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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 (22 available)
Tg(Nes-cre)1Kln mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
(J:67910)
(J:67910)

behavior/neurological
(J:67910)
(J:67910)
(J:67910)
(J:67910)
• develop a stiff, uncoordinated gait (J:67910)
• develop a stiff, uncoordinated gait (J:67910)

craniofacial
• frequently exhibit uneven wearing of the teeth (J:67910)
• frequently exhibit uneven wearing of the teeth (J:67910)

endocrine/exocrine glands
(J:67910)
(J:67910)

growth/size/body
• frequently exhibit uneven wearing of the teeth (J:67910)
• frequently exhibit uneven wearing of the teeth (J:67910)
(J:67910)
(J:67910)

reproductive system
(J:67910)
(J:67910)

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
02/02/2016
MGI 6.02
The Jackson Laboratory