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Gene Expression Data
Assay Details
Assay
Reference: 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
Assay type: Immunohistochemistry
MGI Accession ID: MGI:7425418
Gene symbol: Pou3f2
Gene name: POU domain, class 3, transcription factor 2
Antibody: anti-Brn2 (sc-393324)
Detection system: Secondary antibody coupled to Alexa Fluor
Results
Specimen S4A +/+: embryonic day 18.5 (more )
Structure Cell Type Level Pattern Image Note
TS26: frontal cortex cerebral cortex neuron Present Regionally restricted S4A +/+ Brn2 , S4A +/+ Merged Expression was detected in layer II-V cortical neurons in the motor cortex.

Specimen S4A C215Y/+: embryonic day 18.5; Gnao1em2Katv/Gnao1+ (more )
Structure Cell Type Level Pattern Image Note
TS26: frontal cortex cerebral cortex neuron Present Regionally restricted S4A C215Y/+ Brn2 , S4A C215Y/+ Merged Expression was detected in layer II-V cortical neurons in the motor cortex.

Specimen S4A C215Y/C215Y: embryonic day 18.5; Gnao1em2Katv/Gnao1em2Katv (more )
Structure Cell Type Level Pattern Image Note
TS26: frontal cortex cerebral cortex neuron Present Regionally restricted S4A C215Y/C215Y Merged , S4A C215Y/C215Y Brn2 A decrease in immunopositive cells in layers II-V in the motor cortex was statistically significant for the homozygous mutant compared with wild type.


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)
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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory