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Gene Expression Data
Assay Details
Assay
Reference: J:127117 Pitteloud N, et al., Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proc Natl Acad Sci U S A. 2007 Oct 30;104(44):17447-52
Assay type: RNA in situ
MGI Accession ID: MGI:7488193
Gene symbol: Prokr2
Gene name: prokineticin receptor 2
Probe: Prokr2 probe
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Fluorescence
Results
Specimen 5A: embryonic day 13.5 (more )
Note: Double labeled: green - Prokr2; red - Gnrh1 (assay MGI:7488190).
Structure Level Pattern Image Note
TS22: vomeronasal organ Present 5C , 5A Prokr2 expression did not colocalize with Gnrh1.
Specimen 5D: embryonic day 13.5 (more )
Note: Double labeled: green - Prokr2; red - Gnrh1 (assay MGI:7488190).
Structure Level Pattern Image Note
TS22: basal forebrain Present 5D , 5F Prokr2 expression did not colocalize with Gnrh1.
Specimen 5G: postnatal adult (more )
Note: Double labeled: green - Prokr2; red - Gnrh1 (assay MGI:7488190).
Structure Level Pattern Image Note
TS28: preoptic area Present 5E , 5G Prokr2 expression did not colocalize with Gnrh1.
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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03/18/2025
MGI 6.24 		The Jackson Laboratory