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SLC35A2

靶点ID:TCMBANKGE012721

靶点别名:CDG2M; CDGX; UDP-Gal-Tr; UGALT; UGAT; UGT; UGT1; UGT2; UGTL

靶点描述:solute carrier family 35 member A2

染色体:X

染色体位置:Xp11.23

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:11022

OMIM_Link:314375

Ensembl_Link:ENSG00000102100

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
TCMBANKDI000061	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI000166	-	-	Neoplastic Process	disease
TCMBANKDI001779	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003266	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the digestive system; Abnormality of the integument	Disease or Syndrome	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI003873	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI004086	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006819	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008305	Digestive System Diseases; Infections	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	group
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI010514	-	Abnormality of metabolism/homeostasis	Finding	phenotype
TCMBANKDI011315	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013148	Respiratory Tract Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI013730	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI015336	-	-	Disease or Syndrome	phenotype
TCMBANKDI016288	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI016890	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI018837	Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases	Abnormality of the immune system; Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI019066	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI019915	-	Abnormality of the respiratory system	Anatomical Abnormality	disease
TCMBANKDI023464	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024839	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI026606	Skin and Connective Tissue Diseases	Abnormality of the breast	Anatomical Abnormality	disease
TCMBANKDI028357	Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases	Abnormality of the immune system	Finding	phenotype
TCMBANKDI029054	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI029582	-	Abnormality of the immune system; Abnormality of blood and blood-forming tissues	Finding	phenotype
TCMBANKDI029899	Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases	Neoplasm; Abnormality of blood and blood-forming tissues	Neoplastic Process	group
TCMBANKDI030540	Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases	Abnormality of the genitourinary system; Neoplasm	Neoplastic Process	disease
TCMBANKDI031192	Neoplasms; Male Urogenital Diseases	-	Neoplastic Process	disease
TCMBANKDI031498	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032357	-	Abnormality of the digestive system	Finding	phenotype