Phenotypes Associated with This Genotype

Genotype
MGI:5308942

• Allelic Composition: Sgce^tm1Ygl/Sgce⁺
• Genetic Background: involves: 129S2/SvPas

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

behavior/neurological

impaired coordination ( J:180682 )

• when the allele is inherited paternally

myoclonus ( J:180682 )

• when the allele is inherited paternally

nervous system

myoclonus ( J:180682 )

• when the allele is inherited paternally

abnormal Purkinje cell morphology ( J:180682 )

• abnormal nuclear envelopes with blebbing when the allele is inherited paternally

muscle

myoclonus ( J:180682 )

• when the allele is inherited paternally

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
myoclonic dystonia 11		DOID:0090034	OMIM:159900	J:180682