| Primary Identifier | MGI:3511858 | Allele Type | Chemically induced (ENU) |
| Gene | Myo7a | Strain of Origin | C3HeB/FeJ |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | An A to T transversion at position 531 in exon 6 of Myo7a was identified and is predicted to cause an isoleucine-to-phenylalanine amino acid substitution at position 178, however no evidence of complementation was found when homozygotes were mated with heterozygous Myo7a4626SB. |
