Symbol Name ID |
Nbn
nibrin MGI:1351625 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Dysgammaglobulinemia |
Abnormality of chromosome stability |
Disease(s) Associated with NBN | ||
Nijmegen breakage syndrome |
Mouse Phenotypes | cellular phenotype |
decreased oocyte number |
absent oocytes |
abnormal cell cycle |
abnormal cell cycle checkpoint function |
decreased cellular sensitivity to ionizing radiation |
increased cellular sensitivity to ionizing radiation |
increased cellular sensitivity to gamma-irradiation |
abnormal inner cell mass apoptosis |
increased apoptosis |
abnormal neuron differentiation |
decreased B cell proliferation |
decreased fibroblast proliferation |
decreased inner cell mass proliferation |
absent inner cell mass proliferation |
chromosomal instability |
chromosome breakage |
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Availability | Mouse Genotype | |||||||||||||||||
Nbnem3Jpt/Nbnem3Jpt | ||||||||||||||||||
Nbnem4Jpt/Nbnem4Jpt | ||||||||||||||||||
Nbntm1Jpt/Nbntm1Jpt | * | |||||||||||||||||
Nbntm1Nus/Nbntm1Nus | ||||||||||||||||||
Nbntm1Xu/Nbntm1Xu | ||||||||||||||||||
Nbntm1Zqw/Nbntm1Zqw | ||||||||||||||||||
Nbntm2.1Jpt/Nbntm2.1Jpt | ||||||||||||||||||
Nbntm3Jpt/Nbntm3Jpt | ||||||||||||||||||
Nbntm1Zqw/Nbn+ | ||||||||||||||||||
Nbntm2Zqw/Nbntm2Zqw Tg(Nes-cre)1Wme/0 (conditional) |
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Nbntm1Md/Nbntm1Zqw Tg(Mx1-cre)1Cgn/0 (conditional) |
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Nbntm1Nus/Nbntm2Nus Tg(CD19-cre/ERT2)1Cgn/0 (conditional) |
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Nbntm1Nus/Nbntm2Nus Tg(Spo11-cre)D5Mpel/0 (conditional) |
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Nbntm2Zqw/Nbntm2.1Zqw Tg(Nes-cre)1Wme/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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