Seroatlas · Human Serome Atlas

PIPOX

Peroxisomal sarcosine oxidase

Also known as: LPIPOX, SOX_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q9P0Z9
Gene
PIPOX
Ensembl
ENSG00000179761
Chromosome
17
Canonical length
390 aa
Protein class
Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins

OverviewNCBI Gene

Enables L-pipecolate oxidase activity and sarcosine oxidase activity. Involved in L-lysine catabolic process to acetyl-CoA via L-pipecolate. Located in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

390 residues, UniProt reviewed canonical sequence.

>Q9P0Z9|PIPOX
     1  MAAQKDLWDA IVIGAGIQGC FTAYHLAKHR KRILLLEQFF LPHSRGSSHG QSRIIRKAYL
    61  EDFYTRMMHE CYQIWAQLEH EAGTQLHRQT GLLLLGMKEN QELKTIQANL SRQRVEHQCL
   121  SSEELKQRFP NIRLPRGEVG LLDNSGGVIY AYKALRALQD AIRQLGGIVR DGEKVVEINP
   181  GLLVTVKTTS RSYQAKSLVI TAGPWTNQLL RPLGIEMPLQ TLRINVCYWR EMVPGSYGVS
   241  QAFPCFLWLG LCPHHIYGLP TGEYPGLMKV SYHHGNHADP EERDCPTART DIGDVQILSS
   301  FVRDHLPDLK PEPAVIESCM YTNTPDEQFI LDRHPKYDNI VIGAGFSGHG FKLAPVVGKI
   361  LYELSMKLTP SYDLAPFRIS RFPSLGKAHL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PIPOX 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)
0.23
Highest tissue expression
474 nTPM

Expression across tissuesHPA

Tissue

  • liver: 474 nTPM
  • kidney: 136 nTPM
  • epididymis: 23 nTPM
  • midbrain: 16 nTPM
  • duodenum: 13 nTPM
  • basal ganglia: 12 nTPM

Single-cell type

  • late spermatids: 864 nCPM
  • hepatocytes: 271 nCPM
  • early spermatids: 190 nCPM
  • bergmann glia: 57 nCPM
  • late primary spermatocytes: 56 nCPM
  • epididymal principal cells: 44 nCPM

Immune cell

  • myeloid DC: 1.8 nTPM
  • neutrophil: 1 nTPM
  • basophil: 0.9 nTPM
  • naive CD8 T-cell: 0.7 nTPM
  • memory CD8 T-cell: 0.4 nTPM
  • T-reg: 0.4 nTPM

Brain region

  • cerebellum: 18 nTPM
  • basal ganglia: 18 nTPM
  • midbrain: 16 nTPM
  • thalamus: 16 nTPM
  • hypothalamus: 14 nTPM
  • medulla oblongata: 13 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)
1.26
gnomAD pLI
0
gnomAD missense Z
0.24
DepMap mean gene effect
-0.08
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

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

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

Canonical record: https://seroatlas.com/gene/PIPOX. 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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