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Phenotypes Associated with This Genotype
Genotype
MGI:7266261
Allelic
Composition
Mecp2tm1Nlnd/Y
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Nlnd mutation (0 available); any Mecp2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• males die prematurely, with an average lifespan of 97 days

growth/size/body
• males are lighter

behavior/neurological
• males become progressively symptomatic with Rett-like features after weaning, with worsening of the general condition, tremors, hind limb clasping and highly variable altered mobility
• hind limb clasping appears with age
• tremor is the first symptom to appear

nervous system
• brains from symptomatic males have a 15.7% weight reduction

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rett syndrome DOID:1206 OMIM:312750
OMIM:613454
J:268051


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
11/12/2024
MGI 6.24
The Jackson Laboratory