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Phenotypes Associated with This Genotype
Genotype
MGI:3624719
Allelic
Composition
Mecp2tm1Bird/Y
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Bird mutation (2 available); any Mecp2 mutation (25 available)
Tg(Nes-cre)1Kln mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• frequently exhibit uneven wearing of the teeth

mortality/aging

behavior/neurological
• develop a stiff, uncoordinated gait

craniofacial
• frequently exhibit uneven wearing of the teeth

endocrine/exocrine glands

growth/size/body
• frequently exhibit uneven wearing of the teeth

reproductive system

Mouse Models of Human Disease
OMIM ID Ref(s)
Rett Syndrome; RTT 312750 J:67910


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
07/19/2016
MGI 6.04
The Jackson Laboratory