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Gene Expression Data
Assay Details
Assay
Reference: 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
Assay type: Immunohistochemistry
MGI Accession ID: MGI:7284157
Gene symbol: Nefm
Gene name: neurofilament, medium polypeptide
Antibody: anti-neurofilament clone 2H3
Detection system: Secondary antibody coupled to Alexa Fluor
Results
Specimen S1C P3: postnatal day 3 (more )
Note: Double labeled: green - Nefm; magenta - Slc7a14 (assay MGI:7284092).
Structure Cell Type Level Pattern Image Note
TS27: cochlear ganglion spiral ganglion neuron Present S1C P3
Specimen S1C P14: postnatal day 14 (more )
Note: Double labeled: green - Nefm; magenta - Slc7a14 (assay MGI:7284092).
Structure Cell Type Level Pattern Image Note
TS28: cochlear ganglion spiral ganglion neuron Present S1C P14
Specimen S1C P30: postnatal day 30 (more )
Note: Double labeled: green - Nefm; magenta - Slc7a14 (assay MGI:7284092).
Structure Cell Type Level Pattern Image Note
TS28: cochlear ganglion spiral ganglion neuron Present S1C P30
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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Send questions and comments to User Support. 		last database update
10/29/2024
MGI 6.24 		The Jackson Laboratory