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. 2018 Jul 11;8:10439. doi: 10.1038/s41598-018-28714-1

Table 2.

Neural tube, visceral and cardiovascular defects identified in mouse Zic2 mutants.

iso TALEN Trans-hets
iso/iso A5/A5 A10/A10 & A17/A17 A19/A19 iso/A5 iso/A8
Neural Tube Defects Exencephaly 17/17 10/10 3/3 3/3 2/2 2/2
Holoprosencephaly Alobar 13/16 5/7 3/3 2/3 2/2 2/2
Semilobar 3/16 2/7 0/3 1/3 0/2 0/2
Lobar 0/16 0/7 0/3 0/3 0/2 0/2
Eyes Cyclopia 8/17 3/7 1/3 2/3 1/2 2/2
Hypotelorism 6/17 3/7 1/3 0/3 0/2 0/2
Absent 3/17 0/7 1/3 1/3 1/2 0/2
Spina bifida 17/17 10/10 3/3 3/3 2/2 2/2
Curly tail 17/17 10/10 3/3 3/3 2/2 2/2
Viscera Lungs Right Isomerism 13/17 6/10 2/3 3/3 1/2 2/2
Left Isomerism 0/17 1/10 0/3 0/3 0/2 0/2
Reversed 0/17 0/10 0/3 0/3 0/2 0/2
Normal 4/17 3/10 1/3 0/3 1/2 0/2
Spleen Reduced or absent 1/6 4/7 0/2 0/0 0/1 0/0
Duplicated 0/6 0/7 0/2 0/0 0/1 0/0
Right sided 2/6 0/7 0/2 0/0 0/1 0/0
Heart Dextrocardia 4/16 4/10 0/3 2/3 0/2 1/2
Mesocardia 7/16 2/10 0/3 1/3 2/2 1/2
Stomach Right sided 7/17 2/10 0/3 0/3 0/2 2/2
Pancreas Right sided 5/14 2/7 0/3 0/2 0/2 0/0
Atria & Veins Bilateral systemic venous sinus 10/15 4/10 1/3 3/3 1/2 2/2
Left sided Inferior vena cava 5/16 3/10 0/3 1/3 0/2 2/2
Hepatic vein drainage direct to atria 2/16 3/10 0/3 3/3 0/2 0/2
Atrial septal defect 8/11 5/10 1/3 2/2 1/2 2/2
Ventricles & Arteries Abnormal ventricular topology 6/13 6/10 0/3 1/2 1/2 2/2
Great artery transposition 0/13 0/10 1/3 0/3 0/2 0/2
Double outlet right ventricle 5/13 5/9 0/3 2/3 0/2 2/2
Ventricular septal defect 11/15 7/10 0/3 1/1 2/2 2/2
Rightward looped aortic arch 5/17 3/10 1/3 2/3 0/2 0/2

A summary of the phenotypes observed by MRI and µCT imaging in all Zic2 mutants examined including both the original iso line and TALEN-generated lines. All embryos are homozygous mutants, except for those labelled “trans-hets” which carry one iso allele and one TALEN allele as a test of complementarity. For each phenotype described, the first number indicates the number of embryos observed with that phenotype, while the second indicates the number examined. The latter number differs for different phenotypes because it was not possible to assess every phenotype in every embryo due to limitations of imaging.