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FGA

靶点ID:TCMBANKGE010980

靶点别名:Fib2

靶点描述:fibrinogen alpha chain

染色体:4

染色体位置:4q31.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:3661

OMIM_Link:134820

Ensembl_Link:ENSG00000171560

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

TCMBANKDI000068	Neoplasms; Stomatognathic Diseases	Neoplasm; Abnormality of head or neck	Neoplastic Process	group
TCMBANKDI000088	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	group
TCMBANKDI000771	Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of the immune system	Sign or Symptom	phenotype
TCMBANKDI002231	Digestive System Diseases	Abnormality of the digestive system	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
TCMBANKDI005092	Neoplasms; Nutritional and Metabolic Diseases; Immune System Diseases	-	Neoplastic Process	disease
TCMBANKDI005318	Digestive System Diseases; Chemically-Induced Disorders	-	Disease or Syndrome	disease
TCMBANKDI006259	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI006828	-	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI007832	Cardiovascular Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI012144	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI013453	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI013541	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI018635	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI021272	Cardiovascular Diseases	-	Pathologic Function	phenotype
TCMBANKDI023498	Skin and Connective Tissue Diseases; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI025396	-	-	Finding	phenotype
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
TCMBANKDI031139	Nervous System Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI031189	Neoplasms	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI031190	Cardiovascular Diseases	-	Pathologic Function	phenotype