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Gene Expression Data
Assay Details
Assay
Reference: J:299667 Calame DJ, et al., Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic Dyskinesia. Neuroscience. 2020 Nov 10;448:272-286
Assay type: Immunohistochemistry
MGI Accession ID: MGI:7610589
Gene symbol: Slc17a7
Gene name: solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7
Antibody: VGLUT1 antibody (135 316)
Detection system: Secondary antibody coupled to Alexa Fluor 555
Results
Specimen 4D +/+: postnatal (more )
Note: Double labeled: red - Slc17a7; green - Prrt2 (assay MGI:7610588).
Structure Level Pattern Image Note
TS28: cerebellum granule cell layer Present 4D +/+ merge , 4D +/+ VGLUT1 Expressed in pre-synaptic locations.
TS28: cerebellum molecular layer Present 4D +/+ merge , 4D +/+ VGLUT1 Expressed in pre-synaptic locations.

Specimen 4D -/-: postnatal; Prrt2tm1d(KOMP)Wtsi/Prrt2tm1d(KOMP)Wtsi (more )
Note: Double labeled: red - Slc17a7; green - Prrt2 (assay MGI:7610588).
Structure Level Pattern Image Note
TS28: cerebellum granule cell layer Present 4D -/- merge , 4D -/- VGLUT1
TS28: cerebellum molecular layer Present 4D -/- merge , 4D -/- VGLUT1


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
04/23/2024
MGI 6.23
The Jackson Laboratory