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Gene : ALDH8A1 Homo sapiens

Name  ? aldehyde dehydrogenase 8 family member A1 Cytological Location  6q23.3
Brief Description  aldehyde dehydrogenase 8 family member A1
description  This gene encodes a member of the aldehyde dehydrogenase family of proteins. The encoded protein has been implicated in the synthesis of 9-cis-retinoic acid and in the breakdown of the amino acid tryptophan. This enzyme converts 9-cis-retinal into the retinoid X receptor ligand 9-cis-retinoic acid, and has approximately 40-fold higher activity with 9-cis-retinal than with all-trans-retinal. In addition, this enzyme has been shown to catalyze the conversion of 2-aminomuconic semialdehyde to 2-aminomuconate in the kynurenine pathway of tryptophan catabolism. [provided by RefSeq, Jul 2018]
  • synonyms:
  • NM_001193480,
  • HGNC:15471,
  • AL021939,
  • OTTHUMG00000015623,
  • uc003qew.3,
  • ALDH8A1,
  • DJ352A20.2,
  • ALDH12,
  • ALDH12,
  • aldehyde dehydrogenase 8 family, member A1
  • identifiers:
  • 64577,
  • ENSG00000118514,
  • ALDH8A1

Genome feature

Region: gene ? Length: 32733  
Location: 6:134917390-134950122 reverse strand Cyto location: 6q23.3


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Proteins

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SNPs

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Disease

0 Diseases

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Expression

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2011 SN Ps

5 Cross References

15 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results