WDR83OS
PAT complex subunit Asterix
Also known as: ASTER_HUMAN, Asterix, C19orf56, PTD008
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y284
- Gene
- WDR83OS
- Ensembl
- ENSG00000105583
- Chromosome
- 19
- Canonical length
- 106 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Endoplasmic reticulum
OverviewNCBI Gene
Enables protein folding chaperone. Involved in multi-pass transmembrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane. Part of multi-pass translocon complex and protein folding chaperone complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
106 residues, UniProt reviewed canonical sequence.
>Q9Y284|WDR83OS
1 MSTNNMSDPR RPNKVLRYKP PPSECNPALD DPTPDYMNLL GMIFSMCGLM LKLKWCAWVA
61 VYCSFISFAN SRSSEDTKQM MSSFMLSISA VVMSYLQNPQ PMTPPWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against WDR83OS 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 3
- Mean surface accessibility (rSASA)
- 0.52
- Highest tissue expression
- 261 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 261 nTPM
- kidney: 252 nTPM
- skeletal muscle: 249 nTPM
- adrenal gland: 243 nTPM
- ovary: 237 nTPM
- pancreas: 224 nTPM
Single-cell type
- oligodendrocytes: 15 nCPM
- other brain neurons: 9 nCPM
- microglia: 7.7 nCPM
- brain excitatory neurons: 5.6 nCPM
- oligodendrocyte progenitor cells: 4.7 nCPM
- ependymal cells: 3.9 nCPM
Immune cell
- total PBMC: 636 nTPM
- basophil: 616 nTPM
- non-classical monocyte: 506 nTPM
- classical monocyte: 505 nTPM
- eosinophil: 494 nTPM
- neutrophil: 489 nTPM
Brain region
- white matter: 113 nTPM
- spinal cord: 102 nTPM
- cerebellum: 93 nTPM
- basal ganglia: 92 nTPM
- hypothalamus: 91 nTPM
- thalamus: 90 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about WDR83OS.
Disease | AllUniProt
Conditions WDR83OS is implicated in, by any mechanism.
- Neurodevelopmental disorder with variable familial hypercholanemia (NEDFHCA) MIM:621016
Disease | GeneticClinVar
5 pathogenic / likely-pathogenic of 33 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Hypercholanemia, familial
- Neurodevelopmental disorder with variable familial hypercholanemia
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)
- 1.65
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.7
- DepMap mean gene effect
- -0.15
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- PAT complex subunit Asterix
- PAT complex subunit Asterix
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads WDR83OS as an antibody target. Whether an autoantibody or antibody against WDR83OS could matter depends on whether native WDR83OS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
WDR83OS 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 WDR83OS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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