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ARSB

靶点ID:TCMBANKGE013449

靶点别名:ASB; G4S; MPS6

靶点描述:arylsulfatase B

染色体:5

染色体位置:5q14.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:714

OMIM_Link:611542

Ensembl_Link:ENSG00000113273

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

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000088		Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	group
TCMBANKDI003353		Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI004145		Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	group
TCMBANKDI004646		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI005244		-	-	Finding	disease
TCMBANKDI008043		Cardiovascular Diseases	Abnormality of the cardiovascular system	Anatomical Abnormality	disease
TCMBANKDI008217		-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI011265		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI012157		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	group
TCMBANKDI016946		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases	-	Disease or Syndrome	disease
TCMBANKDI021622		Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI023906		Eye Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI027908		Infections	-	Disease or Syndrome	disease
TCMBANKDI028400		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI029152		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI030874		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI032226		-	Abnormality of the skeletal system; Growth abnormality	Finding	phenotype