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CFL2

靶点ID:TCMBANKGE002618

靶点别名:NEM7

靶点描述:cofilin 2

染色体:14

染色体位置:14q13.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:1875

OMIM_Link:601443

Ensembl_Link:ENSG00000165410

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

TCMBANKIN014187	seo-wenyujinacid B		C2H6OS or HSCH2CH2OH		C(CS)O
TCMBANKIN058970	elaterin		C32H44O8		CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000054		Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI004576		Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI007343		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI013927		Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI013994		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI015863		-	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI018929		Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI018939		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI020257		Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI022380		Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI022442		Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI025401		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	-	Pathologic Function	phenotype
TCMBANKDI027406		-	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI027418		-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI027721		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI032109		Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease