About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Clp1em1Slac
endonuclease-mediated mutation 1, Susan L Ackerman
MGI:6759435
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Clp1em1Slac/Clp1em1Slac C57BL/6J-Clp1em1Slac/J MGI:6771475
ht2
Clp1em1Slac/Clp1em2Slac C57BL/6J-Clp1em1Slac/Clp1em2Slac MGI:6771478


Genotype
MGI:6771475
hm1
Allelic
Composition
Clp1em1Slac/Clp1em1Slac
Genetic
Background
C57BL/6J-Clp1em1Slac/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Clp1em1Slac mutation (1 available); any Clp1 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• females, but not males, weight less than wild-type mice at 1 month of age
• both females and males weigh 21-30% less than wild-type mice at 5 and 9 months of age

behavior/neurological
• mice develop a mild tremor by 4 months of age
• 5-month-old mice, but not 1-month-old mice, perform poorly on the accelerating rotarod test, with rotarod durations of 51% of wild-type values
• 5-month-old mice, but not 1-month-old mice, perform poorly on the rolling wire-hang test, with wire hang durations of 39% of wild-type values
• mice develop a halting gait by 4 months of age
• 5-month-old mice, but not 1-month-old mice, perform poorly on the treadmill task, with treadmill walking percentages of 28% of wild-type values

nervous system
• large neurons in the dentate nuclei are less abundant in 9-month-old mice
• however, aged mice exhibit normal cerebellar measurements

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
pontocerebellar hypoplasia type 10 DOID:0060279 OMIM:615803
J:311491




Genotype
MGI:6771478
ht2
Allelic
Composition
Clp1em1Slac/Clp1em2Slac
Genetic
Background
C57BL/6J-Clp1em1Slac/Clp1em2Slac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Clp1em1Slac mutation (1 available); any Clp1 mutation (22 available)
Clp1em2Slac mutation (1 available); any Clp1 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than the expected number of pups are seen at 1-2 weeks of age, but not at P0, indicating increased mortality during the first 2 weeks after birth

growth/size/body
• mice weigh less than wild-type mice at 1 month of age, but not at P14, and are half the weight of wild-type mice at 5 months of age

behavior/neurological
• mice develop a tremor by 1 month of age
• 1-month-old mice perform poorly on the accelerating rotarod test, with a latency to fall of 20% of that of wild-type mice
• 5-month-old mice are incapable of performing the accelerating rotarod test
• 1-month-old mice exhibit decreased grip strength in the rolling wire-hang test, with no mice reaching the halfway point of the trail in ability to hang from the wire loop
• 5-month-old mice are incapable of performing the rolling wire-hang test
• 5-month-old mice exhibit rigid, splayed hindlimbs
• mice develop an altered gait by 1 month of age
• 1-month-old mice are impaired on the treadmill task, with the average mouse walking for less than 1/3 of the time
• 5-month-old mice are incapable of performing the treadmill task

limbs/digits/tail
• 5-month-old mice exhibit curled forepaws

nervous system
• cross-sectional area of the cerebellar hemispheres is decreased at 1 month of age, but not at P14
• cross-sectional area of the vermis is decreased at 1 month of age, but not at P14
• mice exhibit death of neurons in the deep cerebellar nuclei, with large neurons in the dentate nuclei being 85% less numerous at 5 months of age, but not at P14
• loss of deep cerebellar nuclei neurons in the fastigial and interposed nuclei, with 73% and 79% fewer larger neurons at 5 months of age
• mice show degeneration of spinal cord neurons, having 28% and 45% fewer cervical spinal motor neurons at 3 and 5 months of age, respectively and 14% fewer NeuN+ cells
• however. mice have normal numbers of cervical spinal motor neurons at P14 and 1 month of age
• spinal cord appears smaller

skeleton
• severe kyphosis by 5 months of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
pontocerebellar hypoplasia type 10 DOID:0060279 OMIM:615803
J:311491





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory