搜索结果
靶点ID:TCMBANKGE012462
靶点别名:MCOP3; RX
靶点描述:retina and anterior neural fold homeobox
染色体:18
染色体位置:18q21.32
靶点类型:protein-coding
HERB_ID:-
HGNC_Link:18662
OMIM_Link:601881
Ensembl_Link:ENSG00000134438
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 |
|---|
| TCMBANKDI000835 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | - | Congenital Abnormality | disease | |
| TCMBANKDI009479 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Abnormality of head or neck | Anatomical Abnormality | disease | |
| TCMBANKDI014253 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI014359 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | - | Congenital Abnormality | group | |
| TCMBANKDI016840 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Abnormality of the eye | Congenital Abnormality | disease | |
| TCMBANKDI019309 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Abnormality of the eye | Congenital Abnormality | disease |
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Dai SX Lab