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EVC2

靶点ID:TCMBANKGE013585

靶点别名:LBN; WAD

靶点描述:EvC ciliary complex subunit 2

染色体:4

染色体位置:4p16.2

靶点类型:protein-coding

HERB_ID:HBTAR010951

HGNC_Link:19747

OMIM_Link:607261

Ensembl_Link:ENSG00000173040

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

TCMBANKDI000153	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI000403	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003547	-	Abnormality of limbs; Abnormality of the skeletal system	Acquired Abnormality	disease
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
TCMBANKDI004458	-	Abnormality of the genitourinary system	Finding	phenotype
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
TCMBANKDI007314	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI008217	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI008368	Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI009827	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI017355	-	Abnormality of the genitourinary system	Anatomical Abnormality	disease
TCMBANKDI019900	-	-	Laboratory Procedure	phenotype
TCMBANKDI019974	Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI021455	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI024870	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Congenital Abnormality	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028991	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI029289	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI029546	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease