Showing entry for Bone morphogenetic protein receptor type-1A


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT009939
Protein NameBone morphogenetic protein receptor type-1A
Uniport IdP36894
GeneBMPR1A
Gene Id657
DomainActivin_recp; Pkinase_Tyr; TGF_beta_GS
Pfam PF01064   PF07714   PF08515  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
3. Environmental Information Processing 3.3 Signaling molecules and interaction hsa04060 Cytokine-cytokine receptor interaction
3. Environmental Information Processing 3.2 Signal transduction hsa04350 TGF-beta signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04390 Hippo signaling pathway
4. Cellular Processes 4.3 Cellular community - eukaryotes hsa04550 Signaling pathways regulating pluripotency of stem cells
6. Human Diseases 6.6 Cardiovascular diseases hsa05418 Fluid shear stress and atherosclerosis
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0030509 BMP signaling pathway
Biological Process GO:0061312 BMP signaling pathway involved in heart development
Biological Process GO:0003161 cardiac conduction system development
Biological Process GO:0003215 cardiac right ventricle morphogenesis
Biological Process GO:0071773 cellular response to BMP stimulus
Biological Process GO:0071363 cellular response to growth factor stimulus
Biological Process GO:0002062 chondrocyte differentiation
Biological Process GO:0048589 developmental growth
Biological Process GO:0009950 dorsal/ventral axis specification
Biological Process GO:0009953 dorsal/ventral pattern formation
Biological Process GO:0035912 dorsal aorta morphogenesis
Biological Process GO:0007398 ectoderm development
Biological Process GO:0042733 embryonic digit morphogenesis
Biological Process GO:0048568 embryonic organ development
Biological Process GO:0003272 endocardial cushion formation
Biological Process GO:0003203 endocardial cushion morphogenesis
Biological Process GO:1905285 fibrous ring of heart morphogenesis
Biological Process GO:0060914 heart formation
Biological Process GO:0035137 hindlimb morphogenesis
Biological Process GO:0006955 immune response
Biological Process GO:0001701 in utero embryonic development
Biological Process GO:0048368 lateral mesoderm development
Biological Process GO:0030324 lung development
Biological Process GO:0048382 mesendoderm development
Biological Process GO:0001707 mesoderm formation
Biological Process GO:0003183 mitral valve morphogenesis
Biological Process GO:0001880 Mullerian duct regression
Biological Process GO:0050768 negative regulation of neurogenesis
Biological Process GO:0014912 negative regulation of smooth muscle cell migration
Biological Process GO:0014032 neural crest cell development
Biological Process GO:0021998 neural plate mediolateral regionalization
Biological Process GO:0042475 odontogenesis of dentin-containing tooth
Biological Process GO:0003151 outflow tract morphogenesis
Biological Process GO:0003148 outflow tract septum morphogenesis
Biological Process GO:0048352 paraxial mesoderm structural organization
Biological Process GO:0061626 pharyngeal arch artery morphogenesis
Biological Process GO:0021983 pituitary gland development
Biological Process GO:0030501 positive regulation of bone mineralization
Biological Process GO:0060045 positive regulation of cardiac muscle cell proliferation
Biological Process GO:1904414 positive regulation of cardiac ventricle development
Biological Process GO:0050679 positive regulation of epithelial cell proliferation
Biological Process GO:0002053 positive regulation of mesenchymal cell proliferation
Biological Process GO:0045669 positive regulation of osteoblast differentiation
Biological Process GO:0010862 positive regulation of pathway-restricted SMAD protein phosphorylation
Biological Process GO:1902895 positive regulation of pri-miRNA transcription by RNA polymerase II
Biological Process GO:0060391 positive regulation of SMAD protein signal transduction
Biological Process GO:0045944 positive regulation of transcription by RNA polymerase II
Biological Process GO:1904707 positive regulation of vascular associated smooth muscle cell proliferation
Biological Process GO:0006468 protein phosphorylation
Biological Process GO:0060043 regulation of cardiac muscle cell proliferation
Biological Process GO:2000772 regulation of cellular senescence
Biological Process GO:0048378 regulation of lateral mesodermal cell fate specification
Biological Process GO:0060021 roof of mouth development
Biological Process GO:0001756 somitogenesis
Biological Process GO:0019827 stem cell population maintenance
Biological Process GO:0007179 transforming growth factor beta receptor signaling pathway
Biological Process GO:0003186 tricuspid valve morphogenesis
Biological Process GO:0003223 ventricular compact myocardium morphogenesis
Biological Process GO:0003222 ventricular trabecula myocardium morphogenesis
molecular function GO:0005524 ATP binding
molecular function GO:0098821 BMP receptor activity
molecular function GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific
molecular function GO:0046872 metal ion binding
