Gene

ELO3

Species
Saccharomyces cerevisiae
Symbol
ELO3
Name
fatty acid ELOngation
Synonyms
  • APA1
  • SRE1
Biotype
protein coding gene
Automated Description
Enables fatty acid elongase activity. Involved in late endosome to vacuole transport via multivesicular body sorting pathway; lipid biosynthetic process; and post-Golgi vesicle-mediated transport. Located in endoplasmic reticulum. Human ortholog(s) of this gene implicated in corneal dystrophy; spinocerebellar ataxia type 34; and spinocerebellar ataxia type 38. Orthologous to several human genes including ELOVL1 (ELOVL fatty acid elongase 1) and ELOVL4 (ELOVL fatty acid elongase 4).
SGD Description
Elongase; involved in fatty acid and sphingolipid biosynthesis; synthesizes very long chain 20-26-carbon fatty acids from C18-CoA primers; involved in regulation of sphingolipid biosynthesis; lethality of the elo2 elo3 double null mutation is functionally complemented by human ELOVL1 and weakly complemented by human ELOVL3 or ELOV7
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11157:SF157
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

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    Disease Associations

    Cases where the expected disease association was NOT found
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    Alleles and Variants

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      Transgenic Alleles

      Species
      (carrying the transgene)
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          R64-5-1
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          Sequence Details

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          Expression

          Primary Sources
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          ELO3 molecule type
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            Genetic Interactions

            ELO3 role
            ELO3 genetic perturbation
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