ALDH1A2

Aldehyde dehydrogenase 1 family, member A2

PDB rendering based on 1bi9.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols ALDH1A2 ; RALDH(II); RALDH2; RALDH2-T
External IDs OMIM: 603687 MGI: 107928 HomoloGene: 68368 GeneCards: ALDH1A2 Gene
EC number 1.2.1.36
Orthologs
Species Human Mouse
Entrez 8854 19378
Ensembl ENSG00000128918 ENSMUSG00000013584
UniProt O94788 Q62148
RefSeq (mRNA) NM_001206897 NM_009022
RefSeq (protein) NP_001193826 NP_033048
Location (UCSC) Chr 15:
57.95 – 58.5 Mb
Chr 9:
71.22 – 71.3 Mb
PubMed search

Aldehyde dehydrogenase 1 family, member A2, also known as ALDH1A2 or retinaldehyde dehydrogenase 2 (RALDH2), is an enzyme that in humans is encoded by the ALDH1A2 gene.[1][2]

This protein belongs to the aldehyde dehydrogenase family of proteins. The product of this gene is an enzyme that catalyzes the synthesis of retinoic acid (RA) from retinaldehyde. Retinoic acid, the active derivative of vitamin A (retinol), is a paracrine hormone signaling molecule that functions in developing and adult tissues.[3] The studies of a similar mouse gene suggest that this enzyme and the cytochrome CYP26A1, concurrently establish local embryonic retinoic acid levels that facilitate posterior organ development and prevent spina bifida. Three transcript variants encoding distinct isoforms have been identified for this gene.[2]

References

Further reading

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