| Human Disease |
Nijmegen Breakage Syndrome OMIM ID: 251260 |
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| Synonyms | Ataxia-Telangiectasia Variant V1; AT-V1; Microcephaly with Normal Intelligence, Immunodeficiency, and Lymphoreticular Malignancies; NBS; Nonsyndromal Microcephaly, Autosomal Recessive, with Normal Intelligence; Seemanova Syndrome II | |||||||||||||||||||||
| View all models | View ALL (7) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Nbntm1Xu/Nbntm1Xu |
Not Specified | J:75272 | View |
| Nbntm1Zqw/Nbntm1Zqw |
involves: 129S2/SvPas * C57BL/6 | J:86563 | View |
| Nbntm1.1Md/Nbntm1.1Md |
involves: 129/Sv * 129P2/OlaHsd | J:93598 | View |
| Nbntm1Jpt/Nbntm1Jpt |
involves: 129S7/SvEvBrd | J:75956 | View |
| Nbntm1Zqw/Nbn+ |
involves: 129S2/SvPas * C57BL/6 | J:86563 | View |
| Nbntm1Nus/Nbntm2Nus Tg(CD19-cre/ERT2)1Cgn/0 |
Not Specified | J:96102 | View |
| Nbntm1Md/Nbntm1Zqw Tg(Mx1-cre)1Cgn/0 |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA | J:93598 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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