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11p11.2 copy number variation syndrome
Singleton SuperPath
1
Pathway
in the
11p11.2 copy number variation syndrome
SuperPath
11p11.2 copy number variation syndrome
144
Genes
in the
11p11.2 copy number variation syndrome
SuperPath
GNPDA1
MICA
ADAM10
DDX39A
CDKN1A
TNIP1
HOXB13
CREB3
HYOU1
OLFM4
RBCK1
ATE1
CHRM5
LARGE2
CNTF
FITM2
CRY2
FREY1
TMCO5A
CUX1
NIPAL1
IQUB
NOP9
HBEGF
EMX1
ERCC3
ESR1
ESR2
EXT1
EXT2
FABP4
TMEM218
FHL2
FOXE1
OBSL1
CRB1
RIGI
YIPF3
VIRMA
TCTN3
GATA4
INVS
GNB1
FFAR2
GRM2
GTF2H3
GTF2H4
ANXA7
HLA-DMA
HLA-DMB
HLA-DRA
FOXA1
FOXA3
HNF4A
HNRNPL
HOXA3
HOXB6
HOXD3
PRMT2
BIRC2
IFNA6
RBPJ
CXCL8
ITGA6
ITGA3
ITGA4
ITGB1
ITGB2
CD82
ACCSL
LGALS3BP
MAOA
CXCL9
NUP88
PHF21A
GSKIP
ACP1
PFDN1
MANSC1
TTC19
RNF31
GIMAP5
SLC35C1
ZNF331
PRDM11
MARCHF4
SYT13
AFAP1
RNF4
ALX4
RPS27
RPS29
BDKRB2
ATXN1
CCL1
PARVG
SLC22A2
SMN1
SNCG
SOX2
ELOC
TIMP1
TK1
TSPAN8
TP53
GTF2H2C
UQCRB
KXD1
TNIP2
LONRF3
RBFA
TCTN2
ALX1
VANGL1
H4C1
TMEM120A
ADGRA1
ACCS
USP30
SMIM3
FBF1
CHST1
STK16
RAB11A
TSPAN18
ACBD5
IL1RL1
NEK9
CD4
CD9
CD19
MS4A1
PEX16
MAPK8IP1
TP53I11
CD53
CD63
CD151
RAB27A
RAB10
RAB27B
SLC25A17
PEX3
NRXN1
*Darkness represents the genes rank within the SuperPath, via the multiplicity of each gene in the constituent pathways.
STRING interaction network
for
11p11.2 copy number variation syndrome
SuperPath