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Gene Expression Data
Assay Details
Assay
Reference: J:297493 Matos-Rodrigues GE, et al., Progenitor death drives retinal dysplasia and neuronal degeneration in a mouse model of ATRIP-Seckel syndrome. Dis Model Mech. 2020 Oct 30;13(10):dmm045807
Assay type: Immunohistochemistry
MGI Accession ID: MGI:6506432
Gene symbol: Stx1a
Gene name: syntaxin 1A (brain)
Results
Specimen 3C AtripCtrl: postnatal day 14 (more )
Structure Level Pattern Image Note
TS28: neural retina Present Regionally restricted Expression was detected in amacrine cells.

Specimen 3C Atripalpha-Cre: postnatal day 14; Atriptm1.1Pof/Atriptm1.1Pof, Tg(Pax6-cre,GFP)2Pgr/0 (more )
Note: Conditional mutant.
Structure Level Pattern Image Note
TS28: neural retina Present Regionally restricted There was a slight increase in the proportion of immunopositive cells in the mutant.


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
04/16/2024
MGI 6.23
The Jackson Laboratory