molecular function GO:0042803 protein homodimerization activity
molecular function GO:0004674 protein serine/threonine kinase activity
molecular function GO:0046332 SMAD binding
molecular function GO:0005025 transforming growth factor beta receptor activity, type I
molecular function GO:0004675 transmembrane receptor protein serine/threonine kinase activity
cellular component GO:0030425 dendrite
cellular component GO:0009897 external side of plasma membrane
cellular component GO:1990712 HFE-transferrin receptor complex
cellular component GO:0016021 integral component of membrane
cellular component GO:0043025 neuronal cell body
cellular component GO:0005886 plasma membrane
cellular component GO:0043235 receptor complex
Reactome
Pathway Id Pathway Name
R-HSA-162582 Signal Transduction
R-HSA-201451 Signaling by BMP
R-HSA-9006936 Signaling by TGFB family members
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000737 BXGD000005 Abdominal Pain Pathological Conditions, Signs and Symptoms
C0001816 BXGD000079 Agnosia Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
C0002871 BXGD000132 Anemia Hemic and Lymphatic Diseases
C0002893 BXGD000150 Refractory anemias Hemic and Lymphatic Diseases
C0003467 BXGD000194 Anxiety Behavior and Behavior Mechanisms
C0005890 BXGD000345 Body Height
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006625 BXGD000401 Cachexia Pathological Conditions, Signs and Symptoms
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007113 BXGD000430 Rectal Carcinoma Digestive System Diseases; Neoplasms
C0007137 BXGD000445 Squamous cell carcinoma Neoplasms
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0009080 BXGD000580 Clubbed Fingers Musculoskeletal Diseases
C0009363 BXGD000599 Congenital ocular coloboma (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0009375 BXGD000602 Colonic Neoplasms Digestive System Diseases; Neoplasms
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009806 BXGD000633 Constipation Pathological Conditions, Signs and Symptoms
C0010068 BXGD000648 Coronary heart disease Cardiovascular Diseases
C0010278 BXGD000660 Craniosynostosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0011581 BXGD000733 Depressive disorder Mental Disorders
C0013274 BXGD000809 Patent ductus arteriosus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0013362 BXGD000817 Dysarthria Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0013384 BXGD000826 Dyskinetic syndrome Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0013481 BXGD000846 Ebstein Anomaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0013604 BXGD000859 Edema Pathological Conditions, Signs and Symptoms
C0015393 BXGD000981 Eye Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0015672 BXGD001011 Fatigue Pathological Conditions, Signs and Symptoms
C0017181 BXGD001103 Gastrointestinal Hemorrhage Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0018524 BXGD001200 Hallucinations Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
C0018553 BXGD001203 Hamartoma Syndrome, Multiple Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
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
C0018817 BXGD001235 Atrial Septal Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0018862 BXGD001242 Heberden node Musculoskeletal Diseases
C0018916 BXGD001245 Hemangioma Neoplasms
C0018932 BXGD001251 Hematochezia Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0020492 BXGD001404 Hyperostosis Musculoskeletal Diseases
C0020502 BXGD001410 Hyperparathyroidism Endocrine System Diseases
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0020621 BXGD001449 Hypokalemia Nutritional and Metabolic Diseases
C0021933 BXGD001524 Intussusception Digestive System Diseases
C0022107 BXGD001530 Irritable Mood Behavior and Behavior Mechanisms
C0022408 BXGD001544 Arthropathy Musculoskeletal Diseases
C0023467 BXGD001658 Leukemia, Myelocytic, Acute Neoplasms
C0023508 BXGD001675 White Blood Cell Count procedure
C0024117 BXGD001734 Chronic Obstructive Airway Disease Respiratory Tract Diseases
C0024523 BXGD001781 Malabsorption Syndrome Digestive System Diseases; Nutritional and Metabolic Diseases
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0025222 BXGD001838 Melena Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0026034 BXGD001887 Microstomia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0026106 BXGD001889 Mild Mental Retardation Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0026764 BXGD001928 Multiple Myeloma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0026826 BXGD001935 Muscle Hypertonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0026827 BXGD001936 Muscle hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0027498 BXGD001994 Nausea and vomiting Pathological Conditions, Signs and Symptoms
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027672 BXGD002020 Neoplastic Syndromes, Hereditary Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0027708 BXGD002025 Nephroblastoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027819 BXGD002043 Neuroblastoma Neoplasms
