Advanced search

Combine gene, variant, phenotype, region and year filters

Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

Transparent by designEvery result links extracted entities to its source sentence and publication identifier.
About your search

GLE1 and spinal muscular atrophy are reported together in 1 article.

Gene

GLE1

HGNC
HGNC:4315
2articles
2mentions
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

1 records shown · first 60

The 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
TypeEntitySource evidenceConfidenceExtractor
geneGLE1“The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.”0.98hgnc_dict_v1
phenotypespinal muscular atrophy“The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.”0.98phenotype_alias_lexicon_v2
geneSMN1“The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.”0.98hgnc_dict_v1
geneFUS“The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.”0.98hgnc_dict_v1