PABIR1
PPP2R1A-PPP2R2A-interacting phosphatase regulator 1
Also known as: C9orf42, FAM122A, MGC17347, PBIR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96E09
- Gene
- PABIR1
- Ensembl
- ENSG00000187866
- Chromosome
- 9
- Canonical length
- 287 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
Enables protein phosphatase 2A binding activity and protein serine/threonine phosphatase inhibitor activity. Involved in mitotic G2/M transition checkpoint; positive regulation of cell growth; and positive regulation of proteasomal ubiquitin-dependent protein catabolic process. Located in cytoplasm and nuclear body. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
287 residues, UniProt reviewed canonical sequence.
>Q96E09|PABIR1
1 MAQEKMELDL ELPPGTGGSP AEGGGSGGGG GLRRSNSAPL IHGLSDTSPV FQAEAPSARR
61 NSTTFPSRHG LLLPASPVRM HSSRLHQIKQ EEGMDLINRE TVHEREVQTA MQISHSWEES
121 FSLSDNDVEK SASPKRIDFI PVSPAPSPTR GIGKQCFSPS LQSFVSSNGL PPSPIPSPTT
181 RFTTRRSQSP INCIRPSVLG PLKRKCEMET EYQPKRFFQG ITNMLSSDVA QLSDPGVCVS
241 SDTLDGNSSS AGSSCNSPAK VSTTTDSPVS PAQAASPFIP LDELSSKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PABIR1 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)
- 0.7
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 11 nTPM
- parathyroid gland: 10 nTPM
- placenta: 9.5 nTPM
- liver: 9.2 nTPM
- breast: 9.1 nTPM
- cervix: 9.1 nTPM
Single-cell type
- basal keratinocytes: 0.3 nCPM
- endometrial secretory cells: 0.3 nCPM
- late spermatids: 0.2 nCPM
- megakaryocyte-erythroid progenitors: 0.2 nCPM
- alveolar cells type 1: 0.1 nCPM
- early spermatids: 0.1 nCPM
Immune cell
- naive CD4 T-cell: 3.6 nTPM
- plasmacytoid DC: 2.6 nTPM
- naive B-cell: 2.5 nTPM
- myeloid DC: 2.2 nTPM
- classical monocyte: 2 nTPM
- naive CD8 T-cell: 2 nTPM
Brain region
- choroid plexus: 30 nTPM
- cerebellum: 15 nTPM
- midbrain: 9.2 nTPM
- hypothalamus: 9.1 nTPM
- hippocampal formation: 9 nTPM
- cerebral cortex: 8.9 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)
- 0.79
- gnomAD pLI
- 0.49
- DepMap mean gene effect
- -0.3
- DepMap dependency class
- selective
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
Biological processes
- mitotic G2/M transition checkpoint
- positive regulation of cell growth
- positive regulation of proteasomal ubiquitin-dependent protein catabolic process
Molecular functions
- protein phosphatase 2A binding
- protein phosphatase inhibitor activity
- protein serine/threonine phosphatase inhibitor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PABIR1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PABIR1 as an antibody target. Whether an autoantibody or antibody against PABIR1 could matter depends on whether native PABIR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PABIR1 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 PABIR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...