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PHKG2

靶点ID:TCMBANKGE008411

靶点别名:GSD9C

靶点描述:phosphorylase kinase catalytic subunit gamma 2

染色体:16

染色体位置:16p11.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:8931

OMIM_Link:172471

Ensembl_Link:ENSG00000156873

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

TCMBANKDI002231		Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI011265		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI013347		Pathological Conditions, Signs and Symptoms	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI013599		-	Growth abnormality	Disease or Syndrome	phenotype
TCMBANKDI016382		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI017308		Endocrine System Diseases	Abnormality of the endocrine system; Growth abnormality	Pathologic Function	phenotype
TCMBANKDI018731		Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI019397		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI020119		Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020373		-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI020794		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI023751		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024083		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI030411		Digestive System Diseases	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI030468		Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease