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GNPTAB

靶点ID:TCMBANKGE013569

靶点别名:GNPTA; ICD

靶点描述:N-acetylglucosamine-1-phosphate transferase subunits alpha and beta

染色体:12

染色体位置:12q23.2

靶点类型:protein-coding

HERB_ID:HBTAR009415

HGNC_Link:29670

OMIM_Link:607840

Ensembl_Link:ENSG00000111670

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

TCMBANKDI001050	-	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI001708	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002626	Infections; Respiratory Tract Diseases	Abnormality of the immune system; Abnormality of head or neck; Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI003044	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003261	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI003539	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Mental or Behavioral Dysfunction	phenotype
TCMBANKDI003657	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003746	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI004284	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI005868	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI007856	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI007956	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal 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
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI014215	Infections; Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI018332	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases	Constitutional symptom; Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI020637	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the voice	Sign or Symptom	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI023906	Eye Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI024012	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications	Abnormality of the digestive system; Abnormality of connective tissue	Disease or Syndrome	phenotype
TCMBANKDI026235	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI026423	Neoplasms	Abnormality of the integument	Neoplastic Process	disease
TCMBANKDI028701	Pathological Conditions, Signs and Symptoms	Growth abnormality	Finding	phenotype
TCMBANKDI029038	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease