Key:

hm	homozygous	ht	heterozygous	tg	involves transgenes	√	phenotype observed
cn	conditional genotype	cx	complex: > 1 genome feature	ot	other: hemizygous, indeterminate,...	N	normal phenotype

Genotype/
Background:

Phenotypes:

Affected Systems	cn1	cn2
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craniofacial	√	√
abnormal tooth development	√
abnormal dental mesenchyme morphology	√
abnormal secondary palate development		√
palatal shelf hypoplasia		√
abnormal palatine aponeurosis morphology		√
small levator veli palatini muscle		√
abnormal palatopharyngeus muscle morphology		√
small tensor veli palatini muscle		√
cleft palate	√
digestive/alimentary system	√	√
abnormal secondary palate development		√
palatal shelf hypoplasia		√
abnormal palatine aponeurosis morphology		√
small levator veli palatini muscle		√
abnormal palatopharyngeus muscle morphology		√
small tensor veli palatini muscle		√
cleft palate	√
embryo	√
abnormal dental mesenchyme morphology	√
growth/size/body	√	√
abnormal tooth development	√
abnormal dental mesenchyme morphology	√
abnormal secondary palate development		√
palatal shelf hypoplasia		√
abnormal palatine aponeurosis morphology		√
small levator veli palatini muscle		√
abnormal palatopharyngeus muscle morphology		√
small tensor veli palatini muscle		√
cleft palate	√
mortality/aging	√
neonatal lethality	√
muscle		√
small levator veli palatini muscle		√
abnormal palatopharyngeus muscle morphology		√
small tensor veli palatini muscle		√
abnormal superior pharyngeal constrictor muscle morphology		√
respiratory system		√
abnormal superior pharyngeal constrictor muscle morphology		√
skeleton	√
abnormal tooth development	√
abnormal dental mesenchyme morphology	√