Gene Expression Data
Assay Details
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Assay
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Reference:
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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
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Assay type:
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RNA in situ
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MGI Accession ID:
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MGI:7857180
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Gene symbol:
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Fgfr2
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Gene name:
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fibroblast growth factor receptor 2
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Probe:
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Fgfr2 probe
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Probe preparation:
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labelled with digoxigenin RNA
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Results
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Specimen
S6B:
embryonic day 14.5
(more  )
Specimen
S6B:
(close  )
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Genetic Background:
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Not Specified
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Age:
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embryonic day 14.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Cryosection
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Specimen
S6F:
(close )
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Genetic Background:
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involves: 129S4/SvJae * C57BL/6
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Mutant Allele(s):
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Esrp1tm1.2Rpc/Esrp1tm1.2Rpc
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Age:
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embryonic day 14.5
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Sex:
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Not Specified
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Type:
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section
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Fixation:
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4% Paraformaldehyde
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Embedding:
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Cryosection
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| Structure |
Level |
Pattern |
Image |
Note |
| TS22: cochlear duct |
Present |
Regionally restricted |
S6F
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Ectopic expression along lateral cochlear epithelium.
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Analysis Tools
