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LRRC56

靶点ID:TCMBANKGE003203

靶点别名:CILD39

靶点描述:leucine rich repeat containing 56

染色体:11

染色体位置:11p15.5

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:25430

OMIM_Link:618227

Ensembl_Link:ENSG00000161328

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

TCMBANKIN021186	hexitol	Allitol; ZINC03831017; InChI=1/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H; 488-44-8; (2R,3R,4S,5S)-hexane-1,2,3,4,5,6-hexol; GALACTITOL (D)	C6H14O6	182.17	C(C(C(C(C(CO)O)O)O)O)O
TCMBANKIN060958	oleic acid;cis-oleic acid;oleinic acid		C18H34O2	282.46	CCCCCCCCC=CCCCCCCCC(=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

TCMBANKDI002340		Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI003394		Pathological Conditions, Signs and Symptoms	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI004102		Pathological Conditions, Signs and Symptoms	Constitutional symptom; Abnormality of head or neck	Sign or Symptom	phenotype
TCMBANKDI004646		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI004655		-	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI006620		-	-	Finding	phenotype
TCMBANKDI008867		Otorhinolaryngologic Diseases	Abnormality of the immune system; Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI010048		Infections; Respiratory Tract Diseases	Abnormality of the immune system; Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI025090		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI025171		Otorhinolaryngologic Diseases	Abnormality of the immune system; Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI025668		Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI025832		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype