adisease

Showing entry for Spastic paraplegia 10, autosomal dominant

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD015821
Disease Name	Spastic paraplegia 10, autosomal dominant
Disease CUI Id	C1858712
MeSH Codes	C16 C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7
Disease Ontology Class Name	genetic 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
P26447	BXGT009114	Protein S100-A4	6275	reviewed	Calcium-binding protein
P33176	BXGT009699	Kinesin-1 heavy chain	3799	reviewed	Cellular structure
Q12756	BXGT013261	Kinesin-like protein KIF1A	547	reviewed	Cellular structure
Q12840	BXGT013269	Kinesin heavy chain isoform 5A	3798	reviewed	Cellular structure
Q8WXF7	BXGT019011	Atlastin-1	51062	reviewed	Enzyme modulator
Q9NZ09	BXGT021267	Ubiquitin-associated protein 1	51271	reviewed
Q9UBP0	BXGT023601	Spastin	6683	reviewed	Cellular structure

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}