DAOA
D-amino acid oxidase regulator
Also known as: DAOA_HUMAN, G72
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P59103
- Gene
- DAOA
- Ensembl
- ENSG00000182346
- Chromosome
- 13
- Canonical length
- 153 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein that may function as an activator of D-amino acid oxidase, which degrades the gliotransmitter D-serine, a potent activator of N-methyl-D-aspartate (NMDA) type glutamate receptors. Studies also suggest that one encoded isoform may play a role in mitochondrial function and dendritic arborization. Polymorphisms in this gene have been implicated in susceptibility to schizophrenia and bipolar affective disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Mar 2011]
Canonical amino-acid sequenceUniProt
153 residues, UniProt reviewed canonical sequence.
>P59103|DAOA
1 MLEKLMGADS LQLFRSRYTL GKIYFIGFQR SILLSKSENS LNSIAKETEE GRETVTRKEG
61 WKRRHEDGYL EMAQRHLQRS LCPWVSYLPQ PYAELEEVSS HVGKVFMARN YEFLAYEASK
121 DRRQPLERMW TCNYNQQKDQ SCNHKEITST KAELocalizationUniProt · AlphaFold · HPA
Whether an antibody against DAOA 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)
- 0.45
- Highest tissue expression
- 0 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
- appendix: 0 nTPM
- basal ganglia: 0 nTPM
- blood vessel: 0 nTPM
Single-cell type
- early spermatids: 0.4 nCPM
- late primary spermatocytes: 0.3 nCPM
- mesothelial cells: 0.3 nCPM
- colonocytes: 0.1 nCPM
- distal convoluted tubule cells: 0.1 nCPM
- ependymal cells: 0.1 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DAOA.
Disease | AllUniProt
Conditions DAOA is implicated in, by any mechanism.
- Schizophrenia (SCZD) MIM:181500
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)
- 1.7
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.43
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 1% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of protein catabolic process
- D-amino acid metabolic process
Cellular components
Protein domainsUniProt · Pfam · InterPro
- D-amino acid oxidase regulator
- D-amino acid oxidase activator
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DAOA 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 DAOA as an antibody target. Whether an autoantibody or antibody against DAOA could matter depends on whether native DAOA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DAOA 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 DAOA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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