Phenotypes Associated with This Genotype

Genotype
MGI:5584182

• Allelic Composition: Del(XArmcx5-Nxf3)3Jw/+
• Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

mortality/aging

postnatal lethality, incomplete penetrance ( J:210663 )

♀

growth/size/body

cleft palate ( J:210663 )

♀

postnatal growth retardation ( J:210663 )

♀ • postnatal developmental delay

nervous system

environmentally induced seizures ( J:210663 )

♀ • handling seizures

behavior/neurological

environmentally induced seizures ( J:210663 )

♀ • handling seizures

craniofacial

cleft palate ( J:210663 )

♀

digestive/alimentary system

cleft palate ( J:210663 )

♀

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
chromosomal deletion syndrome		DOID:0060388		J:210663