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Gene Expression Data
Assay Details
Assay
Reference: J:236441 Ruzzo EK, et al., Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron. 2013 Oct 16;80(2):429-41
Assay type: RT-PCR
MGI Accession ID: MGI:6113836
Gene symbol: Asns
Gene name: asparagine synthetase
Probe: Mm00803785_m1
Assay notes: Quantitative RT-PCR. Relative levels were normalized to Gapdh.
Results Image: 5A
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified (a) Amount Genetic BackgroundMutant Allele(s)Sex
Asns+/+ P m 3-4 TS28: cerebral hemisphere Present Not Specified; total RNA C57BL/6N Not Specified
Asns+/- P m 3-4 TS28: cerebral hemisphere Present Not Specified; total RNA C57BL/6N-Asnstm1a(EUCOMM)Wtsi Asnstm1a(EUCOMM)Wtsi/Asns+Not Specified
Asns-/- P m 3-4 TS28: cerebral hemisphere Present Not Specified; total RNA C57BL/6N-Asnstm1a(EUCOMM)Wtsi Asnstm1a(EUCOMM)Wtsi/Asnstm1a(EUCOMM)WtsiNot Specified
Notes:
(a) Both mutant genotypes were significantly different from wild type mRNA levels and significantly different from each other. The data demonstrate that the genetrap mouse is a hypomorph with ~20% of the normal level of mRNA being expressed.

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory