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ZNF423

靶点ID:TCMBANKGE002292

靶点别名:Ebfaz; JBTS19; NPHP14; OAZ; Roaz; ZFP423; Zfp104; hOAZ

靶点描述:zinc finger protein 423

染色体:16

染色体位置:16q12.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:16762

OMIM_Link:604557

Ensembl_Link:ENSG00000102935

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

TCMBANKIN059452	ethyl aldehyde		C2H4O	44.05 g/mol	CC=O
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

TCMBANKDI000009	Neoplasms	Abnormality of the nervous system; Neoplasm	Neoplastic Process	disease
TCMBANKDI000023	Skin and Connective Tissue Diseases; Immune System Diseases	Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI002572	-	-	Finding	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002742	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	group
TCMBANKDI004191	Chemically-Induced Disorders; Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI004857	Nervous System Diseases	-	Disease or Syndrome	group
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007314	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI008874	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010717	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011883	-	-	Mental Process	phenotype
TCMBANKDI015186	-	Abnormality of the nervous system	Anatomical Abnormality	phenotype
TCMBANKDI017183	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI018716	Chemically-Induced Disorders; Mental Disorders	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024380	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease