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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