ALDH1L1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

10-formyltetrahydrofolate dehydrogenase is an enzyme that in humans is encoded by the ALDH1L1 gene.[5]

PDBOrtholog search: PDBe RCSB
AliasesALDH1L1, 10-FTHFDH, 10-fTHF, FDH, FTHFD, aldehyde dehydrogenase 1 family member L1
Quick facts Available structures, PDB ...
ALDH1L1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesALDH1L1, 10-FTHFDH, 10-fTHF, FDH, FTHFD, aldehyde dehydrogenase 1 family member L1
External IDsOMIM: 600249; MGI: 1340024; HomoloGene: 122031; GeneCards: ALDH1L1; OMA:ALDH1L1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001270364
NM_001270365
NM_012190
NM_144776

NM_027406
NM_001356412

RefSeq (protein)

NP_001257293
NP_001257294
NP_036322

NP_081682
NP_001343341

Location (UCSC)Chr 3: 126.1 – 126.2 MbChr 6: 90.46 – 90.58 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene catalyzes the conversion of 10-formyltetrahydrofolate, nicotinamide adenine dinucleotide phosphate (NADP), and water to tetrahydrofolate, NADPH, and carbon dioxide. The encoded protein belongs to the aldehyde dehydrogenase family and is responsible for formate oxidation in vivo. Deficiencies in this gene can result in an accumulation of formate and subsequent methanol poisoning.[5]

References

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