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GP1BA

靶点ID:TCMBANKGE015014

靶点别名:BDPLT1; BDPLT3; BSS; CD42B; CD42b-alpha; DBPLT3; GP1B; GPIbA; GPIbalpha; VWDP

靶点描述:glycoprotein Ib platelet subunit alpha

染色体:17

染色体位置:17p13.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:4439

OMIM_Link:606672

Ensembl_Link:ENSG00000185245

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

TCMBANKDI000068	Neoplasms; Stomatognathic Diseases	Neoplasm; Abnormality of head or neck	Neoplastic Process	group
TCMBANKDI000265	-	-	Disease or Syndrome	disease
TCMBANKDI001226	-	-	Disease or Syndrome	disease
TCMBANKDI001279	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases	Abnormality of the nervous system; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI005139	-	-	Finding	phenotype
TCMBANKDI005635	Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI007003	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI007123	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI008003	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Finding	phenotype
TCMBANKDI009773	Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases	Abnormality of the immune system; Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI011883	-	-	Mental Process	phenotype
TCMBANKDI012000	-	Abnormality of the integument; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI012976	Neoplasms; Stomatognathic Diseases	-	Neoplastic Process	disease
TCMBANKDI014193	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI018513	-	Abnormality of the genitourinary system	Anatomical Abnormality	phenotype
TCMBANKDI021272	Cardiovascular Diseases	-	Pathologic Function	phenotype
TCMBANKDI021599	-	Abnormality of blood and blood-forming tissues	Laboratory or Test Result	phenotype
TCMBANKDI024717	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI024817	Pathological Conditions, Signs and Symptoms; Digestive System Diseases	Abnormality of the digestive system; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system	Sign or Symptom	phenotype
TCMBANKDI026223	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI026250	-	-	Laboratory Procedure	phenotype
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI029861	Neoplasms; Hemic and Lymphatic Diseases	-	Neoplastic Process	disease
TCMBANKDI031190	Cardiovascular Diseases	-	Pathologic Function	phenotype
TCMBANKDI031381	Neoplasms; Hemic and Lymphatic Diseases	-	Neoplastic Process	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease