YEM Search

搜索结果

FGB

靶点ID:TCMBANKGE000708

靶点别名:HEL-S-78p

靶点描述:fibrinogen beta chain

染色体:4

染色体位置:4q31.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:3662

OMIM_Link:134830

Ensembl_Link:ENSG00000171564

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

TCMBANKIN032291	Hydroxyproline		C5H9NO3	131.13 g/mol	C1C(CNC1C(=O)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

TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003353		Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003411		-	-	Disease or Syndrome	disease
TCMBANKDI003733		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases	Abnormality of the nervous system; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system	Pathologic Function	phenotype
TCMBANKDI004388		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI006828		-	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI007520		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007832		Cardiovascular Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI013541		Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI014161		Stomatognathic Diseases	Abnormality of the immune system; Abnormality of head or neck	Disease or Syndrome	group
TCMBANKDI025416		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025420		Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI029962		-	-	Disease or Syndrome	disease
TCMBANKDI031190		Cardiovascular Diseases	-	Pathologic Function	phenotype
TCMBANKDI031297		Cardiovascular Diseases	-	Disease or Syndrome	group