YEM Search

搜索结果

CUL7

靶点ID:TCMBANKGE003179

靶点别名:3M1; CUL-7; KIAA0076; dJ20C7.5

靶点描述:cullin 7

染色体:6

染色体位置:6p21.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:21024

OMIM_Link:609577

Ensembl_Link:ENSG00000044090

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]

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI001068	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases	-	Disease or Syndrome	disease
TCMBANKDI002107	-	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI003657	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI006182	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI007110	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI009697	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010203	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI011339	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI012074	Neoplasms; Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth; Abnormality of the genitourinary system; Neoplasm	Neoplastic Process	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI012620	-	Abnormality of the nervous system; Abnormality of the cardiovascular system	Anatomical Abnormality	disease
TCMBANKDI013599	-	Growth abnormality	Disease or Syndrome	phenotype
TCMBANKDI017569	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI021038	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI022768	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI024199	-	Abnormality of limbs; Abnormality of the skeletal system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI025291	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI027274	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI031591	Respiratory Tract Diseases	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI032419	-	Growth abnormality	Finding	phenotype