Gene

Gba1b

Species
Drosophila melanogaster
Symbol
Gba1b
Name
Glucocerebrosidase 1b
Synonyms
  • CG10299
  • CG31414
Biotype
protein coding gene
Automated Description
Enables glucosylceramidase activity. Involved in several processes, including adult locomotory behavior; cellular response to unfolded protein; and determination of adult lifespan. Is expressed in adult head. Used to study Gaucher's disease; Lewy body dementia; and Parkinson's disease. Human ortholog(s) of this gene implicated in Gaucher's disease (multiple); Lewy body dementia; Parkinson's disease (multiple); and Parkinsonism. Orthologous to human GBA1 (glucosylceramidase beta 1).
FB Description
Glucocerebrosidase 1b (Gba1b) encodes a lysosomal acid beta glucocerebrosidase that catalyzes the hydrolysis of glucosylceramide to ceramide and glucose.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11069
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

Primary Sources
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Annotation details
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    Disease Associations

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

    Allele/Variant Symbol
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      Transgenic Alleles

      Species
      (carrying the transgene)
      Allele symbol
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          R6
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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

          Gba1b molecule type
          Interactor gene
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            Genetic Interactions

            Gba1b role
            Gba1b genetic perturbation
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