmitis | Currarino Syndrome | Heimler Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Pterygium | Thymoma, Malignant | X-linked Creatine Transporter Deficiency | Urea Cycle Disorder | Meesmann Corneal Dystrophy | Nanophthalmos | Familial Mediterranean Fever | Dermatomyositis | Urofacial Syndrome | Camptocormia | Learning Disability | Xeroderma Pigmentosum | Cancer, Bladder | Mannosidase Deficiency Diseases | 3-methylglutaconic Aciduria Type I | Osteogenesis Imperfecta Type VI | Congenital Dyserythropoietic Anemia Type 1 | Spinal Muscular Atrophy | Sponastrime Dysplasia | Thrombasthenia | Primary Hyperoxaluria Type 1 | Spinal Muscular Atrophy Type 3 | Anti-NMDA Receptor Encephalitis | Acute Kidney Injury | Kaposi Sarcoma | Polyomavirus Nephropathy | Benign Hereditary Chorea | Supravalvular Aortic Stenosis | Epidermolysis Bullosa Simplex, Localized | Anal Fissure | Chondromyxoid Fibroma | Astigmatism | Juvenile Xanthogranuloma | Anosmia, Congenital | Necrotizing Autoimmune Myopathy | Choriocarcinoma | Hereditary Multiple Exostoses | Intellectual Disability, Autosomal Dominant 5 | Progressive External Ophthalmoplegia | Hypertension, Essential | Bronchiectasis | Snyder-Robinson Syndrome | Spinocerebellar Ataxia Type 20 | Hyperparathyroidism | Cole-Carpenter Syndrome | Rubeosis Iridis | Obesity, Morbid | Emery-Dreifuss Muscular Dystrophy | Spermatocele | Glutathione Synthetase Deficiency | COACH Syndrome | Allergic Contact Dermatitis | Acute Leukemia | Lentigo | Optic Neuropathy, Anterior Ischemic | Dengue Shock Syndrome | Alveolar Capillary Dysplasia | Canavan Disease | Hyperostosis | Osteogenesis Imperfecta Type I | Creatine Deficiency Syndrome Due To AGAT Deficiency