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Gene Expression Data
Assay Details
Assay
Reference: J:245876 Rohacek AM, et al., ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development. Dev Cell. 2017 Nov 06;43(3):318-331.e5
Assay type: RT-PCR
MGI Accession ID: MGI:7857237
Gene symbol: Fgfr3
Gene name: fibroblast growth factor receptor 3
Probe: Fgfr3-pF, Fgfr3-pR
Probe preparation: labelled with SYBR green
Assay notes: Quantitative RT-PCR. Relative expression was normalized to B2m.
Results Image: 6F Fgfr3
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
Control E16.5 TS24: cochlea epithelium Present Not Specified; total RNA Not Specified Not Specified
Esrp1-/- E16.5 TS24: cochlea epithelium Present Not Specified; total RNA involves: 129S4/SvJae * C57BL/6 Esrp1tm1.2Rpc/Esrp1tm1.2RpcNot Specified
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
03/25/2025
MGI 6.24 		The Jackson Laboratory