搜索结果
靶点ID:TCMBANKGE012974
靶点别名:C20orf59; POROK8; VNUT
靶点描述:solute carrier family 17 member 9
染色体:20
染色体位置:20q13.33
靶点类型:protein-coding
HERB_ID:-
HGNC_Link:16192
OMIM_Link:612107
Ensembl_Link:ENSG00000101194
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 |
|---|
靶点对应的疾病
| 疾病ID | 疾病名 | MeSH名 | HPO名 | UMLS名 | 疾病类型 |
|---|
| TCMBANKDI000166 | - | - | Neoplastic Process | disease | |
| TCMBANKDI000802 | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Abnormality of the integument | Finding | phenotype | |
| TCMBANKDI003248 | Nutritional and Metabolic Diseases; Endocrine System Diseases | Abnormality of metabolism/homeostasis; Abnormality of the endocrine system | Disease or Syndrome | disease | |
| TCMBANKDI017642 | Neoplasms | Abnormality of the integument; Neoplasm | Neoplastic Process | disease | |
| TCMBANKDI020449 | Skin and Connective Tissue Diseases | Abnormality of the integument | Pathologic Function | phenotype | |
| TCMBANKDI025420 | Digestive System Diseases; Neoplasms | Abnormality of the digestive system; Neoplasm | Neoplastic Process | disease | |
| TCMBANKDI027592 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | - | Congenital Abnormality | disease | |
| TCMBANKDI029343 | Pathological Conditions, Signs and Symptoms | - | Sign or Symptom | phenotype |
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