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The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
[中文简述(自动翻译):]  
CHD2基因(以及对应的蛋白质)的细胞分布位置:
CHD2基因的本体(GO)信息:
| 疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
| EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | 0.24 | 1 | 5 | CLINVAR_UNIPROT |
| Epilepsy | 0.121628651 | 6 | 0 | BeFree_CTD_human |
| Lennox-Gastaut syndrome | 0.12 | 0 | 0 | ORPHANET |
| CHARGE Syndrome | 0.080542884 | 2 | 0 | BeFree_MGD |
| Tobacco Use Disorder | 0.002367032 | 1 | 0 | GAD |
| Seizures | 0.000814326 | 3 | 0 | BeFree |
| Epileptic encephalopathy | 0.000814326 | 3 | 0 | BeFree |
| PHOTOPAROXYSMAL RESPONSE 1 | 0.000542884 | 2 | 0 | BeFree |
| Intellectual Disability | 0.000542884 | 2 | 0 | BeFree |
| Azoospermia | 0.000271442 | 1 | 0 | BeFree |
| Epilepsy, Generalized | 0.000271442 | 1 | 0 | BeFree |
| Epilepsies, Myoclonic | 0.000271442 | 1 | 0 | BeFree |
| HIV Infections | 0.000271442 | 1 | 0 | BeFree |
| Chronic Lymphocytic Leukemia | 0.000271442 | 1 | 0 | BeFree |
| Moderate mental retardation (I.Q. 35-49) | 0.000271442 | 1 | 0 | BeFree |
| Encephalopathies | 0.000271442 | 1 | 0 | BeFree |
| Generalized seizures | 0.000271442 | 1 | 0 | BeFree |
| Congenital diaphragmatic hernia | 0.000271442 | 1 | 0 | BeFree |
| Obesity, Abdominal | 0.000271442 | 1 | 0 | BeFree |
| Reflex Epilepsy, Photosensitive | 0.000271442 | 1 | 0 | BeFree |
| Myoclonic Encephalopathy | 0.000271442 | 1 | 0 | BeFree |
| Infantile Severe Myoclonic Epilepsy | 0.000271442 | 1 | 0 | BeFree |
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