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ANKH

靶点ID:TCMBANKGE010034

靶点别名:ANK; CCAL2; CMDJ; CPPDD; HANK; MANK; SLC62A1

靶点描述:ANKH inorganic pyrophosphate transport regulator

染色体:5

染色体位置:5p15.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:15492

OMIM_Link:605145

Ensembl_Link:ENSG00000154122

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

TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003411		-	-	Disease or Syndrome	disease
TCMBANKDI005137		Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	group
TCMBANKDI006900		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010306		-	Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI014248		-	-	Laboratory Procedure	group
TCMBANKDI014359		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	group
TCMBANKDI015238		Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI016670		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI017577		-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI018117		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI020574		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI021387		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	phenotype
TCMBANKDI023464		Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI024668		Musculoskeletal Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025764		-	Abnormality of head or neck; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI027609		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI029783		-	-	Diagnostic Procedure	phenotype
TCMBANKDI031083		-	Abnormality of the skeletal system	Finding	phenotype