LINC00518
Putative uncharacterized protein encoded by LINC00518
Also known as: CF218_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for LINC00518 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
118 residues, UniProt reviewed canonical sequence.
>Q8N0U6|LINC00518
1 MDSSDETGSS FMSFWPHLQS DDLARNGITG FPYFSFIILN ESDQILELDG TLVKIWLLVP
61 SHQPATHFKF EETKTHGPYV ITGDYPRSLW QKSASSLPAS PPCLWYFLPT LGCFCDHTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LINC00518 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about LINC00518.
Disease | ImmuneIEDB
Conditions an epitope on LINC00518 was assayed in.
- melanoma T cell
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LINC00518 as an antibody target. Whether an autoantibody or antibody against LINC00518 could matter depends on whether native LINC00518 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LINC00518 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 LINC00518 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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