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STAT6 and hearing loss are reported together in 1 article.

Gene

STAT6

HGNC
HGNC:11368
20articles
20mentions
3variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype

Hearing loss

HPO
HP:0000365
663articles
663mentions
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

Malignant solitary fibrous tumor of the temporal bone with NAB2 ex6::STAT6 ex16 fusion: a case report with literature review.

PMID 41413814 | PMCID PMC12829090 | DOI 10.1186/s12957-025-04160-y · World journal of surgical oncology · 2025 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneSTAT6“Malignant solitary fibrous tumor of the temporal bone with NAB2 ex6::STAT6 ex16 fusion: a case report with literature review.”0.98hgnc_dict_v1
phenotypehearing loss“CASE PRESENTATION: A 69-year-old female patient presented to the ENT clinic in 2021 with a three-week history of right-sided otalgia and hearing loss.”0.98phenotype_alias_lexicon_v2
geneNAB2“Malignant solitary fibrous tumor of the temporal bone with NAB2 ex6::STAT6 ex16 fusion: a case report with literature review.”0.98hgnc_dict_v1
geneBCL2“Tumor cells were reactive for STAT6, BCL2, and CD99, while CD34 was negative.”0.98hgnc_dict_v1