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TRIP11

靶点ID:TCMBANKGE012769

靶点别名:ACG1A; CEV14; GMAP-210; GMAP210; ODCD; TRIP-11; TRIP230

靶点描述:thyroid hormone receptor interactor 11

染色体:14

染色体位置:14q32.12

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:12305

OMIM_Link:604505

Ensembl_Link:ENSG00000100815

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

TCMBANKDI000044	Infections	-	Disease or Syndrome	group
TCMBANKDI001064	-	Growth abnormality	Finding	phenotype
TCMBANKDI002459	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002490	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI002742	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	group
TCMBANKDI003657	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI008036	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI010306	-	Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI011402	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012098	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013664	Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system; Abnormality of connective tissue	Acquired Abnormality	disease
TCMBANKDI013896	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI016026	Neoplasms; Eye Diseases	Neoplasm; Abnormality of the eye	Neoplastic Process	disease
TCMBANKDI016579	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017527	-	Abnormality of limbs	Anatomical Abnormality	phenotype
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
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
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI024685	-	Abnormality of prenatal development or birth	Finding	phenotype
TCMBANKDI025832	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI028005	-	Abnormality of prenatal development or birth	Finding	phenotype
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028648	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI028669	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	disease
TCMBANKDI030411	Digestive System Diseases	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI031591	Respiratory Tract Diseases	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI032226	-	Abnormality of the skeletal system; Growth abnormality	Finding	phenotype