Gene

ADPRS

Species
Homo sapiens
Symbol
ADPRS
Name
ADP-ribosylserine hydrolase
Synonyms
  • [Protein ADP-ribosylarginine] hydrolase-like protein 2
  • [Protein ADP-ribosylserine] hydrolase
Biotype
protein coding gene
Automated Description
Enables O-acetyl-ADP-ribose deacetylase activity; hydrolase activity, acting on glycosyl bonds; and magnesium ion binding activity. Involved in DNA repair; cellular response to superoxide; and peptidyl-serine ADP-deribosylation. Located in mitochondrion; nuclear body; and site of DNA damage. Implicated in stress-induced childhood-onset neurodegeneration with variable ataxia and seizures.
RGD Description
This gene encodes a member of the ADP-ribosylglycohydrolase family. The encoded enzyme catalyzes the removal of ADP-ribose from ADP-ribosylated proteins. This enzyme localizes to the mitochondria, in addition to the nucleus and cytoplasm.[provided by RefSeq, Feb 2009]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR16222
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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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
          GRCh38
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          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          ADPRS molecule type
          Interactor gene
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            Genetic Interactions

            ADPRS role
            ADPRS genetic perturbation
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