Related Experiment Video
Updated: Jan 28, 2026

Isolation of Chondrocytes and Chondroprogenitors Using Fibronectin Adhesion and Migratory Assay
Published on: October 4, 2024
A novel variant in FN1 in a family with fibronectin glomerulopathy
Nabeel Aslam1, Anshika Singh1, Cherise Cortese2
11Division of Nephrology and Hypertension, Mayo Clinic, Jacksonville, FL USA.
Abstract:
Glomerulopathy with fibronectin deposits (GFND) is a rare glomerular disorder. We report a 28-year-old male diagnosed with GFND by mass spectrometry on kidney biopsy tissue. Whole-exome sequencing (WES) identified that a previously undescribed FN1 gene mutation (c.3051G > T, p.W1017C) was likely responsible for this patient's fibronectin glomerulopathy. We discuss the implications of this novel variant of FN1 and the importance of WES to identify a mutation in a gene of interest.
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