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PDE6B

靶点ID:TCMBANKGE001687

靶点别名:CSNB3; CSNBAD2; GMP-PDEbeta; PDEB; RP40; rd1

靶点描述:phosphodiesterase 6B

染色体:4

染色体位置:4p16.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:8786

OMIM_Link:180072

Ensembl_Link:ENSG00000133256

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

TCMBANKIN031363	dimethyl sulfoxide		C2H6OS	78.14 g/mol	CS(=O)C
TCMBANKIN046636	sophoflavescenol	216450-65-6; CHEMBL77651; SCHEMBL14563970; LMPK12112538; MolPort-039-339-033; AK685650; 3,7-Dihydroxy-2-(4-hydroxy-phenyl)-5-methoxy-8-(3-methyl-but-2-enyl)-chromen-4-one; CS-6033; ZINC4199939; BDBM50116711; 3,7-dihydroxy-2-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)-4H-chromen-4-one; HY-N2284; D00QCL; SOPHOFLAVESCENOL; AKOS032945037	C21H20O6	368.4 g/mol	CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI005749		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI006900		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI011730		Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI014624		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	group
TCMBANKDI016758		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI017045		-	-	Disease or Syndrome	disease
TCMBANKDI017965		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018251		-	-	Disease or Syndrome	disease
TCMBANKDI021278		Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI022182		Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI022434		-	-	Disease or Syndrome	disease
TCMBANKDI026106		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI028908		Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI032191		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI032498		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease