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Gene Expression Data
Assay Details
Assay
Reference: 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
Assay type: RNA in situ
MGI Accession ID: MGI:2153929
Gene symbol: Pax3
Gene name: paired box 3
Probe: Pax3 probe2
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen 6A: embryonic day 11.5 (more )
Structure Level Pattern Image Note
TS19: future spinal cord Present Regionally restricted 6A Expression is in the dorsal half.

Specimen 6B: embryonic day 11.5; Ptch1tm1Mps/Ptch1+ (more )
Structure Level Pattern Image Note
TS19: future spinal cord Present Regionally restricted 6B Expression is in the dorsal half. Expression in this mutant is the same as in wild-type embryos.

Specimen 6C: embryonic day 11.5; Ptch1mes/Ptch1mes (more )
Structure Level Pattern Image Note
TS19: future spinal cord Present Regionally restricted 6C Expression is in the dorsal half. Expression in this mutant is the same as in wild-type embryos.

Specimen 6D: embryonic day 11.5; Ptch1mes/Ptch1tm1Mps (more )
Structure Level Pattern Image Note
TS19: future spinal cord Present Regionally restricted 6D Expression is in the dorsal half. Expression in this mutant is the same as in wild-type embryos.


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
03/25/2025
MGI 6.24
The Jackson Laboratory