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FBXO32 and Duchenne muscular dystrophy are reported together in 1 article.
Gene
FBXO32
- HGNC
- HGNC:16731
5articles
5mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Duchenne muscular dystrophy
40articles
40mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Exploring novel natural compound-based therapies for Duchenne muscular dystrophy management: insights from network pharmacology, QSAR modeling, molecular dynamics, and free energy calculations.
PMID 39415830 | PMCID PMC11481126 | DOI 10.3389/fphar.2024.1395014 · Frontiers in pharmacology · 2024 · 9 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | FBXO32 | “These key genes include DMD, TTN, PLEC, DTNA, PKP2, SLC24A, FBXO32, SNTA1, SMAD3, and NOS1.” | 0.98 | hgnc_dict_v1 |
| phenotype | Duchenne muscular dystrophy | “Exploring novel natural compound-based therapies for Duchenne muscular dystrophy management: insights from network pharmacology, QSAR modeling, molecular dynamics, and free energy calculations.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TTN | “These key genes include DMD, TTN, PLEC, DTNA, PKP2, SLC24A, FBXO32, SNTA1, SMAD3, and NOS1.” | 0.98 | hgnc_dict_v1 |
| gene | PLEC | “These key genes include DMD, TTN, PLEC, DTNA, PKP2, SLC24A, FBXO32, SNTA1, SMAD3, and NOS1.” | 0.98 | hgnc_dict_v1 |