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Gene Expression Data
Assay Details
Assay
Reference: J:75954 Dunwoodie SL, et al., Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development. 2002 Apr;129(7):1795-806
Assay type: RNA in situ
MGI Accession ID: MGI:2178634
Gene symbol: Sptbn1
Gene name: spectrin beta, non-erythrocytic 1
Probe: pSPORT-beta-spectrin2
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen 5G,H: embryonic day 8.5; Dll3tm1Rbe/Dll3+ (more )
Structure Level Pattern Image Note
TS13: trunk somite Present Regionally restricted 5H , 5G Authors state that expression in the center of somites marks epithelialization of mesenchyme to form somites.

Specimen 5I,K: embryonic day 8.5; Dll3tm1Rbe/Dll3tm1Rbe (more )
Structure Level Pattern Image Note
TS13: trunk somite Present Regionally restricted 5J , 5I Authors report that expression in somites is diffuse.

Specimen 5K,L: embryonic day 8.5; Dll3tm1Rbe/Dll3tm1Rbe (more )
Structure Level Pattern Image Note
TS13: trunk somite Present Regionally restricted 5K , 5L Authors report that expression in somites is diffuse.


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
04/30/2024
MGI 6.23
The Jackson Laboratory