| Human Disease |
Immunodeficiency with Hyper-IgM, Type 1; HIGM1 OMIM ID: 308230 |
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| Synonyms | Hyper-Igm Immunodeficiency, X-Linked; XHIM; Hyper-Igm Syndrome 1; Hyper-Igm Syndrome; HIGM; IHIS | |||||||||||||||||||||
| View all models | View ALL (4) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI. | |||||||||||||||||||||
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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 |
| Cd40lgtm1Flv/Cd40lgtm1Flv |
involves: 129S2/SvPas * C57BL/6 | J:25010 | View |
| Cd40lgtm1Imx/Y |
involves: 129S2/SvPas * C57BL/6 | J:21137 | View |
| Cd40lgtm1Flv/Cd40lgtm1Flv Tg(APPSWE)2576Kha/0 |
involves: 129S2/SvPas * C57BL/6 * SJL | J:80429 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Cd40tm1Kik/Cd40tm1Kik Traf3ip2tm1.1Lix/Traf3ip2tm1.1Lix |
involves: 129 * 129P2/OlaHsd * BALB/c | J:93923 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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