2 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
βGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
14PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLETranscription Factor
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
protein bindingidentical protein bindingnucleusregulation of cytokine productionprostate carcinomaalopeciaprostate cancerbenign neoplasm of eye
Based on limited published evidence, ZNF572 is a zinc finger protein predicted to function in transcriptional regulation. UniProt annotations indicate DNA-binding transcription repressor activity specific to RNA polymerase II, with roles in negative regulation of transcription and immune system processes. ZNF572 localizes to the nucleus and nucleoplasm. Genome-wide association studies have identified genetic variants near ZNF572 associated with postpartum depression 1 and altered expression in amniotic fluid linked to preterm birth risk 2, suggesting involvement in perinatal health outcomes, though mechanistic details remain unclear.
1
Genetic variant rs188907279 near ZNF572 was significantly associated with postpartum depression in GWAS of Japanese perinatal women
PMID: 392879322
ZNF572 expression was upregulated in amniotic fluid from preterm birth cases and increased under oxidative stress and infection conditions in trophoblast cells
PMID: 35361790β Limited data available β This gene has 2 indexed publications. Summary and analysis may be incomplete.
prostate carcinomaOpen Targets
prostate cancerOpen Targets
benign neoplasm of eyeOpen Targets
cardiomyopathyOpen Targets
atrial fibrillationOpen Targets
joint diseaseOpen Targets
hypertrophic cardiomyopathyOpen Targets
heart failureOpen Targets
dilated cardiomyopathyOpen Targets
Down syndromeOpen Targets
cholelithiasisOpen Targets
ataxia telangiectasiaOpen Targets
progressive pseudorheumatoid arthropathy of childhoodOpen Targets
Townes-Brocks syndromeOpen Targets
intrahepatic cholestasisOpen Targets
No pathogenic variants reported on ClinVar for this gene.