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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Scyl2tm1.1Spel
targeted mutation 1.1, Stephane Pelletier
MGI:5752500
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Scyl2tm1.1Spel/Scyl2tm1.1Spel involves: 129S6/SvEvTac * C57BL/6 MGI:5752572
cn2
Baxtm2Sjk/Baxtm2Sjk
Scyl2tm1.1Spel/Scyl2tm1.1Spel
Tg(Nes-cre)1Kln/0
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * SJL MGI:5752574
cn3
Scyl2tm1.1Spel/Scyl2tm1.1Spel
Tg(Nes-cre)1Kln/0
involves: 129S6/SvEvTac * C57BL/6 * SJL MGI:5752573


Genotype
MGI:5752572
hm1
Allelic
Composition
Scyl2tm1.1Spel/Scyl2tm1.1Spel
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scyl2tm1.1Spel mutation (0 available); any Scyl2 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are viable, fertile, and exhibit no overt abnormalities




Genotype
MGI:5752574
cn2
Allelic
Composition
Baxtm2Sjk/Baxtm2Sjk
Scyl2tm1.1Spel/Scyl2tm1.1Spel
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Baxtm2Sjk mutation (1 available); any Bax mutation (23 available)
Scyl2tm1.1Spel mutation (0 available); any Scyl2 mutation (36 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected mice are present at weaning

growth/size/body

behavior/neurological
N
• mice do not exhibit limb clasping as in Scyl2tm1.1Spel/Scyl2tm1.1Spel Tg(Nes-cre)1Kln mice

nervous system
N
• mice exhibit nor brain abnormalities unlike in Scyl2tm1.1Spel/Scyl2tm1.1Spel Tg(Nes-cre)1Kln mice




Genotype
MGI:5752573
cn3
Allelic
Composition
Scyl2tm1.1Spel/Scyl2tm1.1Spel
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scyl2tm1.1Spel mutation (0 available); any Scyl2 mutation (36 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• just over half of mice die within 24 h of birth due to malnutrition

reproductive system
• in mice that survive beyond the neonatal period

nervous system
• in the CA3 region
• in the CA3 region
• of pyramidal CA3 neurons at P4.5, P6.5 and P8.5
• in the granular layer of the cerebellum of P6.5
• decreased cellularity by P14.5 and P21.5
• near complete absence of pyramidal CA3 neurons beginning between P6.5 and P8.5
• near complete absence of pyramidal CA3 neurons
• however, CA3 neuron loss is prevented by treatment with MK-801, an irreversible NMDA receptor antagonist
• however, the CA1 region is normal in cellularity
• decreased field excitatory postsynaptic potential in hippocampal slices

behavior/neurological
• sensory-motor deficits and abnormal behaviors in mice that survive beyond the neonatal period
• depression-like behavior (lower latency to immobility in a tail suspension test) in mice that survive beyond the neonatal period
• however, time spent immobile is normal
• in mice that survive beyond the neonatal period
• in mice that survive beyond the neonatal period
• detected using an inverted cage grid in mice that survive beyond the neonatal period

growth/size/body
• detected at 2 weeks in mice that survive beyond the neonatal period
• detected at 2 weeks in mice that survive beyond the neonatal period

hematopoietic system
• in the CA3 region

cellular
• in the CA3 region
• in the CA3 region
• of pyramidal CA3 neurons at P4.5, P6.5 and P8.5
• in the granular layer of the cerebellum of P6.5

immune system
• in the CA3 region





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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory