| Allele |
Construct |
Type |
Affected Genomic Region(s) |
| sa23054 |
|
Point Mutation |
hmx3a
|
| su1Tg |
Tg(evx1:EGFP)
|
Transgenic Insertion |
|
| su2Tg |
Tg(evx1-Mmu.Fos:GAL4-VP16,UAS:EGFP)
|
Transgenic Insertion |
|
| su3 |
|
Indel |
hmx3a
|
| su35 |
|
Insertion |
hmx2
|
| su36 |
|
Small Deletion |
hmx2
|
| su37 |
|
Small Deletion |
hmx2
|
| su38 |
|
Small Deletion |
hmx2
|
| su39 |
|
Indel |
hmx2
|
| su42 |
|
Small Deletion |
hmx3a
|
| su43Tg |
Tg4(hsp70l:GAL4)
|
Transgenic Insertion |
hmx3a
|
| Df(Chr17:hmx3a,hmx2)su44 |
|
Deficiency |
hmx2, 
hmx3a
|
| Df(Chr17:hmx3a,hmx2)su45 |
|
Deficiency |
hmx2, 
hmx3a
|
| ta52b |
|
Point Mutation |
mib1
|
| tpl2Tg |
Tg(14xUAS:mRFP,Xla.Cryg:GFP)
|
Transgenic Insertion |
|