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BTD

靶点ID:TCMBANKGE009679

靶点别名:-

靶点描述:biotinidase

染色体:3

染色体位置:3p25.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:1122

OMIM_Link:609019

Ensembl_Link:ENSG00000169814

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

TCMBANKIN008336	indole-3-acetonitrile	indole-3-acetonitrile	C10H8N2	156.18 g/mol	C1=CC=C2C(=C1)C(=CN2)CC#N
TCMBANKIN022090	oxalaceticacid		C4H4O5	132.07 g/mol	C(C(=O)C(=O)O)C(=O)O
TCMBANKIN057975	lysine acid		C6H14N2O2	146.19 g/mol	C(CCN)CC(C(=O)O)N

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000771		Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of the immune system	Sign or Symptom	phenotype
TCMBANKDI003122		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Pathologic Function	phenotype
TCMBANKDI003266		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the digestive system; Abnormality of the integument	Disease or Syndrome	phenotype
TCMBANKDI005318		Digestive System Diseases; Chemically-Induced Disorders	-	Disease or Syndrome	disease
TCMBANKDI007770		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI009080		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI010752		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI014388		-	Abnormality of the immune system	Finding	phenotype
TCMBANKDI014748		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI017155		Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI018053		Eye Diseases; Skin and Connective Tissue Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI022361		Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI023156		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024083		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI026710		-	Abnormality of the integument	Finding	phenotype
TCMBANKDI031156		Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease