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
- 19,647,291–19,685,881 (+)
- 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
Glycolysis / Gluconeogenesis - Homo sapiens (human)Ascorbate and aldarate metabolism - Homo sapiens (human)Fatty acid degradation - Homo sapiens (human)Valine, leucine and isoleucine degradation - Homo sapiens (human)Lysine degradation - Homo sapiens (human)Arginine and proline metabolism - Homo sapiens (human)Histidine metabolism - Homo sapiens (human)Tryptophan metabolism - Homo sapiens (human)beta-Alanine metabolism - Homo sapiens (human)Glycerolipid metabolism - Homo sapiens (human)
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
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 55458
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/224
- genomic end
- 19685760
- genomic start
- 19551449
- chromosome
- human chromosome 17
- cytogenetic location
- 17p11.2
- genetic association
- Sjogren-Larsson syndrome
via Wikidata · CC0