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SBDS

靶点ID:TCMBANKGE008873

靶点别名:CGI-97; SDS; SWDS

靶点描述:SBDS ribosome maturation factor

染色体:7

染色体位置:7q11.21

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:19440

OMIM_Link:607444

Ensembl_Link:ENSG00000126524

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

TCMBANKDI000294	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI001068	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases	-	Disease or Syndrome	disease
TCMBANKDI003261	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI007135	-	-	Disease or Syndrome	disease
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI007737	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI010589	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI013495	Hemic and Lymphatic Diseases	Neoplasm; Abnormality of blood and blood-forming tissues	Neoplastic Process	group
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI018151	Digestive System Diseases; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI018425	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI019362	-	-	Disease or Syndrome	disease
TCMBANKDI020058	Immune System Diseases	-	Disease or Syndrome	disease
TCMBANKDI020614	-	Abnormality of blood and blood-forming tissues	Finding	phenotype
TCMBANKDI020764	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	group
TCMBANKDI021273	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI021339	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	group
TCMBANKDI024262	-	-	Neoplastic Process	phenotype
TCMBANKDI025832	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI028357	Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases	Abnormality of the immune system	Finding	phenotype
TCMBANKDI029220	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI029546	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI031523	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031591	Respiratory Tract Diseases	Abnormality of the respiratory system	Finding	phenotype