Xla Wt + fzd7 MO has 5 phenotype(s)

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Sources

Experiment + Assay

Phenotypes

Human Diseases

fig.2.f

Zhang Z et al. (2013)

Xla Wt + fzd7 MO

NF20 (in situ hybridization)

Expression Phenotype
decreased amount hhex.L expression in foregut

fig.2.i

Zhang Z et al. (2013)

Xla Wt + fzd7 MO

NF35/36 (in situ hybridization)

Anatomical Phenotype
abnormal head morphology obsolete abnormally edematous pharyngeal region

Expression Phenotype
decreased amount nr1h5.L expression in liver decreased amount pdx1.L expression in duodenum decreased amount pdx1.L expression in pancreas

fig.2.o

Zhang Z et al. (2013)

Xla Wt + fzd7 MO

NF35/36 (morphology)

Anatomical Phenotype
abnormally decreased coiling of small intestine abnormally decreased length of alimentary system obsolete abnormally edematous foregut

fig.2.q

Zhang Z et al. (2013)

Xla Wt + fzd7 MO

NF42 (morphology)

Anatomical Phenotype
absent liver absent stomach decreased size of the heart

fig.2.s

Zhang Z et al. (2013)

Xla Wt + fzd7 MO

NF42 (morphology)

Anatomical Phenotype
abnormally decreased length of intestine absent liver absent pancreas absent stomach