Table 1.
Gene | Myosin | Locus1 | MIM | Reference |
---|---|---|---|---|
MYO3A | myosin 3a | DFNB30 | 607101 | Walsh et al., 2002 |
MYO6 | myosin 6 | DFNB37/DFNA22 | 607821/606346 | Melchionda et al., 2001; Ahmed et al., 2003 |
MYO7A | myosin 7a | DFNB2/DFNA11/USH1B | 600060/601317/276900 | Liu et al., 1997a; Liu et al., 1997b; Weil et al., 1997 |
MYH9 | myosin 9 | DFNA17 | 603622 | Lalwani et al., 2000 |
MYH14 | myosin 14 | DFNA4 | 600652 | Donaudy et al., 2004 |
MYO15A | myosin 15 | DFNB3 | 600316 | Friedman et al., 1995; Wang et al., 1998 |
DFNA locus mapped in a family segregating nonsyndromic deafness as a dominant trait. A DFNB locus mapped in a family segregating nonsyndromic deafness as a recessive trait. USH1B is a locus for Usher syndrome type 1 (OMIM# 276900). Mutations of MYO7A are associated with DFNA, DFNB or USH.