2 sources retrieved · Most recent: April 2026 · Index updated 16 days ago
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21PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingspinal stenosisOral ulcerRomano-Ward syndromeGriscelli disease
Based on limited published evidence, REX1BD is a protein with binding capacity involved in heterochromatin organization. REX1BD regulates position-dependent silencing within heterochromatin repeats through interaction with 14-3-3 protein, coordinating RNAi and HDAC pathways to modulate epigenetic landscapes 1. REX1BD was identified as a component of the RISK4LEP blood transcriptomic signature, which prospectively predicts leprosy development 4-61 months before clinical diagnosis in household contacts of leprosy patients 2. The specific molecular mechanisms underlying its role in disease pathogenesis remain unclear.
1
REX1BD is required for position-dependent silencing within heterochromatin repeats and interacts with 14-3-3 protein to regulate heterochromatin organization via RNAi and HDAC pathways
PMID: 386797592
REX1BD is one of four genes in the RISK4LEP signature that prospectively predicts leprosy development before clinical onset
PMID: 34090257⚠Limited data available — This gene has 2 indexed publications. Summary and analysis may be incomplete.
spinal stenosisOpen Targets
Romano-Ward syndromeOpen Targets
Griscelli diseaseOpen Targets
familial atrial fibrillationOpen Targets
Arrhythmogenic right ventricular dysplasiaOpen Targets
Brugada syndromeOpen Targets
Familial short QT syndromeOpen Targets
Griscelli disease type 3Open Targets
Griscelli syndrome type 3Open Targets
atrial fibrillationOpen Targets
hypertrophic cardiomyopathyOpen Targets
Familial progressive cardiac conduction defectOpen Targets
Rare familial disorder with hypertrophic cardiomyopathyOpen Targets
uncombable hair syndromeOpen Targets
arrhythmogenic right ventricular dysplasia 12Open Targets
Brugada syndrome 9Open Targets
familial sick sinus syndromeOpen Targets
Wolff-Parkinson-White SyndromeOpen Targets
long QT syndrome 10Open Targets
No pathogenic variants reported on ClinVar for this gene.