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LPIN2

靶点ID:TCMBANKGE005922

靶点别名:-

靶点描述:lipin 2

染色体:18

染色体位置:18p11.31

靶点类型:protein-coding

HERB_ID:HBTAR005365

HGNC_Link:14450

OMIM_Link:605519

Ensembl_Link:ENSG00000101577

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

TCMBANKIN004707	phosphatidic acid		C35H69O8P	648.9 g/mol	CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCC

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002512		Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003394		Pathological Conditions, Signs and Symptoms	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI009749		Respiratory Tract Diseases	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI009912		Pathological Conditions, Signs and Symptoms	Abnormality of metabolism/homeostasis	Sign or Symptom	phenotype
TCMBANKDI010589		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI012261		Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	Abnormality of connective tissue	Disease or Syndrome	disease
TCMBANKDI012986		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI013383		Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of the immune system	Finding	phenotype
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
TCMBANKDI016159		Infections; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI018151		Digestive System Diseases; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI021278		Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI022485		-	-	Diagnostic Procedure	phenotype
TCMBANKDI022565		-	-	Finding	phenotype
TCMBANKDI025090		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype