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SLC2A10 and stroke are reported together in 1 article.
Gene
SLC2A10
- HGNC
- HGNC:13444
8articles
8mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype
Stroke
555articles
555mentions
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 60Arterial tortuosity syndrome: 40 new families and literature review.
PMID 29323665 | DOI 10.1038/gim.2017.253 · Genetics in medicine : official journal of the American College of Medical Genetics · 2018 · 2 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | SLC2A10 | “PURPOSE: We delineate the clinical spectrum and describe the histology in arterial tortuosity syndrome (ATS), a rare connective tissue disorder characterized by tortuosity of the large and medium-sized arteries, caused by mutations in SLC2A10.” | 0.98 | hgnc_dict_v1 |
| phenotype | stroke | “Severe but rare vascular complications include early and aggressive aortic root aneurysms, neonatal intracranial bleeding, ischemic stroke, and gastric perforation.” | 0.98 | phenotype_alias_lexicon_v2 |