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TRIP12

靶点ID:TCMBANKGE005925

靶点别名:MRD49; TRIP-12; TRIPC; ULF

靶点描述:thyroid hormone receptor interactor 12

染色体:2

染色体位置:2q36.3

靶点类型:protein-coding

HERB_ID:HBTAR005155

HGNC_Link:12306

OMIM_Link:604506

Ensembl_Link:ENSG00000153827

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

TCMBANKDI000011	Pathological Conditions, Signs and Symptoms	Abnormality of the digestive system; Constitutional symptom	Sign or Symptom	phenotype
TCMBANKDI001342	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI002268	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI006146	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI007444	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI008914	Digestive System Diseases; Nervous System Diseases; Mental Disorders	Abnormality of the digestive system	Sign or Symptom	phenotype
TCMBANKDI011173	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018008	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	phenotype
TCMBANKDI018145	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI018761	-	-	Diagnostic Procedure	phenotype
TCMBANKDI020637	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the voice	Sign or Symptom	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024934	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI029054	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI030017	-	Abnormality of the ear	Anatomical Abnormality	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032419	-	Growth abnormality	Finding	phenotype