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PLS3 and spinal muscular atrophy are reported together in 2 articles.

Gene

PLS3

HGNC
HGNC:9091
3articles
3mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
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

2 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
genePLS3“As plastin 3 (PLS3) has been demonstrated as a modifier of spinal muscular atrophy, the aim of the current study was to evaluate the neuroprotective effect of PLS3 in NSC-34 cells.”0.98hgnc_dict_v1
phenotypespinal muscular atrophy“BACKGROUND: Spinal muscular atrophy is a rare genetic disease, which primarily affects motor neurons and predominantly occurs in children.”0.98phenotype_alias_lexicon_v2

Plastin 3 Promotes Motor Neuron Axonal Growth and Extends Survival in a Mouse Model of Spinal Muscular Atrophy.

PMID 29552580 | PMCID PMC5852384 | DOI 10.1016/j.omtm.2018.01.007 · Molecular therapy. Methods & clinical development · 2018 · 3 validated mentions
TypeEntitySource evidenceConfidenceExtractor
genePLS3“The actin-binding protein plastin 3 (PLS3) has been reported as a modifier for SMA, making it a potential therapeutic target.”0.98hgnc_dict_v1
phenotypespinal muscular atrophy“Plastin 3 Promotes Motor Neuron Axonal Growth and Extends Survival in a Mouse Model of Spinal Muscular Atrophy.”0.98phenotype_alias_lexicon_v2
geneSMN1“SMA is caused by mutations in the survival motor neuron gene (SMN1), leading to reduced levels of SMN protein in the CNS.”0.98hgnc_dict_v1