Gene Expression Data
Assay Details
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Assay
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Reference:
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J:326355
Bademci G, et al., Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice. Proc Natl Acad Sci U S A. 2022 Jun 28;119(26):e2204084119
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Assay type:
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In situ reporter (knock in)
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MGI Accession ID:
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MGI:7329767
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Gene symbol:
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Minar2
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Gene name:
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membrane integral NOTCH2 associated receptor 2
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Results
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Specimen
3C:
(close  )
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Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Minar2tm1b(KOMP)Wtsi/Minar2+
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Age:
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postnatal day 1
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Sex:
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Not Specified
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Type:
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optical section
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Fixation:
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4% Paraformaldehyde
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| Structure |
Level |
Pattern |
Image |
Note |
| TS27: cochlea |
Present |
Regionally restricted |
3C
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Expression in interdental cells, organ of Corti and spiral ganglion.
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Specimen
3D:
(close )
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Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Minar2tm1b(KOMP)Wtsi/Minar2+
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Age:
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postnatal day 1
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Sex:
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Not Specified
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Type:
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optical section
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Fixation:
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4% Paraformaldehyde
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| Structure |
Cell Type |
Level |
Pattern |
Image |
Note |
| TS27: cochlea |
interdental cell of cochlea |
Present |
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3D
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Specimen
3E:
(close )
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Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Minar2tm1b(KOMP)Wtsi/Minar2+
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Age:
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postnatal day 1
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Sex:
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Not Specified
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Type:
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optical section
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Fixation:
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4% Paraformaldehyde
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Specimen
3F:
(close )
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Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Minar2tm1b(KOMP)Wtsi/Minar2+
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Age:
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postnatal day 1
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Sex:
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Not Specified
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Type:
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optical section
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Fixation:
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4% Paraformaldehyde
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Analysis Tools
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