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Gene Expression Data
Assay Details
Assay
Reference: J:275842 Garnai SJ, et al., Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. PLoS Genet. 2019 May;15(5):e1008130
Assay type: RT-PCR
MGI Accession ID: MGI:6360491
Gene symbol: Myrf
Gene name: myelin regulatory factor
Probe: Myrf-pC, Myrf-pD
Assay notes: Taqman Assay system with inventoried probe was used. This assay is a quantitative RT-PCR. Hprt1 was used as the standard.
Results
Image: 8A Myrf ©

 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex Note
Myrf+/fl P7 TS28: eye Present Not Specified involves: 129P2/OlaHsd * C57BL/6J Myrftm1Barr/Myrf+Not Specified
Rxcre;Myrf+/fl P7 TS28: eye Present (a) Not Specified involves: 129P2/OlaHsd * C57BL/6J Myrftm1Barr/Myrf+, Tg(rx3-icre)1Mjam/0Not Specified Conditional mutant.
Rxcre;Myrf fl/fl P7 TS28: eye Absent (b) Not Specified involves: 129P2/OlaHsd * C57BL/6J Myrftm1Barr/Myrftm1Barr, Tg(rx3-icre)1Mjam/0Not Specified Conditional mutant.
- Other lane(s) in blot assay different gene(s)
Notes:
(a) Reduced expression compared with control.
(b) Nearly absent.
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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04/16/2024
MGI 6.23 		The Jackson Laboratory