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XYLT2

靶点ID:TCMBANKGE012543

靶点别名:PXYLT2; SOS; XT-II; XT2; xylT-II

靶点描述:xylosyltransferase 2

染色体:17

染色体位置:17q21.33

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:15517

OMIM_Link:608125

Ensembl_Link:ENSG00000015532

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

TCMBANKDI000078	Neoplasms; Skin and Connective Tissue Diseases	Abnormality of the integument; Neoplasm	Neoplastic Process	group
TCMBANKDI000432	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Congenital Abnormality	disease
TCMBANKDI001110	Neoplasms	Neoplasm	Neoplastic Process	disease
TCMBANKDI001279	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases	Abnormality of the nervous system; Abnormality of blood and blood-forming tissues; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI002459	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002742	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	group
TCMBANKDI002916	-	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI004195	Chemically-Induced Disorders; Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI005094	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Sign or Symptom	phenotype
TCMBANKDI006358	Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI009571	Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI010081	Musculoskeletal Diseases	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI010935	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI011174	Infections	-	Disease or Syndrome	group
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI015605	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI018053	Eye Diseases; Skin and Connective Tissue Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI018731	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI021531	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	phenotype
TCMBANKDI022361	Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI022757	Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI023498	Skin and Connective Tissue Diseases; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI026360	Infections	-	Disease or Syndrome	disease
TCMBANKDI027040	Immune System Diseases	-	Disease or Syndrome	disease
TCMBANKDI028799	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI032226	-	Abnormality of the skeletal system; Growth abnormality	Finding	phenotype