Seroatlas · Human Serome Atlas

C22orf39

Synaptic plasticity regulator PANTS

Also known as: CV039_HUMAN, MGC74441

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q6P5X5
Gene
C22orf39
Ensembl
ENSG00000242259
Chromosome
22
Canonical length
105 aa
Protein class
Predicted intracellular proteins
Subcellular location
Endoplasmic reticulum
Secretome location
Intracellular and membrane

OverviewNCBI Gene

Predicted to be involved in negative regulation of long-term synaptic potentiation. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

105 residues, UniProt reviewed canonical sequence.

>Q6P5X5|C22orf39
     1  MADGSGWQPP RPCEAYRAEW KLCRSARHFL HHYYVHGERP ACEQWQRDLA SCRDWEERRN
    61  AEAQQSLCES ERARVRAARK HILVWAPRQS PPPDWHLPLP QEKDE

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against C22orf39 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)
0.46
Highest tissue expression
90 nTPM

Expression across tissuesHPA

Tissue

  • skeletal muscle: 90 nTPM
  • tongue: 42 nTPM
  • amygdala: 42 nTPM
  • midbrain: 41 nTPM
  • cerebral cortex: 39 nTPM
  • heart muscle: 39 nTPM

Single-cell type

  • megakaryocytes: 74 nCPM
  • parietal cells: 58 nCPM
  • late primary spermatocytes: 46 nCPM
  • gastric chief cells: 36 nCPM
  • hofbauer cells: 36 nCPM
  • enterocytes: 33 nCPM

Immune cell

  • eosinophil: 72 nTPM
  • neutrophil: 43 nTPM
  • plasmacytoid DC: 39 nTPM
  • basophil: 37 nTPM
  • T-reg: 35 nTPM
  • intermediate monocyte: 34 nTPM

Brain region

  • thalamus: 34 nTPM
  • pons: 33 nTPM
  • spinal cord: 32 nTPM
  • midbrain: 31 nTPM
  • amygdala: 31 nTPM
  • cerebral cortex: 30 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)
1.77
gnomAD pLI
0
gnomAD missense Z
-0.2
DepMap mean gene effect
-0.18
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • Plasticity-Associated Neural Transcript Short/Early meiotic induction protein 1-like
  • Synaptic plasticity regulator PANTS-like

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of C22orf39 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 C22orf39 as an antibody target. Whether an autoantibody or antibody against C22orf39 could matter depends on whether native C22orf39 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

C22orf39 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 C22orf39 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/C22orf39. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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