Analysis Tools|
Name ID |
C57BL/6N-Axin2tm1b(KOMP)Wtsi/Bay MGI:5812969 |
| Darker colors indicate more annotations |
This is the default dialog which is useful for displaying information. The dialog window can be moved, resized and closed with the 'x' icon.
| Mouse Phenotypes | abnormal eyelid fusion |
abnormal retina blood vessel morphology |
anophthalmia |
microphthalmia |
persistence of hyaloid vascular system |
|
| Availability | Mouse Genotype | |||||
| Axin2tm1b(KOMP)Wtsi/Axin2+ | ||||||
| Axin2tm1b(KOMP)Wtsi/Axin2tm1b(KOMP)Wtsi | ||||||

