Showing entry for Cartilage oligomeric matrix protein


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT010732
Protein NameCartilage oligomeric matrix protein
Uniport IdP49747
GeneCOMP
Gene Id1311
DomainCOMP; EGF_CA; TSP_3; TSP_C
Pfam PF11598   PF07645   PF02412   PF05735  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
4. Cellular Processes 4.1 Transport and catabolism hsa04145 Phagosome
3. Environmental Information Processing 3.2 Signal transduction hsa04151 PI3K-Akt signaling pathway
4. Cellular Processes 4.3 Cellular community - eukaryotes hsa04510 Focal adhesion
3. Environmental Information Processing 3.3 Signaling molecules and interaction hsa04512 ECM-receptor interaction
6. Human Diseases 6.10 Infectious diseases: Parasitic hsa05144 Malaria
6. Human Diseases 6.9 Infectious diseases: Viral hsa05165 Human papillomavirus infection
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0009887 animal organ morphogenesis
Biological Process GO:0010260 animal organ senescence
Biological Process GO:0006915 apoptotic process
Biological Process GO:0048844 artery morphogenesis
Biological Process GO:0030509 BMP signaling pathway
Biological Process GO:0030282 bone mineralization
Biological Process GO:0002063 chondrocyte development
Biological Process GO:0035988 chondrocyte proliferation
Biological Process GO:0030199 collagen fibril organization
Biological Process GO:0030198 extracellular matrix organization
Biological Process GO:0003417 growth plate cartilage development
Biological Process GO:0060173 limb development
Biological Process GO:0010259 multicellular organism aging
Biological Process GO:0035264 multicellular organism growth
Biological Process GO:0048747 muscle fiber development
Biological Process GO:0050881 musculoskeletal movement
Biological Process GO:0043066 negative regulation of apoptotic process
Biological Process GO:1900047 negative regulation of hemostasis
Biological Process GO:0050905 neuromuscular process
Biological Process GO:0070527 platelet aggregation
Biological Process GO:1902732 positive regulation of chondrocyte proliferation
Biological Process GO:0016485 protein processing
Biological Process GO:0009306 protein secretion
Biological Process GO:0030500 regulation of bone mineralization
Biological Process GO:0010468 regulation of gene expression
Biological Process GO:0006986 response to unfolded protein
Biological Process GO:0001501 skeletal system development
Biological Process GO:0043588 skin development
Biological Process GO:0035989 tendon development
Biological Process GO:0097084 vascular associated smooth muscle cell development
Biological Process GO:0014829 vascular associated smooth muscle contraction
molecular function GO:0036122 BMP binding
molecular function GO:0005509 calcium ion binding
molecular function GO:0005518 collagen binding
molecular function GO:0005201 extracellular matrix structural constituent
molecular function GO:0043395 heparan sulfate proteoglycan binding
molecular function GO:0008201 heparin binding
molecular function GO:0005178 integrin binding
molecular function GO:0002020 protease binding
molecular function GO:0043394 proteoglycan binding
cellular component GO:0062023 collagen-containing extracellular matrix
cellular component GO:0070062 extracellular exosome
cellular component GO:0031012 extracellular matrix
cellular component GO:0005576 extracellular region
cellular component GO:0005615 extracellular space
cellular component GO:0032991 protein-containing complex
Reactome
Pathway Id Pathway Name
R-HSA-1474244 Extracellular matrix organization
R-HSA-216083 Integrin cell surface interactions
R-HSA-3000178 ECM proteoglycans
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0002066 BXGD000101 Alkaptonuria Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0002312 BXGD000107 alpha-Thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0002793 BXGD000130 Anaplasia Pathological Conditions, Signs and Symptoms; Neoplasms
C0003486 BXGD000197 Aortic Aneurysm Cardiovascular Diseases
C0003850 BXGD000225 Arteriosclerosis Cardiovascular Diseases
C0003862 BXGD000230 Arthralgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0003864 BXGD000231 Arthritis Musculoskeletal Diseases
C0003872 BXGD000235 Arthritis, Psoriatic Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0003873 BXGD000236 Rheumatoid Arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C0004096 BXGD000252 Asthma Respiratory Tract Diseases; Immune System Diseases
C0004153 BXGD000260 Atherosclerosis Cardiovascular Diseases
C0004238 BXGD000262 Atrial Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0005941 BXGD000353 Bone Diseases, Developmental Musculoskeletal Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006309 BXGD000392 Brucellosis Infections
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007193 BXGD000451 Cardiomyopathy, Dilated Cardiovascular Diseases
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0007302 BXGD000460 Cartilage Diseases Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0008479 BXGD000544 Chondrosarcoma Neoplasms
C0009319 BXGD000596 Colitis Digestive System Diseases
C0009375 BXGD000602 Colonic Neoplasms Digestive System Diseases; Neoplasms
C0010054 BXGD000647 Coronary Arteriosclerosis Cardiovascular Diseases
C0010068 BXGD000648 Coronary heart disease Cardiovascular Diseases
C0010346 BXGD000664 Crohn Disease Digestive System Diseases
C0011570 BXGD000729 Mental Depression Behavior and Behavior Mechanisms
C0011581 BXGD000733 Depressive disorder Mental Disorders
C0011603 BXGD000734 Dermatitis Skin and Connective Tissue Diseases
C0011644 BXGD000744 Scleroderma Skin and Connective Tissue Diseases
C0011847 BXGD000749 Diabetes Endocrine System Diseases
C0011849 BXGD000751 Diabetes Mellitus Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011884 BXGD000762 Diabetic Retinopathy Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0017638 BXGD001132 Glioma Neoplasms
C0019158 BXGD001293 Hepatitis Digestive System Diseases
C0019159 BXGD001294 Hepatitis A Digestive System Diseases; Infections
C0019559 BXGD001335 Hip joint pain Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0020445 BXGD001386 Hypercholesterolemia, Familial Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0020456 BXGD001392 Hyperglycemia Nutritional and Metabolic Diseases
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0021051 BXGD001475 Immunologic Deficiency Syndromes Immune System Diseases
C0022408 BXGD001544 Arthropathy Musculoskeletal Diseases
C0022410 BXGD001545 Joint Instability Musculoskeletal Diseases
C0022548 BXGD001551 Keloid Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0022821 BXGD001590 Kyphosis deformity of spine Musculoskeletal Diseases
C0023223 BXGD001621 Leg Ulcer Skin and Connective Tissue Diseases
C0023234 BXGD001622 Legg-Calve-Perthes Disease Musculoskeletal Diseases
C0023798 BXGD001702 Lipoma Neoplasms
C0023890 BXGD001713 Liver Cirrhosis Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0024003 BXGD001726 Lordosis Musculoskeletal Diseases
C0025149 BXGD001826 Medulloblastoma Neoplasms
C0025202 BXGD001832 melanoma Neoplasms
C0025517 BXGD001875 Metabolic Diseases Nutritional and Metabolic Diseases
C0025995 BXGD001885 Micromelia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0026707 BXGD001922 Mucopolysaccharidosis IV Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0026760 BXGD001927 Multiple Epiphyseal Dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0026847 BXGD001940 Spinal Muscular Atrophy Nervous System Diseases
C0027051 BXGD001963 Myocardial Infarction Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0027543 BXGD001997 Avascular necrosis of bone Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027765 BXGD002033 nervous system disorder Nervous System Diseases
C0028259 BXGD002073 Nodule
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0029172 BXGD002120 Oral Submucous Fibrosis Stomatognathic Diseases
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0029410 BXGD002138 Osteoarthritis of hip Musculoskeletal Diseases
C0029422 BXGD002142 Osteochondrodysplasias Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0029456 BXGD002157 Osteoporosis Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029463 BXGD002160 Osteosarcoma Neoplasms
C0030193 BXGD002191 Pain Pathological Conditions, Signs and Symptoms
C0030499 BXGD002232 Parasitic Diseases Infections
C0031069 BXGD002279 Familial Mediterranean Fever Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0036420 BXGD002612 Localized scleroderma Skin and Connective Tissue Diseases
C0036421 BXGD002613 Systemic Scleroderma Skin and Connective Tissue Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0036690 BXGD002632 Septicemia Pathological Conditions, Signs and Symptoms; Infections
C0039103 BXGD002791 Synovitis Musculoskeletal Diseases
C0039585 BXGD002821 Androgen-Insensitivity Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0041834 BXGD002935 Erythema Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0042373 BXGD002978 Vascular Diseases Cardiovascular Diseases
C0085435 BXGD003176 Arthritis, Reactive Infections; Musculoskeletal Diseases
C0086437 BXGD003282 Joint laxity Musculoskeletal Diseases
