MYO1E

A gene on chromosome 15q21-q22 that encodes an actin-based molecular motor with ATPase activity, which belongs to the unconventional myosin protein family.

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The mutations in podocyte genes result in either autosomal recessive FSGS (NPHS1, NPHS2, LAMB2, PLCE1, ARGHDIA, MYO1E and other genes) or autosomal dominant FSGS (ACTN4, CD2AP, INF2, TRPC6, WT1, ARHGAP24 and other genes) or mitochondrial disorders (CoQ6, tRNALeu, tRNATyr, tRNAIle).

Understanding the pathogenesis of focal segmental glomerulosclerosis: morphology vs. molecules

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