# Apolipoprotein L1 High-Risk Genotypes are Associated With Lupus Nephritis Incidence

**Authors:** Samir Patel, Hadi Rabee, Amrita Ramnarine, Dalvir Kular, Evangelos Kougiouris, Mark D. Russell, Mohammad Al-Agil, Maryam Adas, Chris Wincup, Jonathan Dick, Sam Norton, James Galloway, Patrick Gordon, Kate Bramham

PMC · DOI: 10.1016/j.ekir.2026.106344 · 2026-02-04

## Full-text entities

- **Genes:** IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, APOL1 (apolipoprotein L1) [NCBI Gene 8542] {aka APO-L, APOL, APOL-I, FSGS4}, MYH9 (myosin heavy chain 9) [NCBI Gene 4627] {aka BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA}
- **Diseases:** kidney disease (MESH:D007674), collapsing glomerulopathy (MESH:D001261), focal segmental glomerulosclerosis (MESH:D005923), proteinuria (MESH:D011507), SLE (MESH:D008180), MDR (MESH:D018088), LN (MESH:D008181), kidney failure (MESH:D051437), chronic kidney disease (MESH:D051436)
- **Chemicals:** creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** p.N264K

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12966666/full.md

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Source: https://tomesphere.com/paper/PMC12966666