DERA
Deoxyribose-phosphate aldolase
Also known as: CGI-26, DEOC, DEOC_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y315
- Gene
- DERA
- Ensembl
- ENSG00000023697
- Chromosome
- 12
- Canonical length
- 318 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables deoxyribose-phosphate aldolase activity. Involved in deoxyribonucleoside catabolic process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
318 residues, UniProt reviewed canonical sequence.
>Q9Y315|DERA
1 MSAHNRGTEL DLSWISKIQV NHPAVLRRAE QIQARRTVKK EWQAAWLLKA VTFIDLTTLS
61 GDDTSSNIQR LCYKAKYPIR EDLLKALNMH DKGITTAAVC VYPARVCDAV KALKAAGCNI
121 PVASVAAGFP AGQTHLKTRL EEIRLAVEDG ATEIDVVINR SLVLTGQWEA LYDEIRQFRK
181 ACGEAHLKTI LATGELGTLT NVYKASMIAM MAGSDFIKTS TGKETVNATF PVAIVMLRAI
241 RDFFWKTGNK IGFKPAGGIR SAKDSLAWLS LVKEELGDEW LKPELFRIGA STLLSDIERQ
301 IYHHVTGRYA AYHDLPMSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DERA 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
- 98 nTPM
Expression across tissuesHPA
Tissue
- liver: 98 nTPM
- kidney: 69 nTPM
- small intestine: 51 nTPM
- rectum: 40 nTPM
- duodenum: 39 nTPM
- colon: 37 nTPM
Single-cell type
- platelets: 463 nCPM
- enterocytes: 220 nCPM
- esophageal apical cells: 213 nCPM
- melanocytes: 201 nCPM
- cone photoreceptor cells: 178 nCPM
- endometrial glandular cells: 167 nCPM
Immune cell
- non-classical monocyte: 77 nTPM
- myeloid DC: 75 nTPM
- intermediate monocyte: 69 nTPM
- classical monocyte: 59 nTPM
- NK-cell: 46 nTPM
- total PBMC: 42 nTPM
Brain region
- choroid plexus: 29 nTPM
- medulla oblongata: 19 nTPM
- white matter: 19 nTPM
- hypothalamus: 18 nTPM
- cerebellum: 17 nTPM
- basal ganglia: 17 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)
- 0.91
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.13
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- carbohydrate catabolic process
- deoxyribonucleotide catabolic process
- pentose-phosphate shunt
- deoxyribonucleoside catabolic process
- deoxyribose phosphate catabolic process
Molecular functions
- deoxyribose-phosphate aldolase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Aldolase-type TIM barrel
- DeoC/FbaB/LacD aldolase
- Deoxyribose-phosphate aldolase
- DeoC/LacD family aldolase
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DERA 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 DERA as an antibody target. Whether an autoantibody or antibody against DERA could matter depends on whether native DERA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DERA 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 DERA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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