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SAMD9

靶点ID:TCMBANKGE005497

靶点别名:C7orf5; DRIF1; MIRAGE; NFTC; OEF1; OEF2

靶点描述:sterile alpha motif domain containing 9

染色体:7

染色体位置:7q21.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:1348

OMIM_Link:610456

Ensembl_Link:ENSG00000205413

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

TCMBANKDI000009	Neoplasms	Abnormality of the nervous system; Neoplasm	Neoplastic Process	disease
TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI003140	-	Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003411	-	-	Disease or Syndrome	disease
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004086	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI004474	Nutritional and Metabolic Diseases	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI005588	Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI005681	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI006326	Pathological Conditions, Signs and Symptoms	-	Congenital Abnormality	group
TCMBANKDI006383	Nervous System Diseases	-	Sign or Symptom	phenotype
TCMBANKDI007003	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	disease
TCMBANKDI007110	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013495	Hemic and Lymphatic Diseases	Neoplasm; Abnormality of blood and blood-forming tissues	Neoplastic Process	group
TCMBANKDI014688	Endocrine System Diseases	Abnormality of the endocrine system	Disease or Syndrome	phenotype
TCMBANKDI015504	-	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI021339	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	group
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI024989	Hemic and Lymphatic Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI026020	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Finding	phenotype
TCMBANKDI028701	Pathological Conditions, Signs and Symptoms	Growth abnormality	Finding	phenotype
TCMBANKDI030268	Neoplasms	-	Neoplastic Process	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
TCMBANKDI031973	Pathological Conditions, Signs and Symptoms; Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease