Disease

Primary Biliary Cholangitis

About the Disease
Primary Biliary Cholangitis, also known as primary biliary cirrhosis, is related to gastrointestinal system disease and non-alcoholic fatty liver disease. An important gene associated with Primary Biliary Cholangitis is PBC2 (Biliary Cirrhosis, Primary, 2), and among its related pathways/superpathways are miRNAs involved in DNA damage response and Cell differentiation - expanded index. The drugs Abatacept and Meropenem have been mentioned in the context of this disorder. Affiliated tissues include Umbilical Cord, liver and bone, and related phenotypes are cirrhosis and biliary cirrhosis

Common Targets
PUS10 | RPS6KA4 | GPBAR1 | CLCNKA | IL21-AS1 | TTC27 | LOC105372988 | SLC22A1 | CD3 Complex (T Cell Receptor Complex) | FUNDC2 | HORMAD2 | PDE4B | TNPO3 | PPARA | CYP7A1 | HLA-B | TMEM39A | G4780 | UBE2A | OR52B2 | TYK2 | TRAF3 | FAM110D | PNPLA3 | LOC105377551 | CD58 | KCNH5 | HLA-DRB1 | TPMT | HLA-DQA1 | LYVE1 | RUNX3 | CTSS | BMX | DLAT | BRD4 | SIGLEC8 | PIK3CD | EPS8L1 | PPARG | CTNNA2 | CTSL | PLCL2 | CLN3 | CASP10 | CSF3R | G7124 | PLCL1 | PRKRIP1 | NOTCH4 | SCNN1D | NOX4 | SEZ6L | S1PR4 | HSD11B1 | IQCN | NUDT15 | GABA(A) receptor | ZNF614 | HLA-A | CD40 | ZSCAN5B | UBE2L3 | PPARD | ELP1 | G3605 | SERPINA7 | MMEL1 | LACC1 | G4137 | CD244 | SHC1 | NR3C1 | CCDC113 | ACHE | ULK4 | DCHS1 | G3480 | GIPR | HLA-DRA | FCRL3 | OBSL1 | ITGA11 | IL12RB2 | G3630 | Interleukin-12 (IL-12) | SLC22A23 | LILRA1 | EPG5 | USP2 | GCKR | DENND1B | PIK3CA | SYNGR1 | ELMO1 | ZGPAT | NR1H4 | ADORA3 | TIMMDC1 | C1orf94 | G4233 | CCNY | MS4A1 | VDR | CXCR3 | Vascular endothelial growth factor receptor (VEGFR) (nonspecified subtype) | HIVEP2 | CTLA4 | NADSYN1 | LINC02513 | WHAMM | STAT4 | ARID3A | LOC285626 | CHIA | CD80 | IL10 | OR8G5 | IKZF3 | ELF1 | PRKCB | BTG4 | CLEC16A | TLR9 | MED4 | IL16 | Integrin alphavbeta6 receptor | S1PR5 | IL12A | PAPPA | APOA1 | NOX1 | ZNF865 | CXCL10 | SLC10A2 | IL12A-AS1 | CREBBP | SPIB | HLA-DPB1 | TNFSF15 | LINC01100 | HNF4A | CLDN14 | CTSB | OR52W1 | Integrin alphavbeta1 | ABCB11 | SH2B3 | TRIM32 | SRSF12 | FER1L6 | JAK1 | JAK2 | MANBA | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | CTNNB1 | ZNF683 | TNFRSF1A | GLP1R | ACACA | HLA-DQB1 | EXOC3L4 | TEAD1 | FGF2 | PIK3CG | PPARGC1A | USP37 | MRGPRX4 | GPR65 | PER3 | HECW2 | RELN | Interleukin 23 complex (IL-23) | CAPSL | LOC105379031 | NF-kappaB (NFkB) | G6774 | UMAD1 | CMA1 | ZMIZ1 | RAD51B | G6647 | NFKB1 | DKK2 | IL21R | GCGR | ZNF292 | FCRL4 | TNFSF4 | LOC105377139 | Phosphodiesterase (nonspecified subtype) | POLD1 | IL12B | URM1 | BTK | FGFR2 | NCOR1 | CX3CL1 | LOC101927745

