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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mecp2tm1Pplt
targeted mutation 1, Patrick P L Tam
MGI:3800596
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Mecp2tm1Pplt/Mecp2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3801488
ot2
Mecp2tm1Pplt/Y involves: 129S1/Sv * 129X1/SvJ MGI:3801486
ot3
Mecp2tm1Pplt/Y involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn MGI:3801485
ot4
Mecp2tm1Pplt/Y involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3801487
ot5
Mecp2tm1Pplt/0 involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn MGI:3801484


Genotype
MGI:3801488
ht1
Allelic
Composition
Mecp2tm1Pplt/Mecp2+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Pplt mutation (0 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• motor defect on initial exposure to rotarod test
• rotarod performance normalized when maintained in an "enriched" environment
• rotarod performance improves over 5 days of training
• rotarod performance remains deficient relative to wild-type kept in a standard environment
• coordination improvement acquired with training is lost in the weeks subsequent to training
• "enriched" environment prevents coordination deficiency from developing
• reduced rearing activity regardless of the environment

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rett syndrome DOID:1206 OMIM:312750
OMIM:613454
J:137344




Genotype
MGI:3801486
ot2
Allelic
Composition
Mecp2tm1Pplt/Y
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Pplt mutation (0 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• dead by 5 weeks




Genotype
MGI:3801485
ot3
Allelic
Composition
Mecp2tm1Pplt/Y
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Pplt mutation (0 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• 50% dead by 7 weeks

growth/size/body
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• reported for this background
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• progressive weight loss after 11 weeks of age
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• growth normal until 5 weeks of age
• growth retardation after 5 weeks

behavior/neurological
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• accompanies weight loss

craniofacial
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• reported for this background

skeleton
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• reported for this background




Genotype
MGI:3801487
ot4
Allelic
Composition
Mecp2tm1Pplt/Y
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Pplt mutation (0 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 50% lethality by 8 weeks

growth/size/body
• marked weight loss starting about 1 week before death
• failure to thrive after 5 weeks
• mean weight 15 g at 8 weeks comppared to 21 g for controls

behavior/neurological
N
• general locomotion is normal through 6 weeks of age
• reduced ability to associate foot shock with context
• reduced ability to associate auditory cue to footshock
• as measured on an elevated + maze
• clasping of hind limbs when lifted by the tail
• coordination remains impaired through week 9 (J:137344)
• time spent on an accelerating rotarod about 1/3 that of controls (J:137513)
• no improvement with successive trials (J:137513)
• splayed limbs
• less rearing behavior when maintained in a standard environment
• lower activity levels on free wheels in mice before onset of breathing problems or seizures
• episodes of seizures

nervous system
• episodes of seizures

respiratory system
• labored breathing

integument
• erect whiskers

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rett syndrome DOID:1206 OMIM:312750
OMIM:613454
J:137344




Genotype
MGI:3801484
ot5
Allelic
Composition
Mecp2tm1Pplt/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mecp2tm1Pplt mutation (0 available); any Mecp2 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• 50% dead by 7 weeks

growth/size/body
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• reported for this background
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• progressive weight loss after 11 weeks of age
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• growth normal for first 6-7 weeks of life
• growth retardation after 7 weeks

behavior/neurological
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• accompanies weight loss

craniofacial
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• reported for this background

skeleton
• these mice retain the neo insert in the Mecp2tm1Pplt allele
• reported for this background





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