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   SMARCD2

靶点ID:TCMBANKGE013583


靶点别名:BAF60B; CRACD2; PRO2451; Rsc6p; SGD2


靶点描述:SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2


染色体:17


染色体位置:17q23.3


靶点类型:protein-coding


HERB_ID:-


HGNC_Link:11107


OMIM_Link:601736


Ensembl_Link:ENSG00000108604


   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
TCMBANKIN057911 se selenium H2Se 78.97 g/mol [Se]
TCMBANKIN059684 Vitamin E β- C29H50O2 430.79 CC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
TCMBANKIN059746 α-tocopherol C29H50O2 430.7 g/mol CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C

   靶点对应的疾病
疾病ID 疾病名 MeSH名 HPO名 UMLS名 疾病类型
TCMBANKDI004489 - Abnormality of the ear Congenital Abnormality disease
TCMBANKDI008598 - Abnormality of the ear Finding phenotype
TCMBANKDI009951 Nutritional and Metabolic Diseases; Musculoskeletal Diseases Abnormality of the skeletal system Disease or Syndrome disease
TCMBANKDI010048 Infections; Respiratory Tract Diseases Abnormality of the immune system; Abnormality of the respiratory system Disease or Syndrome disease
TCMBANKDI013495 Hemic and Lymphatic Diseases Neoplasm; Abnormality of blood and blood-forming tissues Neoplastic Process group
TCMBANKDI027465 Neoplasms - Neoplastic Process disease
TCMBANKDI028305 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of limbs; Abnormality of the skeletal system Congenital Abnormality disease