C0086743 BXGD003308 Osteoarthrosis Deformans Musculoskeletal Diseases
C0149521 BXGD003328 Pancreatitis, Chronic Digestive System Diseases
C0149651 BXGD003342 Clubbing
C0151313 BXGD003413 Sensory neuropathy Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0152235 BXGD003567 Congenital genu recurvatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0158486 BXGD003888 Acquired genu recurvatum Musculoskeletal Diseases
C0162298 BXGD003933 Joint stiffness Musculoskeletal Diseases
C0178874 BXGD004037 Tumor Progression Pathological Conditions, Signs and Symptoms
C0205748 BXGD004117 Dysplastic Nevus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0220726 BXGD004333 Diastrophic dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0221357 BXGD004449 Brachydactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0231678 BXGD004506 Ulnar deviation of the wrist
C0231712 BXGD004519 Waddling gait Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0231749 BXGD004520 Knee pain Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0235974 BXGD004796 Pancreatic carcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0239946 BXGD005010 Fibrosis, Liver Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0241521 BXGD005101 Ulnar deviation of hand Musculoskeletal Diseases
C0242231 BXGD005144 Coronary Stenosis Cardiovascular Diseases
C0242350 BXGD005154 Erectile dysfunction Male Urogenital Diseases; Mental Disorders
C0243026 BXGD005210 Sepsis Pathological Conditions, Signs and Symptoms; Infections
C0263661 BXGD005338 Disorder of skeletal system Musculoskeletal Diseases
C0263680 BXGD005344 Chronic arthritis Musculoskeletal Diseases
C0263746 BXGD005346 Osteoarthritis of the hand Musculoskeletal Diseases
C0272002 BXGD006292 alpha^0^ Thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0276623 BXGD006433 Chronic viral hepatitis Digestive System Diseases
C0278510 BXGD006526 Childhood Medulloblastoma Neoplasms
C0278876 BXGD006607 Adult Medulloblastoma Neoplasms
C0332447 BXGD006891 Morphologically abnormal structure (morphologic abnormality)
C0333307 BXGD006946 Superficial ulcer Pathological Conditions, Signs and Symptoms
C0340629 BXGD007354 Aortic aneurysm without mention of rupture NOS Cardiovascular Diseases
C0342649 BXGD007522 Vascular calcification Nutritional and Metabolic Diseases
C0343284 BXGD007613 Chondrodysplasia Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0344315 BXGD007666 Depressed mood Behavior and Behavior Mechanisms
C0346647 BXGD007832 Malignant neoplasm of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0392476 BXGD008046 Epiphyseal dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0403824 BXGD008316 Teratozoospermia Male Urogenital Diseases
C0409959 BXGD008400 Osteoarthritis, Knee Musculoskeletal Diseases
C0410528 BXGD008430 Skeletal dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0410538 BXGD008434 Pseudoachondroplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0410702 BXGD008447 Adolescent idiopathic scoliosis Musculoskeletal Diseases
C0432211 BXGD008737 Spondyloepimetaphyseal disorder Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0432281 BXGD008762 Pseudochondroplasia
C0451840 BXGD008829 Erosive osteoarthrosis Musculoskeletal Diseases
C0472761 BXGD008916 Homozygous alpha thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0541764 BXGD009259 Delayed bone age
C0544755 BXGD009310 Genu varum Musculoskeletal Diseases
C0546964 BXGD009348 Genu recurvatum
C0575081 BXGD009512 Gait abnormality Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0576093 BXGD009525 Knee joint valgus deformity Musculoskeletal Diseases
C0576226 BXGD009527 Short foot
C0585442 BXGD009593 Osteosarcoma of bone Neoplasms
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0699790 BXGD009866 Colon Carcinoma Digestive System Diseases; Neoplasms
C0740394 BXGD009989 Hyperuricemia Pathological Conditions, Signs and Symptoms
C0744483 BXGD010100 growth hormone treatment
C0745103 BXGD010114 Hyperlipoproteinemia Type IIa Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0847415 BXGD010869 facet joint degeneration
C0852866 BXGD010954 Cervical cord compression Nervous System Diseases; Wounds and Injuries
C0877165 BXGD011338 Short phalanx of finger
C0877430 BXGD011347 Asthma chronic
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C0878659 BXGD011380 Disproportionate short stature Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C1145670 BXGD011764 Respiratory Failure Respiratory Tract Diseases
C1184923 BXGD011800 Lumbar hyperlordosis Musculoskeletal Diseases
C1257915 BXGD011813 Intestinal Polyposis Digestive System Diseases
