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Phenotypes Associated with This Genotype
Genotype
MGI:5308942
Allelic
Composition
Sgcetm1Ygl/Sgce+
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sgcetm1Ygl mutation (0 available); any Sgce mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• when the allele is inherited paternally
• when the allele is inherited paternally

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

muscle
• when the allele is inherited paternally

Mouse Models of Human Disease
OMIM ID Ref(s)
Dystonia 11, Myoclonic; DYT11 159900 J:180682


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/17/2016
MGI 6.03
The Jackson Laboratory