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:2153972
Gene symbol: Nkx2-2
Gene name: NK2 homeobox 2
Probe: Nkx2-2 probe1
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen 6E: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: future spinal cord Present Regionally restricted 6E Expression is ventral in the progenitors of the V3 interneurons.

Specimen 6F: embryonic day 10.5; Ptch1tm1Mps/Ptch1+ (more )
Structure Level Pattern Image Note
TS17: future spinal cord Present Regionally restricted 6F Expression is ventral in the progenitors of the V3 interneurons. Expression in this mutant is the same as in wild-type embryos.

Specimen 6G: embryonic day 10.5; Ptch1mes/Ptch1mes (more )
Structure Level Pattern Image Note
TS17: future spinal cord Present Regionally restricted 6G Expression is ventral in the progenitors of the V3 interneurons. Expression in this mutant is the same as in wild-type embryos.

Specimen 6H: embryonic day 10.5; Ptch1mes/Ptch1tm1Mps (more )
Structure Level Pattern Image Note
TS17: future spinal cord Present Regionally restricted 6H Expression is ventral in the progenitors of the V3 interneurons. 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/18/2025
MGI 6.24
The Jackson Laboratory