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GeneE
10 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
DPRX
divergent-paired related homeobox
Chromosome 19 Β· 19q13.42
NCBI Gene: 503834Ensembl: ENSG00000204595.3HGNC: HGNC:32166UniProt: A6NFQ7
5PubMed Papers
10Diseases
0Drugs
1Pathogenic Variants
FUNCTIONAL ROLE
Transcription Factor
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
sequence-specific double-stranded DNA bindingnucleuschromatinDNA-binding transcription factor activity, RNA polymerase II-specificShort statureresponse to antihypertensive drugMyasthenia gravispernicious anemia
✦AI Summary

DPRX (divergent-paired related homeobox) is a PRD-like homeobox transcription factor that functions as a transcriptional repressor during human embryonic development 1. The gene plays a critical role in the maternal-to-zygotic transition (MZT) during early human preimplantation development, where its deficiency severely impairs MZT and lineage specification 2. DPRX acts as part of a two-stage regulatory model of human embryo genome activation, serving as a balancing transcriptional repressor at the 8-cell stage, following the earlier activation by LEUTX at the 4-cell stage 1. The gene is expressed during human preimplantation development and is transcribed during the transition from four- to eight-cell stage 3. DPRX deficiency leads to aberrant retention of histone acetylation and contributes to cleavage-stage embryonic arrest, though this can be partially rescued by reversing the acetylation retention 2. Notably, DPRX has been lost in the mouse lineage during evolution, making it a human-specific contributor to early embryonic development 4. The gene can also be involved in oncogenic fusions in thyroid cancer, where TG::DPRX fusions drive aberrant DPRX overexpression 5.

Sources cited
1
DPRX is a PRD-like homeobox transcription factor that acts as a powerful repressor and balances LEUTX activation at the 8-cell stage
PMID: 27578796
2
DPRX deficiency severely impairs maternal-to-zygotic transition and lineage specification, leading to aberrant histone acetylation retention and cleavage-stage arrest
PMID: 39809281
3
DPRX is transcribed during the transition from four- to eight-cell stage in human preimplantation development
PMID: 26360614
4
DPRX has been lost in the mouse evolutionary lineage but retained in humans
PMID: 21679462
5
TG::DPRX fusions in thyroid cancer drive aberrant DPRX overexpression
PMID: 39878559
Disease Associationsβ“˜10
Short statureOpen Targets
0.33Weak
response to antihypertensive drugOpen Targets
0.13Weak
Myasthenia gravisOpen Targets
0.05Suggestive
pernicious anemiaOpen Targets
0.05Suggestive
Hodgkins lymphomaOpen Targets
0.03Suggestive
alcohol drinkingOpen Targets
0.02Suggestive
gastric cancerOpen Targets
0.00Suggestive
liver cancerOpen Targets
0.00Suggestive
lung cancerOpen Targets
0.00Suggestive
nonpapillary renal cell carcinomaOpen Targets
0.00Suggestive
Pathogenic Variants1
NM_001012728.2(DPRX):c.466C>T (p.Arg156Ter)Pathogenic
Short stature
β˜†β˜†β˜†β˜†2001β†’ Residue 156
View on ClinVar β†—
Related Genes
LEUTXProtein interaction82%DUXBProtein interaction78%NANOGNBProtein interaction72%TPRX1Protein interaction65%ARGFXCo-mentioned in literature40%DUXACo-mentioned in literature20%
Tissue Expression6 tissues
Lung
100%
Ovary
25%
Brain
25%
Bone Marrow
0%
Heart
0%
Liver
0%
Gene Interaction Network
Click a node to explore
DPRXLEUTXDUXBNANOGNBTPRX1ARGFXDUXA
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted Β· UniProt A6NFQ7
View on AlphaFold β†—
RankingsWhere DPRX stands among ~20K protein-coding genes
  • #18,319of 20,598
    Most Researched5
  • #5,493of 5,498
    Most Pathogenic Variants1
Genes detectedDPRX
Sources retrieved10 papers
Response timeβ€”
πŸ“„ Sources
10β–Ό
1
Allelic transcriptomic profiling identifies the role of PRD-like homeobox genes in human embryonic-cleavage-stage arrest.
PMID: 39809281
Dev Cell Β· 2025
1.00
2
Spectrum and carcinogenic properties of thyroglobulin gene fusions in thyroid.
PMID: 39878559
Endocr Relat Cancer Β· 2025
0.90
3
Human-specific contributors to cleavage-stage embryonic arrest during maternal to zygotic transition.
PMID: 40328227
Dev Cell Β· 2025
0.80
4
The dynamics of vertebrate homeobox gene evolution: gain and loss of genes in mouse and human lineages.
PMID: 21679462
BMC Evol Biol Β· 2011
0.70
5
Patient-specific thresholds of intracranial pressure in severe traumatic brain injury.
PMID: 24506248
J Neurosurg Β· 2014
0.60