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 |
|