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TACO1

靶点ID:TCMBANKGE014989

靶点别名:CCDC44

靶点描述:translational activator of cytochrome c oxidase I

染色体:17

染色体位置:17q23.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:24316

OMIM_Link:612958

Ensembl_Link:ENSG00000136463

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

TCMBANKDI002213	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI011209	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI013453	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI016371	-	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020466	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI021233	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI025832	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI028663	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI030700	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031716	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI031753	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI032413	Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease