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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:7488192
Gene symbol: Prokr2
Gene name: prokineticin receptor 2
Probe: Prokr2 probe
Probe preparation: Antisense labelled with digoxigenin RNA
Results
Specimen 4a: embryonic day 13.5 (more )
Structure Level Pattern Image Note
TS22: vomeronasal organ Present 4a , 4b
TS22: basal forebrain Present 4a , 4c
Specimen 4d: postnatal adult (more )
Structure Level Pattern Image Note
TS28: preoptic area Present 4d , 4e
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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05/07/2024
MGI 6.23 		The Jackson Laboratory