疾病靶点研报
Primary biliary cholangitis

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

Other Diseases

Pemphigus Vulgaris | Granular Corneal Dystrophy | Diabetic Macular Edema | Vitreoretinopathy, Proliferative | IMAGe Syndrome | Strabismus | Hereditary Hemorrhagic Telangiectasia Type 2 | 3C Syndrome | Imerslund-Grasbeck Syndrome | Oculocutaneous Albinism | Fetal And Neonatal Alloimmune Thrombocytopenia | Metachromatic Leukodystrophy | Globozoospermia | Gyrate Atrophy Of The Choroid And Retina | Long QT Syndrome Type 1 | Tremor | Aphasia | Cervicitis | Rickets | Tinea Versicolor | Niemann-Pick Disease, Type A | Polydactyly | Analgesia | Cryptococcal Meningitis | Cranial Nerve Disease | Corneal Ulcer | Conjunctivitis | Encephalopathy, Glycine | Nail Disorder, Nonsyndromic Congenital | Follicular Dendritic Cell Sarcoma | Gilbert Syndrome | Empyema | Lipoma | Sarcomatoid Carcinoma Of The Lung | Hyperacusis | Nephroblastoma | HUPRA Syndrome | Paraplegia | Focal Cortical Dysplasia Type 2 | Spondylo-ocular Syndrome | Glycogen Storage Disease | Primary Hyperoxaluria Type 1 | Pemphigus | Basal Ganglia Disease, Biotin-responsive | Aicardi-Goutieres Syndrome | Mabry Syndrome | Campomelic Dysplasia | Glycogen Storage Disease Type 6 | LRBA Deficiency | Epidermolysis Bullosa Acquisita | Alpha-1 Antitrypsin Deficiency | Cirrhosis | Rhabdomyosarcoma | Hemoglobinopathies | Stiff-man Syndrome | Hyperlipidemia | Hyperoxaluria | Cholera | Hyper IgE Syndrome | Giant Axonal Neuropathy | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Nutrition Disorders | Cerebellofaciodental Syndrome | Spinocerebellar Ataxia Type 16 | Hypotonia-cystinuria Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Esophagitis | Usher Syndrome Type I | Angioedema, Acquired | Acute Anterior Uveitis | Fuchs Dystrophy | Neurofibroma | Acromegaly | Bipolar Disorder | Acne | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Lymphoma, Mantle Cell | Large Granular Lymphocytic Leukemia | T-cell Leukemia | Epidermodysplasia Verruciformis | Hyperthermia, Malignant | Anovulation | Glycogen Storage Disease Type 3 | Congenital Stationary Night Blindness | Asthma, Nocturnal | Diabetes Type 1 | Polymyalgia Rheumatica | Leukoplakia | Hypohidrotic Ectodermal Dysplasia | Spinocerebellar Ataxia Type 21 | Overactive Bladder | Impetigo | Colitis, Microscopic | Central Core Disease | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Anti-NMDA Receptor Encephalitis | Stevens-Johnson Syndrome | Autosomal Recessive Bestrophinopathy | Rhinitis | Nager Acrofacial Dysostosis | Mucolipidosis Type II | Arrhythmogenic Right Ventricular Cardiomyopathy | Familial Advanced Sleep Phase Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Angiosarcoma Of The Breast | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Glycogen Storage Disease Type 0 | Nanophthalmos | Myocardial Infarction | Beare-Stevenson Syndrome | Pneumococcal Meningitis | Bloom Syndrome | Snyder-Robinson Syndrome | Lateral Meningocele Syndrome | Aneurysm, Thoracic Aortic | PASLI Disease | Chondrodysplasia Punctata | Prediabetes | Intracerebral Hemorrhage | Spinocerebellar Ataxia Type 31 | Alopecia | Spinocerebellar Ataxia Type 13 | Neurofibrosarcoma | Superficial Spreading Melanoma | Pontocerebellar Hypoplasia | Lennox-Gastaut Syndrome | Varices | Bronchitis | Myositis, Focal | NDH Syndrome | Canavan Disease | Congenital Adrenal Hyperplasia 1 | Basal Ganglia Disease | Atopic Dermatitis | Ocular Surface Squamous Neoplasia | Colon Adenoma | Adenocarcinoma | TARP Syndrome | Klinefelter Syndrome | Infantile Spasm | Fabry's Disease | Bronchitis, Chronic | Pneumonia, Mycoplasma | Fibromuscular Dysplasia | Parkinson's Disease | Antiphospholipid Syndrome | Osmotic Demyelination Syndrome | Rhabdomyosarcoma, Alveolar | Methemoglobinemia Type IV | Sensory Neuropathy | Anti-glomerular Basement Membrane Disease | Peutz-Jeghers Syndrome | Autoimmune Hemolytic Anemia | Gliosarcoma | Hemophilia | Multiple Sclerosis, Chronic Progressive | Familial Isolated Hyperparathyroidism | Smith-Kingsmore Syndrome | Cleidocranial Dysplasia | Hepatitis, Autoimmune | Panniculitis | Usher Syndrome Type III | Pitt-Hopkins Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Lymphedema | Hyperglycemia | Wolfram Syndrome | Juvenile Myelomonocytic Leukemia | Juvenile Myoclonic Epilepsy | Sclerosteosis 2 | Coma | Encephalitis | Trigonocephaly | Mucolipidosis Type IV | Intracranial Hypertension | Patent Ductus Arteriosus | Anorexia Nervosa | Eating Disorder | Pneumonia, Bacterial | Exfoliative Dermatitis | Epidermolytic Hyperkeratosis | Encephalopathy | Focal Segmental Glomerulosclerosis | Fontaine Progeroid Syndrome | Tyrosinemia | Thrombophlebitis | Palsy, Cerebral | Erysipelas | Acrodysostosis | Biotinidase Deficiency | Nephrosclerosis | Ileitis | Cantu Syndrome | Hypotrichosis Simplex | Neuroblastoma | Gastroschisis | Chylothorax, Congenital | Pericarditis | Inflammatory Myopathy | Cold-induced Sweating Syndrome | Diabetes Insipidus | Keratoconus | Zollinger-Ellison Syndrome | Hemorrhagic Disorders | Citrullinemia | Cri-du-chat Syndrome | Lafora Disease | Micro Syndrome | Glaucoma | Lipodystrophy | Inborn Errors Of Metabolism | Angioedema | Common Variable Immunodeficiency | Geleophysic Dysplasia | Kaposi Sarcoma | Achondrogenesis | Bronchiolitis | Paraganglioma | Pleurisy | Metabolic Diseases | Diastrophic Dysplasia | Amenorrhea | Fucosidosis | Micropenis | Tuberculous Meningitis | Coffin-Lowry Syndrome | Vitreoretinal Degeneration, Snowflake Type | Autoimmune Disease | Trichomegaly | Hereditary Multiple Exostoses | Angina Pectoris | Ellis-Van Creveld Syndrome | Thrombosis | Takotsubo Cardiomyopathy | Diabetes Mellitus, Transient Neonatal | Parvovirus B19 Infection | Werner's Syndrome | Myotonic Disorders | Infertility, Male | Nemaline Myopathy | Non-proliferative Diabetic Retinopathy | REM Sleep Behavior Disorder | Hodgkin Lymphoma | Infantile Nephropathic Cystinosis | Sialidosis Type I | Basan Syndrome | Hoyeraal-Hreidarsson Syndrome | Treacher Collins Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Crimean-Congo Hemorrhagic Fever | Infantile Refsum Disease | Cushing Syndrome | Maternally Inherited Diabetes And Deafness | LMNA-related Congenital Muscular Dystrophy | Reflex Epilepsy | Osteogenesis Imperfecta Type V | Spondylosis | Multiple Sclerosis, Secondary Progressive | Hemolytic Uremic Syndrome | Hepatitis, Alcoholic | Glycogen Storage Disease Type 4 | Batten Disease | Carcinoid Syndrome | Congenital Central Hypoventilation Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Down Syndrome | Chorea | Congenital Heart Block | Epithelial-myoepithelial Carcinoma | Toxoplasmosis | Intestinal Tuberculosis | Postpartum Depression | Autism Spectrum