abnormal epigenetic regulation of gene expression Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process that modulates the frequency, rate or extent of gene expression, in which the process is mitotically or meiotically heritable, or is stably self-propagated in the cytoplasm of a resting cell, and does not entail a change in DNA sequence (Mammalian Phenotype Ontology, MP_0012167)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012167
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Genes

61 gene mutations causing the abnormal epigenetic regulation of gene expression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIRN antisense of IGF2R non-protein coding RNA
ASCL2 achaete-scute family bHLH transcription factor 2
ASIP agouti signaling protein
ASZ1 ankyrin repeat, SAM and basic leucine zipper domain containing 1
AXIN1 axin 1
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CHD7 chromodomain helicase DNA binding protein 7
CITED1 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1
CUL4B cullin 4B
DIO3 deiodinase, iodothyronine, type III
DLK1 delta-like 1 homolog (Drosophila)
DNMT1 DNA (cytosine-5-)-methyltransferase 1
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
DPPA3 developmental pluripotency associated 3
EHMT2 euchromatic histone-lysine N-methyltransferase 2
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
G6PD glucose-6-phosphate dehydrogenase
GCM2 glial cells missing homolog 2 (Drosophila)
GNAS GNAS complex locus
GRB10 growth factor receptor-bound protein 10
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HELLS helicase, lymphoid-specific
IGF2 insulin-like growth factor 2
IGF2R insulin-like growth factor 2 receptor
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
KMT2B lysine (K)-specific methyltransferase 2B
MAEL maelstrom spermatogenic transposon silencer
MAGEL2 melanoma antigen family L2
MBD4 methyl-CpG binding domain protein 4
MDGA2 MAM domain containing glycosylphosphatidylinositol anchor 2
MECP2 methyl CpG binding protein 2
MEG3 maternally expressed 3 (non-protein coding)
MEST mesoderm specific transcript
MIS18A MIS18 kinetochore protein A
MOV10L1 Mov10 RISC complex RNA helicase like 1
NDN necdin, melanoma antigen (MAGE) family member
PEG10 paternally expressed 10
PEG3 paternally expressed 3
PHLDA2 pleckstrin homology-like domain, family A, member 2
PIWIL2 piwi-like RNA-mediated gene silencing 2
PLAC1 placenta-specific 1
PLAGL1 pleiomorphic adenoma gene-like 1
PLD6 phospholipase D family, member 6
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
RLIM ring finger protein, LIM domain interacting
RNF4 ring finger protein 4
SETD1A SET domain containing 1A
SGCE sarcoglycan, epsilon
SMCHD1 structural maintenance of chromosomes flexible hinge domain containing 1
SNRPN small nuclear ribonucleoprotein polypeptide N
SP3 Sp3 transcription factor
TDG thymine-DNA glycosylase
TDRD9 tudor domain containing 9
TDRKH tudor and KH domain containing
TSIX TSIX transcript, XIST antisense RNA
UBE3A ubiquitin protein ligase E3A
UHRF1 ubiquitin-like with PHD and ring finger domains 1
XIST X inactive specific transcript (non-protein coding)
ZBTB16 zinc finger and BTB domain containing 16
ZFP42 ZFP42 zinc finger protein
ZFP57 ZFP57 zinc finger protein