Gene Expression Data
Assay Details
Assay
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Reference:
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J:299667
Calame DJ, et al., Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic Dyskinesia. Neuroscience. 2020 Nov 10;448:272-286
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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:7610563
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Gene symbol:
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Prrt2
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Gene name:
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proline-rich transmembrane protein 2
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Reporter:
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lacZ
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Direct Detection
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Results
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Specimen
1A:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal
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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
1B P7:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal day 7
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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
1B P15:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal day 15
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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
1B P30:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal day 30
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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
1B P90:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal day 90
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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
1C:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal
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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
S2:
(close )
Genetic Background:
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involves: C57BL/6N
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Mutant Allele(s):
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Prrt2tm1a(KOMP)Wtsi/Prrt2tm1a(KOMP)Wtsi
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Age:
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postnatal adult
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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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Coronal sections from anterior to posterior brain.
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