Disorders | Ovarian Sex Cord-stromal Tumor | Necrobiosis Lipoidica | Xeroderma Pigmentosum | Deafness, Dystonia, And Cerebral Hypomyelination | Acanthosis Nigricans | Retinal Degeneration | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Limb Girdle Muscular Dystrophy | CHARGE Syndrome | Familial Digital Arthropathy-brachydactyly | Nephrocalcinosis | Congenital Absence Of Vas Deferens | Pompe Disease | Spondyloarthritis | Marinesco-Sjogren Syndrome | Borderline Personality Disorder | Osteosarcoma | Primary Sclerosing Cholangitis | Spinocerebellar Ataxia Type 40 | Hypotrichosis | Neural Tube Defect | Hypermetropia | Cystinosis | Primary Pigmented Nodular Adrenocortical Disease | Corticobasal Syndrome | Cramp Fasciculation Syndrome | Amish Infantile Epilepsy Syndrome | Histoplasmosis | Multisystemic Smooth Muscle Dysfunction Syndrome | Hypotension, Orthostatic | Waardenburg Syndrome Type 4A | Sarcoma, Alveolar Soft Part | Major Depression | Osteogenesis Imperfecta | Guttate Psoriasis | Liver Failure, Acute Infantile | Borjeson-Forssman-Lehmann Syndrome | Congenital Sodium Diarrhea | Erythromelalgia | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Pain | Placenta Previa | Cocaine-Related Disorders | Leukoplakia, Oral | Behcet's Disease | Frank-ter Haar Syndrome | Usher Syndrome Type IIC | Sclerosteosis | Miyoshi Myopathy | 3-hydroxy-3-methylglutaric Aciduria | Nephropathy | Familial Episodic Pain Syndrome | Triple A Syndrome | Restrictive Dermopathy | Obesity | Astrocytoma, Anaplastic | Diabetic Encephalopathy | Glaucomatocyclitic Crisis | Pheochromocytoma | Scleritis | Spondyloperipheral Dysplasia | Chorea-acanthocytosis | Hereditary Mixed Polyposis Syndrome | Syndactyly | Craniometaphyseal Dysplasia | Auriculocondylar Syndrome | Brachial Plexus Neuropathy | Generalized Epilepsy And Paroxysmal Dyskinesia | Porphyria Cutanea Tarda | Gastrointestinal Disorders | Acquired Partial Lipodystrophy | Cerebrotendinous Xanthomatosis | Acrodermatitis | Early Infantile Epileptic Encephalopathy 1 | Lewy Body Dementia | Holoprosencephaly | Myoclonic Epilepsy With Ragged Red Fibers | Spermatocele | Pre-eclampsia | Periodic Limb Movement Disorder | Spinocerebellar Ataxia Type 3 | Autosomal Recessive Spastic Paraplegia Type 75 | Parkinson Disease 6, Autosomal Recessive Early-onset | Glutaric Aciduria Type 2 | Rash | Chronic Thromboembolic Pulmonary Hypertension | Pernicious Anemia | Glutathione Synthetase Deficiency | Incontinentia Pigmenti | Psoriasis | Echinococcosis | Raine Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Torticollis | Pancytopenia | Neuropathy | Hypercalciuria | Periventricular Leukomalacia | Vascular Calcification | Dementia | Cataplexy | Bacterial Meningitis | Mitochondrial DNA Depletion Syndrome 13 | Membranous Nephropathy | Alstrom Syndrome | Spondylolisthesis | Dysthymia | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Tuberculosis | Headache | Congenital Myasthenic Syndrome | Myopia | Restless Legs Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Epidermolytic Palmoplantar Keratoderma | Encephalopathy, Hepatic | Aarskog-Scott Syndrome | Polyarteritis Nodosa | Branchiootorenal Syndrome | Sponastrime Dysplasia | Atopy | Congenital Disorders Of Glycosylation | Anxiety Disorders | Keratitis-ichthyosis-deafness Syndrome | Arthritis, Reactive | Trichotillomania | Angioimmunoblastic T-cell Lymphoma