Madelaine et al., 2018 - A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human. Nucleic acids research   46(7):3517-3531 Full text @ Nucleic Acids Res.
11 Genes / Markers
Marker Type Symbol Name
miRNA Gene dre-mir-9-1 microRNA 9-1
Gene mef2cb myocyte enhancer factor 2cb
miRNA Gene mir9-2 microRNA 9-2
miRNA Gene mir9-3 microRNA 9-3
miRNA Gene mir9-4 microRNA 9-4
miRNA Gene mir9-5 microRNA 9-5
miRNA Gene mir9-6 microRNA 9-6
miRNA Gene mir9-7 microRNA 9-7
NC Conserved Region (CNE, CNS) nccr.mef2cb-tmem161b.cne1 non-coding conserved region between mef2cb and tmem161b
lincRNA Gene si:ch211-202e12.3 si:ch211-202e12.3
Gene tmem161b transmembrane protein 161B
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