Gene Expression Data
Assay Details
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Assay
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Reference:
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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
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Assay type:
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RNA in situ
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MGI Accession ID:
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MGI:2178635
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Gene symbol:
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Lfng
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Gene name:
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LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
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Probe:
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Lfng probe-1
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Probe preparation:
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Antisense labelled with digoxigenin RNA
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Visualized with:
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Alkaline phosphatase
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Results
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Specimen
6A:
embryonic day 9.5; Dll3tm1Rbe/Dll3 +
(more  )
Specimen
6A:
(close  )
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Genetic Background:
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involves: 129P2/Ola * C57BL/6
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Mutant Allele(s):
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Dll3tm1Rbe/Dll3+
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Age:
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embryonic day 9.5
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Age Note:
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Age of embryo at noon of plug day not specified in reference.
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Sex:
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Not Specified
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Type:
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whole mount
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Fixation:
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Bouin's Fixative
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| Structure |
Level |
Pattern |
Image |
Note |
| TS15: tail unsegmented mesenchyme |
Present |
Regionally restricted |
6A
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Two domains of expression: rostrally, 1 or 2 bands (the anteriormost just caudal to the forming somite boundary); caudally, extending to the primitive streak.
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Specimen
6B:
(close )
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Genetic Background:
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involves: 129P2/Ola * C57BL/6
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Mutant Allele(s):
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Dll3tm1Rbe/Dll3tm1Rbe
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Age:
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embryonic day 9.5
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Age Note:
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Age of embryo at noon of plug day not specified in reference.
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Sex:
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Not Specified
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Type:
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whole mount
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Fixation:
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Bouin's Fixative
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Analysis Tools