Gene Expression Data
Assay Details
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Assay
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Reference:
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J:114410
Jumlongras D, et al., A nonsense mutation in MSX1 causes Witkop syndrome. Am J Hum Genet. 2001 Jul;69(1):67-74
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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:6116300
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Gene symbol:
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Msx1
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Gene name:
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msh homeobox 1
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Probe:
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Msx1 cDNA18
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Probe preparation:
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Antisense labelled with P33 RNA
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Visualized with:
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Autoradiography
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Results
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Specimen
3B:
embryonic day 16.5
(more  )
Specimen
3B:
(close  )
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Genetic Background:
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involves: 129S4/SvJae * BALB/c
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Age:
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embryonic day 16.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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| Structure |
Level |
Pattern |
Image |
Note |
| TS24: digit mesenchyme |
Present |
Regionally restricted |
3B
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Expression is in the mesenchyme subjacent to the epithelium of the nail bed.
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Analysis Tools
