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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: Immunohistochemistry
MGI Accession ID: MGI:7857198
Gene symbol: Bsnd
Gene name: barttin CLCNK type accessory beta subunit
Antibody: anti-Barttin
Detection system: Secondary antibody coupled to Alexa Fluor 488
Results
Specimen 5J: embryonic day 18.5 (more )
Structure Cell Type Level Pattern Image Note
TS26: cochlea epithelium strial marginal cell Present 5J

Specimen 5Q: embryonic day 18.5; Esrp1tm1.2Rpc/Esrp1tm1.2Rpc (more )
Structure Cell Type Level Pattern Image Note
TS26: cochlea epithelium strial marginal cell Trace 5Q Expression reduced or absent compared to control.

Specimen 7E: embryonic day 18.5 (more )
Structure Cell Type Level Pattern Image Note
TS26: cochlea epithelium strial marginal cell Present 7E

Specimen 7L: embryonic day 18.5; Esrp1tm1.2Rpc/Esrp1tm1.2Rpc (more )
Structure Cell Type Level Pattern Image Note
TS26: cochlea epithelium strial marginal cell Trace 7L Expression reduced or absent compared to control.

Specimen 7S: embryonic day 18.5; Esrp1tm1.2Rpc/Esrp1tm1.2Rpc, Fgf9tm1b(KOMP)Wtsi/Fgf9+ (more )
Structure Cell Type Level Pattern Image Note
TS26: cochlea epithelium strial marginal cell Present 7S Authors report recovery of strial marginal 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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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory