Primary Identifier | MGI:5514275 | Allele Type | Spontaneous |
Attribute String | Dominant negative, Null/knockout | Gene | Slc25a13 |
Inheritance Mode | Recessive | Strain of Origin | SJL/J |
Is Recombinase | false | Is Wild Type | false |
molecularNote | The hyperspin mutation is a spontaneous 123.6 kb deletion of Chromosome 6: 5.86-6.66 Mb (GRCm38) that begins in intron 3 of Slc25a13 and ends in exon 17, an interval that includes an enhancer of Dlx5 and, in addition to creating a null allele of Slc25a13, diminishes otocyst expression of Dlx5. |