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KCNE1

靶点ID:TCMBANKGE003231

靶点别名:ISK; JLNS; JLNS2; LQT2/5; LQT5; MinK

靶点描述:potassium voltage-gated channel subfamily E regulatory subunit 1

染色体:21

染色体位置:21q22.12

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:6240

OMIM_Link:176261

Ensembl_Link:ENSG00000180509

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

TCMBANKIN060183	ginsenoside- Re		C48H82O18	947.15	CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C(C)(CCC=C(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O)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

TCMBANKDI002657		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI003177		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI003411		-	-	Disease or Syndrome	disease
TCMBANKDI003957		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the cardiovascular system	Sign or Symptom	phenotype
TCMBANKDI004131		-	-	Finding	phenotype
TCMBANKDI004384		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI005748		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI006612		Neoplasms; Female Urogenital Diseases and Pregnancy Complications	Abnormality of the genitourinary system; Neoplasm	Neoplastic Process	disease
TCMBANKDI009702		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	phenotype
TCMBANKDI009943		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI014716		Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI020129		Skin and Connective Tissue Diseases	Abnormality of the integument; Neoplasm	Neoplastic Process	disease
TCMBANKDI020942		-	-	Laboratory Procedure	phenotype
TCMBANKDI021369		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI024355		Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025428		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025502		-	-	Laboratory Procedure	phenotype
TCMBANKDI026511		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI029321		Cardiovascular Diseases	-	Disease or Syndrome	group