DHRSX
Polyprenol dehydrogenase
Also known as: DHRS5X, DHRS5Y, DHRSX_HUMAN, DHRSXY, DHRSY, SDR46C1, SDR7C6
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N5I4
- Gene
- DHRSX
- Ensembl
- ENSG00000169084
- Chromosome
- X
- Canonical length
- 330 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Mitotic spindle,Cytosol
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Enables dolichal reductase [NAD(P)+] activity and polyprenol dehydrogenase activity. Involved in dolichol biosynthetic process and positive regulation of autophagy. Located in extracellular region. Is active in lipid droplet. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
330 residues, UniProt reviewed canonical sequence.
>Q8N5I4|DHRSX
1 MSPLSAARAA LRVYAVGAAV ILAQLLRRCR GGFLEPVFPP RPDRVAIVTG GTDGIGYSTA
61 KHLARLGMHV IIAGNNDSKA KQVVSKIKEE TLNDKVEFLY CDLASMTSIR QFVQKFKMKK
121 IPLHVLINNA GVMMVPQRKT RDGFEEHFGL NYLGHFLLTN LLLDTLKESG SPGHSARVVT
181 VSSATHYVAE LNMDDLQSSA CYSPHAAYAQ SKLALVLFTY HLQRLLAAEG SHVTANVVDP
241 GVVNTDVYKH VFWATRLAKK LLGWLLFKTP DEGAWTSIYA AVTPELEGVG GHYLYNEKET
301 KSLHVTYNQK LQQQLWSKSC EMTGVLDVTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DHRSX 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.23
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- liver: 29 nTPM
- pancreas: 21 nTPM
- heart muscle: 19 nTPM
- choroid plexus: 17 nTPM
- stomach: 16 nTPM
- adrenal gland: 15 nTPM
Single-cell type
- neutrophils: 984 nCPM
- syncytiotrophoblasts: 328 nCPM
- myonuclei: 267 nCPM
- proximal tubule cells: 255 nCPM
- cdc: 199 nCPM
- pancreatic acinar cells: 196 nCPM
Immune cell
- neutrophil: 57 nTPM
- classical monocyte: 38 nTPM
- myeloid DC: 35 nTPM
- eosinophil: 35 nTPM
- intermediate monocyte: 31 nTPM
- plasmacytoid DC: 28 nTPM
Brain region
- choroid plexus: 33 nTPM
- medulla oblongata: 33 nTPM
- thalamus: 31 nTPM
- midbrain: 30 nTPM
- spinal cord: 26 nTPM
- pons: 26 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DHRSX.
Disease | AllUniProt
Conditions DHRSX is implicated in, by any mechanism.
- Congenital disorder of glycosylation 1DD (CDG1DD) MIM:301133
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 232 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Congenital disorder of glycosylation, type 1DD
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)
- 1.2
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
OntologyGO
Biological processes
Molecular functions
- alcohol dehydrogenase (NADP+) activity
- dolichal reductase (NADPH) activity
- polyprenol dehydrogenase (NAD+) activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DHRSX as an antibody target. Whether an autoantibody or antibody against DHRSX could matter depends on whether native DHRSX is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DHRSX is annotated as secreted, so native DHRSX circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label DHRSX as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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