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ACVR2B

靶点ID:TCMBANKGE010677

靶点别名:ACTRIIB; ActR-IIB; HTX4

靶点描述:activin A receptor type 2B

染色体:3

染色体位置:3p22.2

靶点类型:protein-coding

HERB_ID:HBTAR000053

HGNC_Link:174

OMIM_Link:602730

Ensembl_Link:ENSG00000114739

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

TCMBANKIN058460	pedatisectine b		C5H5N5	135.13 g/mol	C1=NC2=NC=NC(=C2N1)N
TCMBANKIN060889	delta(9)-tetrahydrocannabinol		C21H30O2	314.5 g/mol	CCCCCC1=CC(=C2C3C=C(CCC3C(OC2=C1)(C)C)C)O
TCMBANKIN060892	tetrahydrocannabinol delta8				CCCCCC1=CC2=C(C3C=C(CCC3C(O2)(C)C)C)C(=C1)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI005407		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI011557		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI013171		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases	Growth abnormality	Congenital Abnormality	disease
TCMBANKDI018731		Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI018761		-	-	Diagnostic Procedure	phenotype
TCMBANKDI019138		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI020603		Pathological Conditions, Signs and Symptoms	-	Anatomical Abnormality	phenotype
TCMBANKDI021798		-	-	Disease or Syndrome	disease
TCMBANKDI027494		-	Abnormality of the genitourinary system	Anatomical Abnormality	disease
TCMBANKDI028459		Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the digestive system; Abnormality of the cardiovascular system; Growth abnormality	Congenital Abnormality	disease
TCMBANKDI029791		Nutritional and Metabolic Diseases	-	Disease or Syndrome	phenotype