Showing entry for RETINITIS PIGMENTOSA 2 (disorder)



                               
General Disease Information
BXGD IdBXGD017424
Disease NameRETINITIS PIGMENTOSA 2 (disorder)
Disease CUI IdC2681923
MeSH Codes C16   C11  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations
The  disease-related  target proteins
Proteins
Uniport Id BXGT Id Protein Name Gene Status Protein Class
Uniport Id BXGT Id Protein name Gene Status Protein class
P10275 BXGT007552 Androgen receptor 367 reviewed Nuclear receptor
P20936 BXGT008619 Ras GTPase-activating protein 1 5921 reviewed Enzyme modulator
Q2M1P5 BXGT014129 Kinesin-like protein KIF7 374654 reviewed
Q92834 BXGT019381 X-linked retinitis pigmentosa GTPase regulator 6103 reviewed
The  disease-related  compounds
Compounds
BXGC Id Compound Name Structure Molecular Weight Number of targets?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease
The  disease-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compounds in food?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease