Diabetic Nephropathy
About the Disease
Microvascular Complications of Diabetes 2, also known as microvascular complications of diabetes, susceptibility to, 2, is related to microvascular complications of diabetes 3 and background diabetic retinopathy. An important gene associated with Microvascular Complications of Diabetes 2 is EPO (Erythropoietin). The drugs Mecobalamin and Hydroxocobalamin have been mentioned in the context of this disorder. Affiliated tissues include kidney, endothelial and retina.
Common Targets
G1801 | G1636 | G105379399 | G3077 | P5755 | G6752 | G83596 | G8817 | G2936 | G387082 | G23389 | G1124 | G3636 | G4306 | G221692 | G5142 | G2915 | G83440 | G5465 | G102724087 | P16092 | G4627 | G4780 | G64122 | G3597 | G7317 | Protein kinase C (nonspecified subtype) | G2350 | G9779 | G4804 | G10800 | G26074 | G9612 | G59272 | G3958 | G4192 | G4842 | G84942 | G284391 | G5651 | G3117 | G5159 | G6559 | G2864 | G3574 | G152687 | G121551 | G388507 | G7295 | G2053 | G2162 | G779 | G93035 | G79809 | G2475 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | G4128 | G1902 | G1950 | G5321 | G693123 | G9212 | G4199 | CDK5/p25 | G7299 | G80704 | G51557 | G5174 | G10280 | G5578 | G11343 | G10320 | G9370 | G183 | Endothelin-Converting Enzymes (ECE) (nonspecified subtype) | G1268 | G5468 | G8883 | P12327 | G406928 | G407040 | G7442 | G142 | G846 | G57495 | G3479 | G1520 | DNA Topoisomerase II (nonspecified subtype) | G4217 | G3163 | G7224 | G9817 | G6352 | G5241 | G1020 | G3383 | G187 | G2645 | G7058 | G8660 | G54901 | G9039 | G84649 | G5742 | G89795 | G10786 | G23158 | G23411 | G1514 | G246175 | G5313 | G116085 | G1374 | G5137 | G221710 | G23607 | G3135 | ADP-Ribosyl Cyclase/cyclic ADP-Ribose Hydrolase (ADPRC) (nonspecified subtype) | G2022 | G10014 | G9429 | G2908 | G128869 | G375248 | G101929129 | G10628 | Transforming growth factor (nonspecified subtype) | G4158 | G43 | G6339 | G442117 | G22986 | G50507 | G51085 | G3795 | G7111 | G9173 | G57572 | G22843 | G105375741 | G1803 | G4773 | G80310 | G8856 | G1490 | G841 | G6510 | G6648 | G4360 | G55504 | G729230 | G5467 | G54875 | G3605 | G100874095 | G9294 | G135 | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | G554 | G5743 | G57619 | G255738 | G27189 | G3630 | P24881 | G7039 | G231 | G8224 | G7046 | G2321 | G54206 | G5770 | G353500 | G5208 | G2876 | G5595 | G952 | G3854 | G7412 | G57466 | P38822 | G7052 | G7498 | G8801 | G3600 | G3643 | G1910 | G283284 | G3375 | G3689 | G4544 | G5243 | G2739 | G3614 | G83858 | P11113 | G2696 | G390260 | G7517 | G57099 | G9971 | G4524 | G219621 | G84310 | G2837 | G55693 | G4598 | G7421 | G3276 | G1903 | G2646 | G5795 | G1192 | G4159 | G122664 | G168090 | Mitogen-Activated Protein Kinase (nonspecified subtype) | G836 | G5287 | G6754 | G5054 | G57205 | G64478 | G114826 | G1278 | G5734 | Na+/K+-ATPase (nonspecified subtype) | G284459 | G93594 | G140 | G5601 | G4846 | G2729 | G9844 | G162466 | G79782 | G5340 | G7225 | G26751 | G102724768 | G5580 | G59307 | G3586 | G7010 | G84898 | Heme Oxygenase (HO) (nonspecified subtype) | G3791 | G100130698 | G11156 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | G29128 | G7466 | G51586 | G26585 | G4311 | P10959 | Phospholipase A2, Cytosolic (nonspecified subtype) | G4313 | G7536 | G833 | G2569 | G150684 | G22852 | G53831 | G56670 | G3552 | G8654 | G9759 | G6833 | G10203 | G10560 | G9734 | G64241 | G646603 | Prostanoid TP receptor (nonspecified subtype) | G1649 | G823 | G29109 | G1147 | G7042 | G2690 | G6568 | G7422 | G2982 | G5933 | G3458 | G3553 | Transforming growth factor beta (nonspecified subtype) | G2153 | G23235 | G101929504 | G5153 | G101929523 | G4843 | G5741 | G54106 | G5579 | G5315 | G28996 | G9991 | G3569 | G2066 | G7296 | G22891 | G79400 | G53407 | G338440 | G2548 | G100288142 | G2846 | G5787 | G50508 | G2246 | G6523 | G185 | G2823 | G10320 | G26047 | G9379 | G5860 | G1234 | P5757 | G6513 | G4973 | G55512 | G335 | G5167 | G440584 | G5345 | G55604 | G6569 | G406938 | G7369 | G32 | G6755 | G10135 | G2879 | G27035 | Inosine 5'-monophosphate dehydrogenase (IMPDH) (nonspecified subtype) | G4744 | G1024 | G5602 | G3115 | G64061 | G4160 | G351 | P16740 | G4862 | G3565 | G3717 | G22925 | G55365 | G177 | G961 | G10855 | G57512 | G8542 | G3718 | G4481 | G1814 | G834 | G120425 | G348 | G186 | G2069 | G3716 | G1889 | G22807 | G10168 | G3146 | G4363 | G79068 | P24924 | G4036 | G7941 | G114548 | G56606 | G3576 | G6347 | P6058 | G51185 | Nitric oxide synthase (NOS) (nonspecified subtype) | G3596 | P5754 | G2740 | G64770 | G1672 | G2764 | G596 | G2149 | G9896 | G29922 | G7515 | G55148 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | G105370003 | G6514 | G162989 | G1585 | G5305 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | alpha-Amylase (nonspecified subtype) | G23564 | G8764 | G10665 | G407051 | G101927438 | G3606 | G50807 | NADPH Oxidase (nonspecified subtype) | G7043 | G7220 | G7804 | G5581 | G105378977 | G3815 | G23171 | G290 | G3162 | P10999 | G6331 | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | G102723341 | G6934 | G5136 | G768206 | G5972 | G137964 | G8639 | G1286 | G80772 | G90134 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | G387 | G6647 | G7040 | G23643 | Superoxide dismutase (SOD) (nonspecified subtype) | G9770 | G1215 | Vasopressin V1 Receptor (nonspecified subtype) | G7809 | G84265 | G54346 | G7099 | G5144 | G7351 | G2621 | Phosphodiesterase (nonspecified subtype) | G7568 | G10413 | Glutathione peroxidase (nonspecified subtype) | G401237 | G1909 | G2642 | G3091 | G3708 | G80776 | G9718 | P5767 | Transforming growth factor (TGF)-beta receptor (nonspecified subtype) | G847 | G29126 | G695 | G130271 | G3684 | G1535 | G55892 | G3655 | G3882 | G3931 | G23097 | G552 | G55867 | G9314 | G6524 | G7124 | G11000 | G151306 | G6916 | G113402 | G55328 | G9989 | G5820 | G102 | G57521 | G4591 | G5176 | G338557 | G6720 | G83639 | G90865 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G10497 | G840 | G55811 | G1436 | G4256
The "Target / Biomarker Review Report" is a comprehensive and customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about the Target(s) / Biomarker(s) of your choice related to Diabetic Nephropathy, including but not limited to:
• general information;
• protein structure and compound binding;
• protein biological mechanisms;
• its importance;
• the target screening and validation;
• expression level;
• disease relevance;
• drug resistance;
• related combination drugs;
• pharmacochemistry experiments;
• related patent analysis;
• advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai
Other Diseases
Diabetic Neuropathy | Diamond-Blackfan Anemia | Diarrhea | Diastrophic Dysplasia | DICER1 Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Diffuse Intrinsic Pontine Glioma | Diffuse Mesangial Sclerosis | Diffuse Palmoplantar Keratoderma | DiGeorge Syndrome | Discoid Lupus Erythematosus | Disseminated Intravascular Coagulation | Disseminated Superficial Actinic Porokeratosis | Distal Myopathy | Distal Myopathy 2 | Distal Spinal Muscular Atrophy | Diverticulitis | DNA Ligase IV Deficiency | DOCK8 Immunodeficiency Syndrome | Dominant Optic Atrophy | Donnai-Barrow Syndrome | Double Outlet Right Ventricle | Dowling-Degos Disease | Down Syndrome | DRESS Syndrome | Duane Retraction Syndrome | Dubin-Johnson Syndrome | Duchenne Muscular Dystrophy | Duodenal Atresia | Dupuytren Disease | Dwarfism | Dyggve-Melchior-Clausen Disease | Dysequilibrium Syndrome | Dysferlinopathy | Dysfibrinogenemia | Dysgerminoma | Dyskeratosis Congenita | Dyslexia | Dyslipidemia | Dysmorphophobia | Dysplastic Nevus | Dysthymia | Dystonia | Dystonia Musculorum Deformans | Dystonia-parkinsonism, X-linked | Dystrophy, Cone-rod | Early Infantile Epileptic Encephalopathy | Early Infantile Epileptic Encephalopathy 1 | Early Infantile Epileptic Encephalopathy 13 | Early Infantile Epileptic Encephalopathy 28 | Early Infantile Epileptic Encephalopathy 4 | Eating Disorder | Ebstein Anomaly | Eccrine Porocarcinoma | Echinococcosis | Eclampsia | Ectodermal Dysplasia | Ectopia Lentis, Isolated, Autosomal Recessive | Ectrodactyly | Eczema | Ehlers-Danlos Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Eiken Syndrome | Ellis-Van Creveld Syndrome | Emery-Dreifuss Muscular Dystrophy | Empyema | Encephalitis | Encephalitis, Tick-borne | Encephalocele | Encephalopathy | Encephalopathy, Ethylmalonic | Encephalopathy, Glycine | Encephalopathy, Hepatic | Endocarditis | Endometrial Hyperplasia | Endometriosis | Endometritis | Endophthalmitis | Enhanced S-cone Syndrome | Enlarged Vestibular Aqueduct | Enterocolitis, Necrotizing | Eosinophilia | Eosinophilic Asthma | Ependymoma | Epicondylitis | Epidermal Nevus Syndrome | Epidermodysplasia Verruciformis | Epidermolysis Bullosa | Epidermolysis Bullosa Acquisita | Epidermolysis Bullosa Dystrophica | Epidermolysis Bullosa Simplex | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Epidermolysis Bullosa Simplex, Generalized | Epidermolysis Bullosa Simplex, Localized | Epidermolytic Hyperkeratosis | Epidermolytic Ichthyosis, Annular | Epidermolytic Palmoplantar Keratoderma | Epilepsy | Epilepsy Of Infancy With Migrating Focal Seizures | Epilepsy, Generalized | Epiphyseal Chondrodysplasia, Miura Type | Episodic Ataxia | Episodic Ataxia Type 1 | Episodic Ataxia Type 2 | Epithelial-myoepithelial Carcinoma | Epithelioid Hemangioma | Erdheim-Chester Disease | Erectile Dysfunction | Erysipelas | Erythema Multiforme | Erythema Nodosum | Erythematotelangiectatic Rosacea | Erythrokeratodermia Variabilis | Erythromelalgia | Erythropoietic Protoporphyria | Esophageal Adenocarcinoma | Esophageal Carcinoma | Esophageal Motility Disorders | Esophagitis | Esophagitis, Eosinophilic | Esotropia | Essential Fructosuria | Esthesioneuroblastoma | Evans Syndrome | Exfoliative Dermatitis | Exocrine Pancreatic Insufficiency | Exostoses | Exotropia | Extramammary Paget's Disease | Fabry's Disease | Facioscapulohumeral Muscular Dystrophy | Facioscapulohumeral Muscular Dystrophy Type 1 | Facioscapulohumeral Muscular Dystrophy Type 2 | Fahr Disease | Familial Advanced Sleep Phase Syndrome | Familial Cerebral Amyloid Angiopathy | Familial Digital Arthropathy-brachydactyly | Familial Dysautonomia | Familial Episodic Pain Syndrome | Familial Exudative Vitreoretinopathy | Familial Glucocorticoid Deficiency | Familial Hemiplegic Migraine | Familial Hyperaldosteronism | Familial Hypertrophic Cardiomyopathy | Familial Hypobetalipoproteinemia | Familial Isolated Hyperparathyroidism | Familial Male-limited Precocious Puberty | Familial Mediterranean Fever | Familial Partial Lipodystrophy | Familial Pheochromocytoma-paraganglioma | Familial Retinal Arterial Macroaneurysm | Familial Thoracic Aortic Aneurysm | Fanconi Anemia | Fanconi Syndrome | Farber Disease | Fascioliasis | Fatty Aldehyde Dehydrogenase Deficiency | Feingold Syndrome | Fetal Akinesia Deformation Sequence | Fetal Alcohol Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | FG Syndrome | Fibrillation, Atrial | Fibrodysplasia Ossificans Progressiva | Fibromuscular Dysplasia | Fibromyalgia | Fibronectin Glomerulopathy | Fibrosarcoma | Fibrosis | Filariasis | Focal Cortical Dysplasia Type 2 | Focal Dermal Hypoplasia | Focal Facial Dermal Dysplasia | Focal Segmental Glomerulosclerosis | Follicular Dendritic Cell Sarcoma | Fontaine Progeroid Syndrome | Fowler's Syndrome | Fragile X Syndrome | Frank-ter Haar Syndrome | Fraser Syndrome | Frontometaphyseal Dysplasia | Frontotemporal Dementia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Fuchs Dystrophy | Fuchs Heterochromic Iridocyclitis | Fucosidosis | Fukuyama Congenital Muscular Dystrophy | Fundus Albipunctatus | Galactosemia | Galactosialidosis | Galloway-Mowat Syndrome | Gallstones | Ganglioglioma | Ganglioneuroma | Gangliosidosis | Gangliosidosis, GM1 | GAPO Syndrome | Gardner Syndrome | Gastric Atrophy | Gastritis | Gastritis, Atrophic | Gastroenteritis | Gastroenteritis, Eosinophilic | Gastrointestinal Disorders | Gastroschisis | GATA2 Deficiency | Gaucher Disease | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Geleophysic Dysplasia | Genee-Wiedemann Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Generalized Epilepsy With Febrile Seizures Plus | Genitopatellar Syndrome | Gerodermia Osteodysplastica | Gerstmann-Straussler-Scheinker Syndrome | Gestational Trophoblastic Disease | Ghosal Syndrome | Giant Axonal Neuropathy | Giant Cell Arteritis | Giant Cell Glioblastoma | Gigantism | Gilbert Syndrome | Gingivitis | Gitelman Syndrome | Glanzmann Thrombasthenia | Glaucoma | Glaucoma, Congenital | Glaucomatocyclitic Crisis | Glioblastoma | Glioblastoma Multiforme | Glioma | Gliosarcoma | Globozoospermia | Glomerulonephritis | Glomerulonephritis, Membranoproliferative | Glomerulonephritis, Membranous | Glucagonoma | GLUT1 Deficiency Syndrome | Glutaric Aciduria Type 1 | Glutaric Aciduria Type 2 | Glutaric Aciduria Type 3 | Glutathione Synthetase Deficiency | Glycogen Storage Disease | Glycogen Storage Disease Type 0 | Glycogen Storage Disease Type 0, Muscle | Glycogen Storage Disease Type 1 | Glycogen Storage Disease Type 1a | Glycogen Storage Disease Type 1b | Glycogen Storage Disease Type 3 | Glycogen Storage Disease Type 4 | Glycogen Storage Disease Type 5 | Glycogen Storage Disease Type 6 | Glycogen Storage Disease Type 9 | GM2-gangliosidosis AB Variant | Gnathodiaphyseal Dysplasia | GNE Myopathy | Goiter | Goiter, Nodular | Goldenhar Syndrome | Gout | Graft-versus-host Disease | Granular Corneal Dystrophy | Granular Corneal Dystrophy Type 1 | Granuloma Annulare | Graves Disease | Gray Platelet Syndrome | Greenberg Dysplasia | Greig Cephalopolysyndactyly Syndrome | Growth Hormone Excess | Guanidinoacetate Methyltransferase Deficiency | Guillain-Barre Syndrome | Guttate Psoriasis | Gynecomastia | Gyrate Atrophy Of The Choroid And Retina | H Syndrome | Haim-Munk Syndrome | Hairy Cell Leukemia | Hamartoma | HANAC Syndrome | Harlequin Ichthyosis | Hartnup Disease | Hartsfield Syndrome | Hashimoto Thyroiditis | Headache | Heart Block | Heart Failure | Heart Septal Defects | Heavy Chain Disease | Heimler Syndrome | HELLP Syndrome | Hemangioblastoma | Hemangioendothelioma | Hemangioma | Hemimegalencephaly | Hemochromatosis | Hemochromatosis Type 1 | Hemochromatosis Type 2 | Hemoglobinopathies | Hemolytic Anemia | Hemolytic Uremic Syndrome | Hemolytic Uremic Syndrome, Atypical | Hemophagocytic Lymphohistiocytosis | Hemophilia | Hemorrhage | Hemorrhagic Disorders | Hemorrhoids | Hemosiderosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Hepatic Adenomatosis | Hepatic Steatosis | Hepatic Veno-occlusive Disease | Hepatitis | Hepatitis A | Hepatitis B, Chronic | Hepatitis C, Chronic | Hepatitis D | Hepatitis E | Hepatitis, Alcoholic | Hepatitis, Autoimmune | Hepatitis, Chronic | Hepatoblastoma | Hepatopulmonary Syndrome | Hepatorenal Syndrome | Hereditary Coproporphyria | Hereditary Elliptocytosis | Hereditary Folate Malabsorption | Hereditary Hemorrhagic Telangiectasia | Hereditary Hemorrhagic Telangiectasia Type 2 | Hereditary Inclusion Body Myopathy | Hereditary Mixed Polyposis Syndrome | Hereditary Multiple Exostoses | Hereditary Neuropathy With Liability To Pressure Palsies | Hereditary Pyropoikilocytosis | Hereditary Sensory And Autonomic Neuropathy | Hereditary Sensory Neuropathy Type 1 | Hereditary Spastic Paraplegia | Hereditary Spherocytosis | Hereditary Xerocytosis | Hermansky-Pudlak Syndrome | Hernia, Inguinal | Heroin Dependence | Herpes Genitalis | Herpes Simplex Dermatitis | Heterotaxy | Heterotopic Ossification | HIBCH Deficiency | Hidradenitis | Hidradenitis Suppurativa | High Molecular Weight Kininogen Deficiency | Histiocytic Sarcoma | Histiocytosis | Histoplasmosis | Hodgkin Lymphoma | Holoprosencephaly | Holt-Oram Syndrome | Homocystinuria | Hoyeraal-Hreidarsson Syndrome | Huntington's Disease | Huntington's Disease-like 2 | HUPRA Syndrome | Hydrocephalus | Hydrocephalus, Normal Pressure | Hydrolethalus Syndrome | Hydronephrosis | Hydrops Fetalis | Hyper IgE Syndrome | Hyperacusis | Hyperammonemia | Hyperandrogenemia | Hyperbilirubinemia | Hyperbilirubinemia, Neonatal | Hypercalcemia | Hypercalciuria | Hypercholesterolemia | Hypercholesterolemia, Familial | Hyperekplexia | Hypereosinophilic Syndrome | Hyperferritinemia-cataract Syndrome | Hyperglycemia | Hyperhomocysteinemia | Hyperinsulinemia | Hyperinsulinemic Hypoglycemia | Hyperinsulinism-hyperammonemia Syndrome | Hyperkalemic Periodic Paralysis | Hyperkeratosis | Hyperlipidemia | Hyperlipidemia Type V | Hyperlipidemia, Familial Combined | Hypermethioninemia | Hypermetropia | Hyperostosis | Hyperoxaluria | Hyperparathyroidism | Hyperparathyroidism, Primary | Hyperparathyroidism, Secondary | Hyperparathyroidism-jaw Tumor Syndrome | Hyperphenylalaninemia | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Hyperprolactinemia
