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GAPDH and spinal muscular atrophy are reported together in 1 article.
Gene
GAPDH
- HGNC
- HGNC:4141
34articles
34mentions
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 60The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.
PMID 30565205 | DOI 10.5603/FHC.a2018.0022 · Folia histochemica et cytobiologica · 2018 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | GAPDH | “GAPDH as internal control gene.” | 0.98 | hgnc_dict_v1 |
| phenotype | spinal muscular atrophy | “The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | SMN1 | “The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.” | 0.98 | hgnc_dict_v1 |
| gene | GLE1 | “The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.” | 0.98 | hgnc_dict_v1 |