| 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
|