Symbol Name ID |
Chd7
chromodomain helicase DNA binding protein 7 MGI:2444748 |
Darker colors indicate more annotations |
Human Phenotypes | Facial palsy |
Hypotonia |
Disease(s) Associated with CHD7 | ||
CHARGE syndrome |
Mouse Phenotypes | abnormal myocardial trabeculae morphology |
abnormal myocardium compact layer morphology |
thin ventricle myocardium compact layer |
thin myocardium |
decreased fetal cardiomyocyte proliferation |
increased cardiomyocyte apoptosis |
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Availability | Mouse Genotype | ||||||
Chd7tm2a(EUCOMM)Wtsi/Chd7tm2a(EUCOMM)Wtsi | |||||||
Chd7tm2a(EUCOMM)Wtsi/Chd7tm2a(EUCOMM)Wtsi Mesp1tm2(cre)Ysa/Mesp1+ (conditional) |
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Chd7tm2a(EUCOMM)Wtsi/Chd7tm2a(EUCOMM)Wtsi Tg(Tek-cre)1Ywa/0 (conditional) |
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 04/16/2024 MGI 6.23 |
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