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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: Immunohistochemistry
MGI Accession ID: MGI:6360319
Gene symbol: Mfrp
Gene name: membrane frizzled-related protein
Antibody: Mouse MFRP Antibody
Detection system: Secondary antibody coupled to Alexa Fluor
Results
Specimen S11 left: postnatal adult; Myrftm1Barr/Myrf+ (more )
Structure Level Pattern Image Note
TS28: pigmented retinal epithelium Present S11_left
Specimen S11 right: postnatal adult; Myrftm1Barr/Myrftm1Barr, Tg(rx3-icre)1Mjam/0 (more )
Note: Conditional mutant.
Structure Level Pattern Image Note
TS28: pigmented retinal epithelium Present S11_right No distinguishable difference compared with the control.
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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04/23/2024
MGI 6.23 		The Jackson Laboratory