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Symbol Name ID |
Cdh2
cadherin 2 MGI:88355 |
| Darker colors indicate more annotations |
| Human Phenotypes | Axial hypotonia |
| Disease(s) Associated with CDH2 | |
| agenesis of corpus callosum, cardiac, ocular, and genital syndrome |
| Mouse Phenotypes | abnormal myocardium layer morphology |
abnormal myocardial fiber morphology |
abnormal intercalated disk morphology |
decreased ventricle muscle contractility |
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| Availability | Mouse Genotype | ||||
| Cdh2tm1Hyn/Cdh2tm1Hyn | |||||
| Cdh2tm1Glr/Cdh2Gt(OST49160)Lex A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (conditional) |
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| Cdh2tm1Glr/Cdh2tm1Hyn A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (conditional) |
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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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