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ZBTB20

靶点ID:TCMBANKGE003855

靶点别名:DPZF; HOF; ODA-8S; PRIMS; ZNF288

靶点描述:zinc finger and BTB domain containing 20

染色体:3

染色体位置:3q13.31

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:13503

OMIM_Link:606025

Ensembl_Link:ENSG00000181722

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

TCMBANKIN059452	ethyl aldehyde	C2H4O	44.05 g/mol	CC=O
TCMBANKIN059684	Vitamin E β-	C29H50O2	430.79	CC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
TCMBANKIN059746	α-tocopherol	C29H50O2	430.7 g/mol	CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C
TCMBANKIN060111	17alpha-estradiol	C18H24O2	272.4 g/mol	CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000061	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI002092	-	Abnormality of the ear	Finding	phenotype
TCMBANKDI002881	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI004832	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006146	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI009697	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010203	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI012119	Pathological Conditions, Signs and Symptoms	Abnormality of the nervous system	Cell or Molecular Dysfunction	phenotype
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI015605	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI015991	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI016360	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI016890	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI017066	-	Abnormality of the integument	Congenital Abnormality	phenotype
TCMBANKDI017469	Skin and Connective Tissue Diseases	Abnormality of the breast	Disease or Syndrome	disease
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI018731	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI021493	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI025420	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI027669	-	-	Finding	phenotype
TCMBANKDI029054	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI029520	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI029712	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI030467	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease