PSMG2
Proteasome assembly chaperone 2
Also known as: CLAST3, HCCA3, HsT1707, MDS003, MGC15092, PAC2, PSMG2_HUMAN, TNFSF5IP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q969U7
- Gene
- PSMG2
- Ensembl
- ENSG00000128789
- Chromosome
- 18
- Canonical length
- 264 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
Enables molecular adaptor activity. Involved in chaperone-mediated protein complex assembly. Located in nucleus. Part of protein folding chaperone complex. Implicated in proteosome-associated autoinflammatory syndrome 4. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
264 residues, UniProt reviewed canonical sequence.
>Q969U7|PSMG2
1 MFVPCGESAP DLAGFTLLMP AVSVGNVGQL AMDLIISTLN MSKIGYFYTD CLVPMVGNNP
61 YATTEGNSTE LSINAEVYSL PSRKLVALQL RSIFIKYKSK PFCEKLLSWV KSSGCARVIV
121 LSSSHSYQRN DLQLRSTPFR YLLTPSMQKS VQNKIKSLNW EEMEKSRCIP EIDDSEFCIR
181 IPGGGITKTL YDESCSKEIQ MAVLLKFVSE GDNIPDALGL VEYLNEWLQI LKPLSDDPTV
241 SASRWKIPSS WRLLFGSGLP PALFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PSMG2 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)
- 0.28
- Highest tissue expression
- 82 nTPM
Expression across tissuesHPA
Tissue
- testis: 82 nTPM
- bone marrow: 70 nTPM
- blood vessel: 68 nTPM
- epididymis: 63 nTPM
- adipose tissue: 62 nTPM
- ovary: 62 nTPM
Single-cell type
- late primary spermatocytes: 797 nCPM
- early spermatids: 529 nCPM
- esophageal apical cells: 304 nCPM
- oocytes: 272 nCPM
- differentiating spermatogonia: 249 nCPM
- migrating cytotrophoblasts: 218 nCPM
Immune cell
- non-classical monocyte: 98 nTPM
- T-reg: 92 nTPM
- intermediate monocyte: 85 nTPM
- total PBMC: 78 nTPM
- classical monocyte: 78 nTPM
- eosinophil: 76 nTPM
Brain region
- cerebellum: 47 nTPM
- white matter: 39 nTPM
- cerebral cortex: 38 nTPM
- basal ganglia: 35 nTPM
- pons: 34 nTPM
- medulla oblongata: 34 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PSMG2.
Disease | AllUniProt
Conditions PSMG2 is implicated in, by any mechanism.
- Proteasome-associated autoinflammatory syndrome 4 (PRAAS4) MIM:619183
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 248 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Proteasome-associated autoinflammatory syndrome 4
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)
- 1.44
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.44
- DepMap mean gene effect
- -0.68
- DepMap dependency class
- common
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
- chaperone-mediated protein complex assembly
- mitotic spindle assembly checkpoint signaling
- negative regulation of apoptotic process
- proteasome assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Proteasome assembly chaperone 2, eukaryotic
- Proteasome assembly chaperone 2
- Proteasome assembly chaperone 2 superfamily
- PAC2 family
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PSMG2 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 PSMG2 as an antibody target. Whether an autoantibody or antibody against PSMG2 could matter depends on whether native PSMG2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PSMG2 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 PSMG2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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