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Gene Expression Data
Assay Details
Assay
Reference: J:158434 Liu X, et al., Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2. Am J Hum Genet. 2010 Jan;86(1):65-71
Assay type: RNA in situ
MGI Accession ID: MGI:4440487
Gene symbol: Prps1
Gene name: phosphoribosyl pyrophosphate synthetase 1
Results
Specimen 4A: embryonic day 18.5 (more )
Structure Level Pattern Image Note
TS26: cochlear duct epithelium Present Regionally restricted 4A Expression is in the cochlear hair cells, the Claudius cells, and the greater epithelial ridge, but not in other cochlear supporting cells.
TS26: cochlear duct mesenchyme Absent 4A
Specimen 4C: postnatal day 6 (more )
Structure Level Pattern Image Note
TS28: cochlear duct Present Regionally restricted 4C Expression is in the cochlear hair cells, the Claudius cells, and is reduced in the greater epithelial ridge.
TS28: cochlear ganglion Present 4C
Specimen Not shown: embryonic day 18.5 (more )
Structure Level Pattern Image Note
TS26: crista ampullaris Present Regionally restricted Expression is in crista hair cells.
TS26: utricle epithelium Present Regionally restricted Expression is in hair cells.
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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory