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EOGT

靶点ID:TCMBANKGE007853

靶点别名:AER61; AOS4; C3orf64; EOGT1

靶点描述:EGF domain specific O-linked N-acetylglucosamine transferase

染色体:3

染色体位置:3p14.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:28526

OMIM_Link:614789

Ensembl_Link:ENSG00000163378

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

TCMBANKIN061382	sarcosine	N- methyl glycine	C3H7NO2	89.09 g/mol	CNCC(=O)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI004646		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI007618		Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI009080		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI011730		Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI013730		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI014088		Respiratory Tract Diseases; Cardiovascular Diseases	Abnormality of the respiratory system; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI014740		Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system	Disease or Syndrome	phenotype
TCMBANKDI016031		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI018553		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI022048		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases; Cardiovascular Diseases; Wounds and Injuries	Abnormality of the integument; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI027322		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI027961		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI028305		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028951		-	-	Finding	phenotype