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FERMT1

靶点ID:TCMBANKGE004126

靶点别名:C20orf42; DTGCU2; KIND1; UNC112A; URP1

靶点描述:fermitin family member 1

染色体:20

染色体位置:20p12.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:15889

OMIM_Link:607900

Ensembl_Link:ENSG00000101311

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

TCMBANKIN057911	se	selenium	H2Se	78.97 g/mol	[Se]
TCMBANKIN059684	Vitamin E β-		C29H50O2	430.79	CC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
TCMBANKIN059746	α-tocopherol		C29H50O2	430.7 g/mol	CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000061	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI000088	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	group
TCMBANKDI002512	Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI002533	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI007394	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	group
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI010346	Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI011167	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI011743	Neoplasms; Skin and Connective Tissue Diseases	Neoplasm; Abnormality of the breast	Neoplastic Process	group
TCMBANKDI011827	Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI012238	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI014215	Infections; Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI016216	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	-	Congenital Abnormality	disease
TCMBANKDI016890	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI017642	Neoplasms	Abnormality of the integument; Neoplasm	Neoplastic Process	disease
TCMBANKDI019825	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI020449	Skin and Connective Tissue Diseases	Abnormality of the integument	Pathologic Function	phenotype
TCMBANKDI022101	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Anatomical Abnormality	phenotype
TCMBANKDI023220	Male Urogenital Diseases	-	Finding	phenotype
TCMBANKDI025826	Pathological Conditions, Signs and Symptoms; Neoplasms; Skin and Connective Tissue Diseases	Abnormality of the integument	Anatomical Abnormality	disease
TCMBANKDI031189	Neoplasms	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI031407	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype