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   FA2H

靶点ID:TCMBANKGE001922


靶点别名:FAAH; FAH1; FAXDC1; SCS7; SPG35


靶点描述:fatty acid 2-hydroxylase


染色体:16


染色体位置:16q23.1


靶点类型:protein-coding


HERB_ID:-


HGNC_Link:21197


OMIM_Link:611026


Ensembl_Link:ENSG00000103089


   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
TCMBANKIN057905 ferrum iron Fe 55.84 g/mol [Fe]
TCMBANKIN060889 delta(9)-tetrahydrocannabinol C21H30O2 314.5 g/mol CCCCCC1=CC(=C2C3C=C(CCC3C(OC2=C1)(C)C)C)O
TCMBANKIN060892 tetrahydrocannabinol delta8 CCCCCC1=CC2=C(C3C=C(CCC3C(O2)(C)C)C)C(=C1)O

   靶点对应的疾病
疾病ID 疾病名 MeSH名 HPO名 UMLS名 疾病类型
TCMBANKDI000076 Neoplasms - Neoplastic Process group
TCMBANKDI000121 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system; Abnormality of the musculature Finding phenotype
TCMBANKDI000690 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI001889 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system Finding phenotype
TCMBANKDI002718 - - Finding phenotype
TCMBANKDI002974 Neoplasms - Neoplastic Process disease
TCMBANKDI003957 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the cardiovascular system Sign or Symptom phenotype
TCMBANKDI006815 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI007228 - - Finding phenotype
TCMBANKDI010792 Mental Disorders - Mental or Behavioral Dysfunction disease
TCMBANKDI010896 Nervous System Diseases Abnormality of the nervous system Disease or Syndrome group
TCMBANKDI011730 Eye Diseases; Nervous System Diseases Abnormality of the eye Disease or Syndrome disease
TCMBANKDI011776 Digestive System Diseases Abnormality of the digestive system; Constitutional symptom Disease or Syndrome disease
TCMBANKDI012119 Pathological Conditions, Signs and Symptoms Abnormality of the nervous system Cell or Molecular Dysfunction phenotype
TCMBANKDI016438 Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Mental Disorders; Behavior and Behavior Mechanisms Abnormality of the genitourinary system Mental or Behavioral Dysfunction disease
TCMBANKDI016612 Mental Disorders Abnormality of the nervous system Mental or Behavioral Dysfunction phenotype
TCMBANKDI016700 Mental Disorders - Mental or Behavioral Dysfunction disease
TCMBANKDI018939 Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Abnormality of the musculature Finding phenotype
TCMBANKDI018962 Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI020119 Mental Disorders Abnormality of the nervous system Finding phenotype
TCMBANKDI023957 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system Finding phenotype
TCMBANKDI025420 Digestive System Diseases; Neoplasms Abnormality of the digestive system; Neoplasm Neoplastic Process disease
TCMBANKDI025632 Mental Disorders - Mental or Behavioral Dysfunction disease
TCMBANKDI027026 Neoplasms; Skin and Connective Tissue Diseases - Neoplastic Process disease
TCMBANKDI028005 - Abnormality of prenatal development or birth Finding phenotype
TCMBANKDI028480 - Abnormality of the nervous system Finding phenotype
TCMBANKDI031189 Neoplasms Neoplasm; Abnormality of the respiratory system Neoplastic Process disease
TCMBANKDI032275 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system Anatomical Abnormality disease