| Primary Identifier | MGI:1856555 | Allele Type | Spontaneous |
| Gene | Myo6 | Inheritance Mode | Recessive |
| Strain of Origin | B10.HA/(33NX)Sn | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | On the basis of a series of southern blots, this mutation appears to involve a 1.1 kb intragenic deletion. Gene transcripts could be detected by RT-PCR. Sequence analysis of these transcripts identified a 150 bp deletion corresponding to nucleotides 2456-2585. The deletion results in a frame shift which introduces a stop codon at the beginning of the neck region. |
