RPL13AP3
Putative ribosomal protein uL13-like
Also known as: R13P3_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for RPL13AP3 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
102 residues, UniProt reviewed canonical sequence.
>Q6NVV1|RPL13AP3
1 MLRHKTKRGH ASLDCLKVFD GIPPPYDKKK RMVVPAALKV VRLKPTRKFA LLGRQAQEVR
61 WKYQAVTATL EEKRKEKAKI HYWKKKQLMR LRKQAEKNVK KNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPL13AP3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.52
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RPL13AP3 as an antibody target. Whether an autoantibody or antibody against RPL13AP3 could matter depends on whether native RPL13AP3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPL13AP3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label RPL13AP3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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