| Human Disease |
Tay-Sachs Disease; TSD OMIM ID: 272800 |
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| Synonyms | B Variant Gm2-Gangliosidosis; GM2-Gangliosidosis, Type I; Hexosaminidase A Deficiency | |||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Hexatm1Rlp/Hexatm1Rlp |
involves: 129S4/SvJae * C57BL/6 | J:21008 | View |
| Hexatm1Grv/Hexatm1Grv |
involves: 129P2/Ola * C57BL/6J | J:30899 | View |
| Hexatm1Cota/Hexatm1Cota |
involves: 129S2/SvPas * C57BL/6 | J:30435 | 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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