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Gene : ALDH3A2 Homo sapiens

Name  ? aldehyde dehydrogenase 3 family member A2 Cytological Location  17p11.2
Brief Description  aldehyde dehydrogenase 3 family member A2
description  Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • NM_000382,
  • SLS,
  • uc002gwb.2,
  • ALDH10,
  • SLS,
  • OTTHUMG00000059471,
  • ALDH10,
  • ALDH3A2,
  • L47162,
  • HGNC:403,
  • FALDH,
  • FALDH,
  • fatty aldehyde dehydrogenase,
  • aldehyde dehydrogenase 3 family, member A2
  • identifiers:
  • 224,
  • ENSG00000072210,
  • ALDH3A2

Genome feature

Region: gene ? Length: 29451  
Location: 17:19648146-19677596 Cyto location: 17p11.2


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

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Other

796 SN Ps

5 Cross References

19 Data Sets

11 Homologues

0 Located Features

90 Rna Seq Results