Showing entry for Desmoplakin


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT008171
Protein NameDesmoplakin
Uniport IdP15924
GeneDSP
Gene Id1832
DomainPlectin; SH3_10; Spectrin_like
Pfam PF00681   PF17902   PF18373  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
6. Human Diseases 6.6 Cardiovascular diseases hsa05412 Arrhythmogenic right ventricular cardiomyopathy (ARVC)
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0034332 adherens junction organization
Biological Process GO:0086073 bundle of His cell-Purkinje myocyte adhesion involved in cell communication
Biological Process GO:0098609 cell-cell adhesion
Biological Process GO:0070268 cornification
Biological Process GO:0002934 desmosome organization
Biological Process GO:0008544 epidermis development
Biological Process GO:0090136 epithelial cell-cell adhesion
Biological Process GO:0045104 intermediate filament cytoskeleton organization
Biological Process GO:0045109 intermediate filament organization
Biological Process GO:0031424 keratinization
Biological Process GO:0030216 keratinocyte differentiation
Biological Process GO:0043312 neutrophil degranulation
Biological Process GO:0018149 peptide cross-linking
Biological Process GO:0150105 protein localization to cell-cell junction
Biological Process GO:0086091 regulation of heart rate by cardiac conduction
Biological Process GO:0098911 regulation of ventricular cardiac muscle cell action potential
Biological Process GO:0043588 skin development
Biological Process GO:0003223 ventricular compact myocardium morphogenesis
Biological Process GO:0042060 wound healing
molecular function GO:0086083 cell adhesive protein binding involved in bundle of His cell-Purkinje myocyte communication
molecular function GO:0005080 protein kinase C binding
molecular function GO:0003723 RNA binding
molecular function GO:0097110 scaffold protein binding
molecular function GO:0005200 structural constituent of cytoskeleton
molecular function GO:0005198 structural molecule activity
cellular component GO:0016323 basolateral plasma membrane
cellular component GO:0030054 cell junction
cellular component GO:0001533 cornified envelope
cellular component GO:0005737 cytoplasm
cellular component GO:0030057 desmosome
cellular component GO:0070062 extracellular exosome
cellular component GO:0005916 fascia adherens
cellular component GO:0101003 ficolin-1-rich granule membrane
cellular component GO:0014704 intercalated disc
cellular component GO:0005882 intermediate filament
cellular component GO:0016020 membrane
cellular component GO:0005634 nucleus
cellular component GO:0005886 plasma membrane
Reactome
Pathway Id Pathway Name
R-HSA-109581 Apoptosis
R-HSA-111465 Apoptotic cleavage of cellular proteins
R-HSA-1266738 Developmental Biology
R-HSA-168249 Innate Immune System
R-HSA-168256 Immune System
R-HSA-351906 Apoptotic cleavage of cell adhesion proteins
R-HSA-5357801 Programmed Cell Death
R-HSA-6798695 Neutrophil degranulation
R-HSA-6805567 Keratinization
R-HSA-6809371 Formation of the cornified envelope
R-HSA-75153 Apoptotic execution phase
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000887 BXGD000017 Acantholysis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0001418 BXGD000050 Adenocarcinoma Neoplasms
C0002170 BXGD000105 Alopecia Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0003811 BXGD000222 Cardiac Arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0006267 BXGD000383 Bronchiectasis Respiratory Tract Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007131 BXGD000441 Non-Small Cell Lung Carcinoma Neoplasms; Respiratory Tract Diseases
C0007137 BXGD000445 Squamous cell carcinoma Neoplasms
C0007193 BXGD000451 Cardiomyopathy, Dilated Cardiovascular Diseases
C0007194 BXGD000452 Hypertrophic Cardiomyopathy Cardiovascular Diseases
C0008031 BXGD000511 Chest Pain Pathological Conditions, Signs and Symptoms
C0009080 BXGD000580 Clubbed Fingers Musculoskeletal Diseases
C0010200 BXGD000653 Coughing Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0010346 BXGD000664 Crohn Disease Digestive System Diseases
C0011071 BXGD000696 Sudden death Pathological Conditions, Signs and Symptoms
C0011603 BXGD000734 Dermatitis Skin and Connective Tissue Diseases
C0011606 BXGD000735 Exfoliative dermatitis Skin and Connective Tissue Diseases
C0011991 BXGD000766 Diarrhea Pathological Conditions, Signs and Symptoms
C0013575 BXGD000854 Ectodermal Dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0013604 BXGD000859 Edema Pathological Conditions, Signs and Symptoms
C0014493 BXGD000919 Epidemic keratoconjunctivitis Infections; Eye Diseases
C0014518 BXGD000921 Toxic Epidermal Necrolysis Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders; Stomatognathic Diseases
C0014527 BXGD000923 Epidermolysis Bullosa Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0014742 BXGD000945 Erythema Multiforme Skin and Connective Tissue Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0017168 BXGD001101 Gastroesophageal reflux disease Digestive System Diseases
C0017572 BXGD001121 Gingival Recession Stomatognathic Diseases
C0018500 BXGD001196 Hair Diseases Skin and Connective Tissue Diseases
C0018790 BXGD001221 Cardiac Arrest Cardiovascular Diseases
C0018798 BXGD001223 Congenital Heart Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0018801 BXGD001226 Heart failure Cardiovascular Diseases
C0018802 BXGD001227 Congestive heart failure Cardiovascular Diseases
C0020608 BXGD001443 Hypodontia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0020678 BXGD001463 Hypotrichosis Skin and Connective Tissue Diseases
C0020757 BXGD001466 Ichthyoses Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0020758 BXGD001467 Congenital ichthyosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0022579 BXGD001558 Keratoderma Skin and Connective Tissue Diseases
C0022595 BXGD001562 Keratosis Follicularis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0022596 BXGD001563 Palmoplantar Keratosis Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0023212 BXGD001616 Left-Sided Heart Failure Cardiovascular Diseases
C0023434 BXGD001643 Chronic Lymphocytic Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023976 BXGD001724 Long QT Syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0024117 BXGD001734 Chronic Obstructive Airway Disease Respiratory Tract Diseases
C0024121 BXGD001735 Lung Neoplasms Neoplasms; Respiratory Tract Diseases
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0025202 BXGD001832 melanoma Neoplasms
C0025286 BXGD001850 Meningioma Neoplasms; Nervous System Diseases
C0027443 BXGD001992 Natal Teeth
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0030436 BXGD002221 Parakeratosis Skin and Connective Tissue Diseases
C0030805 BXGD002256 Bullous pemphigoid Skin and Connective Tissue Diseases; Immune System Diseases
C0030807 BXGD002257 Pemphigus Skin and Connective Tissue Diseases; Immune System Diseases
C0030809 BXGD002258 Pemphigus Vulgaris Skin and Connective Tissue Diseases; Immune System Diseases
C0031538 BXGD002305 Phimosis Male Urogenital Diseases
C0034067 BXGD002456 Pulmonary Emphysema Respiratory Tract Diseases
C0034069 BXGD002458 Pulmonary Fibrosis Respiratory Tract Diseases
C0034088 BXGD002461 Pulmonary Valve Insufficiency Cardiovascular Diseases
C0034642 BXGD002485 Rales Pathological Conditions, Signs and Symptoms
C0036391 BXGD002608 Schwartz-Jampel Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0037116 BXGD002666 Silicosis Respiratory Tract Diseases; Occupational Diseases
C0037274 BXGD002676 Dermatologic disorders Skin and Connective Tissue Diseases
C0037277 BXGD002677 Skin Diseases, Genetic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0039075 BXGD002788 Syndactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0039231 BXGD002799 Tachycardia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0041834 BXGD002935 Erythema Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0042345 BXGD002977 Varicosity Cardiovascular Diseases
C0042510 BXGD002987 Ventricular Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0042514 BXGD002989 Tachycardia, Ventricular Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0042834 BXGD003004 Vital capacity
C0079153 BXGD003064 Hyperkeratosis, Epidermolytic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0085084 BXGD003121 Motor Neuron Disease Nervous System Diseases
C0085106 BXGD003124 Familial benign pemphigus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0085298 BXGD003155 Sudden Cardiac Death Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0085612 BXGD003204 Ventricular arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0085786 BXGD003252 Hamman-Rich syndrome Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases
