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PRMT1 and spinal muscular atrophy are reported together in 1 article.
Gene
PRMT1
- HGNC
- HGNC:5187
3articles
3mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Spinal muscular atrophy
45articles
45mentions
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 60Nucleolar reorganization after cellular stress is orchestrated by SMN shuttling between nuclear compartments.
PMID 37968267 | PMCID PMC10652021 | DOI 10.1038/s41467-023-42390-4 · Nature communications · 2023 · 2 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | PRMT1 | “This shuttling is important for nucleolar homeostasis and relies on the presence of Coilin and the activity of PRMT1.” | 0.98 | hgnc_dict_v1 |
| phenotype | spinal muscular atrophy | “Spinal muscular atrophy is an autosomal recessive neuromuscular disease caused by mutations in the multifunctional protein Survival of Motor Neuron, or SMN.” | 0.98 | phenotype_alias_lexicon_v2 |