YEM Search

搜索结果

NUMA1

靶点ID:TCMBANKGE010446

靶点别名:NMP-22; NUMA

靶点描述:nuclear mitotic apparatus protein 1

染色体:11

染色体位置:11q13.4

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:8059

OMIM_Link:164009

Ensembl_Link:ENSG00000137497

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

TCMBANKIN059684	Vitamin E β-		C29H50O2	430.79	CC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
TCMBANKIN059746	α-tocopherol		C29H50O2	430.7 g/mol	CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000011		Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system; Constitutional symptom	Sign or Symptom	phenotype
TCMBANKDI003879		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI006828		-	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI007618		Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI009912		Pathological Conditions, Signs and Symptoms	Abnormality of metabolism/homeostasis	Sign or Symptom	phenotype
TCMBANKDI011229		Stomatognathic Diseases	Abnormality of the immune system; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI011743		Neoplasms; Skin and Connective Tissue Diseases	Neoplasm; Abnormality of the breast	Neoplastic Process	group
TCMBANKDI014645		Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI016252		Skin and Connective Tissue Diseases; Immune System Diseases	-	Disease or Syndrome	disease
TCMBANKDI022565		-	-	Finding	phenotype
TCMBANKDI023630		-	Abnormality of blood and blood-forming tissues; Abnormality of head or neck	Pathologic Function	phenotype
TCMBANKDI025416		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025502		-	-	Laboratory Procedure	phenotype
TCMBANKDI027961		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI028561		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Neoplastic Process	disease
TCMBANKDI028701		Pathological Conditions, Signs and Symptoms	Growth abnormality	Finding	phenotype
TCMBANKDI031523		Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease