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ANKS6 and renal failure are reported together in 1 article.
Gene
ANKS6
- HGNC
- HGNC:26724
1articles
1mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Renal failure
523articles
523mentions
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 60ANKS6 Variants Underlie Polycystic Kidneys in Prenatal and Neonatal Cases.
PMID 39596574 | PMCID PMC11593910 | DOI 10.3390/genes15111374 · Genes · 2024 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ANKS6 | “ANKS6 Variants Underlie Polycystic Kidneys in Prenatal and Neonatal Cases.” | 0.98 | hgnc_dict_v1 |
| phenotype | renal failure | “BACKGROUND: Nephronophthisis (NPHP) is an autosomal recessive genetic disorder that can cause early-onset kidney failure.” | 0.93 | phenotype_alias_lexicon_v2 |
| phenotype | polycystic kidney disease | “CONCLUSIONS: We identified homozygous ANKS6 variants in three families presenting with antenatal polycystic kidney disease.” | 0.98 | phenotype_alias_lexicon_v2 |
| population | Saudi Arabia | “Here, we report the detection of ANKS6 variants in consanguineous families with polycystic kidney antenatally and in the early stages of life. METHODS: Three unrelated Saudi Arabian patients (two prenatal patients and one neonate) were investigated.” | 0.95 | saudi_context_rules_v1 |