About   Help   FAQ
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:2153856
Gene symbol: Shh
Gene name: sonic hedgehog
Probe: Shh cDNA2
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Assay notes: Fixation for the whole mounted embryos in this assay was in 3.5% paraformaldehyde.
Results
Specimen 3D: embryonic day 12.0; Ptch1tm1Mps/Ptch1+ (more )
Structure Level Pattern Image Note
TS20: hindlimb Present Regionally restricted 3D Expression is in the posterior mesenchyme. Expression in this mutant is the same as in wild-type embryos.

Specimen 3E: embryonic day 12.0; Ptch1mes/Ptch1tm1Mps (more )
Structure Level Pattern Image Note
TS20: hindlimb Present Regionally restricted 3E There is ectopic expression at the anterior margin ot the limb bud. This expression is very weak in some cases. There is also normal expression in the posterior.

Specimen 5E: embryonic day 11.5; Ptch1tm1Mps/Ptch1+ (more )
Structure Level Pattern Image Note
TS19: neural tube floor plate Present 5E
TS19: notochord Present 5E

Specimen 5F: embryonic day 11.5; Ptch1mes/Ptch1tm1Mps (more )
Structure Level Pattern Image Note
TS19: neural tube floor plate Present 5F
TS19: notochord Present 5F


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/30/2025
MGI 6.24
The Jackson Laboratory