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POU3F4

靶点ID:TCMBANKGE004971

靶点别名:BRAIN-4; BRN-4; BRN4; DFN3; DFNX2; OCT-9; OTF-9; OTF9

靶点描述:POU class 3 homeobox 4

染色体:X

染色体位置:Xq21.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:9217

OMIM_Link:300039

Ensembl_Link:ENSG00000196767

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

TCMBANKIN059114	PAU	b-Alanine, N-[(2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl]- (9CI); 3-[[(2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl]amino]propanoic acid; PANTOTHENOIC ACID; BRN 1727064; (D,+)-N(alpha-gamma-Dihydroxy-beta,beta-dimethylbutyryl)-beta-alanine; N-(2,4-Dihydroxy-3,3-dimethylbutyryl)-beta-alanine; beta-Alanine, N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-, (R)-; Pantothenic acid, D- (8CI); Chick antidermatitis factor; 3-[[(2R)-2,4-dihydroxy-3,3-dimethyl-butanoyl]amino]propionic acid; beta-Alanine, N-[(2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl]-; Pantothenic acid, D-; 3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoic acid; 4-04-00-02569 (Beilstein Handbook Reference); beta-Alanine, N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-, (R)- (9CI); CHEBI:46905; EINECS 201-229-0; (D)-(+)-Pantothenic acid; 3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]propanoic acid; HSDB 1020; Kyselina pantothenova [Czech]; C00864; D(+)-N-(2,4-Dihydroxy-3,3-dimethylbutyryl)-beta-alanine; (R)-pantothenic acid; 3-[[(2R)-2,4-dihydroxy-3,3-dimethyl-butanoyl]amino]propanoic acid; 10-20-8; N-[(2R)-2,4-DIHYDROXY-3,3-DIMETHYLBUTANOYL]-BETA-ALANINE; (R)-N-(2,4-Dihydroxy-3,3-dimethyl-1-oxobutyl)-beta-alanine; 3563-85-7; (+)-Pantothenic acid;pantothenic acid	C9H17NO5	219.24	CC(C)(CO)C(C(=O)NCCC(=O)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

TCMBANKDI000054		Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI002657		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI003183		-	Abnormality of the ear	Finding	phenotype
TCMBANKDI004835		-	Abnormality of the eye	Finding	phenotype
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI009727		Infections	-	Disease or Syndrome	disease
TCMBANKDI009827		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI009860		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI011730		Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011867		Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017878		-	Abnormality of the ear	Finding	phenotype
TCMBANKDI018117		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI020914		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of limbs; Abnormality of the musculature	Finding	phenotype
TCMBANKDI021293		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases	Abnormality of the genitourinary system; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI026767		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032419		-	Growth abnormality	Finding	phenotype