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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:2178633
Gene symbol: Mesp2
Gene name: mesoderm posterior 2
Probe: MesP2 cDNA2
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen 5A,B: embryonic day 9.5; Dll3tm1Rbe/Dll3+ (more )
Structure Level Pattern Image Note
TS15: tail unsegmented mesenchyme Present Regionally restricted 5B , 5A Anterior boundary of expression approximately 1 somite width caudal to the posterior boundary of the last formed somite.

Specimen 5C,D: embryonic day 9.5; Dll3tm1Rbe/Dll3tm1Rbe (more )
Structure Level Pattern Image Note
TS15: tail unsegmented mesenchyme Present Regionally restricted 5D , 5C Expression boundary approximately 3 somite widths posterior to the last formed somite.

Specimen 5E,F: embryonic day 9.5; Dll3tm1Rbe/Dll3tm1Rbe (more )
Structure Level Pattern Image Note
TS15: tail unsegmented mesenchyme Present Regionally restricted 5E , 5F No epithelial somites were detected in this -/- embryo; authors state the band of expression is an equivalent position to that seen in the +/- embryo.


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
05/21/2024
MGI 6.23
The Jackson Laboratory