C1261473 BXGD011855 Sarcoma Neoplasms
C1269955 BXGD012005 Tumor Cell Invasion
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1328407 BXGD012465 Hip Dysplasia Musculoskeletal Diseases; Wounds and Injuries
C1332986 BXGD012574 Childhood Osteosarcoma Neoplasms
C1335302 BXGD012775 Pancreatic Ductal Adenocarcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C1442965 BXGD013064 Avascular necrosis of the capital femoral epiphysis Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C1449563 BXGD013086 Cardiomyopathy, Familial Idiopathic Cardiovascular Diseases
C1456873 BXGD013129 alpha^+^ Thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C1510586 BXGD013176 Autism Spectrum Disorders Mental Disorders
C1561643 BXGD013363 Chronic Kidney Diseases Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1611743 BXGD013456 Familial (FPAH)
C1623038 BXGD013475 Cirrhosis Pathological Conditions, Signs and Symptoms
C1739135 BXGD013733 Progression of prostate cancer
C1800706 BXGD013755 Idiopathic Pulmonary Fibrosis Respiratory Tract Diseases
C1836184 BXGD014088 Short femoral neck
C1836308 BXGD014107 Generalized joint laxity
C1837084 BXGD014195 Short metacarpal
C1838280 BXGD014307 Epiphyseal dysplasia, multiple, 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1839829 BXGD014413 Short distal phalanx of finger
C1842153 BXGD014499 Irregular vertebral endplates
C1843108 BXGD014556 Short palm
C1844704 BXGD014665 Platyspondyly
C1846439 BXGD014817 Hypoplasia of the odontoid process Musculoskeletal Diseases
C1846449 BXGD014819 Irregular epiphyses
C1846803 BXGD014840 Small epiphyses
C1848673 BXGD014963 Hypoplastic feet
C1849016 BXGD014995 Broad femoral neck
C1849937 BXGD015091 Disproportionate short-limb short stature
C1851542 BXGD015217 Limited hip movement
C1854912 BXGD015441 Short long bone
C1855665 BXGD015524 Ovoid vertebral bodies
C1856599 BXGD015619 Beaking of vertebral bodies
C1856637 BXGD015622 Spatulate ribs
C1857108 BXGD015677 Limitation of joint mobility
C1863749 BXGD016195 Carpal bone hypoplasia
C1865200 BXGD016298 Delayed epiphyseal ossification
C1867103 BXGD016438 Limited elbow extension
C1867487 BXGD016462 Childhood onset short-limb short stature
C1867494 BXGD016463 Fragmented, irregular epiphyses
C1956346 BXGD016627 Coronary Artery Disease Cardiovascular Diseases
C2118460 BXGD016927 Acute colitis Digestive System Diseases
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C2745959 BXGD017570 Spondyloepiphyseal dysplasia, congenita Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C3150077 BXGD018291 Mild short stature
C3160814 BXGD018477 Cannabis use
C3161174 BXGD018505 Hemoglobin H Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C3272802 BXGD018631 Hamartomatous polyposis Pathological Conditions, Signs and Symptoms; Neoplasms
C3489413 BXGD018931 Lipomatosis, Multiple Neoplasms
C3495559 BXGD018994 Juvenile arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C3539878 BXGD019087 Triple Negative Breast Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C3544347 BXGD019116 Intestinal fibrosis
C3553368 BXGD019170 Limited hip extension
C3553764 BXGD019187 Joint hyperflexibility
C3714757 BXGD019430 Juvenile rheumatoid arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C3811653 BXGD019662 Experimental Organism Basal Cell Carcinoma Neoplasms
C3840085 BXGD019794 Disorder of Achilles tendon
C3887524 BXGD019892 Skin Erosion Skin and Connective Tissue Diseases
C4016660 BXGD020356 EPIPHYSEAL DYSPLASIA, MULTIPLE, 1, SEVERE
C4021305 BXGD020608 Small epiphyses of the phalanges of the hand
C4021611 BXGD020697 Abnormality of epiphysis morphology
C4021688 BXGD020730 Ulnar metaphyseal irregularity
C4021692 BXGD020731 Radial metaphyseal irregularity
C4021735 BXGD020743 Abnormality of the hip bone
C4022253 BXGD020893 Fragmented epiphyses
C4024934 BXGD021484 Cerebellar medulloblastoma Neoplasms
C4025401 BXGD021658 Irregular carpal bones
C4025674 BXGD021725 Flared femoral metaphysis
C4025814 BXGD021806 Abnormality of the metaphysis
C4275061 BXGD022360 Multiple epiphyseal dysplasia type 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C4310948 BXGD022688 PSEUDOACHONDROPLASIA, SEVERE
C4551516 BXGD023333 Hip pain Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C4551686 BXGD023391 Malignant neoplasm of soft tissue Neoplasms
C4551915 BXGD023441 Gait Disturbance, CTCAE
C4721806 BXGD023772 Carcinoma, Basal Cell Neoplasms
C4722518 BXGD023806 Triple-Negative Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002586 Calcium 40.08
BXGC0050194 alpha-D-Mannose 180.06
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