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RLBP1

靶点ID:TCMBANKGE010015

靶点别名:CRALBP

靶点描述:retinaldehyde binding protein 1

染色体:15

染色体位置:15q26.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:10024

OMIM_Link:180090

Ensembl_Link:ENSG00000140522

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

TCMBANKIN032138	rhodopsin	C20H28O	284.4 g/mol	CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=O)C)C
TCMBANKIN059684	Vitamin E β-	C29H50O2	430.79	CC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
TCMBANKIN059714	Vitamin A aldehyde	C20H28O	284.4 g/mol	CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=O)C)C
TCMBANKIN059715	vitamin a	C20H30O	286.5 g/mol	CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C
TCMBANKIN059746	α-tocopherol	C29H50O2	430.7 g/mol	CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)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
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI004835	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI005344	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI006349	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008166	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI010221	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI013348	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI019586	Eye Diseases	Abnormality of metabolism/homeostasis; Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI024946	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI026106	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI027197	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI028799	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI031630	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI032498	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease