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CENPI and dyslipidemia are reported together in 1 article.
Gene
CENPI
- HGNC
- HGNC:3968
1articles
1mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Dyslipidemia
338articles
338mentions
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 60Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome.
PMID 31912435 | DOI 10.1007/s40620-019-00692-1 · Journal of nephrology · 2020 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CENPI | “Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome.” | 0.98 | hgnc_dict_v1 |
| phenotype | dyslipidemia | “BACKGROUND: Individuals with proteinuria in association with hypoalbuminemia, edema, and hyperlipidemia are considered as having nephrotic syndrome (NS).” | 0.93 | phenotype_alias_lexicon_v2 |
| phenotype | nephrotic syndrome | “Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | c.383G>A | “An unbiased and hypothesis-free exome data analysis identified a missense variant (c.383G>A; p.Arg128Gln) in the CENPI gene.” | 0.95 | hgvs_regex_v1 |