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STX16

靶点ID:TCMBANKGE012190

靶点别名:SYN16

靶点描述:syntaxin 16

染色体:20

染色体位置:20q13.32

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:11431

OMIM_Link:603666

Ensembl_Link:ENSG00000124222

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

TCMBANKIN003665	evoden				C1CCN(CC1)CCOC2=CC=C(C=C2)C(=O)C3=C(SC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002606		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI007343		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI007678		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI009572		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	phenotype
TCMBANKDI012677		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI014953		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI014969		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI016310		-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI021138		-	Abnormality of the digestive system	Sign or Symptom	phenotype
TCMBANKDI023514		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI026626		-	Abnormality of the endocrine system	Finding	phenotype
TCMBANKDI027324		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI027669		-	-	Finding	phenotype
TCMBANKDI028111		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	disease