Human Disease and Mouse Model Detail
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Human Disease
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Spinal Muscular Atrophy, X-Linked 2; SMAX2
OMIM ID: 301830
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Synonyms
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AMC, Distal, X-Linked;
Arthrogryposis Multiplex Congenita, Distal, X-Linked;
Arthrogryposis, X-Linked, Type I; AMCX1;
Spinal Muscular Atrophy, Infantile X-Linked; XLSMA;
Spinal Muscular Atrophy, X-Linked Lethal Infantile
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Uba1
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UBA1*
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1:1 Homology
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Analysis Tools