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DSP

靶点ID:TCMBANKGE012516

靶点别名:DCWHKTA; DP

靶点描述:desmoplakin

染色体:6

染色体位置:6p24.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:3052

OMIM_Link:125647

Ensembl_Link:ENSG00000096696

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

TCMBANKDI000076	Neoplasms	-	Neoplastic Process	group
TCMBANKDI000088	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	group
TCMBANKDI000092	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI000372	Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI002512	Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI002533	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI005474	Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI005587	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI006835	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI008314	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI008939	Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI009080	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI009657	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	group
TCMBANKDI009702	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	phenotype
TCMBANKDI009943	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI010589	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI011000	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI011480	Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI011741	-	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI012976	Neoplasms; Stomatognathic Diseases	-	Neoplastic Process	disease
TCMBANKDI014106	Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases	-	Neoplastic Process	disease
TCMBANKDI016216	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	-	Congenital Abnormality	disease
TCMBANKDI016439	Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI017642	Neoplasms	Abnormality of the integument; Neoplasm	Neoplastic Process	disease
TCMBANKDI020257	Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI022482	-	-	Finding	phenotype
TCMBANKDI022675	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	-	Pathologic Function	phenotype
TCMBANKDI023220	Male Urogenital Diseases	-	Finding	phenotype
TCMBANKDI024040	Congenital, Hereditary, and Neonatal Diseases and Abnormalities	-	Disease or Syndrome	disease
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI024696	-	-	Disease or Syndrome	disease
TCMBANKDI024870	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Congenital Abnormality	disease
TCMBANKDI025090	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI025420	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI025428	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025668	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI026511	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI026625	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	group
TCMBANKDI028192	Skin and Connective Tissue Diseases; Immune System Diseases	-	Disease or Syndrome	disease
TCMBANKDI029038	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI029289	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI029509	-	-	Disease or Syndrome	disease
TCMBANKDI029701	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI030490	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI030947	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031104	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	-	Congenital Abnormality	disease
TCMBANKDI031217	Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	group
TCMBANKDI032138	Pathological Conditions, Signs and Symptoms	-	Pathologic Function	phenotype