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CEP120

靶点ID:TCMBANKGE002686

靶点别名:CCDC100; JBTS31; SRTD13

靶点描述:centrosomal protein 120

染色体:5

染色体位置:5q23.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:26690

OMIM_Link:613446

Ensembl_Link:ENSG00000168944

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

TCMBANKDI001317	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI002581	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002791	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI003536	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the digestive system; Abnormality of connective tissue	Congenital 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
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007314	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI008874	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI010717	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI011167	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI017183	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI017681	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI019267	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI019358	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI022361	Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI023838	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI026143	-	Abnormality of the cardiovascular system	Finding	phenotype
TCMBANKDI027961	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI029064	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI029870	-	Abnormality of head or neck; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI030837	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI031221	-	Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease