Table 3 Proposed causative mutations identified by WGS
Allele NameStrain IDMutationGene DescriptionGene ID (v5.5)
adf1-2Finst et al. 1998G692fsX714TRP15Cre09.g396142
adf1-3Finst et al. 1998Δ chromosome 9: 4743360–4745263
adf1-4Finst et al. 1998Unidentified
adf1-5Finst et al. 1998Unidentified
adf1-6Finst et al. 1998A1724D
adf1-7E1 P19 C5Unidentified
adf1-12E6.1 P3 A4P1133F
adf1-13E6.1 P3 A7Unidentified
adf1-14E12 M20W560L
adf1-15E20 G2L139fsX221
adf1-16E21B5Unidentified
adf1-17E21 C13P1155L
adf3-1E3.1 P15 B4c.2731–1G > A (Splice site acceptor, exon 20)FAP16Cre06.g303400
adf3-2E21 C7Y841*
fa1-6E12 AN8K1014FSFA1Cre06.g257600
fa1-7E15.2 P12 E6c.2610–2A > G (Splice site acceptor, exon 16)
fa2-5E12 AA8Q129*FA2Cre07.g351150
fa2-6E12 AC10G163R
fa2-7E12 AE48G592FS