Aliases ALDH16A1 Ensembl ENSG00000161618 | Entrez 126133 | |
External IDs MGI: 1916998 HomoloGene: 34938 GeneCards: ALDH16A1 | ||
Aldehyde dehydrogenase 16 family, member A1 also known as ALDH16A1 is an aldehyde dehydrogenase gene.
Clinical significance
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.
References
ALDH16A1 Wikipedia(Text) CC BY-SA