Xla Wt + fzd7 MO has 5 phenotype(s)
Images 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
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