Showing entry for Myelin P2 protein


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT005919
Protein NameMyelin P2 protein
Uniport IdP02689
GenePMP2
Gene Id5375
DomainLipocalin
Pfam PF00061  
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:0061024 membrane organization
molecular function GO:0015485 cholesterol binding
molecular function GO:0005504 fatty acid binding
cellular component GO:0005737 cytoplasm
cellular component GO:0070062 extracellular exosome
cellular component GO:0043209 myelin sheath
Reactome
Pathway Id Pathway Name
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007959 BXGD000507 Charcot-Marie-Tooth Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0025202 BXGD001832 melanoma Neoplasms
C0027813 BXGD002041 Neuritis Nervous System Diseases
C0031117 BXGD002285 Peripheral Neuropathy Nervous System Diseases
C0036341 BXGD002600 Schizophrenia Mental Disorders
C0039273 BXGD002806 Talipes cavus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0085436 BXGD003177 Meningitis, Cryptococcal Infections; Nervous System Diseases
C0311394 BXGD006884 Difficulty walking Pathological Conditions, Signs and Symptoms
C0427149 BXGD008608 Gait, Drop Foot Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0442874 BXGD008814 Neuropathy Nervous System Diseases
C0751036 BXGD010299 Hereditary Motor and Sensory Neuropathy Type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0850703 BXGD010905 Frequent falls Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1269955 BXGD012005 Tumor Cell Invasion
C1847906 BXGD014897 Onion bulb formation
C1854494 BXGD015409 Slow progression
C1859198 BXGD015861 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C3854222 BXGD019826 Human immunodeficiency virus (HIV) II infection category B1
C4721453 BXGD023744 Peripheral Nervous System Diseases Nervous System Diseases
C4748940 BXGD024041 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000436 Glycerol 92.09
BXGC0002195 Elaidic acid 282.46
BXGC0002196 Vaccenic acid 282.46
BXGC0003705 Chloride 35.45
BXGC0004187 D-Malic acid 134.09
BXGC0005513 Hexadecanoic acid 256.42
BXGC0006198 Citric acid 192.12
BXGC0042373 N,N-Dimethyldodecan-1-Amine Oxide 229.24
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