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SLC26A2

靶点ID:TCMBANKGE004881

靶点别名:D5S1708; DTD; DTDST; EDM4; MST153; MSTP157

靶点描述:solute carrier family 26 member 2

染色体:5

染色体位置:5q32

靶点类型:protein-coding

HERB_ID:HBTAR001122

HGNC_Link:10994

OMIM_Link:606718

Ensembl_Link:ENSG00000155850

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

TCMBANKIN003665	evoden				C1CCN(CC1)CCOC2=CC=C(C=C2)C(=O)C3=C(SC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O
TCMBANKIN058277	2-hydroxybenzoic acid	O-hydroxybenzoic acid; 3- coffee acid; Thick-stemmed black base	C7H6O3 or HOC6H4COOH	138.12 g/mol	C1=CC=C(C(=C1)C(=O)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

TCMBANKDI000088	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	group
TCMBANKDI001064	-	Growth abnormality	Finding	phenotype
TCMBANKDI001706	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI002456	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002459	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002490	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003657	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003746	-	Abnormality of the skeletal system	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
TCMBANKDI005153	Female Urogenital Diseases and Pregnancy Complications	-	Disease or Syndrome	disease
TCMBANKDI005977	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI007871	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI010094	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI010896	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	group
TCMBANKDI011167	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI012098	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI012888	-	Neoplasm; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013664	Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system; Abnormality of connective tissue	Acquired Abnormality	disease
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI014359	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	group
TCMBANKDI015420	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI015801	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI016579	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017267	Endocrine System Diseases	Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI020637	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the voice	Sign or Symptom	phenotype
TCMBANKDI020764	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	group
TCMBANKDI020911	Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases	-	Disease or Syndrome	disease
TCMBANKDI021094	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI021924	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI022473	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI023088	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024293	Neoplasms	Neoplasm	Neoplastic Process	disease
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI025420	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	disease
TCMBANKDI027966	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028400	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI028669	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	disease
TCMBANKDI029152	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI029611	Neoplasms	Neoplasm; Abnormality of the cardiovascular system	Neoplastic Process	disease
TCMBANKDI030411	Digestive System Diseases	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI031116	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases	Abnormality of the respiratory system	Finding	phenotype