PYM1
Partner of Y14 and mago
Also known as: PYM, PYM1_HUMAN, WIBG
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BRP8
- Gene
- PYM1
- Ensembl
- ENSG00000170473
- Chromosome
- 12
- Canonical length
- 204 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Cell Junctions,Cytosol
OverviewNCBI Gene
Enables ribosome binding activity. Involved in exon-exon junction complex disassembly; nuclear-transcribed mRNA catabolic process, nonsense-mediated decay; and positive regulation of translation. Located in cell junction; cytosol; and nuclear lumen. Part of exon-exon junction complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
204 residues, UniProt reviewed canonical sequence.
>Q9BRP8|PYM1
1 MEAAGSPAAT ETGKYIASTQ RPDGTWRKQR RVKEGYVPQE EVPVYENKYV KFFKSKPELP
61 PGLSPEATAP VTPSRPEGGE PGLSKTAKRN LKRKEKRRQQ QEKGEAEALS RTLDKVSLEE
121 TAQLPSAPQG SRAAPTAASD QPDSAATTEK AKKIKNLKKK LRQVEELQQR IQAGEVSQPS
181 KEQLEKLARR RALEEELEDL ELGLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PYM1 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)
- 0.54
- Highest tissue expression
- 70 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 70 nTPM
- liver: 41 nTPM
- skin: 40 nTPM
- epididymis: 39 nTPM
- tonsil: 37 nTPM
- salivary gland: 32 nTPM
Single-cell type
- esophageal apical cells: 487 nCPM
- esophageal suprabasal cells: 196 nCPM
- epididymal principal cells: 109 nCPM
- migrating cytotrophoblasts: 101 nCPM
- cytotrophoblasts: 99 nCPM
- esophageal basal cells: 97 nCPM
Immune cell
- T-reg: 180 nTPM
- myeloid DC: 117 nTPM
- memory CD4 T-cell: 98 nTPM
- memory B-cell: 91 nTPM
- intermediate monocyte: 91 nTPM
- total PBMC: 84 nTPM
Brain region
- choroid plexus: 20 nTPM
- hypothalamus: 16 nTPM
- pons: 15 nTPM
- spinal cord: 15 nTPM
- medulla oblongata: 15 nTPM
- white matter: 15 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
- gnomAD pLI
- 0.02
- DepMap mean gene effect
- -0.31
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
- positive regulation of translation
- exon-exon junction complex disassembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- WIBG, Mago-binding
- WIBG, N-terminal domain superfamily
- Partner of Y14 and mago
- Mago binding
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PYM1 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 PYM1 as an antibody target. Whether an autoantibody or antibody against PYM1 could matter depends on whether native PYM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PYM1 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 PYM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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