Xla Wt + Nf2 MO has 4 phenotype(s)

Images

Sources

Experiment + Assay

Phenotypes

Human Diseases

fig.3.c

Zhu X et al. (2015)

Xla Wt + Nf2 MO

NF10.5 (morphology)

Anatomical Phenotype
abnormal development of eye decreased size of the head

fig.4.c, d

Zhu X et al. (2015)

Xla Wt + Nf2 MO

NF15 (immunohistochemistry)

Anatomical Phenotype
abnormal Wnt signaling pathway

Expression Phenotype
mislocalised ctnnb1.L expression in neural plate

fig.3.d

Zhu X et al. (2015)

Xla Wt + Nf2 MO

NF23-24 (in situ hybridization)

Expression Phenotype
decreased amount six3.L expression in retinal neural layer increased amount hoxc9-like.L expression in spinal cord mislocalised hoxc9-like.L expression in spinal cord mislocalised six3.L expression in retinal neural layer

fig.3.e

Zhu X et al. (2015)

Xla Wt + Nf2 MO

NF23-24 (in situ hybridization)

Expression Phenotype
decreased amount rax.L expression in retinal neural layer mislocalised egr2.L expression in hindbrain mislocalised en2.L expression in presumptive midbrain-hindbrain boundary