| Human Disease |
MASA Syndrome OMIM ID: 303350 |
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| Synonyms | Adducted Thumb with Mental Retardation; Clasped Thumb and Mental Retardation; CRASH Syndrome; Gareis-Mason Syndrome; Mental Retardation, Aphasia, Shuffling Gait, and Adducted Thumbs; Spastic Paraplegia 1, X-Linked; SPG1; Thumb, Congenital Clasped, with Mental Retardation | |||||||||||||||||||||
| 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 |
| L1camtm1Mtei/Y |
either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv) | J:43838 | 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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