Gene Expression Data
Assay Details
Assay
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Reference:
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J:242353
Pichery M, et al., PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier. Hum Mol Genet. 2017 May 15;26(10):1787-1800
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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:7461577
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Gene symbol:
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Pnpla1
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Gene name:
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patatin-like phospholipase domain containing 1
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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
S3C Skin:
(close )
Genetic Background:
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B6NTac;B6N-Atm1Brd Pnpla1tm1a(KOMP)Wtsi/Ics
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Mutant Allele(s):
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Pnpla1tm1a(KOMP)Wtsi/Pnpla1tm1a(KOMP)Wtsi
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Age:
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embryonic day 18.5
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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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Embedding:
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Cryosection
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Specimen
S3C Digestive Tract:
(close )
Genetic Background:
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B6NTac;B6N-Atm1Brd Pnpla1tm1a(KOMP)Wtsi/Ics
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Mutant Allele(s):
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Pnpla1tm1a(KOMP)Wtsi/Pnpla1tm1a(KOMP)Wtsi
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Age:
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embryonic day 18.5
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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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Embedding:
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Cryosection
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