搜索结果
靶点ID:TCMBANKGE005959
靶点别名:EPIM; EPM; STX2A; STX2B; STX2C
靶点描述:syntaxin 2
染色体:12
染色体位置:12q24.33
靶点类型:protein-coding
HERB_ID:-
HGNC_Link:3403
OMIM_Link:132350
Ensembl_Link:ENSG00000111450
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 |
|---|
| TCMBANKIN004686 | realgar | AsHS | 0 | S[As] | |
| TCMBANKIN058588 | coixan C | coixan A | C17H18FN3O3 | C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=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 |
|---|
| TCMBANKDI000092 | Respiratory Tract Diseases | Abnormality of the respiratory system | Disease or Syndrome | disease | |
| TCMBANKDI000166 | - | - | Neoplastic Process | disease | |
| TCMBANKDI000533 | Digestive System Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI003502 | - | - | Laboratory Procedure | phenotype | |
| TCMBANKDI007618 | Hemic and Lymphatic Diseases | Abnormality of blood and blood-forming tissues | Disease or Syndrome | phenotype | |
| TCMBANKDI009827 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases | Abnormality of head or neck | Congenital Abnormality | disease | |
| TCMBANKDI015485 | Mental Disorders | Abnormality of the nervous system | Mental or Behavioral Dysfunction | disease | |
| TCMBANKDI019558 | Infections | Abnormality of the immune system | Disease or Syndrome | group | |
| TCMBANKDI022160 | Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI025152 | Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases | - | Disease or Syndrome | disease |
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