Table 3. Proposed causative mutations identified by WGS.
| Allele Name | Strain ID | Mutation | Gene Description | Gene ID (v5.5) |
|---|---|---|---|---|
| adf1-2 | Finst et al. 1998 | G692fsX714 | TRP15 | Cre09.g396142 |
| adf1-3 | Finst et al. 1998 | Δ chromosome 9: 4743360–4745263 | ||
| adf1-4 | Finst et al. 1998 | Unidentified | ||
| adf1-5 | Finst et al. 1998 | Unidentified | ||
| adf1-6 | Finst et al. 1998 | A1724D | ||
| adf1-7 | E1 P19 C5 | Unidentified | ||
| adf1-12 | E6.1 P3 A4 | P1133F | ||
| adf1-13 | E6.1 P3 A7 | Unidentified | ||
| adf1-14 | E12 M20 | W560L | ||
| adf1-15 | E20 G2 | L139fsX221 | ||
| adf1-16 | E21B5 | Unidentified | ||
| adf1-17 | E21 C13 | P1155L | ||
| adf3-1 | E3.1 P15 B4 | c.2731–1G > A (Splice site acceptor, exon 20) | FAP16 | Cre06.g303400 |
| adf3-2 | E21 C7 | Y841* | ||
| fa1-6 | E12 AN8 | K1014FS | FA1 | Cre06.g257600 |
| fa1-7 | E15.2 P12 E6 | c.2610–2A > G (Splice site acceptor, exon 16) | ||
| fa2-5 | E12 AA8 | Q129* | FA2 | Cre07.g351150 |
| fa2-6 | E12 AC10 | G163R | ||
| fa2-7 | E12 AE48 | G592FS |