ALDH16A1

Mutations in the SPG21 (ACP33/maspardin) gene are associated with the mast syndrome, a type of spastic paraplegia. The protein encoded by the SPG21 gene has been shown to interact with the ALDH16A1 enzyme.{{cite journal | vauthors = Hanna MC, Blackstone C | title = Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1 | journal = Neurogenetics | volume = 10| issue = 3| pages = 217–28|date=January 2009 | pmid = 19184135 | doi = 10.1007/s10048-009-0172-6 | pmc = 5585778 }}

{{Reflist}}

• {{UCSC gene info|ALDH16A1}}

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{{Aldehyde dehydrogenases}}

{{gene-19-stub}}