Gene Expression Data
Assay Details
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Assay
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Reference:
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J:323825
Giffen KP, et al., Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction. Sci Adv. 2022 Apr 8;8(14):eabk0942
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Assay type:
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Immunohistochemistry
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MGI Accession ID:
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MGI:7284171
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Gene symbol:
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Ctbp2
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Gene name:
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C-terminal binding protein 2
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Results
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Specimen
not shown wild type:
postnatal month 3.5
(more  )
Specimen
not shown wild type:
(close  )
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Genetic Background:
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C57BL/6J
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Age:
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postnatal month 3.5
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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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Formalin
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Embedding:
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Paraffin
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| Structure |
Cell Type |
Level |
Pattern |
Image |
Note |
| TS28: cochlea |
cochlear inner hair cell |
Present |
Punctate |
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Expression was detected in synaptic ribbons.
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Specimen
not shown knock-in:
(close )
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Genetic Background:
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C57BL/6J-Slc7a14em1Jin
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Mutant Allele(s):
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Slc7a14em1Jin/Slc7a14em1Jin
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Age:
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postnatal month 3.5
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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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Formalin
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Embedding:
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Paraffin
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| Structure |
Cell Type |
Level |
Pattern |
Image |
Note |
| TS28: cochlea |
cochlear inner hair cell |
Present |
Punctate |
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There was no measurable difference of immunopositive puncta between the knock-in and wild type inner hair cells in the apical or low apical cochlear turns.
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Analysis Tools
