GO:0032259 methylation (117)

GeneInput weightStandardRank
KMT2A1.0116
ATRX--136
SUV420H11.01173
RAB6A--351
CTCF0.51396
SETD20.251672
FBXO11--741
SMARCA4--801
PRMT8--817
SATB1--828
ETF1--832
BTG1--1000
WHSC1L1--11055
SUZ12--1188
KMT2E0.511234
BAZ2A--1312
EED--1566
FOS--1680
KDM6A--1766
PCMT1--1813
GNAS--11842
ATF7IP--1980
RAB3B--1982
KMT2C1.012003
PAXIP1--2915
EHMT2--3182
SETD1B--3231
CTCFL--3489
TDRD1--3754
PRDM5--3909
DNMT3A--4002
PRMT1--4008
MAT2A--4189
MAEL--4472
BHMT0.2514707
CARM1--4755
TDRD9--4819
PIWIL2--4828
WDR82--4909
MEN1--14917
ASZ1--5809
GSPT1--6042
CYP1A2--6074
GATAD2A--6570
KMT2D--6700
PRDM9--6886
EHMT10.517204
TDRD5--7375
TRMT112--7690
BAGE3--7700
CXXC1--7956
DOT1L--7980
BAGE4--7982
DNMT3L--8034
BAGE5--8527
PIWIL4--8984
RBBP5--9373
SMYD2--9412
PICK1--11315
TRDMT1--12254
ZFP57--12704
AHCY--113030
METTL14--13112
DNMT1--13233
COMT0.25113475
SETD3--13578
PRMT2--13677
SETD6--13985
NSD10.25114116
DNMT3B--14663
SETD8--14849
MAT2B--15319
SETD7--18622
CMTR1--18629
ALKBH8--19453
HENMT1--19491
LCMT1--19950
SUV420H2--19960
SUV39H2--20238
KDM1B--20503
RAB3D--21252
FTSJ1--21450
PLD6--21953
MAT1A--21961
GAMT--22050
TRMT61B--22080
NDUFAF7--22163
WBSCR22--22239
ASH2L--22257
WDR92--22279
DMAP1--22351
SMYD3--22549
EZH2--22623
SETDB20.25122691
PRMT7--22847
METTL3--22948
HELLS--22974
DPY30--23146
TGS1--23201
N6AMT1--23284
TPMT--23732
MGMT--24063
NSUN2--24176
PRMT6--24226
SUV39H1--24290
NTMT1--24513
WDR5--24720
HEMK1--24743
COPRS--24936
ICMT--24975
TRMT61A--25140
PRMT3--25447
FTSJ2--25611
FTSJ3--25622
NNMT--25643
MTR0.25125646
PRMT5--25692

Network

GO:0032259

Network
Enrichment
NameDescriptionExternal IDs
KMT2Alysine (K)-specific methyltransferase 2A Entrez:4297  HPRD: 01162  HGNC: 7132  Ensembl: ENSG00000118058 
ATRXalpha thalassemia/mental retardation syndrome X-linked Entrez:546  HPRD: 02069  HGNC: 886  Ensembl: ENSG00000085224 
SUV420H1suppressor of variegation 4-20 homolog 1 (Drosophila) Entrez:51111  HPRD: 11616  HGNC: 24283  Ensembl: ENSG00000110066 
RAB6ARAB6A, member RAS oncogene family Entrez:5870  HPRD: 01543  HGNC: 9786  Ensembl: ENSG00000175582 
CTCFCCCTC-binding factor (zinc finger protein) Entrez:10664  HPRD: 05005  HGNC: 13723  Ensembl: ENSG00000102974 
GenesetTypeFreq. (Network vs Genome)P-Value (FDR Corrected)Genes
GeneDescriptionAvg. edge score to queryRankIn genesetIn query
KMT2Alysine (K)-specific methyltransferase 2A
ATRXalpha thalassemia/mental retardation syndrome X-linked
SUV420H1suppressor of variegation 4-20 homolog 1 (Drosophila)
RAB6ARAB6A, member RAS oncogene family
CTCFCCCTC-binding factor (zinc finger protein)
Query geneGeneGene descriptionEdge score
KMT2AKMT2Alysine (K)-specific methyltransferase 2A
ATRXATRXalpha thalassemia/mental retardation syndrome X-linked
SUV420H1SUV420H1suppressor of variegation 4-20 homolog 1 (Drosophila)
RAB6ARAB6ARAB6A, member RAS oncogene family
CTCFCTCFCCCTC-binding factor (zinc finger protein)