Xla Wt + sia1 MO + sia2 MO has 7 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
fig.6.h^1

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF10.5 (in situ hybridization)
Expression Phenotype
decreased amount gsc.L expression in upper blastopore lip
fig.6.i^1

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF10.5 (in situ hybridization)
Expression Phenotype
decreased amount chrd.1.S expression in upper blastopore lip
fig.6.j^1

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF10.5 (in situ hybridization)
Expression Phenotype
increased amount wnt8a.L expression in upper blastopore lip
mislocalised wnt8a.L expression in upper blastopore lip
fig.6.l^1

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF10.5 (in situ hybridization)
Expression Phenotype
decreased amount zic1.S expression in neural plate
fig.6.i

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF31 (morphology)
Anatomical Phenotype
absent head
decreased length of anterior-posterior axis
decreased size of the tail
decreased size of the trunk
fig.6.k

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF31 (morphology)
Anatomical Phenotype
abnormal dorsal/ventral axis specification
absent notochord
fused somites
fig.6.l

Bae S et al. (2011)
Xla Wt + sia1 MO + sia2 MO

NF31 (morphology)
Anatomical Phenotype
abnormal dorsal/ventral axis specification
absent neural tube
absent notochord
absent somite
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