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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:7857236
Gene symbol: Fgfr2
Gene name: fibroblast growth factor receptor 2
Probe: Fgfr2-pF, Fgfr2-pR
Probe preparation: labelled with SYBR green
Assay notes: Quantitative RT-PCR. Relative expression was normalized to B2m.
Results Image: 6F Fgfr2
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
Control E16.5 TS24: cochlea epithelium Present (a) Not Specified; total RNA Not Specified Not Specified
Esrp1-/- E16.5 TS24: cochlea epithelium Present (b) Not Specified; total RNA involves: 129S4/SvJae * C57BL/6 Esrp1tm1.2Rpc/Esrp1tm1.2RpcNot Specified
Notes:
(a) Predominant expression of epithelial Fgfr2-IIIb isoform.
(b) Predominant expression of mesenchymal Fgfr2-IIIc isoform.
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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03/25/2025
MGI 6.24 		The Jackson Laboratory