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Gene : ALDH1L2 Homo sapiens

Name  ? aldehyde dehydrogenase 1 family member L2 Cytological Location  12q23.3
Brief Description  aldehyde dehydrogenase 1 family member L2
Description  This gene encodes a member of both the aldehyde dehydrogenase superfamily and the formyl transferase superfamily. This member is the mitochondrial form of 10-formyltetrahydrofolate dehydrogenase (FDH), which converts 10-formyltetrahydrofolate to tetrahydrofolate and CO2 in an NADP(+)-dependent reaction, and plays an essential role in the distribution of one-carbon groups between the cytosolic and mitochondrial compartments of the cell. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2010]
  • synonyms:
  • mtFDH,
  • mtFDH,
  • uc001tlc.4,
  • HGNC:26777,
  • ALDH1L2,
  • aldehyde dehydrogenase 1 family, member L2,
  • FLJ38508,
  • OTTHUMG00000169823,
  • NM_001034173,
  • mitochondrial 10-formyltetrahydrofolate dehydrogenase,
  • AK095827
  • identifiers:
  • 160428,
  • ENSG00000136010,
  • ALDH1L2

Genome feature

Region: gene ? Length: 64826  
Location: 12:105019784-105084609 reverse strand Cyto location: 12q23.3

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0 Diseases

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3740 SNPs

5 Cross References

14 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results