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Gene Expression Data
Assay Details
Reference: J:272028 O'Connell AE, et al., Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation. PLoS Genet. 2019 Feb;15(2):e1007917
Assay type: RT-PCR
MGI Accession ID: MGI:6361187
Gene symbol: Hbs1l
Gene name: Hbs1-like (S. cerevisiae)
Probe: Hbs1l-pA, Hbs1l-pB
Probe preparation: labelled with other - see notes
Assay notes: This assay is a quantitative RT-PCR. B2m was used as the standard. TaqMan probe Mm03807425_g1 was used in this Real-Time PCR.
Image: 9B ©

 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
WT E9.5 TS15: embryo Present 0.2 µg; total RNA involves: C57BL/6N Not Specified
Het E9.5 TS15: embryo Present 0.2 µg; total RNA C57BL/6N-Hbs1ltm1a(KOMP)Wtsi/Wtsi Hbs1ltm1a(KOMP)Wtsi/Hbs1l+Not Specified
KO E9.5 TS15: embryo Weak (a) 0.2 µg; total RNA C57BL/6N-Hbs1ltm1a(KOMP)Wtsi/Wtsi Hbs1ltm1a(KOMP)Wtsi/Hbs1ltm1a(KOMP)WtsiNot Specified
(a) 10% residual expression.

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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MGI 6.17
The Jackson Laboratory