Gene: MYRF ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 745
Gene Symbol: MYRF
MYRF 		0.320 Biomarker disease GENOMICS_ENGLAND Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. 31048900 2019
Entrez Id: 745
Gene Symbol: MYRF
MYRF 		0.320 Biomarker disease BEFREE The underlying mechanism of MYRF in the development of nanophthalmos needs to be further investigated. 31266062 2019
Entrez Id: 745
Gene Symbol: MYRF
MYRF 		0.320 GeneticVariation disease BEFREE Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. 31048900 2019
Entrez Id: 745
Gene Symbol: MYRF
MYRF 		0.320 Biomarker disease GENOMICS_ENGLAND Using Myc-MYRF chromatin immunoprecipitation data from rat oligodendrocytes, <i>MYRF</i> was found to bind immediately upstream of the transcriptional start site of <i>Tmem98</i>, a gene that itself has been implicated in autosomal dominant nanophthalmos. 31700225 2019