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22q11.2 copy number variation syndrome
Singleton SuperPath
1
Pathway
in the
22q11.2 copy number variation syndrome
SuperPath
22q11.2 copy number variation syndrome
130
Genes
in the
22q11.2 copy number variation syndrome
SuperPath
KRT18P62
RNY1P9
CDH15
LINC01637
PAK4
TXNRD2
NPRL2
RN7SL812P
RNU6-225P
RN7SL168P
MALT1
SNORA77B
RCC1
TANGO2
SLC9A3P2
COMT
CLDN3
CRKL
NKX2-5
LINC00896
AIFM3
CYP26A1
DRD2
EGFR
FGF8
FGF10
FGFR1
FGFR2
FOXC1
FOXC2
SEPTIN8
CBX5
TSSK2
ASF1A
DGCR5
GBX2
TRMT2A
GLUD1
GP1BA
GP1BB
GP5
GP9
EMC10
DROSHA
GSC2
ZDHHC8
SERPIND1
FOXA2
HES1
CYP26C1
KPNB1
TNPO1
CCDC188
LRRC74B
BMAL1
MAG
ARVCF
OAT
PRKN
PAX3
MED15
PI4KA
PITX2
PLK1
SEPTIN5
POLR2A
DGCR8
GNB1L
PPP1CB
SEPTIN11
PRODH
RELN
CYP26B1
RTN4
RAF1
ACTA2
RAN
RANBP1
RANGAP1
BCL2
TSKS
RORC
SMPD4P1
TUBA3GP
SHH
MRPL40
RTN4R
SLC2A4
SLC7A4
SLC25A1
SREBF1
SREBF2
SRF
TBX1
ACTC1
CLDN5
TP53
KRT18P5
HIRA
UFD1
VWF
XPO1
ZNF74
RTL10
SHOC2
THAP7
NPRL3
LZTR1
CLTCL1
ESS2
CDC45
H4C1
CUL3
HIRIP3
KLHL22
DGCR6L
CHRD
ALDH4A1
HDAC3
ALDH1A2
CLDN1
SCARF2
P2RX6
SNAP29
HAND2
NCOR1
DEPDC5
RBX1
CDC42
DGCR2
*Darkness represents the genes rank within the SuperPath, via the multiplicity of each gene in the constituent pathways.
STRING interaction network
for
22q11.2 copy number variation syndrome
SuperPath