Table 5.
Gene name | Reported pathogenic mutation | Reference | |
---|---|---|---|
Autosomal dominant inheritance mutations | |||
ACTG1 | NM_001199954:c.A353T:p.K118M | Zhu et al. (2003) | |
ACTG1 | NM_001199954:c.G721A:p.E241K | Morín et al. (2009) | |
KCNQ4 | NM_004700:c.C546G:p.F182L | Su et al. (2007) | |
KCNQ4 | NM_004700:c.C546G:p.F182L | Su et al. (2007) | |
KCNQ4 | NM_004700:c.C546G:p.F182L | Su et al. (2007) | |
MYH9 | NM_002473:c.G2114A:p.R705H | Dong et al. (2005) | |
TECTA | NM_005422:c.C5597T:p.T1866M | Sagong et al. (2010) | |
WFS1 | NM_001145853:c.G1846T:p.A616S | Liu et al. (2005) | |
WFS1 | NM_001145853:c.G2185A:p.D729N | Domènech et al. (2002) | |
WFS1 | NM_001145853:c.G2590A:p.E864K | Eiberg et al. (2006) |
Gene name | Reported pathogenic mutation | Novel mutation found by MPS | Reference |
---|---|---|---|
Autosomal recessive inheritance mutations | |||
CDH23 | NM_001171930:c.C805T:p.R269W | NM_001171933:c.C2407T:p.R803W | Oshima et al. (2006) |
MYO7A | NM_000260:c.G635A:p.R212H | NM_000260:c.G3475A:p.G1159S | Weil et al. (1997) |
MYO15A | NM_016239:c.G6731A:p.G2244E | NM_016239:c.6457delG:p.A2153fs | Nal et al. (2007) |
SLC26A4 | NM_000441:c.T2228A:p.L743X | NM_000441:c.C1208A:p.A403D | Yuan et al. (2009) |
Among the autosomal recessive causative genes, only the reported pathogenic variants with other mutation candidates in the same genes detected by MPS were listed.