该基因编码的蛋白质包含一个环（c3hc4）锌指基序和几个c3h锌指基序。这个基因是无内含子和印记的，只有来自父系等位基因的表达。该位点印记的破坏可能导致普拉德-威利综合征。已发现一个功能未知的反义rna与该基因重叠。[由RefSeq提供，2008年7月]
The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene. [provided by RefSeq, Jul 2008]
| 基因名： | MKRN3 |
| 别名： | CPPB2,D15S9,RNF63,ZFP127,ZNF127 |
| 基因ID： | 7681 |
| Chromosome： (GRCh37) | 15 Start: 23810454 End: 23820764 Strand: |
| 信号通路： |
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