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SLC40A1

靶点ID:TCMBANKGE009398

靶点别名:FPN1; HFE4; IREG1; MST079; MSTP079; MTP1; SLC11A3

靶点描述:solute carrier family 40 member 1

染色体:2

染色体位置:2q32.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:10909

OMIM_Link:604653

Ensembl_Link:ENSG00000138449

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

TCMBANKIN057905	ferrum	iron	Fe	55.84 g/mol	[Fe]

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000011	Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system; Constitutional symptom	Sign or Symptom	phenotype
TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	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
TCMBANKDI009278	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI009702	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	phenotype
TCMBANKDI011094	Musculoskeletal Diseases	-	Acquired Abnormality	disease
TCMBANKDI011446	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	disease
TCMBANKDI011458	Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI011758	-	-	Laboratory Procedure	phenotype
TCMBANKDI012175	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI016255	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI018731	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI021455	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI022757	Nutritional and Metabolic Diseases	-	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
TCMBANKDI027339	Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases	Neoplasm; Abnormality of blood and blood-forming tissues	Neoplastic Process	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
TCMBANKDI028810	Pathological Conditions, Signs and Symptoms	-	Pathologic Function	disease
TCMBANKDI029791	Nutritional and Metabolic Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI031083	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031606	-	-	Disease or Syndrome	disease
TCMBANKDI032496	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease