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Phenotypes Associated with This Genotype
Genotype
MGI:5584025
Allelic
Composition
Mecp2tm1.1Dhy/Y
Genetic
Background
C57BL/6N-Mecp2tm1.1Dhy
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1.1Dhy mutation (1 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die between 7 and 31 weeks

behavior/neurological
• by 6 weeks, mice exhibit neurological defects (determined by scoring of level of grooming, ambulation, presence of skin sores, abdomen size and response to tail suspension) as in Mecp2tm1.1Bird mice
• in an elevated plus maze, mice spend more time in the open arms compared with wild-type mice
• stereotypic over grooming
• mice exhibit slower running pace and reduced variability in rear paw placement distance compared with wild-type mice
• in a three-chambered assay, mice spend less time interacting with a test mice compared with wild-type mice
• possible seizure activity

nervous system
• possible seizure activity
• smaller nuclei than in wild-type mice

integument
• on flanks, chest and tail region
• skin loss on flanks, chest and tail region

growth/size/body
N
• mice exhibit normal weight, body length and body mass index

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rett syndrome DOID:1206 OMIM:312750
OMIM:613454
J:209069


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory