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BMPR1B

靶点ID:TCMBANKGE010320

靶点别名:ALK-6; ALK6; AMDD; BDA1D; BDA2; CDw293

靶点描述:bone morphogenetic protein receptor type 1B

染色体:4

染色体位置:4q22.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:1077

OMIM_Link:603248

Ensembl_Link:ENSG00000138696

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

TCMBANKIN000705	Flavopiridol	flavopiridol	C21H20ClNO5	401.8 g/mol	CN1CCC(C(C1)O)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4Cl)O)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000403	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI001064	-	Growth abnormality	Finding	phenotype
TCMBANKDI002456	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002974	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI003129	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI004926	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI005587	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI012416	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI012581	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI012924	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013133	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI013169	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI014359	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	group
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI017720	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI018090	-	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI022433	Respiratory Tract Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI023021	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	group
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; 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
TCMBANKDI031083	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031498	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031644	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI031811	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease