Allele |
Construct |
Type |
Affected Genomic Region(s) |
hsc9 |
|
Small Deletion |
ptk7a
|
hsc12Tg |
Tg(foxj1a:ptk7a,cryaa:EGFP)
|
Transgenic Insertion |
|
hsc13Tg |
Tg(foxj1a:ptk7a,cryaa:EGFP)
|
Transgenic Insertion |
|
hsc14Tg |
Tg(foxj1a:ptk7a,cryaa:EGFP)
|
Transgenic Insertion |
|
hsc15Tg |
Tg(foxj1a:ptk7a,cryaa:EGFP)
|
Transgenic Insertion |
|
hsc16Tg |
Tg(foxj1a:EGFP)
|
Transgenic Insertion |
|
hsc17Tg |
Tg(foxj1a:EGFP)
|
Transgenic Insertion |
|
hsc18Tg |
Tg(foxj1a:EGFP)
|
Transgenic Insertion |
|
pr13 |
|
Indel |
dnaaf4
|
tm304 |
|
Point Mutation |
cfap298
|
to237b |
|
Point Mutation |
ccdc40
|
ts272 |
|
Unknown |
odad3
|