搜索结果
靶点ID:TCMBANKGE007894
靶点别名:HSPC139; SSMDF
靶点描述:CXXC repeat containing interactor of PDZ3 domain
染色体:2
染色体位置:2p21
靶点类型:protein-coding
HERB_ID:-
HGNC_Link:14312
OMIM_Link:604594
Ensembl_Link:ENSG00000119878
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 |
|---|
| TCMBANKDI002718 | - | - | Finding | phenotype | |
| TCMBANKDI004056 | - | - | Laboratory or Test Result | phenotype | |
| TCMBANKDI005528 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | - | Congenital Abnormality | disease | |
| TCMBANKDI005587 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Abnormality of limbs; Abnormality of the skeletal system | Congenital Abnormality | disease | |
| TCMBANKDI007228 | - | - | Finding | phenotype | |
| TCMBANKDI009951 | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Abnormality of the skeletal system | Disease or Syndrome | disease | |
| TCMBANKDI013067 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Abnormality of limbs | Congenital Abnormality | disease | |
| TCMBANKDI021278 | Eye Diseases | Abnormality of the eye | Disease or Syndrome | disease | |
| TCMBANKDI028305 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Abnormality of limbs; Abnormality of the skeletal system | Congenital Abnormality | disease | |
| TCMBANKDI028357 | Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases | Abnormality of the immune system | Finding | phenotype |
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Dai SX Lab