YEM Search

搜索结果

MAN2B1

靶点ID:TCMBANKGE007164

靶点别名:LAMAN; MANB

靶点描述:mannosidase alpha class 2B member 1

染色体:19

染色体位置:19p13.13

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:6826

OMIM_Link:609458

Ensembl_Link:ENSG00000104774

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

TCMBANKIN018611	swainsonine		C8H15NO3	173.21	C1CC(C2C(C(CN2C1)O)O)O
TCMBANKIN031363	dimethyl sulfoxide		C2H6OS	78.14 g/mol	CS(=O)C
TCMBANKIN057911	se	selenium	H2Se	78.97 g/mol	[Se]

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI010203		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010896		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	group
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
TCMBANKDI011758		-	-	Laboratory Procedure	phenotype
TCMBANKDI017965		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024559		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI026785		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI028799		Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease