About   Help   FAQ
Gene Expression Data
Assay Details
Assay
Reference: J:307192 Yadav PS, et al., Stat3 loss in mesenchymal progenitors causes Job syndrome-like skeletal defects by reducing Wnt/beta-catenin signaling. Proc Natl Acad Sci U S A. 2021 Jun 29;118(26):e2020100118
Assay type: RNA in situ
MGI Accession ID: MGI:6831054
Gene symbol: Phex
Gene name: phosphate regulating endopeptidase homolog, X-linked
Probe: Phex probe1
Probe preparation: Antisense labelled with digoxigenin RNA
Results
Specimen S6B Prrx1Cre;Stat3C/+: embryonic day 16.5; Stat3tm1Flv/Stat3+, Tg(Prrx1-cre)1Cjt/0 (more )
Note: Conditional mutant.
Structure Level Pattern Image Note
TS24: humerus Present Regionally restricted S6B Phex Prrx1Cre;Stat3C/+ Expression is in osetocytes.
Specimen S6B Prrx1Cre;Stat3C/C: embryonic day 16.5; Stat3tm1Flv/Stat3tm1Flv, Tg(Prrx1-cre)1Cjt/0 (more )
Note: Conditional mutant.
Structure Level Pattern Image Note
TS24: humerus Weak Regionally restricted S6B Phex Prrx1Cre;Stat3C/C
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
05/07/2024
MGI 6.23 		The Jackson Laboratory