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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mecp2tm1.1Jtc
targeted mutation 1.1, Joseph T Coyle
MGI:5568206
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mecp2tm1.1Jtc/Mecp2tm1.1Jtc involves: 129S6/SvEvTac * 129/SvJ MGI:5568215
ht2
Mecp2tm1.1Jtc/Mecp2+ involves: 129S6/SvEvTac * C57BL/6 MGI:5568998
ot3
Mecp2tm1.1Jtc/Y involves: 129S6/SvEvTac * 129/SvJ MGI:5568214
ot4
Mecp2tm1.1Jtc/Y involves: 129S6/SvEvTac * C57BL/6 MGI:5568994


Genotype
MGI:5568215
hm1
Allelic
Composition
Mecp2tm1.1Jtc/Mecp2tm1.1Jtc
Genetic
Background
involves: 129S6/SvEvTac * 129/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1.1Jtc mutation (1 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• female mice exhibit hindlimb clasping by 6 months of age

mortality/aging
• most females die before a year, however, some females survive to more than a year
• lifespan is longer than in males

respiratory system
• female mice exhibit breathing irregularities by 6 months of age




Genotype
MGI:5568998
ht2
Allelic
Composition
Mecp2tm1.1Jtc/Mecp2+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1.1Jtc mutation (1 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• object memory is intact at 1 hour, but impaired at 24 hours after object training, however, the impairment occurs to a lesser degree than in males
• females freeze for a larger percentage of time during the acquisition phase of the associative fear conditioning task as compared to wild type on day 80, but not on postnatal day 40
• reduced latency to fall from rotarod as compared to wild type on postnatal day 30
• reduced ambulatory movements (two consecutive beam breaks) as compared to wild type on postnatal day 63
• reduced fine motor movements (repeated breaking of same beam) as compared to wild type on postnatal day 63
• tonic-clonic seizures observed in 3.7% (5/136) of females
• seizures appear to be stimulated by touch
• mice die within a month of seizures

growth/size/body
• reduced body weight as compared to wild type on postnatal day 64

nervous system
• tonic-clonic seizures observed in 3.7% (5/136) of females
• seizures appear to be stimulated by touch
• mice die within a month of seizures

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rett syndrome DOID:1206 OMIM:312750
OMIM:613454
J:209637




Genotype
MGI:5568214
ot3
Allelic
Composition
Mecp2tm1.1Jtc/Y
Genetic
Background
involves: 129S6/SvEvTac * 129/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1.1Jtc mutation (1 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• male mice exhibit hindlimb clasping by 7 weeks of age
• male mice exhibit hypoactivity
• male mice exhibit forelimb stereotypies

growth/size/body
• male mice exhibit great variability in weight
• some male mice exhibit failure to thrive
• a subset of male mice have excessive weight gain

mortality/aging
• average lifespan in males is 85.8 +/-24.2 days

respiratory system
• male mice exhibit breathing irregularities by 7 weeks of age




Genotype
MGI:5568994
ot4
Allelic
Composition
Mecp2tm1.1Jtc/Y
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1.1Jtc mutation (1 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice appear lethargic by postnatal day 50
• object memory is intact at 1 hour, but impaired 24 hours after object training
• increased time spent in open arms as compared to wild type on postnatal day 25
• increased number of open arm entries as compared to wild type on on postnatal day 25
• increased travel distance in zero maze as compared to wild type control on postnatal day 25
• males freeze for a larger percentage of time as compared to wild type on postnatal day 35, however, males freeze for smaller percentage of time on both context and cued memory tasks
• reduced latency to fall from rotarod as compared to wild type on postnatal day 29
• decreased forelimb grip strength as compared to wild type on postnatal day 25
• reduced ambulatory movements (two consecutive beam breaks) as compared to wild type first observed at postnatal day 24
• reduced fine motor movements (repeated breaking of same beam) as compared to wild type observed at postnatal day 43

growth/size/body
• reduced body weight as compared to wild type on postnatal day 25

integument
• ruffled fur observed by postnatal day 50

respiratory system
• respiratory abnormalities observed by postnatal day 50

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rett syndrome DOID:1206 OMIM:312750
OMIM:613454
J:209637





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory