ALDH3A2 Back

aldehyde dehydrogenase 3 family, member A2

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NCBI Description of ALDH3A2

Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Community Annotation of ALDH3A2 Add / Edit ALDH3A2: Annotations

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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

ALDH3A2 is highly significantly mutated in
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ALDH3A2 is significantly mutated in
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ALDH3A2 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for ALDH3A2