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COG8

靶点ID:TCMBANKGE009188

靶点别名:CDG2H; DOR1

靶点描述:component of oligomeric golgi complex 8

染色体:16

染色体位置:16q22.1

靶点类型:protein-coding

HERB_ID:HBTAR010069

HGNC_Link:18623

OMIM_Link:606979

Ensembl_Link:ENSG00000213380

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

TCMBANKIN057911	se	selenium	H2Se	78.97 g/mol	[Se]

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000309		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI003097		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003797		Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	group
TCMBANKDI004086		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI004558		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI005528		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI005868		-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI006146		-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI006165		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI012000		-	Abnormality of the integument; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI013067		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI016195		-	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI016890		Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI020373		-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI021867		Digestive System Diseases	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024934		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI027721		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease