搜索结果


   TPM2

靶点ID:TCMBANKGE002337


靶点别名:AMCD1; DA1; DA2B; DA2B4; HEL-S-273; NEM4; TMSB


靶点描述:tropomyosin 2


染色体:9


染色体位置:9p13.3


靶点类型:protein-coding


HERB_ID:-


HGNC_Link:12011


OMIM_Link:190990


Ensembl_Link:ENSG00000198467


   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
TCMBANKIN057906 mercury hydrargyrum Hg 200.59 g/mol [Hg]
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
TCMBANKDI000061 Digestive System Diseases; Neoplasms Abnormality of the digestive system; Neoplasm Neoplastic Process group
TCMBANKDI000121 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system; Abnormality of the musculature Finding phenotype
TCMBANKDI000166 - - Neoplastic Process disease
TCMBANKDI000248 Musculoskeletal Diseases; Nervous System Diseases - Congenital Abnormality disease
TCMBANKDI002840 Musculoskeletal Diseases; Nervous System Diseases - Disease or Syndrome; Congenital Abnormality disease
TCMBANKDI003411 - - Disease or Syndrome disease
TCMBANKDI003685 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of prenatal development or birth Disease or Syndrome disease
TCMBANKDI003879 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Abnormality of the genitourinary system Congenital Abnormality disease
TCMBANKDI004489 - Abnormality of the ear Congenital Abnormality disease
TCMBANKDI005398 Eye Diseases - Disease or Syndrome disease
TCMBANKDI006028 - Abnormality of the musculature Finding phenotype
TCMBANKDI006900 - Abnormality of head or neck Finding phenotype
TCMBANKDI007043 Musculoskeletal Diseases Abnormality of the skeletal system Congenital Abnormality disease
TCMBANKDI007163 Musculoskeletal Diseases; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI007343 Pathological Conditions, Signs and Symptoms; Nervous System Diseases - Finding phenotype
TCMBANKDI007610 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Abnormality of head or neck Congenital Abnormality disease
TCMBANKDI008156 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature Disease or Syndrome disease
TCMBANKDI008874 - Abnormality of head or neck Finding phenotype
TCMBANKDI009025 Musculoskeletal Diseases; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI009106 Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases - Disease or Syndrome disease
TCMBANKDI009575 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases - Disease or Syndrome disease
TCMBANKDI009751 - - Finding phenotype
TCMBANKDI013067 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of limbs Congenital Abnormality disease
TCMBANKDI013169 - Abnormality of the skeletal system Anatomical Abnormality disease
TCMBANKDI013913 Nervous System Diseases Abnormality of the musculature Sign or Symptom phenotype
TCMBANKDI013927 Respiratory Tract Diseases Abnormality of the respiratory system Pathologic Function phenotype
TCMBANKDI013994 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system Finding phenotype
TCMBANKDI015863 - Abnormality of the nervous system; Abnormality of the musculature Finding phenotype
TCMBANKDI016031 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of limbs Congenital Abnormality disease
TCMBANKDI016890 Digestive System Diseases; Neoplasms - Neoplastic Process disease
TCMBANKDI017642 Neoplasms Abnormality of the integument; Neoplasm Neoplastic Process disease
TCMBANKDI017813 Musculoskeletal Diseases Abnormality of limbs Anatomical Abnormality disease
TCMBANKDI017869 Nervous System Diseases Abnormality of the nervous system; Abnormality of the musculature Disease or Syndrome disease
TCMBANKDI018020 - Abnormality of the musculature Finding phenotype
TCMBANKDI018929 Eye Diseases Abnormality of the eye Disease or Syndrome disease
TCMBANKDI018930 Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Abnormality of limbs; Abnormality of the musculature Finding phenotype
TCMBANKDI018939 Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Abnormality of the musculature Finding phenotype
TCMBANKDI019650 Pathological Conditions, Signs and Symptoms; Nervous System Diseases - Disease or Syndrome phenotype
TCMBANKDI020119 Mental Disorders Abnormality of the nervous system Finding phenotype
TCMBANKDI020373 - Abnormality of the musculature Pathologic Function phenotype
TCMBANKDI020574 Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature Disease or Syndrome disease
TCMBANKDI020764 Digestive System Diseases Abnormality of the digestive system Disease or Syndrome group
TCMBANKDI022380 Female Urogenital Diseases and Pregnancy Complications Abnormality of prenatal development or birth Pathologic Function phenotype
TCMBANKDI022448 Musculoskeletal Diseases; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI022768 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of the skeletal system Congenital Abnormality disease
TCMBANKDI023100 Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases - Congenital Abnormality disease
TCMBANKDI023319 Musculoskeletal Diseases; Nervous System Diseases - Disease or Syndrome disease
TCMBANKDI023751 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the musculature Finding phenotype
TCMBANKDI024199 - Abnormality of limbs; Abnormality of the skeletal system; Abnormality of the musculature Finding phenotype
TCMBANKDI024239 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of head or neck; Abnormality of the skeletal system Disease or Syndrome disease
TCMBANKDI024595 - - Anatomical Abnormality group
TCMBANKDI025924 - Abnormality of limbs; Abnormality of the skeletal system Sign or Symptom phenotype
TCMBANKDI027248 Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Abnormality of the musculature Finding phenotype
TCMBANKDI027406 - Abnormality of the nervous system; Abnormality of the musculature Finding phenotype
TCMBANKDI027418 - Abnormality of the musculature Finding phenotype
TCMBANKDI027721 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature Disease or Syndrome disease
TCMBANKDI028507 - - Disease or Syndrome disease
TCMBANKDI028664 - - Finding phenotype
TCMBANKDI030017 - Abnormality of the ear Anatomical Abnormality disease
TCMBANKDI031438 Pathological Conditions, Signs and Symptoms; Nervous System Diseases Abnormality of the nervous system Finding phenotype
TCMBANKDI031642 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases - Disease or Syndrome disease
TCMBANKDI031753 - Abnormality of the musculature Finding phenotype
TCMBANKDI031899 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases - Disease or Syndrome; Congenital Abnormality disease
TCMBANKDI032100 - Abnormality of the musculature Disease or Syndrome disease
TCMBANKDI032109 Pathological Conditions, Signs and Symptoms - Disease or Syndrome disease