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PTCH2

靶点ID:TCMBANKGE006521

靶点别名:PTC2

靶点描述:patched 2

染色体:1

染色体位置:1p34.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:9586

OMIM_Link:603673

Ensembl_Link:ENSG00000117425

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

TCMBANKIN060111	17alpha-estradiol		C18H24O2	272.4 g/mol	CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI001342	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI003129	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
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
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI004802	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI006121	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI006900	-	Abnormality of head or neck	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
TCMBANKDI011779	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI014056	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI015452	Neoplasms; Endocrine System Diseases	Abnormality of the endocrine system; Neoplasm	Neoplastic Process	disease
TCMBANKDI019737	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020128	Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI020721	Pathological Conditions, Signs and Symptoms; Neoplasms; Eye Diseases	Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI021455	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI022840	-	Abnormality of the integument; Abnormality of limbs	Finding	phenotype
TCMBANKDI023140	Neoplasms; Endocrine System Diseases	Abnormality of the endocrine system; Neoplasm	Neoplastic Process	disease
TCMBANKDI025495	-	-	Neoplastic Process	disease
TCMBANKDI025826	Pathological Conditions, Signs and Symptoms; Neoplasms; Skin and Connective Tissue Diseases	Abnormality of the integument	Anatomical Abnormality	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028664	-	-	Finding	phenotype
TCMBANKDI028953	-	Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI029783	-	-	Diagnostic Procedure	phenotype
TCMBANKDI030301	Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI030540	Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases	Abnormality of the genitourinary system; Neoplasm	Neoplastic Process	disease
TCMBANKDI030653	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI031221	-	Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI031407	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype