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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Olig2tm1And
targeted mutation 1, David J Anderson
MGI:2179515
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Olig1tm1And/Olig1tm1And
Olig2tm1And/Olig2tm1And
involves: 129 * C57BL/6J MGI:3810327
cx2
Olig1tm1And/Olig1tm1And
Olig2tm1And/Olig2tm1And
Tg(Olig2)#Wdr/?
Not Specified MGI:5696832


Genotype
MGI:3810327
cx1
Allelic
Composition
Olig1tm1And/Olig1tm1And
Olig2tm1And/Olig2tm1And
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Olig1tm1And mutation (0 available); any Olig1 mutation (13 available)
Olig2tm1And mutation (0 available); any Olig2 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• though present at E18.5, no live births are observed

nervous system
• no oligodendrocyte progenitors are detected in the hindbrain and spinal cord
• neuroepithelial cells differentiate into astrocytes instead of oligodendrocytes
• no oligodendrocyte progenitors are detected in the hindbrain and spinal cord
• at E10.5, most Isl1/2+ Hb9+ motor neurons are lost at all axial levels in the spinal cord
• no projecting axons are observed in the ventral root
• at E13.5, somatic and visceral motor neurons are absent from the spinal cord
• at E16.5, somatic but not visceral motor neurons are absent from the hindbrain
• at E10.5 and E13.5, the number of V2 interneurons is increased compared to in wild-type mice and they are expanded ventrally
• however, the numbers and distribution of V1 and V3 interneurons are normal

growth/size/body
• at E18.5

cellular
• no oligodendrocyte progenitors are detected in the hindbrain and spinal cord




Genotype
MGI:5696832
cx2
Allelic
Composition
Olig1tm1And/Olig1tm1And
Olig2tm1And/Olig2tm1And
Tg(Olig2)#Wdr/?
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Olig1tm1And mutation (0 available); any Olig1 mutation (13 available)
Olig2tm1And mutation (0 available); any Olig2 mutation (46 available)
Tg(Olig2)#Wdr mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• oligodendrocyte markers are absent in the spinal cord at E17.5 but present in controls
• oligodendrocyte markers are present at relatively low levels relative to controls at E18.5
• oligodendrocyte markers are present at levels comparable to controls at 3 days of age





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