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.
Knowledge-base search
About your search
KCNJ11 and obesity are reported together in 1 article.
Gene
KCNJ11
- HGNC
- HGNC:6257
27articles
27mentions
3variants with confirmed gene link
Most co-reported phenotypes (articles)
diabetes mellitus 20developmental delay 3epilepsy 3renal failure 2intellectual disability 1obesity 1
Reported variants (articles · ClinVar status)
Phenotype
Obesity
- HPO
- HP:0001513
856articles
856mentions
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 60KCNJ11 (p.Arg192Cys)-associated MODY13 with coexisting autoimmunity in a child, a case report.
PMID 41772505 | PMCID PMC13059244 | DOI 10.1186/s12887-026-06672-2 · BMC pediatrics · 2026 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | KCNJ11 | “KCNJ11 (p.Arg192Cys)-associated MODY13 with coexisting autoimmunity in a child, a case report.” | 0.98 | hgnc_dict_v1 |
| phenotype | obesity | “He presented with hyperglycemia, obesity, and acanthosis nigricans.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | diabetes mellitus | “BACKGROUND: Maturity-onset diabetes of the young type 13 (MODY13) is a rare autosomal dominant monogenic diabetes caused by mutations in the potassium inwardly rectifying channel subfamily J member 11 (KCNJ11) gene.” | 0.93 | phenotype_alias_lexicon_v2 |
| variant | p.Arg192Cys | “KCNJ11 (p.Arg192Cys)-associated MODY13 with coexisting autoimmunity in a child, a case report.” | 0.95 | hgvs_regex_v1 |