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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Immunohistochemistry
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MGI Accession ID:
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MGI:7857192
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Gene symbol:
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Cdkn1b
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Gene name:
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cyclin dependent kinase inhibitor 1B
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Results
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Specimen
S4N:
embryonic day 14.5
(more  )
Note: Base of cochlea.
Specimen
S4N:
(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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Note:
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Base of cochlea.
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| Structure |
Level |
Pattern |
Image |
Note |
| TS22: cochlear duct |
Present |
Regionally restricted |
S4N
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Expression in sensory progenitors.
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Specimen
S4O:
(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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Note:
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Base of cochlea.
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| Structure |
Level |
Pattern |
Image |
Note |
| TS22: cochlear duct |
Present |
Regionally restricted |
S4O
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No difference in expression in sensory progenitors compared to control.
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Analysis Tools