C0027831 BXGD002047 Neurofibromatosis 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0030554 BXGD002239 Paresthesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0032000 BXGD002318 Pituitary Adenoma Neoplasms; Nervous System Diseases; Endocrine System Diseases
C0032460 BXGD002355 Polycystic Ovary Syndrome Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0032580 BXGD002362 Adenomatous Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0032584 BXGD002363 polyps Pathological Conditions, Signs and Symptoms
C0033680 BXGD002414 Protein-Losing Enteropathies Digestive System Diseases
C0034885 BXGD002490 Rectal Neoplasms Digestive System Diseases; Neoplasms
C0034887 BXGD002491 Rectal polyp Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms
C0034888 BXGD002492 Rectal Prolapse Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0038013 BXGD002725 Ankylosing spondylitis Musculoskeletal Diseases
C0040136 BXGD002845 Thyroid Neoplasm Neoplasms; Endocrine System Diseases
C0042076 BXGD002956 Urologic Neoplasms Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0042138 BXGD002962 Uterine Neoplasms Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0043202 BXGD003037 Wolff-Parkinson-White Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0079218 BXGD003066 Fibromatosis, Aggressive Neoplasms
C0079731 BXGD003087 B-Cell Lymphomas Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0085215 BXGD003141 Ovarian Failure, Premature Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0149793 BXGD003366 Amaurosis Fugax Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0149931 BXGD003388 Migraine Disorders Nervous System Diseases
C0151740 BXGD003468 Intracranial Hypertension Nervous System Diseases
C0152021 BXGD003520 Congenital heart disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0157946 BXGD003873 Osteoarthrosis, localized, not specified whether primary or secondary Musculoskeletal Diseases
C0206734 BXGD004279 Hemangioblastoma Neoplasms
C0220620 BXGD004299 Gastrointestinal Carcinoid Tumor Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0220630 BXGD004302 Adult Liver Carcinoma Digestive System Diseases; Neoplasms
C0221273 BXGD004432 Juvenile polyp Pathological Conditions, Signs and Symptoms; Neoplasms
C0221354 BXGD004446 Frontal bossing Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221355 BXGD004447 Macrocephaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0233794 BXGD004618 Memory impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
C0234132 BXGD004623 Pyramidal sign Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0234144 BXGD004625 Dysgraphia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0236048 BXGD004807 Polyposis, Gastric Digestive System Diseases; Neoplasms
C0238463 BXGD004938 Papillary thyroid carcinoma Neoplasms; Endocrine System Diseases
C0238790 BXGD004956 bone destruction
C0239234 BXGD004974 Low set ears
C0239981 BXGD005011 Hypoalbuminemia Hemic and Lymphatic Diseases
C0265326 BXGD005517 Bannayan-Riley-Ruvalcaba Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0266617 BXGD005700 Congenital anomaly of face Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases
C0267373 BXGD005741 Intestinal hemorrhage NOS Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0278701 BXGD006566 Gastric Adenocarcinoma Digestive System Diseases; Neoplasms
C0278804 BXGD006594 Adenocarcinoma of duodenum Digestive System Diseases; Neoplasms
C0279000 BXGD006622 Liver and Intrahepatic Biliary Tract Carcinoma Digestive System Diseases; Neoplasms
C0279702 BXGD006685 Conventional (Clear Cell) Renal Cell Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0281361 BXGD006774 Adenocarcinoma of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0282193 BXGD006798 Iron Overload Nutritional and Metabolic Diseases
C0333068 BXGD006920 Flexion contracture Musculoskeletal Diseases
C0334108 BXGD006994 Multiple polyps Pathological Conditions, Signs and Symptoms
C0338106 BXGD007167 Adenocarcinoma of colon Digestive System Diseases; Neoplasms
C0345893 BXGD007743 Juvenile polyposis syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0345904 BXGD007745 Malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0346957 BXGD007836 Disseminated Malignant Neoplasm Neoplasms
C0347509 BXGD007857 Benign neoplasm of central nervous system Neoplasms; Nervous System Diseases
C0349588 BXGD007933 Short stature
C0375206 BXGD007973 Hemiplegia/hemiparesis
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0376634 BXGD008006 Craniofacial Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0392470 BXGD008044 Anomalous atrioventricular excitation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0409952 BXGD008399 Idiopathic osteoarthritis Musculoskeletal Diseases
C0423110 BXGD008471 Downward slant of palpebral fissure
C0424503 BXGD008532 Dysmorphic facies
C0426891 BXGD008595 Broad thumbs
C0456070 BXGD008863 Growth delay
C0476089 BXGD008977 Endometrial Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0520947 BXGD009126 Clumsiness - motor delay Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0542476 BXGD009276 Forgetful Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0549473 BXGD009384 Thyroid carcinoma Neoplasms; Endocrine System Diseases
