DECR2
Peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing]
Also known as: DECR2_HUMAN, PDCR, SDR17C1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NUI1
- Gene
- DECR2
- Ensembl
- ENSG00000242612
- Chromosome
- 16
- Canonical length
- 292 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Peroxisomes,Microtubules
OverviewNCBI Gene
Enables 2,4-dienoyl-CoA reductase (NADPH) activity and trans-2-enoyl-CoA reductase (NADPH) activity. Involved in unsaturated fatty acid biosynthetic process. Predicted to be located in cytosol and peroxisomal membrane. Predicted to be active in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
292 residues, UniProt reviewed canonical sequence.
>Q9NUI1|DECR2
1 MAQPPPDVEG DDCLPAYRHL FCPDLLRDKV AFITGGGSGI GFRIAEIFMR HGCHTVIASR
61 SLPRVLTAAR KLAGATGRRC LPLSMDVRAP PAVMAAVDQA LKEFGRIDIL INCAAGNFLC
121 PAGALSFNAF KTVMDIDTSG TFNVSRVLYE KFFRDHGGVI VNITATLGNR GQALQVHAGS
181 AKAAVDAMTR HLAVEWGPQN IRVNSLAPGP ISGTEGLRRL GGPQASLSTK VTASPLQRLG
241 NKTEIAHSVL YLASPLASYV TGAVLVADGG AWLTFPNGVK GLPDFASFSA KLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DECR2 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)
- 0.25
- Highest tissue expression
- 174 nTPM
Expression across tissuesHPA
Tissue
- liver: 174 nTPM
- kidney: 39 nTPM
- adrenal gland: 37 nTPM
- skeletal muscle: 37 nTPM
- pancreas: 23 nTPM
- colon: 20 nTPM
Single-cell type
- proximal tubule cells: 25 nCPM
- tuft cells: 12 nCPM
- astrocytes: 6.7 nCPM
- bergmann glia: 6.3 nCPM
- loop of henle epithelial cells: 5.2 nCPM
- renal collecting duct intercalated cells: 4.6 nCPM
Immune cell
- plasmacytoid DC: 7.9 nTPM
- intermediate monocyte: 5.1 nTPM
- myeloid DC: 5.1 nTPM
- classical monocyte: 3.8 nTPM
- NK-cell: 2.9 nTPM
- gdT-cell: 2.8 nTPM
Brain region
- hypothalamus: 4.8 nTPM
- white matter: 3.5 nTPM
- cerebral cortex: 3.2 nTPM
- basal ganglia: 2.8 nTPM
- hippocampal formation: 2.7 nTPM
- medulla oblongata: 2.7 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)
- 1.68
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.19
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
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
- fatty acid beta-oxidation using acyl-CoA oxidase
- fatty acid metabolic process
- unsaturated fatty acid biosynthetic process
Molecular functions
- 2,4-dienoyl-CoA reductase (NADPH) activity
- GTPase binding
- protein-containing complex binding
- trans-2-enoyl-CoA reductase (NADPH) activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Short-chain dehydrogenase/reductase SDR
- NAD(P)-binding domain superfamily
- Ketoreductase domain
- Enoyl-(Acyl carrier protein) reductase
- Peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing]
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DECR2 as an antibody target. Whether an autoantibody or antibody against DECR2 could matter depends on whether native DECR2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DECR2 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 DECR2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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