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EXOSC9

靶点ID:TCMBANKGE009737

靶点别名:PCH1D; PM/Scl-75; PMSCL1; RRP45; Rrp45p; p5; p6

靶点描述:exosome component 9

染色体:4

染色体位置:4q27

靶点类型:protein-coding

HERB_ID:HBTAR003068

HGNC_Link:9137

OMIM_Link:606180

Ensembl_Link:ENSG00000123737

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

TCMBANKIN009173	cytidine		C9H13N3O5	243.22 g/mol	C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)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

TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI003390		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI004489		-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI005528		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006243		-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI007343		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI011758		-	-	Laboratory Procedure	phenotype
TCMBANKDI013927		Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI017965		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI024850		-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI026592		-	-	Disease or Syndrome	disease
TCMBANKDI027388		Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the integument; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI028966		-	Abnormality of the integument; Abnormality of limbs	Finding	phenotype
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease