搜索结果
靶点ID:TCMBANKGE002781
靶点别名:HMSN6B
靶点描述:solute carrier family 25 member 46
染色体:5
染色体位置:5q22.1
靶点类型:protein-coding
HERB_ID:HBTAR010375
HGNC_Link:25198
OMIM_Link:610826
Ensembl_Link:ENSG00000164209
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 |
|---|
| TCMBANKDI001272 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI001889 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Abnormality of the nervous system | Finding | phenotype | |
| TCMBANKDI002718 | - | - | Finding | phenotype | |
| TCMBANKDI006349 | - | Abnormality of the eye | Finding | phenotype | |
| TCMBANKDI007228 | - | - | Finding | phenotype | |
| TCMBANKDI007343 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | - | Finding | phenotype | |
| TCMBANKDI019267 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Abnormality of the nervous system | Sign or Symptom | phenotype | |
| TCMBANKDI020452 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI020466 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI026606 | Skin and Connective Tissue Diseases | Abnormality of the breast | Anatomical Abnormality | disease | |
| TCMBANKDI028664 | - | - | Finding | phenotype | |
| TCMBANKDI031570 | - | Abnormality of the nervous system | Mental or Behavioral Dysfunction | disease |
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