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SLC25A24

靶点ID:TCMBANKGE002190

靶点别名:APC1; SCAMC-1; SCAMC1

靶点描述:solute carrier family 25 member 24

染色体:1

染色体位置:1p13.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:20662

OMIM_Link:608744

Ensembl_Link:ENSG00000085491

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
TCMBANKDI000166	-	-	Neoplastic Process	disease
TCMBANKDI000485	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI002459	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002881	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI005587	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI006835	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI007820	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI008598	-	Abnormality of the ear	Finding	phenotype
TCMBANKDI009657	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	group
TCMBANKDI010203	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI011480	Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011845	-	-	Laboratory Procedure	phenotype
TCMBANKDI011917	-	Abnormality of head or neck	Disease or Syndrome	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI012814	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI014088	Respiratory Tract Diseases; Cardiovascular Diseases	Abnormality of the respiratory system; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI015857	Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI019974	Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI025291	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI027274	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI029546	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI029658	-	Abnormality of the eye	Finding	disease
TCMBANKDI031802	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Disease or Syndrome	disease