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COQ2

靶点ID:TCMBANKGE009255

靶点别名:CL640; COQ10D1; MSA1; PHB:PPT

靶点描述:coenzyme Q2, polyprenyltransferase

染色体:4

染色体位置:4q21.22-q21.23

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:25223

OMIM_Link:609825

Ensembl_Link:ENSG00000173085

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

TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI000121	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI001033	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI001299	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003110	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI004821	Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI011586	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI012119	Pathological Conditions, Signs and Symptoms	Abnormality of the nervous system	Cell or Molecular Dysfunction	phenotype
TCMBANKDI012420	Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI013148	Respiratory Tract Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI014919	Infections	-	Disease or Syndrome	disease
TCMBANKDI015757	Infections	-	Disease or Syndrome	disease
TCMBANKDI015829	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI016712	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018346	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI019267	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI022361	Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI023320	-	-	Disease or Syndrome	disease
TCMBANKDI025774	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases	Abnormality of metabolism/homeostasis	Pathologic Function	phenotype
TCMBANKDI027669	-	-	Finding	phenotype
TCMBANKDI028945	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI029791	Nutritional and Metabolic Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI031523	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease