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   KRT10

靶点ID:TCMBANKGE000722


靶点别名:BCIE; BIE; CK10; EHK; K10; KPP


靶点描述:keratin 10


染色体:17


染色体位置:17q21.2


靶点类型:protein-coding


HERB_ID:-


HGNC_Link:6413


OMIM_Link:148080


Ensembl_Link:ENSG00000186395


   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
TCMBANKIN018754 kinetin AC1L8XK3; N-(furan-2-ylmethyl)-5H-purin-6-amine C10H9N5O 215.21 g/mol C1=COC(=C1)CNC2=NC=NC3=C2NC=N3
TCMBANKIN024475 tretinoin C20H28O2 300.4 g/mol CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC(=O)O)C)C
TCMBANKIN036881 delphinidin delphinidin ; delfinidin; delphinidin-3-glu-coside_qt; Anthocyanin; Delphinidin-3-monoglucoside_qt; 3-O-β-(6-O-malonyl)-D-glucopyranoside_qt C15H11O7+ 303.24 g/mol C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)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
TCMBANKDI000061 Digestive System Diseases; Neoplasms Abnormality of the digestive system; Neoplasm Neoplastic Process group
TCMBANKDI000078 Neoplasms; Skin and Connective Tissue Diseases Abnormality of the integument; Neoplasm Neoplastic Process group
TCMBANKDI000533 Digestive System Diseases - Disease or Syndrome disease
TCMBANKDI002809 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases - Disease or Syndrome disease
TCMBANKDI003353 Pathological Conditions, Signs and Symptoms; Neoplasms - Neoplastic Process phenotype
TCMBANKDI008914 Digestive System Diseases; Nervous System Diseases; Mental Disorders Abnormality of the digestive system Sign or Symptom phenotype
TCMBANKDI008939 Skin and Connective Tissue Diseases Abnormality of the integument; Abnormality of the immune system Disease or Syndrome disease
TCMBANKDI010331 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases - Disease or Syndrome; Congenital Abnormality disease
TCMBANKDI010589 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Abnormality of the integument Disease or Syndrome disease
TCMBANKDI011000 Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Abnormality of the integument Disease or Syndrome disease
TCMBANKDI016890 Digestive System Diseases; Neoplasms - Neoplastic Process disease
TCMBANKDI017642 Neoplasms Abnormality of the integument; Neoplasm Neoplastic Process disease
TCMBANKDI019879 Digestive System Diseases; Neoplasms; Endocrine System Diseases - Neoplastic Process disease
TCMBANKDI020449 Skin and Connective Tissue Diseases Abnormality of the integument Pathologic Function phenotype
TCMBANKDI020451 Neoplasms - Neoplastic Process disease
TCMBANKDI023464 Nervous System Diseases Abnormality of the nervous system Disease or Syndrome disease
TCMBANKDI025507 Skin and Connective Tissue Diseases Abnormality of the integument Disease or Syndrome disease
TCMBANKDI028701 Pathological Conditions, Signs and Symptoms Growth abnormality Finding phenotype
TCMBANKDI030540 Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Abnormality of the genitourinary system; Neoplasm Neoplastic Process disease
TCMBANKDI030775 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases - Disease or Syndrome disease
TCMBANKDI031134 - Abnormality of the integument Finding phenotype
TCMBANKDI031570 - Abnormality of the nervous system Mental or Behavioral Dysfunction disease