Xla Wt + foxi1 MO has 2 phenotype(s)

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Sources

Experiment + Assay

Phenotypes

Human Diseases

fig.5.f

Mir A et al. (2007)

Xla Wt + foxi1 MO

NF23 (in situ hybridization)

Expression Phenotype
decreased amount foxg1.L expression in embryo decreased amount hoxb9.L expression in embryo decreased amount krt12.4.L expression in embryo decreased amount snai2.L expression in embryo decreased amount sox2.S expression in embryo

fig.5.e

Mir A et al. (2007)

Xla Wt + foxi1 MO

NF27 (morphology)

Anatomical Phenotype
abnormal axis elongation abnormally incomplete structure of epidermis decreased length of anterior-posterior axis decreased size of the head