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Gene : ALDH1A3 Homo sapiens

Name  ? aldehyde dehydrogenase 1 family member A3 Cytological Location  15q26.3
Brief Description  aldehyde dehydrogenase 1 family member A3
Description  This gene encodes an aldehyde dehydrogenase enzyme that uses retinal as a substrate. Mutations in this gene have been associated with microphthalmia, isolated 8, and expression changes have also been detected in tumor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
  • synonyms:
  • ALDH1A3,
  • ALDH6,
  • ALDH6,
  • aldehyde dehydrogenase 1 family, member A3,
  • retinaldehyde dehydrogenase 3,
  • NM_000693,
  • HGNC:409,
  • uc002bwn.5,
  • RALDH3,
  • U07919,
  • ALDH1A6,
  • RALDH3,
  • MCOP8,
  • OTTHUMG00000186439
  • identifiers:
  • 220,
  • ENSG00000184254,
  • ALDH1A3

Genome feature

Region: gene ? Length: 36796  
Location: 15:100879831-100916626 Cyto location: 15q26.3

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Gene -> HPO annotation (Human Phenotype Ontology)

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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Ontology

Gene --> GO terms.



78 SNPs

5 Cross References

18 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results