Genes with the highest odds of NM were located on chromosome 5 (5q33.1d; ZNF300, CCDC69, SLC36A1, and SLC36A2) and 14 (14q 11: in gene SLC7A8; 14q13: gene AKAP6; and 14q2: gene CLEC14A). The gene discussed is CLEC14A; the disease is nemaline myopathy.