APRG1
APRG1 tumor suppressor candidate
Also known as: APRG1_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for APRG1 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
170 residues, UniProt reviewed canonical sequence.
>Q8IVJ8|APRG1
1 MKTMATRKRC KLSRTGPEFE NVIKRLLCAR TFHTRIGGDL THGIINRGRR ANAEQMGLQG
61 SAQHFNIFPL DLWTQGKKTE VQKREGTDSI PAAGRSGTAN QPSIAPHRCL FSRGITALDG
121 LKRGRGCNGA AHLVRGDAWK TKLGEPWVSI ALALAGPGAI LILELSWFLGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APRG1 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
- 1
- Mean surface accessibility (rSASA)
- 0.68
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads APRG1 as an antibody target. Whether an autoantibody or antibody against APRG1 could matter depends on whether native APRG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APRG1 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 APRG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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