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TRPS1

靶点ID:TCMBANKGE003957

靶点别名:GC79; LGCR

靶点描述:transcriptional repressor GATA binding 1

染色体:8

染色体位置:8q23.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:12340

OMIM_Link:604386

Ensembl_Link:ENSG00000104447

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

TCMBANKDI000771	Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of the immune system	Sign or Symptom	phenotype
TCMBANKDI000974	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI002107	-	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI002456	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003128	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI003261	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI004208	Neoplasms	Neoplasm; Abnormality of the breast	Neoplastic Process	disease
TCMBANKDI005082	Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006229	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007281	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007598	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI007737	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI007782	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI009080	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI009951	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI010203	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI011743	Neoplasms; Skin and Connective Tissue Diseases	Neoplasm; Abnormality of the breast	Neoplastic Process	group
TCMBANKDI011758	-	-	Laboratory Procedure	phenotype
TCMBANKDI011883	-	-	Mental Process	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI014359	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	group
TCMBANKDI014690	-	-	Laboratory Procedure	phenotype
TCMBANKDI016031	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI016125	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI017106	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases	Neoplasm; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI017251	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017483	Neoplasms	-	Neoplastic Process	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
TCMBANKDI018239	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI019825	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI020097	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI020602	Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI020997	Neoplasms; Animal Diseases	-	Neoplastic Process	disease
TCMBANKDI022521	-	-	Organ or Tissue Function	phenotype
TCMBANKDI022565	-	-	Finding	phenotype
TCMBANKDI023088	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024012	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications	Abnormality of the digestive system; Abnormality of connective tissue	Disease or Syndrome	phenotype
TCMBANKDI024199	-	Abnormality of limbs; Abnormality of the skeletal system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI024381	Stomatognathic Diseases	Abnormality of head or neck	Anatomical Abnormality	disease
TCMBANKDI024934	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI026419	-	Abnormality of the voice	Finding	phenotype
TCMBANKDI027274	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI029154	-	Abnormality of the skeletal system	Finding	phenotype
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
TCMBANKDI029981	-	Abnormality of the voice	Anatomical Abnormality	disease
TCMBANKDI030017	-	Abnormality of the ear	Anatomical Abnormality	disease
TCMBANKDI030556	-	-	Disease or Syndrome	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032058	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI032436	Musculoskeletal Diseases	-	Disease or Syndrome	disease