Gene

RPS26

Species
Homo sapiens
Symbol
RPS26
Name
ribosomal protein S26
Synonyms
  • 40S ribosomal protein S26
  • DBA10
Biotype
protein coding gene
Automated Description
Enables mRNA binding activity. A structural constituent of ribosome. Involved in cytoplasmic translation and negative regulation of RNA splicing. Located in extracellular exosome and membrane. Part of cytosolic small ribosomal subunit. Implicated in Diamond-Blackfan anemia 10.
RGD Description
This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S26E family of ribosomal proteins. Mutations in this gene are found in Diamond-Blackfan anemia 10. There are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Aug 2017]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR12538
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
None
Other Sources

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
GRCh38
Viewer Help
56.0415M56.0420M56.0425M56.0430M56.0435M56.0440M56.0445M

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

Genetic Interactions