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Phenotype Figure Summary
Marker:
olig2
Conditions:
Standard or Control
Publication
Data
Fish
Anatomy
Zannino
et al.
, 2012
Fig. 1
rw0Tg + MO4-olig2
facial nerve motor nucleus motor neuron mislocalised, abnormal
neuron migration disrupted, abnormal
Fig. 2
rw0Tg + MO4-olig2
facial nerve motor nucleus motor neuron mislocalised, abnormal
neuron migration disrupted, abnormal
Fig. 5
rw0Tg + MO4-olig2
facial nerve motor nucleus motor neuron mislocalised, abnormal
neuron migration disrupted, abnormal
Lim
et al.
, 2011
Fig. 7
y1Tg/+ + MO1-olig2
motor neuron lacks parts or has fewer parts of type motor neuron axon, abnormal
parachordal vessel immature, abnormal
parachordal vessel venous endothelial cell migration involved in lymph vessel development arrested, abnormal
Yang
et al.
, 2010
Fig. 7
WT + MO5-olig2
lateral floor plate Kolmer-Agduhr neuron cellular quality, abnormal
spinal cord interneuron cellular quality, abnormal
ventral spinal cord interneuron differentiation disrupted, abnormal
Borodovsky
et al.
, 2009
Fig. 5
WT + MO1-olig2
dopaminergic neuron decreased amount, abnormal
Schebesta
et al.
, 2009
Fig. 8
WT + MO1-olig2
oligodendrocyte development disrupted, abnormal
Zannino
et al.
, 2009
Fig. 6
vu12Tg + MO4-olig2
abducens nucleus development disrupted, abnormal
cranial nerve VI motor neuron decreased amount, abnormal
hindbrain glioblast (sensu Vertebrata) decreased amount, abnormal
Fig. 8
vu12Tg + MO4-olig2
cell differentiation in hindbrain disrupted, abnormal
neuron differentiation disrupted, abnormal
oligodendrocyte differentiation disrupted, abnormal
text only
vu12Tg + MO4-olig2
oligodendrocyte decreased amount, abnormal
spinal cord motor neuron decreased amount, abnormal
Yeo
et al.
, 2007
Fig. 2
zf532Tg + MO3-olig2
spinal cord GABAergic neuron amount, abnormal
Park
et al.
, 2002
Fig. 5
WT + MO1-olig2
spinal cord lacks all parts of type primary motor neuron, abnormal
spinal cord motor neuron differentiation disrupted, abnormal
Fig. 6
WT + MO1-olig2
oligodendrocyte development disrupted, abnormal
spinal cord lacks parts or has fewer parts of type oligodendrocyte, abnormal
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