GO:0040029 regulation of gene expression, epigenetic (115)

GeneInput weightStandardRank
ATRX--136
ARID1A--67
CTCF0.51396
AGO2--490
NR3C1--496
ZCCHC11--737
DICER1--1762
SMARCA4--801
SMAD3--823
PHF20.511030
HAT1--1208
SIRT1--1233
KMT2E0.511234
BAZ2A--1312
HDAC2--1440
EED--1566
FOS--1680
HMGA1--11695
TNRC6A--1752
GNAS--11842
SMAD1--1872
HDAC5--1950
ATF7IP--1980
PHF80.2512109
AGO3--2124
H2AFY0.2512221
CELF1--2232
SMARCD1--2282
EPC1--2533
SMAD2--2694
SIRT3--2700
BAZ1B--2716
AGO1--2764
DIRAS3--3034
ARID1B1.013173
EHMT2--3182
AGO4--3370
CTCFL--3489
TDRD1--3754
DNMT3A--4002
UBR2--4054
UBE2B--4057
RBM4--4069
CREBZF--4129
GSK3A--4141
UBTF--4174
TET1--4338
MAEL--4472
SIRT4--4652
TDRD9--4819
PIWIL2--4828
H2AFY2--4831
SMCHD1--5026
LIN28B--5378
AICDA--5566
ASZ1--5809
GATAD2A--6570
TNP1--6604
KMT2D--6700
ASF1A--6738
LIN28A--7070
EHMT10.517204
TDRD5--7375
KCNQ1--17724
FTO--7782
DNMT3L--8034
DGCR8--8286
PIWIL4--8984
RLIM--9269
PRKRA--9728
PICK1--11315
GPX10.25111644
WTIP--11726
TRDMT1--12254
APOBEC1--12314
SRRT--12400
SNIP1--12657
ZFP57--12704
DNMT1--13233
SIRT5--13673
DROSHA--14199
APOBEC2--14209
TRIM27--14656
DNMT3B--14663
MBD30.25115779
HILS1--16105
GLMN--16462
AJUBA--18146
LIMD1--19839
APOBEC3A--20197
KDM1B--20503
APEX1--20571
SIRT7--20593
SIRT6--21428
PLD6--21953
SIRT2--22147
DMAP1--22351
IGF20.25122401
RRP8--22607
RBM3--22670
PRMT7--22847
HELLS--22974
ALKBH1--23309
APOBEC3C--23560
MOV10--23619
APOBEC3F--23939
ALKBH3--24014
ALKBH2--24050
MGMT--24063
CLP1--24100
SUV39H1--24290
BRCA1--124573
TARBP2--24667
HEMK1--24743
SLC50A1--24980

Network

GO:0040029

Network
Enrichment
NameDescriptionExternal IDs
ATRXalpha thalassemia/mental retardation syndrome X-linked Entrez:546  HPRD: 02069  HGNC: 886  Ensembl: ENSG00000085224 
ARID1AAT rich interactive domain 1A (SWI-like) Entrez:8289  HPRD: 04319  HGNC: 11110  Ensembl: ENSG00000117713 
CTCFCCCTC-binding factor (zinc finger protein) Entrez:10664  HPRD: 05005  HGNC: 13723  Ensembl: ENSG00000102974 
AGO2argonaute RISC catalytic component 2 Entrez:27161  HPRD: 06943  HGNC: 3263  Ensembl: ENSG00000123908 
NR3C1nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) Entrez:2908  HGNC: 7978  HPRD: 00679  Ensembl: ENSG00000113580 
GenesetTypeFreq. (Network vs Genome)P-Value (FDR Corrected)Genes
GeneDescriptionAvg. edge score to queryRankIn genesetIn query
ATRXalpha thalassemia/mental retardation syndrome X-linked
ARID1AAT rich interactive domain 1A (SWI-like)
CTCFCCCTC-binding factor (zinc finger protein)
AGO2argonaute RISC catalytic component 2
NR3C1nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
Query geneGeneGene descriptionEdge score
ATRXATRXalpha thalassemia/mental retardation syndrome X-linked
ARID1AARID1AAT rich interactive domain 1A (SWI-like)
CTCFCTCFCCCTC-binding factor (zinc finger protein)
AGO2AGO2argonaute RISC catalytic component 2
NR3C1NR3C1nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)