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Lamp2

靶点ID:TCMBANKGE000655

靶点别名:CD107b; LGP-B; Lamp II; Lamp-2; Lamp-2a; Lamp-2b; Lamp-2c; Mac3

靶点描述:lysosomal-associated membrane protein 2

染色体:X

染色体位置:X A3.3|X 22.67 cM

靶点类型:protein-coding

HERB_ID:HBTAR012816

HGNC_Link:-

OMIM_Link:-

Ensembl_Link:ENSMUSG00000016534

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

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000002	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI002231	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI002512	Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI002624	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI004922	Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI005794	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI009534	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI009702	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	phenotype
TCMBANKDI010221	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI010491	Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI011174	Infections	-	Disease or Syndrome	group
TCMBANKDI011555	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI012859	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI013541	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI014531	Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases	-	Neoplastic Process	disease
TCMBANKDI019267	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI020257	Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI020602	Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI020826	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders	-	Disease or Syndrome	disease
TCMBANKDI022322	-	-	Disease or Syndrome	disease
TCMBANKDI023044	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI023654	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI024083	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI027248	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI028799	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI029030	Pathological Conditions, Signs and Symptoms	Abnormality of the cardiovascular system	Pathologic Function	phenotype
TCMBANKDI029321	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI031297	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031753	-	Abnormality of the musculature	Finding	phenotype