10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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42PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingtranslation repressor activityribosome bindingnegative regulation of translationschizophreniaAbnormality of the skeletal systemHashimoto's thyroiditisobesity
IFRD2 (interferon related developmental regulator 2) functions as a ribosome-binding protein that acts as an inhibitor of mRNA translation by promoting ribosome inactivation 1. The protein associates with the P- and E-sites of the ribosome and inserts a C-terminal helix into the mRNA exit channel to preclude translation 1. Structural studies reveal that IFRD2 binds ribosomes containing a tRNA occupying a noncanonical 'Z site', providing a mechanism for translational repression during cellular processes requiring reduced protein synthesis 1. Beyond its role in translation control, IFRD2 expression appears to be modulated in disease contexts. In chr3 hepatitis B patients, low IFRD2 expression is associated with poor interferon therapy efficacy 2. The gene has also been implicated in inflammatory bowel disease pathways, where appendicitis-appendectomy modulates IFRD2 expression as part of protective mechanisms against experimental colitis 3. Additionally, IFRD2 has been identified as a potential candidate gene in biliary atresia susceptibility through exome sequencing studies 4. The protein's dual role in translation regulation and immune-inflammatory responses suggests it may serve as a molecular link between cellular stress responses and disease pathogenesis.
1
IFRD2 functions as ribosome-binding protein that inhibits translation by associating with P- and E-sites and inserting C-terminal helix into mRNA exit channel
PMID: 303554412
Low IFRD2 expression is associated with poor interferon therapy efficacy in chronic hepatitis B patients
PMID: 368545513
IFRD2 expression is modulated in appendicitis-appendectomy model that protects against experimental colitis
PMID: 303290494
IFRD2 identified as candidate gene in biliary atresia susceptibility through exome sequencing studies
PMID: 36942736⚠Limited data available — This gene has 4 indexed publications. Summary and analysis may be incomplete.
schizophreniaOpen Targets
Abnormality of the skeletal systemOpen Targets
Hashimoto's thyroiditisOpen Targets
autosomal dominant cerebellar ataxiaOpen Targets
viral diseaseOpen Targets
chronic kidney diseaseOpen Targets
colorectal adenocarcinomaOpen Targets
HypertriglyceridemiaOpen Targets
Other metabolic diseaseOpen Targets
glioma susceptibility 1Open Targets
urinary bladder cancerOpen Targets
No pathogenic variants reported on ClinVar for this gene.