adisease

Showing entry for Galloway Mowat syndrome

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD010768
Disease Name	Galloway Mowat syndrome
Disease CUI Id	C0795949
MeSH Codes	C23 C16 C13 C05 C12 C10
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630
Disease Ontology Class Name	genetic disease
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
O15230	BXGT004138	Laminin subunit alpha-5	3911	reviewed	Enzyme modulator
O43707	BXGT004616	Alpha-actinin-4	81	reviewed
P05556	BXGT006368	Integrin beta-1	3688	reviewed	Receptor
Q96S44	BXGT019738	EKC/KEOPS complex subunit TP53RK	112858	reviewed	Kinase
Q14657	BXGT024111	EKC/KEOPS complex subunit LAGE3	8270	reviewed
Q9BXV9	BXGT024112	EKC/KEOPS complex subunit GON7	84520	reviewed
Q9NPF4	BXGT024113	Probable tRNA N6-adenosine threonylcarbamoyltransferase	55644	reviewed	Enzyme

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}