| Human Disease |
Infantile Sialic Acid Storage Disorder OMIM ID: 269920 |
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| Synonyms | ISSD; N-Acetylneuraminic Acid Storage Disease; Nana Storage Disease; NSD; Sialuria, Infantile Form | |||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Slc17a5tm1Lex/Slc17a5tm1Lex |
involves: 129S5/SvEvBrd * C57BL/6 | J:158444 | 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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