adisease

Showing entry for Autosomal Dominant Myotubular Myopathy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD019263
Disease Name	Autosomal Dominant Myotubular Myopathy
Disease CUI Id	C3661489
MeSH Codes	C05 C10
Disease Class Name	Musculoskeletal Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
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
P06753	BXGT006498	Tropomyosin alpha-3 chain	7170	reviewed	Cellular structure
P21817	BXGT008693	Ryanodine receptor 1	6261	reviewed	Ion channel
P68133	BXGT011578	Actin, alpha skeletal muscle	58	reviewed	Cellular structure
Q13586	BXGT013380	Stromal interaction molecule 1	6786	reviewed
Q96D31	BXGT019635	Calcium release-activated calcium channel protein 1	84876	reviewed	Ion channel

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}