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LRAT

靶点ID:TCMBANKGE014361

靶点别名:LCA14

靶点描述:lecithin retinol acyltransferase

染色体:4

染色体位置:4q32.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:6685

OMIM_Link:604863

Ensembl_Link:ENSG00000121207

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

TCMBANKIN059715	vitamin a		C20H30O	286.5 g/mol	CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C

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
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI005318	Digestive System Diseases; Chemically-Induced Disorders	-	Disease or Syndrome	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007362	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI009877	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI012175	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI013348	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI014624	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	group
TCMBANKDI014798	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI021382	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Finding	phenotype
TCMBANKDI022182	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024118	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI024946	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI026106	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032498	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease