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Symbol Name ID |
Chd7
chromodomain helicase DNA binding protein 7 MGI:2444748 |
| Darker colors indicate more annotations |
| Human Phenotypes | Esophageal atresia |
Tracheoesophageal fistula |
Duodenal atresia |
Dysphagia |
Gastroesophageal reflux |
| Disease(s) Associated with CHD7 | |||||
| CHARGE syndrome |
| Mouse Phenotypes | abnormal secondary palate development |
abnormal palatal shelf fusion at midline |
decreased palatal rugae number |
cleft secondary palate |
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| Availability | Mouse Genotype | ||||
| Chd7Whi/Chd7+ | |||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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