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STAT1 and multiple sclerosis are reported together in 1 article.

Gene

STAT1

HGNC
HGNC:11362
51articles
51mentions
10variants with confirmed gene link (top 10)
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
236articles
236mentions
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

MAPK pathway and B cells overactivation in multiple sclerosis revealed by phosphoproteomics and genomic analysis.

PMID 31004050 | PMCID PMC6510997 | DOI 10.1073/pnas.1818347116 · Proceedings of the National Academy of Sciences of the United States of America · 2019 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneSTAT1“Finally, using flow cytometry, we detected in MS patients increased STAT1, STAT3, TF65, and HSPB1 phosphorylation in CD19+ cells.”0.98hgnc_dict_v1
phenotypemultiple sclerosis“MAPK pathway and B cells overactivation in multiple sclerosis revealed by phosphoproteomics and genomic analysis.”0.98phenotype_alias_lexicon_v2
geneIRF8“Moreover, we identified one SNP located in the PHDGH gene and another on IRF8 gene that were associated with MP2K1 phosphorylation levels, providing a first clue on how this MS risk gene may act.”0.98hgnc_dict_v1
geneSTAT3“Finally, using flow cytometry, we detected in MS patients increased STAT1, STAT3, TF65, and HSPB1 phosphorylation in CD19+ cells.”0.98hgnc_dict_v1