Citations for
1NPAP1, POM121
The imprinted NPAP1 gene in the Prader-Willi syndrome region belongs to a POM121-related family of retrogenes.
Neumann LC, Feiner N, Meyer A, Buiting K, Horsthemke B.
Genome Biol Evol 6(2):344-51. doi: 10.1093/gbe/evu019. 2014
2NPAP1, POM121
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein.
Neumann LC, Markaki Y, Mladenov E, Hoffmann D, Buiting K, Horsthemke B.
Hum Mol Genet 21(18):4038-48. doi: 10.1093/hmg/dds228. 2012
3NPAP1
The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection.
Wawrzik M, Unmehopa UA, Swaab DF, van de Nes J, Buiting K, Horsthemke B.
Neurogenetics 11(2):153-61. doi: 10.1007/s10048-009-0231-z. 2010
4DFNA5, GSDMA, GSDMB, GSDMC, GSDMD, NPAP1, PJVK, PWRN1, PWRN2
C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain.
Buiting K, Nazlican H, Galetzka D, Wawrzik M, Gross S, Horsthemke B.
Genomics 89(5):588-95. Epub 2007 Mar 6. 2007
5NPAP1
Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15.
Farber C, Gross S, Neesen J, Buiting K, Horsthemke B.
Genomics 65(2):174-83. 2000