Gene Expression Data
Assay Details
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Assay
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Reference:
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J:72380
Makino S, et al., A Spontaneous Mouse Mutation, mesenchymal dysplasia (mes), Is Caused by a Deletion of the Most C-Terminal Cytoplasmic Domain of patched (ptc). Dev Biol. 2001 Nov 1;239(1):95-106
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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:2153916
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Gene symbol:
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Ptch1
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Gene name:
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patched 1
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Probe:
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M2-3
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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
5G:
embryonic day 12.5; Ptch1tm1Mps/Ptch1 +
(more  )
Specimen
5G:
(close  )
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Genetic Background:
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involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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Mutant Allele(s):
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Ptch1tm1Mps/Ptch1+
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Age:
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embryonic day 12.5
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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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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Cryosection
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Specimen
5H:
(close )
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Genetic Background:
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involves: 129S1/Sv * 129X1/SvJ * C3HeB/Fe * C57BL/6 * CBA/J
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Mutant Allele(s):
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Ptch1mes/Ptch1tm1Mps
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Age:
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embryonic day 12.5
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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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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Cryosection
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| Structure |
Level |
Pattern |
Image |
Note |
| TS20: trunk mesenchyme |
Present |
Regionally restricted |
5H
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The expression in this mutant is the same as in the heterozygote shown in FIG. 5G.
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Analysis Tools
