Gene Expression Data
Assay Details
Assay
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Reference:
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J:319706
Silachev D, et al., Mouse models characterize GNAO1 encephalopathy as a neurodevelopmental disorder leading to motor anomalies: from a severe G203R to a milder C215Y mutation. Acta Neuropathol Commun. 2022 Jan 28;10(1):9
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:7425418
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Gene symbol:
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Pou3f2
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Gene name:
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POU domain, class 3, transcription factor 2
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Results
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Specimen
S4A +/+:
embryonic day 18.5
(more )
Specimen
S4A +/+:
(close )
Genetic Background:
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involves: C57BL/6J
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Age:
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embryonic day 18.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
S4A C215Y/+:
embryonic day 18.5; Gnao1em2Katv/Gnao1 +
(more )
Specimen
S4A C215Y/+:
(close )
Genetic Background:
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involves: C57BL/6J
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Mutant Allele(s):
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Gnao1em2Katv/Gnao1+
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Age:
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embryonic day 18.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Specimen
S4A C215Y/C215Y:
(close )
Genetic Background:
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involves: C57BL/6J
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Mutant Allele(s):
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Gnao1em2Katv/Gnao1em2Katv
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Age:
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embryonic day 18.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Paraffin
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Structure |
Cell Type |
Level |
Pattern |
Image |
Note |
TS26: frontal cortex |
cerebral cortex neuron |
Present |
Regionally restricted |
S4A C215Y/C215Y Merged
,
S4A C215Y/C215Y Brn2
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A decrease in immunopositive cells in layers II-V in the motor cortex was statistically significant for the homozygous mutant compared with wild type.
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