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GCDH

靶点ID:TCMBANKGE012227

靶点别名:ACAD5; GCD

靶点描述:glutaryl-CoA dehydrogenase

染色体:19

染色体位置:19p13.13

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:4189

OMIM_Link:608801

Ensembl_Link:ENSG00000105607

靶点对应的植物

ID	拉丁名	药名	药用植物名	功能与主治	来源	药用部位	使用民族

靶点对应的化合物

化合物ID	化合物名	别名	分子式	分子质量	Smiles

TCMBANKIN057984	PG	ST5214535; 504-63-2; .beta.-Propylene glycol; PDO; C02457; InChI=1/C3H8O2/c4-2-1-3-5/h4-5H,1-3H; 2-Deoxyglycerol; .omega.-Propanediol; 1,3-Dihydroxypropane; BRN 0969155; Propane-1,3-diol; Trimethylene glycol; beta-Propylene glycol; CHEBI:16109; 2-(Hydroxymethyl)ethanol; 1,3-Propylenediol; 533734_ALDRICH; 81780_FLUKA; 1,3-PROPANDIOL; 4-01-00-02493 (Beilstein Handbook Reference); AI3-01851; NSC 65426; P50404_ALDRICH; 1,3-Propylene glycol; omega-Propanediol; EINECS 207-997-3; 1,3-Propanediol; ZINC01529437; NSC65426; 757125-93-2;1,3-propanediol	C3H8O2	76.09	C(CO)CO

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002275		-	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Disease or Syndrome	phenotype
TCMBANKDI004086		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI008708		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI010896		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	group
TCMBANKDI011758		-	-	Laboratory Procedure	phenotype
TCMBANKDI015290		Nervous System Diseases; Cardiovascular Diseases	Abnormality of the nervous system; Abnormality of the cardiovascular system	Pathologic Function	disease
TCMBANKDI016564		Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI017437		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI025313		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease