| Primary Identifier | MGI:5755140 | Allele Type | Spontaneous |
| Attribute String | Hypomorph | Gene | Ap1g1 |
| Inheritance Mode | Recessive | Strain of Origin | C57BL/6-Tg(APOA1)1Rub/J |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | This spontaneous 6 bp deletion of TTTCTG in exon 13 of NM009677, isoform 1, and exon 12 of Nm002301211, isoform 2, is predicted to cause an in-frame deletion of F391 and L392 of isoform 1, or F388 and L389 of isoform 2, amino acids which are in the adaptin N-terminal homology domain involved in interactions with other subunitos of the AP-1 complex. |
