Allele |
Construct |
Type |
Affected Genomic Region(s) |
b1105 |
|
Point Mutation |
jag1b
|
b1246 |
|
Small Deletion |
prrx1a
|
b1247 |
|
Small Deletion |
prrx1b
|
el10Tg |
Tg(sox10:DsRed)
|
Transgenic Insertion |
|
el49Tg |
Tg(UAS:bmp4,myl7:EGFP)
|
Transgenic Insertion |
|
el249Tg |
Tg(UAS:edn1,cryaa:Cerulean)
|
Transgenic Insertion |
|
el483Tg |
TgBAC(col2a1a:EGFP)
|
Transgenic Insertion |
|
el491 |
|
Insertion |
prrx1b
|
el515 |
|
Indel |
notch2
|
el558 |
|
Small Deletion |
prrx1a
|
fh331 |
|
Point Mutation |
barx1
|
fh332 |
|
Point Mutation |
notch3
|
kca3Tg |
Tg(5xUAS-E1B:6xMYC-notch1a)
|
Transgenic Insertion |
|
kca4Tg |
Tg(-1.5hsp70l:GAL4)
|
Transgenic Insertion |
|
Df(Chr01:hand2)s6 |
|
Deficiency |
hand2
|
tf216b |
|
Point Mutation |
edn1
|
y1Tg |
Tg(fli1:EGFP)
|
Transgenic Insertion |
|