|
Symbol Name ID |
Nbn
nibrin MGI:1351625 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short neck |
Short stature |
Cachexia |
Intrauterine growth retardation |
| Disease(s) Associated with NBN | ||||
| Nijmegen breakage syndrome |
| Mouse Phenotypes | decreased embryo size |
decreased body weight |
postnatal growth retardation |
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| Availability | Mouse Genotype | |||
| Nbntm1Nus/Nbntm1Nus | ||||
| Nbntm1Xu/Nbntm1Xu | ||||
| Nbntm2Zqw/Nbntm2Zqw Tg(Nes-cre)1Wme/0 (conditional) |
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| Nbntm2Zqw/Nbntm2.1Zqw Tg(Nes-cre)1Wme/0 (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 04/23/2024 MGI 6.23 |
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