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靶点ID:TCMBANKGE003467

靶点别名:SHNKND; UGTREL7

靶点描述:solute carrier family 35 member D1

染色体:1

染色体位置:1p31.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:20800

OMIM_Link:610804

Ensembl_Link:ENSG00000116704

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

TCMBANKDI001064		-	Growth abnormality	Finding	phenotype
TCMBANKDI003657		-	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
TCMBANKDI014359		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	group
TCMBANKDI017720		-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI022380		Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI022394		-	-	Laboratory Procedure	phenotype
TCMBANKDI028292		-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI028305		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease