Showing entry for Peripheral myelin protein 22


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT012588
Protein NamePeripheral myelin protein 22
Uniport IdQ01453
GenePMP22
Gene Id5376
DomainPMP22_Claudin
Pfam PF00822  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0032060 bleb assembly
Biological Process GO:0008219 cell death
Biological Process GO:0007268 chemical synaptic transmission
Biological Process GO:0032288 myelin assembly
Biological Process GO:0042552 myelination
Biological Process GO:0007422 peripheral nervous system development
cellular component GO:0016021 integral component of membrane
cellular component GO:0005886 plasma membrane
cellular component GO:0045202 synapse
Reactome
Pathway Id Pathway Name
R-HSA-1266738 Developmental Biology
R-HSA-9619665 EGR2 and SOX10-mediated initiation of Schwann cell myelination
R-HSA-9675108 Nervous system development
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0001418 BXGD000050 Adenocarcinoma Neoplasms
C0001430 BXGD000054 Adenoma Neoplasms
C0002395 BXGD000111 Alzheimer's Disease Nervous System Diseases; Mental Disorders
C0002726 BXGD000125 Amyloidosis Nutritional and Metabolic Diseases
C0004364 BXGD000270 Autoimmune Diseases Immune System Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007097 BXGD000424 Carcinoma Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007107 BXGD000428 Malignant neoplasm of larynx Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0007114 BXGD000431 Malignant neoplasm of skin Neoplasms; Skin and Connective Tissue Diseases
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0007286 BXGD000459 Carpal Tunnel Syndrome Nervous System Diseases; Wounds and Injuries
C0007682 BXGD000471 CNS disorder Nervous System Diseases
C0007959 BXGD000507 Charcot-Marie-Tooth Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0008073 BXGD000518 Developmental Disabilities Mental Disorders
C0009319 BXGD000596 Colitis Digestive System Diseases
C0009324 BXGD000597 Ulcerative Colitis Digestive System Diseases
C0009375 BXGD000602 Colonic Neoplasms Digestive System Diseases; Neoplasms
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009404 BXGD000606 Colorectal Neoplasms Digestive System Diseases; Neoplasms
C0010346 BXGD000664 Crohn Disease Digestive System Diseases
C0011195 BXGD000702 Dejerine-Sottas Disease (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0011303 BXGD000712 Demyelinating Diseases Nervous System Diseases
C0011304 BXGD000713 Demyelination Nervous System Diseases
C0011311 BXGD000714 Dengue Fever Infections
C0011849 BXGD000751 Diabetes Mellitus Nutritional and Metabolic Diseases; Endocrine System Diseases
C0013132 BXGD000799 Drooling Stomatognathic Diseases
C0013264 BXGD000808 Muscular Dystrophy, Duchenne Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0013363 BXGD000818 Dysautonomia Nervous System Diseases
C0013404 BXGD000833 Dyspnea Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0014378 BXGD000912 Enterovirus Infections Infections
C0014550 BXGD000930 Myoclonic Epilepsy Nervous System Diseases
C0016506 BXGD001062 Foot Deformities Musculoskeletal Diseases
C0016579 BXGD001069 Formication Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0017178 BXGD001102 Gastrointestinal Diseases Digestive System Diseases
C0017638 BXGD001132 Glioma Neoplasms
C0018378 BXGD001190 Guillain-Barre Syndrome Immune System Diseases; Nervous System Diseases
C0018784 BXGD001220 Sensorineural Hearing Loss (disorder) Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic 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
C0019100 BXGD001283 Severe Dengue Infections
C0019816 BXGD001348 Hereditary, Type VII, Motor and Sensory Neuropathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0019829 BXGD001350 Hodgkin Disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0021053 BXGD001476 Immune System Diseases Immune System Diseases
C0021390 BXGD001503 Inflammatory Bowel Diseases Digestive System Diseases
C0021841 BXGD001519 Intestinal Neoplasms Digestive System Diseases; Neoplasms
C0022735 BXGD001581 Klinefelter Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0023211 BXGD001615 Left Bundle-Branch Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0023473 BXGD001661 Myeloid Leukemia, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023944 BXGD001723 Locked-In Syndrome Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0023976 BXGD001724 Long QT Syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0025149 BXGD001826 Medulloblastoma Neoplasms
C0026106 BXGD001889 Mild Mental Retardation Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0026499 BXGD001905 Monosomy Pathological Conditions, Signs and Symptoms
C0026764 BXGD001928 Multiple Myeloma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0026769 BXGD001930 Multiple Sclerosis Immune System Diseases; Nervous System Diseases
C0026827 BXGD001936 Muscle hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0026896 BXGD001946 Myasthenia Gravis Neoplasms; Immune System Diseases; Nervous System Diseases
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027743 BXGD002031 Nerve compression syndrome Nervous System Diseases
C0027765 BXGD002033 nervous system disorder Nervous System Diseases
C0027796 BXGD002037 Neuralgia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0027809 BXGD002040 Neurilemmoma Neoplasms
C0027813 BXGD002041 Neuritis Nervous System Diseases
C0027830 BXGD002046 neurofibroma Neoplasms; Nervous System Diseases
C0027831 BXGD002047 Neurofibromatosis 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0027868 BXGD002053 Neuromuscular Diseases Nervous System Diseases
C0027888 BXGD002056 Hereditary Motor and Sensory Neuropathies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0028643 BXGD002079 Numbness Nervous System Diseases; Mental Disorders
C0029132 BXGD002117 Disorder of the optic nerve Eye Diseases; Nervous System Diseases
C0029463 BXGD002160 Osteosarcoma Neoplasms
C0030354 BXGD002214 Papilloma Neoplasms
C0030552 BXGD002238 Paresis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0030554 BXGD002239 Paresthesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0031117 BXGD002285 Peripheral Neuropathy Nervous System Diseases
C0032580 BXGD002362 Adenomatous Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0032587 BXGD002365 Polyradiculoneuropathy Immune System Diseases; Nervous System Diseases
C0032927 BXGD002381 Precancerous Conditions Neoplasms
C0034372 BXGD002480 Quadriplegia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0034933 BXGD002496 Reflex, Abnormal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0035021 BXGD002501 Relapsing Fever Infections
C0035229 BXGD002516 Respiratory Insufficiency Respiratory Tract Diseases
C0036341 BXGD002600 Schizophrenia Mental Disorders
C0036421 BXGD002613 Systemic Scleroderma Skin and Connective Tissue Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0037011 BXGD002656 Shoulder Pain Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0037221 BXGD002673 Situs Inversus Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0037315 BXGD002687 Sleep Apnea Syndromes Respiratory Tract Diseases; Nervous System Diseases
C0039273 BXGD002806 Talipes cavus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0040100 BXGD002840 Thymoma Neoplasms; Hemic and Lymphatic Diseases
C0041296 BXGD002903 Tuberculosis Infections
C0042384 BXGD002979 Vasculitis Cardiovascular Diseases
C0042928 BXGD003014 Vocal Cord Paralysis Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
C0079731 BXGD003087 B-Cell Lymphomas Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0085648 BXGD003221 Synovial Cyst Neoplasms
C0085996 BXGD003260 Child Development Deviations Mental Disorders
C0085997 BXGD003261 Child Development Disorders, Specific Mental Disorders
C0149940 BXGD003391 Sciatic Neuropathy Nervous System Diseases
C0151311 BXGD003412 Cranial nerve palsies Nervous System Diseases
C0151313 BXGD003413 Sensory neuropathy Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0151572 BXGD003442 Reflex, Corneal, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0151786 BXGD003475 Muscle Weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0151888 BXGD003497 Hyporeflexia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0151889 BXGD003498 Hyperreflexia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0152025 BXGD003521 Polyneuropathy Nervous System Diseases
C0152109 BXGD003542 Juvenile Spinal Muscular Atrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0152237 BXGD003569 Talipes Calcaneovalgus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0153382 BXGD003627 Malignant neoplasm of oropharynx Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0153690 BXGD003684 Secondary malignant neoplasm of bone Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases
C0162309 BXGD003934 Adrenoleukodystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
C0175702 BXGD004008 Williams Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
C0178874 BXGD004037 Tumor Progression Pathological Conditions, Signs and Symptoms
C0205711 BXGD004113 Pelizaeus-Merzbacher Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0205713 BXGD004114 Roussy-Levy Syndrome (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0206692 BXGD004243 Carcinoma, Lobular Neoplasms; Skin and Connective Tissue Diseases
C0220597 BXGD004292 Adult Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220644 BXGD004306 Childhood Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220766 BXGD004341 Congenital hypoplasia of adrenal gland Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
C0221052 BXGD004380 Chronic berylliosis Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases; Occupational Diseases; Wounds and Injuries
C0221373 BXGD004454 Claw hand Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0231686 BXGD004508 Gait, Unsteady Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0234146 BXGD004626 Absent reflex Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0234784 BXGD004696 Reflex, Gag, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0235044 BXGD004716 Paresthesia, Distal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0238190 BXGD004890 Inclusion Body Myositis (disorder) Musculoskeletal Diseases; Nervous System Diseases
C0238288 BXGD004905 Muscular Dystrophy, Facioscapulohumeral Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0238463 BXGD004938 Papillary thyroid carcinoma Neoplasms; Endocrine System Diseases
C0240991 BXGD005069 Ataxia, Sensory Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0241772 BXGD005112 Reflex, Deep Tendon, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0242287 BXGD005145 Isaacs syndrome Musculoskeletal Diseases; Nervous System Diseases
C0262576 BXGD005255 Nerve paralysis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0266464 BXGD005676 Polymicrogyria Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0267375 BXGD005742 Chronic colitis Digestive System Diseases
C0270790 BXGD006105 Quadriparesis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0270911 BXGD006128 Charcot-Marie-Tooth Disease, Type Ia (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0270912 BXGD006129 Charcot-Marie-Tooth Disease, Type Ib Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0270913 BXGD006130 Charcot-Marie-Tooth disease, Type 1C Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0270914 BXGD006131 Hereditary Motor and Sensory-Neuropathy Type II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0270921 BXGD006133 Axonal neuropathy Nervous System Diseases
C0270922 BXGD006134 Peripheral demyelinating neuropathy Immune System Diseases; Nervous System Diseases
C0270933 BXGD006135 Inflammatory neuropathy Nervous System Diseases
C0271623 BXGD006222 Hypogonadotropic hypogonadism Endocrine System Diseases
C0271682 BXGD006233 Mixed sensory-motor polyneuropathy Nervous System Diseases
C0271683 BXGD006234 Polyneuropathy, Motor Nervous System Diseases
C0277839 BXGD006481 Hoffman's Reflex Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0277850 BXGD006482 Reflex, Pendular Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0278211 BXGD006507 Reflex, Corneal, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0278502 BXGD006522 recurrent gastric cancer
C0334583 BXGD007124 Pilocytic Astrocytoma Neoplasms
C0338478 BXGD007184 Idiopathic Myoclonic Epilepsy Nervous System Diseases
C0338479 BXGD007185 Symptomatic Myoclonic Epilepsy Nervous System Diseases
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0342482 BXGD007486 X-linked Adrenal Hypoplasia Endocrine System Diseases
C0345392 BXGD007732 Congenital kyphoscoliosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0376544 BXGD008001 Hematopoietic Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C0392553 BXGD008055 Hereditary peripheral neuropathy Nervous System Diseases
C0392699 BXGD008064 Dysesthesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0393695 BXGD008121 Early Childhood Epilepsy, Myoclonic Nervous System Diseases
C0393702 BXGD008124 Myoclonic Astatic Epilepsy Nervous System Diseases
C0393703 BXGD008125 Myoclonic Absence Epilepsy Nervous System Diseases
C0393808 BXGD008148 Charcot-Marie-Tooth disease, X-linked, 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0393814 BXGD008149 Hereditary liability to pressure palsies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0393818 BXGD008150 Congenital hypomyelinating neuropathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0393819 BXGD008151 Polyradiculoneuropathy, Chronic Inflammatory Demyelinating Immune System Diseases; Nervous System Diseases
C0403396 BXGD008276 Steroid-sensitive nephrotic syndrome Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0424605 BXGD008535 Developmental delay (disorder) Mental Disorders
C0426970 BXGD008598 Spastic Quadriplegia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0427065 BXGD008604 Distal muscle weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0427149 BXGD008608 Gait, Drop Foot Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0432072 BXGD008718 Dysmorphic features
