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Gene Expression Data
Assay Details
Assay
Reference: J:72517 Hajihosseini MK, et al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3855-60
Assay type: RNA in situ
MGI Accession ID: MGI:7284945
Gene symbol: Fgfr2
Gene name: fibroblast growth factor receptor 2
Probe: FgfR2IIIb probe3
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen 5E +/+: embryonic day 18.5 (more )
Structure Level Pattern Image Note
TS26: suture Trace 5E +/+ Staining was barely detectable in calvarial sutures in the wild type mice.

Specimen 5E +/delta: embryonic day 18.5; Fgfr2tm2.3Dsn/Fgfr2+ (more )
Structure Level Pattern Image Note
TS26: suture Present Regionally restricted 5E +/delta Calvarial sutures showed elevated expression of the Fgfr2-IIIb isoform in the hemizygote.

Specimen 5I: embryonic day 18.0 (more )
Structure Level Pattern Image Note
TS26: sternebra Strong Regionally restricted 5I Strong expression was detected in the periosteal region of each sternebrae.

Specimen 5J: embryonic day 18.0; Fgfr2tm2.3Dsn/Fgfr2+ (more )
Structure Level Pattern Image Note
TS26: sternebra Strong Regionally restricted 5J Strong expression was detected on the periosteal region of each sternebrae. Expression was also detected in the hemi-sternebrae medial rims in hemizygotes.


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