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. 2013 Aug 14;8(8):e72640. doi: 10.1371/journal.pone.0072640

Table 3. Summary of the genetic and expression of chromosomal region 15q11, 2-13.

Gene name  Description Imprinting status Expression level (Deletion)   Expression level (mUPD)   Comparison in two subtypes
TUBGCP5 tubulin, gamma complex associated protein 5 non-imprinted haploinsufficiency normal different
CYFIP1 cytoplasmic FMR1 interacting protein 1 non-imprinted haploinsufficiency normal different
NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2 non-imprinted haploinsufficiency normal different
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1 non-imprinted haploinsufficiency normal different
GOLGA8E golgin A8 family, member E, pseudogene non-imprinted haploinsufficiency normal different
MKRN3 makorin ring finger protein 3 paternally expressed no expression no expression same
MAGEL2 MAGE-like 2 paternally expressed no expression no expression same
NDN necdin, melanoma antigen (MAGE) family member paternally expressed no expression no expression same
NPAP1 nuclear pore associated protein 1 non-imprinted haploinsufficiency normal different
SNRPN small nuclear ribonucleoprotein polypeptide N paternally expressed no expression no expression same
SNURF SNRPN upstream reading frame paternally expressed no expression no expression same
snoRNAs small nucleolar RNA paternally expressed no expression no expression same
UBE3A ubiquitin protein ligase E3A maternally expressed normal over expression different
ATP10A ATPase, class V, type 10A maternally expressed normal over expression different
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3 paternal biased expression haploinsufficiency haploinsufficiency same
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5 paternal biased expression haploinsufficiency haploinsufficiency same
GABRG3 gamma-aminobutyric acid (GABA) A receptor, gamma 3 non-imprinted haploinsufficiency normal different
OCA2 oculocutaneous albinism II non-imprinted haploinsufficiency normal different
GOLGA8G golgin A8 family, member G non-imprinted haploinsufficiency normal different