Xla Wt + lhx1 MO + otx2 MO has 2 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
fig.S7

Rankin SA et al. (2011)
Xla Wt + lhx1 MO + otx2 MO

NF10.5 (in situ hybridization)
Expression Phenotype
decreased amount chrd.1.L expression in involuted dorsal mesoderm
decreased amount gsc.L expression in involuted dorsal mesoderm
decreased amount hhex.L expression in dorsal endomesoderm
increased amount chrd.1.L expression in involuted dorsal mesoderm
mislocalised chrd.1.L expression in involuted dorsal mesoderm
fig.S1

Rankin SA et al. (2011)
Xla Wt + lhx1 MO + otx2 MO

NF33/34-35 and 36 (morphology)
Anatomical Phenotype
abnormal embryo morphology
abnormal gastrulation