C0149630 BXGD003334 Bicuspid aortic valve Cardiovascular Diseases
C0151295 BXGD003411 Mononeuritis Multiplex Nervous System Diseases
C0151636 BXGD003451 Premature ventricular contractions Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0151970 BXGD003511 Ulcer of esophagus Digestive System Diseases
C0153381 BXGD003626 Malignant neoplasm of mouth Neoplasms; Stomatognathic Diseases
C0153382 BXGD003627 Malignant neoplasm of oropharynx Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0175704 BXGD004010 LEOPARD Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C0206062 BXGD004148 Lung Diseases, Interstitial Respiratory Tract Diseases
C0206623 BXGD004189 Adenosquamous carcinoma Neoplasms
C0220641 BXGD004305 Lip and Oral Cavity Carcinoma Neoplasms; Stomatognathic Diseases
C0221260 BXGD004424 Dystrophia unguium Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0221270 BXGD004430 Acanthosis Pathological Conditions, Signs and Symptoms
C0221505 BXGD004466 Lesion of brain
C0231807 BXGD004524 Dyspnea on exertion Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0241181 BXGD005084 Fragile skin
C0241984 BXGD005130 Honeycomb lung Respiratory Tract Diseases
C0242379 BXGD005157 Malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C0243050 BXGD005212 Cardiovascular Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0263505 BXGD005318 Alopecia universalis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0265004 BXGD005446 Dilatation of aorta Cardiovascular Diseases
C0265610 BXGD005555 Clinodactyly of fingers Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0265992 BXGD005599 alopecia congenita Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0265998 BXGD005600 ANONYCHIA Pathological Conditions, Signs and Symptoms
C0266427 BXGD005665 Testicular regression syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0270922 BXGD006134 Peripheral demyelinating neuropathy Immune System Diseases; Nervous System Diseases
C0279626 BXGD006657 Squamous cell carcinoma of esophagus Digestive System Diseases; Neoplasms
C0282160 BXGD006797 Aplasia Cutis Congenita Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0333873 BXGD006971 Squamous intraepithelial lesion Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0334013 BXGD006978 Phrynoderma Skin and Connective Tissue Diseases
C0343055 BXGD007593 Generalized pustular psoriasis Skin and Connective Tissue Diseases
C0343073 BXGD007597 Wooly hair Skin and Connective Tissue Diseases
C0344893 BXGD007706 Right ventricular dilatation
C0348617 BXGD007877 Other cardiomyopathies Cardiovascular Diseases
C0349788 BXGD007956 Arrhythmogenic Right Ventricular Dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0393819 BXGD008151 Polyradiculoneuropathy, Chronic Inflammatory Demyelinating Immune System Diseases; Nervous System Diseases
C0406709 BXGD008365 Hay-Wells syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases
C0410916 BXGD008452 Neonatal Death Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C0442874 BXGD008814 Neuropathy Nervous System Diseases
C0543816 BXGD009295 Progressive cardiomyopathic lentiginosis syndrome Cardiovascular Diseases
C0553694 BXGD009409 Oropharyngeal disorders Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0595921 BXGD009626 Intraocular pressure disorder Eye Diseases
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0684249 BXGD009790 Carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0699790 BXGD009866 Colon Carcinoma Digestive System Diseases; Neoplasms
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0740281 BXGD009974 Multiple allergies
C0751783 BXGD010592 Lafora Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0853087 BXGD010964 Nail abnormality Pathological Conditions, Signs and Symptoms
C0853945 BXGD010986 Oral mucosal blisters
C0855329 BXGD011084 Electrocardiogram change
C0870082 BXGD011309 Hyperkeratosis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C1142166 BXGD011736 Brugada Syndrome (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1269955 BXGD012005 Tumor Cell Invasion
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1306460 BXGD012362 Primary malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C1333292 BXGD012612 Diffuse infiltrative lymphocytosis syndrome Pathological Conditions, Signs and Symptoms
