1 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
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3PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Swiss-Prot Reviewed
neurodegenerative diseaseAbnormality of the skeletal systemHIV infectionviral disease
Based on limited published evidence, RNF103-CHMP3 readthrough is a readthrough transcript fusion gene located on chromosome 2. Database annotations suggest functional roles in ESCRT-mediated protein sorting and vesicular transport (typical of CHMP3 component). Recent research identifies RNF103-CHMP3 as a key gene associated with diabetic foot ulcers, linked to extracellular interactions and tissue repair mechanisms 1. The gene shows significant downregulation in successfully healed diabetic foot ulcer patients, particularly in NK cells and macrophages 1, suggesting involvement in wound healing and cellular communication.
1
RNF103-CHMP3 identified as key gene associated with diabetic foot ulcers, linked to extracellular interactions and tissue repair; significantly downregulated in cured DFU patients in NK cells and macrophages
PMID: 39543487β Limited data available β This gene has 1 indexed publication. Summary and analysis may be incomplete.
neurodegenerative diseaseOpen Targets
Abnormality of the skeletal systemOpen Targets
HIV infectionOpen Targets
viral diseaseOpen Targets
severe acute respiratory syndromeOpen Targets
major depressive disorderOpen Targets
ocular hypotensionOpen Targets
overnutritionOpen Targets
atrial fibrillationOpen Targets
myeloid leukemiaOpen Targets
Fuchs endothelial corneal dystrophyOpen Targets
hepatocellular carcinomaOpen Targets
Familial ocular anterior segment mesenchymal dysgenesisOpen Targets
granular corneal dystrophy type IOpen Targets
congenital hereditary endothelial dystrophy of corneaOpen Targets
Cataract-microcornea syndromeOpen Targets
Juvenile cataract - microcornea - renal glucosuriaOpen Targets
No pathogenic variants reported on ClinVar for this gene.