搜索结果
靶点ID:TCMBANKGE014939
靶点别名:LGMD1; LGMD1A; MFM3; TTID; TTOD
靶点描述:myotilin
染色体:5
染色体位置:5q31.2
靶点类型:protein-coding
HERB_ID:-
HGNC_Link:12399
OMIM_Link:604103
Ensembl_Link:ENSG00000120729
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 |
|---|
| TCMBANKDI001033 | - | Abnormality of the nervous system | Finding | phenotype | |
| TCMBANKDI002624 | Cardiovascular Diseases | - | Disease or Syndrome | group | |
| TCMBANKDI004277 | - | Abnormality of limbs; Abnormality of the skeletal system | Finding | phenotype | |
| TCMBANKDI006903 | - | Abnormality of limbs; Abnormality of the musculature | phenotype | ||
| TCMBANKDI007343 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | - | Finding | phenotype | |
| TCMBANKDI009625 | - | - | Disease or Syndrome | disease | |
| TCMBANKDI013913 | Nervous System Diseases | Abnormality of the musculature | Sign or Symptom | phenotype | |
| TCMBANKDI013994 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Abnormality of the nervous system | Finding | phenotype | |
| TCMBANKDI016933 | Musculoskeletal Diseases; Nervous System Diseases | - | Disease or Syndrome | disease | |
| TCMBANKDI019267 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Abnormality of the nervous system | Sign or Symptom | phenotype | |
| TCMBANKDI019650 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | - | Disease or Syndrome | phenotype | |
| TCMBANKDI019748 | Musculoskeletal Diseases | Abnormality of the musculature | Disease or Syndrome | disease | |
| TCMBANKDI024159 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Abnormality of the musculature | Sign or Symptom | phenotype | |
| TCMBANKDI024451 | - | Abnormality of the musculature | Disease or Syndrome | disease | |
| TCMBANKDI025401 | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | - | Pathologic Function | phenotype | |
| TCMBANKDI027248 | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases | Abnormality of the musculature | Finding | phenotype | |
| TCMBANKDI028664 | - | - | Finding | phenotype | |
| TCMBANKDI032156 | - | Constitutional symptom; Abnormality of the skeletal system | Sign or Symptom | phenotype |
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