| Allele |
Construct |
Type |
Affected Genomic Region(s) |
| Df(Chr01:cx41.8,dla,msxb,otx1l)b220 |
|
Deficiency |
dla,
msx1b,
otx2a
|
| T(Chr03:eve1,hoxb5a,pyy,rarab,thra)b245 |
|
Translocation |
elavl3,
eve1,
hoxb5a,
pyya,
rarab,
thraa
|
| T(Chr17:gsc)b250 |
|
Translocation |
foxa2,
gsc
|
| Df(Chr23:myb)b316 |
|
Deficiency |
myb
|
| Df(Chr05:tncb)b345 |
|
Deficiency |
tncb
|
| Df(Chr12:dlx3b,dlx4b,tbx6)b380 |
|
Deficiency |
dlx3b,
dlx4b,
tbx6
|
| T(Chr03:eve1,hoxb5a,pyy,rarab,thra)b447 |
|
Translocation |
elavl3,
eve1,
hoxb5a,
pyya,
rarab,
thraa
|
| Df(Chr03:elavl3,hoxb5a)b491 |
|
Deficiency |
elavl3,
hoxb5a
|
| t1 |
|
Point Mutation |
gja5b
|
