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ATP6V1E1

靶点ID:TCMBANKGE012837

靶点别名:ARCL2C; ATP6E; ATP6E2; ATP6V1E; P31; Vma4

靶点描述:ATPase H+ transporting V1 subunit E1

染色体:22

染色体位置:22q11.21

靶点类型:protein-coding

HERB_ID:HBTAR000325

HGNC_Link:857

OMIM_Link:108746

Ensembl_Link:ENSG00000131100

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

TCMBANKIN059815	tanshinone i		C18H12O3	276.3 g/mol	CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C

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
TCMBANKDI002294	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002791	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI002881	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI006165	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008407	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI011339	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI015460	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases	Abnormality of the respiratory system	Congenital Abnormality	disease
TCMBANKDI015857	Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI018634	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI020008	-	Abnormality of the integument; Abnormality of the cardiovascular system	Finding	phenotype
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI021278	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI022473	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI022768	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI027274	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI028701	Pathological Conditions, Signs and Symptoms	Growth abnormality	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032419	-	Growth abnormality	Finding	phenotype