C1335475 BXGD012791 Primary Carcinoma Neoplasms
C1367654 BXGD012886 Marginal Zone B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1449563 BXGD013086 Cardiomyopathy, Familial Idiopathic Cardiovascular Diseases
C1527303 BXGD013265 Chronic Airflow Obstruction Respiratory Tract Diseases
C1611743 BXGD013456 Familial (FPAH)
C1720824 BXGD013686 Sudden Cardiac Arrest Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C1739133 BXGD013732 Mucocutaneous herpes simplex
C1800706 BXGD013755 Idiopathic Pulmonary Fibrosis Respiratory Tract Diseases
C1821417 BXGD013764 RESTING HEART RATE
C1832600 BXGD013861 Naxos disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Cardiovascular Diseases
C1834405 BXGD013970 Nail dysplasia Pathological Conditions, Signs and Symptoms
C1836906 BXGD014177 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1840069 BXGD014433 Sandal gap
C1843292 BXGD014570 Skin Fragility-Woolly Hair Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C1843294 BXGD014571 Palmoplantar keratosis with erythema and scale
C1843300 BXGD014572 Sparse eyelashes
C1843896 BXGD014618 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1852127 BXGD015259 KERATOSIS PALMOPLANTARIS STRIATA II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C1854063 BXGD015378 Cardiomyopathy dilated with Woolly hair and keratoderma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Cardiovascular Diseases
C1858302 BXGD015782 Ectodermal dysplasia/ skin fragility syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C1864826 BXGD016253 Epidermolysis bullosa, lethal acantholytic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C1879286 BXGD016570 Hereditary bundle branch system defect Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C1969236 BXGD016767 Mitten deformity
C1969237 BXGD016768 Tapered distal phalanges of finger
C1969238 BXGD016769 Widely spaced toes
C2063326 BXGD016902 Right ventricular cardiomyopathy Cardiovascular Diseases
C2349952 BXGD017065 Oropharyngeal Carcinoma Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C2931783 BXGD018061 Amelogenesis imperfecta nephrocalcinosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Stomatognathic Diseases
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C3150852 BXGD018342 EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
C3266262 BXGD018600 Multiple Chronic Conditions Pathological Conditions, Signs and Symptoms
C3279947 BXGD018789 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
C3495530 BXGD018990 Congenital alopecia X-linked Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C3809719 BXGD019608 Severe dermatitis, multiple allergies, metabolic wasting syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C3887524 BXGD019892 Skin Erosion Skin and Connective Tissue Diseases
C4014393 BXGD020144 CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS
C4015202 BXGD020193 PALMOPLANTAR KERATODERMA AND WOOLLY HAIR
C4021133 BXGD020563 Left ventricular noncompaction cardiomyopathy Pathological Conditions, Signs and Symptoms
C4021633 BXGD020708 Patchy palmoplantar keratoderma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C4021800 BXGD020790 Abnormality of dental enamel
C4024202 BXGD021303 Reduced number of teeth
C4082304 BXGD022090 Oligodontia
C4227331 BXGD022290 Cardiomyocyte hypertrophy
C4282407 BXGD022423 Sparse and thin eyebrow
C4476639 BXGD022845 Ground-glass opacification on pulmonary HRCT
C4476748 BXGD022859 Reticular pattern on pulmonary HRCT
C4551647 BXGD023381 Long QT Syndrome 1 Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4551675 BXGD023384 Keratoderma, Palmoplantar Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C4703660 BXGD023676 Increased troponin I level in blood
C4707237 BXGD023710 Striate palmoplantar keratoderma Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C4721507 BXGD023747 Alveolitis, Fibrosing Respiratory Tract Diseases
C4721508 BXGD023748 Hamman-Rich Disease Respiratory Tract Diseases
C4721509 BXGD023749 Usual Interstitial Pneumonia Respiratory Tract Diseases
C4721530 BXGD023750 Congenital hypotrichia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C4721952 BXGD023786 Familial Idiopathic Pulmonary Fibrosis Respiratory Tract Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002682 Zinc 65.41
BXGC0051100 dihydroartemisinin 284.16
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein