PMS2P3
Putative postmeiotic segregation increased 2-like protein 3
Also known as: PM2P3_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for PMS2P3 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
168 residues, UniProt reviewed canonical sequence.
>Q13401|PMS2P3
1 MNTLQGPVSF KDVAVDFTQE EWRQLDPDEK IAYGDVMLEN YSHLVSVGYD YHQAKHHHGV
61 EVKEVEQGEE PWIMEGEFPC QHSPEPAKAI KPIDRKSVHQ ICSGPVVLSL STAVKELVEN
121 SLDAGATNID LKLKDYGVDL IEVSDNGCGV EEENFEGLIS FSSETSHMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PMS2P3 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)
- 0.49
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PMS2P3 as an antibody target. Whether an autoantibody or antibody against PMS2P3 could matter depends on whether native PMS2P3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PMS2P3 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 PMS2P3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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