EGLN3
Prolyl hydroxylase EGLN3
Also known as: EGLN3_HUMAN, HIFPH3, PHD3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H6Z9
- Gene
- EGLN3
- Ensembl
- ENSG00000129521
- Chromosome
- 14
- Canonical length
- 239 aa
- Protein class
- Enzymes, FDA approved drug targets, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables peptidyl-proline 4-dioxygenase activity. Involved in protein hydroxylation. Located in cytosol and nucleus. Implicated in renal cell carcinoma. Biomarker of clear cell renal cell carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
239 residues, UniProt reviewed canonical sequence.
>Q9H6Z9|EGLN3
1 MPLGHIMRLD LEKIALEYIV PCLHEVGFCY LDNFLGEVVG DCVLERVKQL HCTGALRDGQ
61 LAGPRAGVSK RHLRGDQITW IGGNEEGCEA ISFLLSLIDR LVLYCGSRLG KYYVKERSKA
121 MVACYPGNGT GYVRHVDNPN GDGRCITCIY YLNKNWDAKL HGGILRIFPE GKSFIADVEP
181 IFDRLLFFWS DRRNPHEVQP SYATRYAMTV WYFDAEERAE AKKKFRNLTR KTESALTEDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EGLN3 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)
- 0.28
- Highest tissue expression
- 114 nTPM
Expression across tissuesHPA
Tissue
- skin: 114 nTPM
- heart muscle: 102 nTPM
- urinary bladder: 51 nTPM
- small intestine: 39 nTPM
- blood vessel: 36 nTPM
- stomach: 36 nTPM
Single-cell type
- esophageal apical cells: 576 nCPM
- melanocytes: 419 nCPM
- urothelial cells: 272 nCPM
- extravillous trophoblasts: 264 nCPM
- respiratory ciliated cells: 239 nCPM
- prostatic club cells: 219 nCPM
Immune cell
- plasmacytoid DC: 26 nTPM
- myeloid DC: 2.6 nTPM
- eosinophil: 1.8 nTPM
- memory CD4 T-cell: 1.2 nTPM
- NK-cell: 1.1 nTPM
- memory CD8 T-cell: 0.9 nTPM
Brain region
- thalamus: 63 nTPM
- basal ganglia: 58 nTPM
- hypothalamus: 55 nTPM
- cerebellum: 54 nTPM
- midbrain: 53 nTPM
- white matter: 47 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)
- 0.93
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.72
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
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
- apoptotic process
- cellular response to hypoxia
- DNA damage response
- negative regulation of ferroptosis
- protein hydroxylation
- protein stabilization
- regulation of neuron apoptotic process
Molecular functions
- 2-oxoglutarate-dependent dioxygenase activity
- ferrous iron binding
- hypoxia-inducible factor-proline dioxygenase activity
- L-ascorbic acid binding
- peptidyl-proline 4-dioxygenase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EGLN3 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 EGLN3 as an antibody target. Whether an autoantibody or antibody against EGLN3 could matter depends on whether native EGLN3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EGLN3 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 EGLN3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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