C0432470 BXGD008792 46, XY female Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0438414 BXGD008802 Myoclonic Encephalopathy Nervous System Diseases
C0442874 BXGD008814 Neuropathy Nervous System Diseases
C0474520 BXGD008953 Myokymia, Generalized Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0476273 BXGD008986 Respiratory distress Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0494165 BXGD009022 Secondary malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0494491 BXGD009032 Mononeuropathies Nervous System Diseases
C0497552 BXGD009067 Congenital neurologic anomalies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0520947 BXGD009126 Clumsiness - motor delay Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0521158 BXGD009130 Recurrent tumor
C0521532 BXGD009141 Diaphragmatic paresis Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0522224 BXGD009198 Paralysed Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0522345 BXGD009201 Reflex, Acoustic, Abnormal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0524851 BXGD009246 Neurodegenerative Disorders Nervous System Diseases
C0541794 BXGD009262 Skeletal muscle atrophy
C0557874 BXGD009444 Global developmental delay
C0558845 BXGD009459 Reflex, Ankle, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0558846 BXGD009460 Reflex, Triceps, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0558847 BXGD009461 Reflex, Biceps, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0575081 BXGD009512 Gait abnormality Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0575157 BXGD009514 Deformity of spine
C0575158 BXGD009515 Kyphoscoliosis deformity of spine Musculoskeletal Diseases
C0576612 BXGD009529 Reflex, Anal, Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0579144 BXGD009555 Cavovarus deformity of foot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0585442 BXGD009593 Osteosarcoma of bone Neoplasms
C0587246 BXGD009616 Muscle weakness of limb Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0588008 BXGD009620 Severe depression Mental Disorders
C0595989 BXGD009632 Carcinoma of larynx Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0596992 BXGD009649 myelinopathy Nervous System Diseases
C0598589 BXGD009667 Inherited neuropathies Nervous System Diseases
C0600033 BXGD009682 Acquired Kyphoscoliosis Musculoskeletal Diseases
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0677932 BXGD009736 Progressive Neoplastic Disease
C0677944 BXGD009738 Sentinel node (disorder)
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0684219 BXGD009789 Myokymia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0686619 BXGD009835 Secondary malignant neoplasm of lymph node Pathological Conditions, Signs and Symptoms; Neoplasms
C0699790 BXGD009866 Colon Carcinoma Digestive System Diseases; Neoplasms
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0728829 BXGD009917 Congenital pes cavus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0740340 BXGD009978 Amyloidosis, Familial Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0743002 BXGD010072 Abnormal Deep Tendon Reflex Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751036 BXGD010299 Hereditary Motor and Sensory Neuropathy Type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0751059 BXGD010308 Cranial Neuropathies, Multiple Nervous System Diseases
C0751120 BXGD010324 Benign Infantile Myoclonic Epilepsy Nervous System Diseases
C0751122 BXGD010325 Infantile Severe Myoclonic Epilepsy Nervous System Diseases
C0751412 BXGD010433 Painful Paresthesias Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751460 BXGD010449 Flaccid Quadriplegia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751461 BXGD010450 Paralysis, Spinal, Quadriplegic Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751468 BXGD010453 Bulbocavernosus Reflex, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751469 BXGD010454 Bulbocavernousus Reflex Absent Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751470 BXGD010455 Palmo-Mental Reflex Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751471 BXGD010456 Reflex, Anal, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751472 BXGD010457 Reflex, Ankle, Abnormal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751473 BXGD010458 Reflex, Ankle, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751474 BXGD010459 Reflex, Biceps, Abnormal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751475 BXGD010460 Reflex, Biceps, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751476 BXGD010461 Reflex, Gag, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751477 BXGD010462 Reflex, Knee, Abnormal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751478 BXGD010463 Reflex, Knee, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751479 BXGD010464 Reflex, Moro, Asymmetric Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751480 BXGD010465 Reflex, Triceps, Abnormal Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751481 BXGD010466 Reflex, Triceps, Decreased Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751690 BXGD010553 Malignant Peripheral Nerve Sheath Tumor Neoplasms; Nervous System Diseases
C0751837 BXGD010604 Gait Ataxia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751922 BXGD010644 Median Neuropathy Nervous System Diseases
C0795864 BXGD010754 Smith-Magenis syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0795865 BXGD010755 Chromosome 17, trisomy 17p Pathological Conditions, Signs and Symptoms
C0917800 BXGD011411 Epilepsy, Myoclonic, Infantile Nervous System Diseases
C1096168 BXGD011606 Chromosome 17 trisomy Pathological Conditions, Signs and Symptoms
C1136179 BXGD011712 Hammer Toe Musculoskeletal Diseases
C1258666 BXGD011825 Myxoid cyst Neoplasms; Skin and Connective Tissue Diseases
C1269955 BXGD012005 Tumor Cell Invasion
C1290871 BXGD012197 Disorder of hand
C1302401 BXGD012303 Adenoma of large intestine Digestive System Diseases; Neoplasms
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1332986 BXGD012574 Childhood Osteosarcoma Neoplasms
C1337013 BXGD012876 Differentiated Thyroid Gland Carcinoma
C1384666 BXGD012948 hearing impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C1408174 BXGD013034 Hypertrophic neuropathy of infancy
C1408182 BXGD013035 Hereditary motor and sensory neuropathy, types I-IV
C1458155 BXGD013136 Mammary Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C1510429 BXGD013161 Entrapment Neuropathies Nervous System Diseases
C1527231 BXGD013261 Adrenomyeloneuropathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
C1611743 BXGD013456 Familial (FPAH)
C1695985 BXGD013499 Lewis-Sumner syndrome
C1737329 BXGD013728 Dysmorphism Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C1806780 BXGD013759 Increased CSF protein
C1832588 BXGD013856 Chromosome 11p11.2 Deletion Syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases
C1832776 BXGD013875 Hypertrophic nerve changes
C1834304 BXGD013965 AMYOTROPHY, HEREDITARY NEURALGIC Nervous System Diseases
C1836150 BXGD014082 Gait imbalance
C1836450 BXGD014117 Distal lower limb muscle weakness
C1837352 BXGD014223 Childhood onset
C1839259 BXGD014363 Bulbo-Spinal Atrophy, X-Linked Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1843057 BXGD014552 Calf muscle hypertrophy
C1843077 BXGD014553 Segmental peripheral demyelination/remyelination
C1843168 BXGD014562 Myelin outfoldings
C1845112 BXGD014711 Hyperkyphosis
C1846176 BXGD014791 Hyperactive deep tendon reflexes Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1847584 BXGD014876 Distal sensory impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1847906 BXGD014897 Onion bulb formation
C1848296 BXGD014918 DOSAGE-SENSITIVE SEX REVERSAL Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C1848736 BXGD014970 Distal amyotrophy
C1849148 BXGD015014 Decreased sensory nerve conduction velocity
C1849193 BXGD015022 PEELING SKIN SYNDROME Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C1854301 BXGD015391 Motor delay Mental Disorders
C1854494 BXGD015409 Slow progression
C1858120 BXGD015774 Generalized hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1858285 BXGD015781 Decreased number of peripheral myelinated nerve fibers
C1858729 BXGD015825 Decreased motor nerve conduction velocity
C1861403 BXGD016045 Variable expressivity
C1861669 BXGD016063 Charcot-Marie-Tooth disease and deafness Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Otorhinolaryngologic Diseases
C1861675 BXGD016064 Cold-induced muscle cramps Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C1866141 BXGD016379 Foot dorsiflexor weakness
C1866636 BXGD016411 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1867138 BXGD016442 Upper limb postural tremor Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1879344 BXGD016574 Biliary papillomatosis Digestive System Diseases; Neoplasms
C2079538 BXGD016914 Charcot-Marie-Tooth disease, Type 2A Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C2118460 BXGD016927 Acute colitis Digestive System Diseases
C2349952 BXGD017065 Oropharyngeal Carcinoma Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C2350019 BXGD017066 Solitary Pulmonary Nodule Respiratory Tract Diseases
C2350037 BXGD017067 Clinically Isolated Syndrome, CNS Demyelinating Nervous System Diseases
C2718001 BXGD017521 Protein Misfolding Disorders Nutritional and Metabolic Diseases
C2750090 BXGD017652 Charcot-Marie-Tooth Disease, Axonal, Type 2n Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C2875300 BXGD017836 Peroneal muscular atrophy (axonal type) (hypertrophic type)
C2919828 BXGD017881 Chronic ulcerative colitis Digestive System Diseases
C2930619 BXGD017890 Sex Differentiation Disorders Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C2931246 BXGD017987 Potocki-Lupski syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C2931686 BXGD018047 Charcot-Marie-Tooth disease, Type 1E Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C2932678 BXGD018098 Inherited Peripheral Neuropathy Nervous System Diseases
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C3266262 BXGD018600 Multiple Chronic Conditions Pathological Conditions, Signs and Symptoms
C3495591 BXGD018999 Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Otorhinolaryngologic Diseases
C3539781 BXGD019086 Progressive cGVHD
C3542501 BXGD019106 Acute Infective Polyneuritis Immune System Diseases; Nervous System Diseases
C3544347 BXGD019116 Intestinal fibrosis
C3714772 BXGD019433 Recurrent fevers
C3887709 BXGD019918 Optic Neuropathy Eye Diseases; Nervous System Diseases
C4016264 BXGD020298 DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
C4016716 BXGD020365 CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, AUTOSOMAL RECESSIVE
C4016717 BXGD020366 CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS
C4020732 BXGD020474 Mitochondrial abnormalities
C4020904 BXGD020492 Myelin tomacula
C4021727 BXGD020736 EMG: neuropathic changes
C4021753 BXGD020758 Abnormality of the immune system
C4023690 BXGD021244 Spontaneous pain sensation
C4024933 BXGD021483 Acute demyelinating polyneuropathy
C4025214 BXGD021595 Sleepy facial expression
C4025799 BXGD021796 Ulnar claw Musculoskeletal Diseases
C4048329 BXGD021904 Immunosuppression
C4083008 BXGD022100 Guillain-Barre Syndrome, Familial Immune System Diseases; Nervous System Diseases
C4255193 BXGD022313 Bilateral Vestibulopathy Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C4477013 BXGD022904 Impaired oropharyngeal swallow response Digestive System Diseases; Otorhinolaryngologic Diseases
C4511452 BXGD023002 Sporadic Parkinson disease Nervous System Diseases
C4518505 BXGD023025 Partial trisomy of chromosome 17
C4551551 BXGD023345 X-linked hereditary motor and sensory neuropathy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C4551910 BXGD023440 Acute Inflammatory Demyelinating Polyneuropathy Immune System Diseases; Nervous System Diseases
C4551915 BXGD023441 Gait Disturbance, CTCAE
C4696948 BXGD023629 Trauma symptoms
C4721453 BXGD023744 Peripheral Nervous System Diseases Nervous System Diseases
C4722085 BXGD023788 Malignant neoplasm of colon and/or rectum
C4722172 BXGD023791 Primary differentiated carcinoma of thyroid gland
C4727002 BXGD023847 Chronic Hemolysis
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000099 3,4-Dihydroxyphenylacetic acid 168.15
BXGC0000130 Estradiol 272.38
BXGC0000205 Theobromine 180.16
BXGC0000530 Hydroquinone 110.11
BXGC0000665 Nonivamide 293.4
BXGC0000895 5-Hydroxyindole-3-acetic acid 191.18
BXGC0001002 1,2-Benzenediol 110.11
BXGC0001325 Progesterone 314.46
BXGC0001623 L-Tryptophan 204.23
BXGC0001767 (E)-Resveratrol 228.25
BXGC0001857 Caffeic acid 180.16
BXGC0001868 Catechin 290.27
BXGC0001899 Daidzein 254.24
BXGC0001940 Daphnetin 178.14
BXGC0002071 Apigenin 270.24
BXGC0002906 Caffeic acid ester 284.31
BXGC0002916 Melatonin 232.28
BXGC0003392 Isoxanthopterin 179.14
BXGC0003610 5-Hydroxy-L-tryptophan 220.22
BXGC0004276 Acetamide 59.07
BXGC0005624 Genistein 270.24
BXGC0005683 Quercetin 302.24
BXGC0005894 Azelaic acid 188.22
BXGC0006306 Myricetin 318.24
BXGC0006362 Estrone 270.37
BXGC0006389 Rotenone 394.42
BXGC0006422 Mercenene 214.05
BXGC0008184 Phloretin 274.27
BXGC0008707 Isoliquiritigenin 256.25
BXGC0009649 Dihydrocapsaicin 307.43
BXGC0012340 L-glutamine 146.14
BXGC0014695 Loratadine 382.14
BXGC0016470 Camptothecin 348.11
BXGC0016681 Hispidin 246.05
BXGC0016886 Papaverine Hydrochloride 339.15
BXGC0017757 Androstenedione 286.19
BXGC0018736 Benzamide 121.05
BXGC0021478 Lipoic Acid 206.04
BXGC0024988 Nifedipine 346.12
BXGC0025757 Calcimycin 523.27
BXGC0027374 Glyburide 493.14
BXGC0027421 Paclitaxel 853.33
BXGC0028001 Beta-Lapachone 242.09
BXGC0028278 Rutaecarpine 287.11
BXGC0034256 Rottlerin 516.18
BXGC0034379 Tetraethylammonium Chloride 130.16
BXGC0042870 Piceatannol 244.07
BXGC0043125 Taxifolin 304.06
BXGC0044857 Sp-600125 220.06
BXGC0045252 Sc-560 352.06
BXGC0045254 Sb-202190 331.11
BXGC0046139 Aminoglutethimide 232.12
BXGC0046510 Tpck 351.07
BXGC0046559 Paraxanthine 180.06
BXGC0048661 Nicardipine Hydrochloride 479.21
BXGC0049738 Dexibuprofen 206.13
BXGC0050471 Fluorouracil 130.02
BXGC0051524 Ouabain 584.28
BXGC0052374 Reserpine 608.27
BXGC0053629 Esatenolol 266.16
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