maternal imprinting Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the establishment of heritable alterations in the activity of a gene that depend on whether it passed through the maternal germline, but that are not encoded by DNA itself (Mammalian Phenotype Ontology, MP_0003122)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003122
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Genes

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

Symbol Name
AIRN antisense of IGF2R non-protein coding RNA
ASIP agouti signaling protein
AXIN1 axin 1
DIO3 deiodinase, iodothyronine, type III
DLK1 delta-like 1 homolog (Drosophila)
GNAS GNAS complex locus
IGF2 insulin-like growth factor 2
IGF2R insulin-like growth factor 2 receptor
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
MAGEL2 melanoma antigen family L2
MEG3 maternally expressed 3 (non-protein coding)
MEST mesoderm specific transcript
NDN necdin, melanoma antigen (MAGE) family member
PEG10 paternally expressed 10
PEG3 paternally expressed 3
PLAGL1 pleiomorphic adenoma gene-like 1
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
SGCE sarcoglycan, epsilon
SNRPN small nuclear ribonucleoprotein polypeptide N