C0575081 BXGD009512 Gait abnormality Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0578477 BXGD009547 Duodenal polyposis
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
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0747845 BXGD010184 early pregnancy
C0750929 BXGD010256 Arnold-Chiari Malformation, Type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0949059 BXGD011568 Polyp of large intestine Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms
C1257915 BXGD011813 Intestinal Polyposis Digestive System Diseases
C1262477 BXGD011882 Weight decreased Pathological Conditions, Signs and Symptoms
C1263846 BXGD011897 Attention deficit hyperactivity disorder Mental Disorders
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1319315 BXGD012415 Adenocarcinoma of large intestine Digestive System Diseases; Neoplasms
C1333015 BXGD012581 Childhood Kidney Wilms Tumor Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1384584 BXGD012943 Generalized osteoarthritis Musculoskeletal Diseases
C1389016 BXGD012962 ATRIOVENTRICULAR CANAL DEFECT Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1403035 BXGD013018 Subcutaneous lipoma Neoplasms; Skin and Connective Tissue Diseases
C1458155 BXGD013136 Mammary Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C1611743 BXGD013456 Familial (FPAH)
C1621958 BXGD013468 Glioblastoma Multiforme Neoplasms
C1720887 BXGD013694 Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications
C1832587 BXGD013855 POLYPOSIS SYNDROME, HEREDITARY MIXED, 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C1832940 BXGD013887 JUVENILE POLYPOSIS OF STOMACH Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C1836542 BXGD014129 Depressed nasal bridge
C1836830 BXGD014165 Developmental regression Mental Disorders
C1837404 BXGD014229 High, narrow palate
C1839783 BXGD014407 Large forehead
C1844530 BXGD014641 Midclavicular hypoplasia
C1854301 BXGD015391 Motor delay Mental Disorders
C1858120 BXGD015774 Generalized hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1862151 BXGD016110 BRACHYDACTYLY, TYPE A1 (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1864730 BXGD016247 Polyposis Syndrome, Hereditary Mixed, 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C1868071 BXGD016483 Adenomatous colonic polyposis Digestive System Diseases; Neoplasms
C1868081 BXGD016485 Juvenile Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C1956346 BXGD016627 Coronary Artery Disease Cardiovascular Diseases
C1959582 BXGD016636 PTEN Hamartoma Tumor Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C1963165 BXGD016685 Malabsorption, CTCAE
C1963167 BXGD016686 Memory Impairment, CTCAE 3.0
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C2677102 BXGD017359 Chromosome 10q23 Deletion Syndrome Pathological Conditions, Signs and Symptoms; Neoplasms
C2677290 BXGD017368 COLORECTAL CANCER, SUSCEPTIBILITY TO, 4
C2677291 BXGD017369 COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 15
C2700617 BXGD017474 Irritation - emotion Behavior and Behavior Mechanisms
C2732838 BXGD017558 Neoplasm of skeletal system
C2919142 BXGD017867 Short Stature, CTCAE
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C2973725 BXGD018205 Pulmonary arterial hypertension Respiratory Tract Diseases; Cardiovascular Diseases
C3203102 BXGD018555 Idiopathic pulmonary arterial hypertension Respiratory Tract Diseases
C3272802 BXGD018631 Hamartomatous polyposis Pathological Conditions, Signs and Symptoms; Neoplasms
C3697248 BXGD019355 Short lower third of face
C3714239 BXGD019404 Bmpr1a-Related Juvenile Polyposis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C3714240 BXGD019405 Smad4-Related Juvenile Polyposis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C3714745 BXGD019427 Malabsorption Digestive System Diseases
C3887875 BXGD019923 Visual field defects Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C3896578 BXGD020039 Familial Colorectal Cancer Type X Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases
C4020965 BXGD020514 Cardiac diverticulum
C4021040 BXGD020530 Freckled genitalia
C4021790 BXGD020782 Abnormality of the skeletal system
C4023006 BXGD021060 Juvenile colonic polyposis
C4023010 BXGD021063 Hyperplastic colonic polyposis
C4023986 BXGD021282 Broad phalanx of the toes
C4025811 BXGD021803 Anemic pallor Pathological Conditions, Signs and Symptoms
C4524092 BXGD023092 Chronic rhinosinusitis with nasal polyps
C4551915 BXGD023441 Gait Disturbance, CTCAE
C4552810 BXGD023525 Irritability, CTCAE
C4553765 BXGD023551 Memory Impairment, CTCAE 5.0
C4721806 BXGD023772 Carcinoma, Basal Cell Neoplasms
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0042376 Picropodophyllotoxin 414.13
BXGC0045254 Sb-202190 331.11
BXGC0047692 Gefitinib 446.15
BXGC0050099 (2E,5S,6S,8Z,11S)-5,6,15-Trihydroxy-17-Methoxy-11-Methyl-12-Oxabicyclo[12.4.0]Octadeca-1(14),2,8,15,17-Pentaene-7,13-Dione 362.14
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