Seroatlas · Human Serome Atlas

CDO1

Cysteine dioxygenase type 1

Also known as: CDO1_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q16878
Gene
CDO1
Ensembl
ENSG00000129596
Chromosome
5
Canonical length
200 aa
Protein class
Enzymes, Metabolic proteins, Predicted intracellular proteins
Subcellular location
Nucleoplasm,Cytosol

OverviewNCBI Gene

Enables cysteine dioxygenase activity; ferrous iron binding activity; and zinc ion binding activity. Predicted to be involved in L-cysteine catabolic process. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

200 residues, UniProt reviewed canonical sequence.

>Q16878|CDO1
     1  MEQTEVLKPR TLADLIRILH QLFAGDEVNV EEVQAIMEAY ESDPTEWAMY AKFDQYRYTR
    61  NLVDQGNGKF NLMILCWGEG HGSSIHDHTN SHCFLKMLQG NLKETLFAWP DKKSNEMVKK
   121  SERVLRENQC AYINDSIGLH RVENISHTEP AVSLHLYSPP FDTCHAFDQR TGHKNKVTMT
   181  FHSKFGIRTP NATSGSLENN

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CDO1 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)
0.27
Highest tissue expression
474 nTPM

Expression across tissuesHPA

Tissue

  • liver: 474 nTPM
  • choroid plexus: 319 nTPM
  • epididymis: 132 nTPM
  • adipose tissue: 112 nTPM
  • seminal vesicle: 69 nTPM
  • blood vessel: 60 nTPM

Single-cell type

  • syncytiotrophoblasts: 716 nCPM
  • cytotrophoblasts: 439 nCPM
  • migrating cytotrophoblasts: 263 nCPM
  • epididymal principal cells: 228 nCPM
  • hepatocytes: 226 nCPM
  • retinal pigment epithelial cells: 200 nCPM

Immune cell

  • memory CD4 T-cell: 1.5 nTPM
  • T-reg: 0.5 nTPM
  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM

Brain region

  • choroid plexus: 200 nTPM
  • hypothalamus: 33 nTPM
  • cerebral cortex: 28 nTPM
  • basal ganglia: 27 nTPM
  • hippocampal formation: 24 nTPM
  • thalamus: 24 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)
0.93
gnomAD pLI
0.01
gnomAD missense Z
0.19
DepMap mean gene effect
0.03
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 CDO1 as an antibody target. Whether an autoantibody or antibody against CDO1 could matter depends on whether native CDO1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CDO1 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 CDO1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CDO1. 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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