ALDH3A2
Sign in to saveAlso known as aldehyde dehydrogenase 3 family, member A2, ALDH10, FALDH, SLS, aldehyde dehydrogenase 3 family member A2
protein-coding gene in the species Homo sapiens
Gene data
ALDH3A2- Name
- aldehyde dehydrogenase 3 family member A2
- Type
- protein-coding
- Position
- 19,647,291–19,685,760 (+)
- Aliases
- ALDH10, FALDH, SLS
- Ensembl
- ENSG00000072210
- RefSeq RNA
- NM_000382.3, NM_001031806.2, NM_001369136.1, NM_001369137.2, NM_001369138.2
- RefSeq protein
- NP_000373.1, NP_001026976.1, NP_001356065.1, NP_001356066.1, NP_001356067.1
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. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
aldehyde dehydrogenase 3 family member A2
- Symbol
- ALDH3A2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:19,647,291-19,685,881
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 55458
- exact match
- identifiers.org/ncbigene/224
- genomic end
- 19685760
- genomic start
- 19551449
- cytogenetic location
- 17p11.2
via Wikidata · CC0