paternal imprinting Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	establishment of heritable alterations in the activity of a gene that depend on whether it passed through the paternal germline, but that are not encoded by DNA itself (Mammalian Phenotype Ontology, MP_0003123)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003123
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Genes

14 gene mutations causing the paternal imprinting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ASCL2	achaete-scute family bHLH transcription factor 2
AXIN1	axin 1
CDKN1C	cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CITED1	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1
G6PD	glucose-6-phosphate dehydrogenase
GNAS	GNAS complex locus
GRB10	growth factor receptor-bound protein 10
H19	H19, imprinted maternally expressed transcript (non-protein coding)
HELLS	helicase, lymphoid-specific
MEG3	maternally expressed 3 (non-protein coding)
PHLDA2	pleckstrin homology-like domain, family A, member 2
PLAC1	placenta-specific 1
RASGRF1	Ras protein-specific guanine nucleotide-releasing factor 1
UBE3A	ubiquitin protein ligase E3A