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TYK2 and inflammatory bowel disease are reported together in 2 articles.

Gene

TYK2

HGNC
HGNC:12440
15articles
15mentions
1variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
693articles
693mentions
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
geneTYK2“Rare variants of CARD9, TYK2, IL4, and NLRP1 genes present in VDZ responders enhance the anti-inflammatory/immune modulation effects.”0.98hgnc_dict_v1
phenotypeinflammatory bowel disease“High-Throughput Whole-Exome Sequencing and Large-Scale Computational Analysis to Identify the Genetic Biomarkers to Predict the Vedolizumab Response Status in Inflammatory Bowel Disease Patients from Saudi Arabia.”0.98phenotype_alias_lexicon_v2
geneNOD2“The rare variant analysis prioritized NOD2, IL23, IL10, IL27, and TRAF1 genes in non-responders.”0.98hgnc_dict_v1
geneIL10“The rare variant analysis prioritized NOD2, IL23, IL10, IL27, and TRAF1 genes in non-responders.”0.98hgnc_dict_v1

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome.

PMID 26304966 | PMCID PMC4577846 | DOI 10.1084/jem.20140280 · The Journal of experimental medicine · 2015 · 3 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneTYK2“Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome.”0.98hgnc_dict_v1
phenotypeinflammatory bowel disease“All eight TYK2-deficient patients displayed impaired but not abolished cellular responses to (a) IL-12 and IFN-α/β, accounting for mycobacterial and viral infections, respectively; (b) IL-23, with normal proportions of circulating IL-17(+) T cells, accounting for their apparent lack of mucocutaneous candidiasis; and (c) IL-10, with no overt clinical consequences, including a lack of inflammatory bowel disease.”0.98phenotype_alias_lexicon_v2
phenotypeatopic dermatitis“Autosomal recessive, complete TYK2 deficiency was previously described in a patient (P1) with intracellular bacterial and viral infections and features of hyper-IgE syndrome (HIES), including atopic dermatitis, high serum IgE levels, and staphylococcal abscesses.”0.98phenotype_alias_lexicon_v2