PABPN1L
Embryonic polyadenylate-binding protein 2
Also known as: EPAB2_HUMAN, ePABP2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NDY0
- Gene
- PABPN1L
- Ensembl
- ENSG00000205022
- Chromosome
- 16
- Canonical length
- 278 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable poly(A) binding activity. Predicted to be involved in nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay. Predicted to act upstream of or within maternal-to-zygotic transition of gene expression; negative regulation of SCF-dependent proteasomal ubiquitin-dependent catabolic process; and negative regulation of protein ubiquitination. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
278 residues, UniProt reviewed canonical sequence.
>A6NDY0|PABPN1L
1 MWPFPSRSLF PPPTQAWLQT VSSDPEAQGW GAWNETKEIL GPEGGEGKEE KEEEEDAEED
61 QDGDAGFLLS LLEQENLAEC PLPDQELEAI KMKVCAMEQA EGTPRPPGVQ QQAEEEEGTA
121 AGQLLSPETV GCPLSGTPEE KVEADHRSVY VGNVDYGGSA EELEAHFSRC GEVHRVTILC
181 DKFSGHPKGY AYIEFATKGS VQAAVELDQS LFRGRVIKVL PKRTNFPGIS STDRGGLRGH
241 PGSRGAPFPH SGLQGRPRLR PQGQNRARGK FSPWFSPYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PABPN1L 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)
- 0.58
- Highest tissue expression
- 2.4 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 2.4 nTPM
- adrenal gland: 2.2 nTPM
- bone marrow: 0.6 nTPM
- basal ganglia: 0.5 nTPM
- spleen: 0.5 nTPM
- pancreas: 0.4 nTPM
Single-cell type
- oocytes: 60 nCPM
- adrenal cortex cells: 1.7 nCPM
- hematopoietic stem cells: 1 nCPM
- granulosa cells: 0.8 nCPM
- pdcs: 0.6 nCPM
- retinal bipolar cells: 0.4 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 2.4 nTPM
- cerebral cortex: 1.4 nTPM
- basal ganglia: 1.1 nTPM
- pons: 1 nTPM
- white matter: 1 nTPM
- amygdala: 0.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.87
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.84
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- maternal-to-zygotic transition of gene expression
- negative regulation of protein ubiquitination
- negative regulation of SCF-dependent proteasomal ubiquitin-dependent catabolic process
- nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PABPN1L as an antibody target. Whether an autoantibody or antibody against PABPN1L could matter depends on whether native PABPN1L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PABPN1L 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 PABPN1L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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