Xla Wt + spry2dn has 1 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
Fig. 1. E., F

Sun J et al. (2020)
Xla Wt + spry2dn

NF 33 (immunohistochemistry)
Anatomical Phenotype
abnormal cell migration
abnormal retina
abnormally decreased number of retinal progenitor cell