Name ID |
C57BL/6N-Axin2tm1b(KOMP)Wtsi/Bay MGI:5812969 |
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Mouse Phenotypes | abnormal eyelid fusion |
abnormal retina blood vessel morphology |
anophthalmia |
microphthalmia |
persistence of hyaloid vascular system |
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Availability | Mouse Genotype | |||||
Axin2tm1b(KOMP)Wtsi/Axin2+ | ||||||
Axin2tm1b(KOMP)Wtsi/Axin2tm1b(KOMP)Wtsi |