12613369748ENSG00000161618ENSMUSG00000007833Q8IZ83Q571I9NM_001145396NM_153329NM_145954NP_001138868NP_699160NP_666066Aldehyde dehydrogenase 16 family, member A1 also known as ALDH16A1 is an aldehyde dehydrogenase gene.

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.

This article on a gene on human chromosome 19 is a stub.

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