| Human Disease |
Spinal Muscular Atrophy, Type III; SMA3 OMIM ID: 253400 |
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| Synonyms | Kugelberg-Welander Syndrome; KWS; Muscular Atrophy, Juvenile; SMA III; Spinal Muscular Atrophy, Mild Childhood and Adolescent Form | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Smn1tm1Msd/Smn1tm1Msd Tg(SMN1*A2G)2023Ahmb/0 Tg(SMN2)89Ahmb/0 |
involves: 129P2/OlaHsd * FVB/N | J:81238 | View |
| Smn1tm1.1Dscd/Smn1tm1.1Dscd |
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 | J:164889 | 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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