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B4GALT7

靶点ID:TCMBANKGE006700

靶点别名:EDSP1; EDSSLA; EDSSPD1; XGALT1; XGPT; XGPT1

靶点描述:beta-1,4-galactosyltransferase 7

染色体:5

染色体位置:5q35.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:930

OMIM_Link:604327

Ensembl_Link:ENSG00000027847

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

TCMBANKDI000199	-	Abnormality of the ear	Congenital Abnormality	phenotype
TCMBANKDI001180	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI002820	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
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
TCMBANKDI006808	-	Abnormality of the integument; Abnormality of limbs	Finding	phenotype
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI008377	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI008407	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI012128	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI012238	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI013182	-	-	Disease or Syndrome	disease
TCMBANKDI014359	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	group
TCMBANKDI016579	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI016840	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease