| Human Disease |
Gaucher Disease, Type I OMIM ID: 230800 |
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| Synonyms | Acid Beta-Glucosidase Deficiency; Gaucher Disease, Noncerebral Juvenile; GBA Deficiency; GD I; Glucocerebrosidase Deficiency | |||||||||||||||||||||
| View all models | View ALL (13) 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 |
| Gbatm1.1Karl/Gbatm1.1Karl |
involves: 129S1/Sv * 129X1/SvJ | J:113751 | View |
| Gbatm1Ggb/Gbatm1Ggb |
involves: 129S5/SvEvBrd * C57BL/6 | J:86334 | View |
| Gbatm2Ggb/Gbatm2Ggb |
involves: 129S5/SvEvBrd * C57BL/6 | J:86334 | View |
| Gbatm3Ggb/Gbatm3Ggb |
involves: 129S5/SvEvBrd | J:86334 | View |
| Gbatm4Ggb/Gbatm4Ggb |
involves: 129S5/SvEvBrd * C57BL/6 | J:86334 | View |
| Gbatm2Ggb/Gbatm1Nsb |
involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6 | J:86334 | View |
| Gbatm3Ggb/Gbatm1Nsb |
involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6 | J:86334 | View |
| Gbatm4Ggb/Gbatm1Nsb |
involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6 | J:86334 | View |
| Gbatm2Ggb/Gbatm2Ggb Psaptm1Suz/Psaptm1Suz |
involves: 129P2/OlaHsd * 129S5/SvEvBrd | J:174780 | View |
| Gbatm1Clk/Gbatm1.1Clk Tg(Tek-cre)12Flv/0 |
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J | J:117763 | View |
| Gbatm1Karl/Gbatm1.1Karl Tg(Mx1-cre)1Cgn/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:113751 | View |
| Gbatm1.1Pmis/Gbatm1.1Pmis Tg(Mx1-cre)1Cgn/0 |
involves: C57BL/6 * CBA | J:167081 | View |
| Gbatm1.1Pmis/Gbatm1.2Pmis Tg(Mx1-cre)1Cgn/0 |
involves: C57BL/6 * CBA | J:167081 | 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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