Xla Wt + DN-SQSTM1 has 3 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
Fig. 6 g

Puvirajesinghe TM et al. (2016)
Xla Wt + dnHsa.SQSTM1

NF13 (RT-PCR)
Expression Phenotype
decreased amount pcdh8.L expression in embryo
Fig. 6 f

Puvirajesinghe TM et al. (2016)
Xla Wt + dnHsa.SQSTM1

NF22-44 (in situ hybridization)
Anatomical Phenotype
abnormal convergent extension involved in axis elongation
abnormal neural tube closure
decreased length of anterior-posterior axis
Fig. 6 f

Puvirajesinghe TM et al. (2016)
Xla Wt + dnHsa.SQSTM1

NF22-44 (whole-mount microscopy)
Anatomical Phenotype
abnormal neural tube closure
decreased length of anterior-posterior axis