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   NDUFAF6

靶点ID:TCMBANKGE013839


靶点别名:C8orf38; MC1DN17


靶点描述:NADH:ubiquinone oxidoreductase complex assembly factor 6


染色体:8


染色体位置:8q22.1


靶点类型:protein-coding


HERB_ID:-


HGNC_Link:28625


OMIM_Link:612392


Ensembl_Link:ENSG00000156170


   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
TCMBANKIN040768 Phytoene 7,8,11,12,7',8',11',12'-octahydro-psi,psi-carotene; NSC378840; 540-04-5; 2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,16,18,22,26,30-nonaene; all-trans-phytoene; NSC 378840; C05413; Lycopene, 7,7',8,8',11,11',12,12'-octahydro-, all-trans-; phytoene; 13832-75-2; 7696-40-4; LMPR01070254; (6E,10E,14E,16E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,16,18,22,26,30-nonaene; .psi.,.psi.-Carotene, 7,7',8,8',11,11',12,12'-octahydro-; psi,psi-Carotene, 7,7',8,8',11,11',12,12'-octahydro-; 7,7',8,8',11,11',12,12'-Octahydro-psi,psi-carotene; CHEBI:8191 545

   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
TCMBANKDI002718 - - Finding phenotype
TCMBANKDI003248 Nutritional and Metabolic Diseases; Endocrine System Diseases Abnormality of metabolism/homeostasis; Abnormality of the endocrine system Disease or Syndrome disease
TCMBANKDI004210 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases - Disease or Syndrome disease
TCMBANKDI007228 - - Finding phenotype
TCMBANKDI007770 Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Abnormality of the respiratory system Sign or Symptom phenotype
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
TCMBANKDI011758 - - Laboratory Procedure phenotype
TCMBANKDI017673 - - Clinical Attribute phenotype
TCMBANKDI017965 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system Finding phenotype
TCMBANKDI018929 Eye Diseases Abnormality of the eye Disease or Syndrome disease
TCMBANKDI020373 - Abnormality of the musculature Pathologic Function phenotype
TCMBANKDI020466 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI023751 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the musculature Finding phenotype
TCMBANKDI028664 - - Finding phenotype
TCMBANKDI029783 - - Diagnostic Procedure phenotype
TCMBANKDI031570 - Abnormality of the nervous system Mental or Behavioral Dysfunction disease
TCMBANKDI032109 Pathological Conditions, Signs and Symptoms - Disease or Syndrome disease