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:2153870
Gene symbol: Gli1
Gene name: GLI-Kruppel family member GLI1
Probe: Gli cDNA1
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Assay notes: The fixation used for this assay was 3.5% paraformaldehyde.
Results
Specimen 3F: embryonic day 11.5; Ptch1tm1Mps/Ptch1+ (more )
Structure Level Pattern Image Note
TS19: hindlimb bud Present Regionally restricted 3F Expression is posterior.

Specimen 3G: embryonic day 11.5; Ptch1mes/Ptch1tm1Mps (more )
Structure Level Pattern Image Note
TS19: hindlimb bud Present Regionally restricted 3G Expression is posterior and there is ectopic expesssion anterior.

Specimen 3H: embryonic day 12.0 (more )
Structure Level Pattern Image Note
TS20: hindlimb Present Regionally restricted 3H Expression is posterior.

Specimen 3I: embryonic day 12.0; Ptch1mes/Ptch1tm1Mps (more )
Structure Level Pattern Image Note
TS20: hindlimb Present Regionally restricted 3I Expression is posterior and there is ectopic expression anterior.


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