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Ribosomal protein S26 pseudogene 13 (RPS26P13)
- Target
- RPS26P13
- Molecular classification
- Other (pseudogene)
01
Overview
Ribosomal protein S26 pseudogene 13 (RPS26P13) is a human pseudogene related to the ribosomal protein S26 gene (RPS26)[2][8]. Unlike the functional RPS26 gene, which encodes a component of the 40S ribosomal subunit implicated in Diamond-Blackfan anemia, RPS26P13 is a processed pseudogene—meaning it is a non-functional DNA sequence with significant similarity to the ancestral protein-coding gene but lacking coding potential and not known to be transcribed or translated into a functional product[2][8]. There are multiple such pseudogenes of ribosomal protein genes found in the genome as a result of evolutionary duplication events[1].
- Other names
- RPS26P13RPS26_4_158
02
Mechanism of action
None
03
Biological functions
None; as a pseudogene, RPS26P13 does not encode a functional protein and has no known biological function or cellular activity[2][8].
04
Disease associations
None specific to RPS26P13. The functional RPS26 gene is associated with Diamond-Blackfan anemia, but there is no evidence that RPS26P13 plays any disease role[1][3][5][4].
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