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SRD5A3

靶点ID:TCMBANKGE009239

靶点别名:CDG1P; CDG1Q; KRIZI; SRD5A2L; SRD5A2L1

靶点描述:steroid 5 alpha-reductase 3

染色体:4

染色体位置:4q12

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:25812

OMIM_Link:611715

Ensembl_Link:ENSG00000128039

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

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

TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002791	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI004267	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms	-	Disease or Syndrome	disease
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI005226	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI006621	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008407	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI009697	-	Abnormality of head or neck	Finding	phenotype
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
TCMBANKDI010081	Musculoskeletal Diseases	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI010589	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI010717	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI011000	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI012238	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI013008	Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI016459	-	-	Neoplastic Process	disease
TCMBANKDI016840	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI022361	Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI023021	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	group
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI025368	Infections; Nervous System Diseases; Mental Disorders	-	Disease or Syndrome	disease
TCMBANKDI029839	-	Abnormality of metabolism/homeostasis	Finding	phenotype
TCMBANKDI031192	Neoplasms; Male Urogenital Diseases	-	Neoplastic Process	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease