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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dnajc11spc
spastic
MGI:5707591
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dnajc11spc/Dnajc11spc B6.Cg-Dnajc11spc MGI:5707632
cx2
Dnajc11spc/Dnajc11spc
Rag2tm1Fwa/Rag2tm1Fwa
involves: 129S6/SvEvTac * C57BL/6J MGI:5707633


Genotype
MGI:5707632
hm1
Allelic
Composition
Dnajc11spc/Dnajc11spc
Genetic
Background
B6.Cg-Dnajc11spc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnajc11spc mutation (1 available); any Dnajc11 mutation (57 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• however, the phenotype is rescued in mice crossing to a line expressing the human gene

hematopoietic system
N
• myeloid populations are normal
• with loss of patchy appearance
• 20% of wild-type in moribund mice
• starting at P10 with massive degeneration and loss of organ architecture
• however, the phenotype is rescued in mice crossing to a line expressing the human gene
• slightly in the thymus
• slightly in the blood
• four-fold in the thymus
• two-fold in the spleen
• four-fold in the thymus
• two-fold in the spleen
• profound in the blood
• however, the phenotype is rescued in mice crossing to a line expressing the human gene
• in the spleen
• starting at P10 with massive degeneration
• however, the phenotype is rescued in mice crossing to a line expressing the human gene

behavior/neurological
• limb tremors
• in hindlimbs as early as P10
• as early as P10

nervous system
• arising from either mitochondria or endoplasmic reticulum in the cell bodies of motor neurons mainly in the medulla
• vacuoles arising from either mitochondria or endoplasmic reticulum are detected in the cell bodies of motor neurons mainly in the medulla
• abnormal mitochondria in the bodies of motor neurons but not the dendrites or synapses
• however, nuclei and nucleoli are normal

growth/size/body
• progressive
• however, the phenotype is rescued in mice crossing to a line expressing the human gene

cellular

endocrine/exocrine glands
• with loss of patchy appearance
• 20% of wild-type in moribund mice
• starting at P10 with massive degeneration and loss of organ architecture
• however, the phenotype is rescued in mice crossing to a line expressing the human gene

immune system
• with loss of patchy appearance
• 20% of wild-type in moribund mice
• starting at P10 with massive degeneration and loss of organ architecture
• however, the phenotype is rescued in mice crossing to a line expressing the human gene
• slightly in the thymus
• four-fold in the thymus
• two-fold in the spleen
• four-fold in the thymus
• two-fold in the spleen
• profound in the blood
• however, the phenotype is rescued in mice crossing to a line expressing the human gene
• in the spleen
• starting at P10 with massive degeneration
• however, the phenotype is rescued in mice crossing to a line expressing the human gene

muscle
• starting at the hindlimb and progressing to the forelimbs
• however, the phenotype is rescued in mice crossing to a line expressing the human gene




Genotype
MGI:5707633
cx2
Allelic
Composition
Dnajc11spc/Dnajc11spc
Rag2tm1Fwa/Rag2tm1Fwa
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnajc11spc mutation (1 available); any Dnajc11 mutation (57 available)
Rag2tm1Fwa mutation (48 available); any Rag2 mutation (117 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice exhibit the same clinical symptoms as in Dnajc11spc homozygotes





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory