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01 DiGeorge Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
DGCR [NCBI] 0.000671319
SCZD4 [NCBI] 0.000571511
TBX1 [NCBI] 0.000464286
DGCR7 [NCBI] 0.000373825
DGCR5 [NCBI] 0.000373825
DGCR10 [NCBI] 0.000373825
DGCR12 [NCBI] 0.000373825
DGCR11 [NCBI] 0.000373825
DGCR9 [NCBI] 0.000373825
TSSK1A [NCBI] 0.000373825
VCF [NCBI] 0.000275285
HIRA [NCBI] 0.000212581
UFD1L [NCBI] 0.000165185
DGCR14 [NCBI] 0.000100151
CDC45L [NCBI] 7.12905e-05
GNB1L [NCBI] 7.05257e-05
GSC2 [NCBI] 6.01081e-05
DGCR6 [NCBI] 5.19002e-05
SEPT5 [NCBI] 4.57281e-05
SLC25A1 [NCBI] 4.50616e-05
HAND2 [NCBI] 4.1865e-05
COMT [NCBI] 4.05586e-05
DGCR2 [NCBI] 3.79209e-05
GSC [NCBI] 3.6854e-05
TBX5 [NCBI] 2.8895e-05
T [NCBI] 2.67745e-05
ZNF74 [NCBI] 2.42507e-05
PRODH [NCBI] 1.94587e-05
TBX3 [NCBI] 1.79271e-05
PAX3 [NCBI] 1.75401e-05
HIST1H4A [NCBI] 1.50077e-05
NPLOC4 [NCBI] 1.50077e-05
DVL1L1 [NCBI] 1.50077e-05
ZNF160 [NCBI] 1.50077e-05
FOXC2 [NCBI] 1.45015e-05
FGF8 [NCBI] 1.4354e-05
HIRIP3 [NCBI] 1.26275e-05
DGCR6L [NCBI] 1.26275e-05
LZTR1 [NCBI] 1.26275e-05
TSSK2 [NCBI] 1.26275e-05
CTNND1 [NCBI] 1.21645e-05
XPO5 [NCBI] 1.17292e-05
CLTCL1 [NCBI] 1.1146e-05
GGT5 [NCBI] 1.1146e-05
HIST1H2BD [NCBI] 1.1146e-05
DGCR8 [NCBI] 1.1146e-05
SLC7A4 [NCBI] 1.1146e-05
PTPLA [NCBI] 1.07124e-05
HIST1H2BK [NCBI] 1.07124e-05
ECEL1 [NCBI] 1.07124e-05
DNAJA2 [NCBI] 1.07124e-05
RANBP1 [NCBI] 1.03669e-05
MED15 [NCBI] 1.03669e-05
ZDHHC8 [NCBI] 1.00797e-05
ORC2L [NCBI] 1.00797e-05
DVL1 [NCBI] 9.83379e-06
ARVCF [NCBI] 9.83379e-06
HIST2H2BE [NCBI] 9.25621e-06
TXNRD2 [NCBI] 9.25621e-06
EIF2C2 [NCBI] 9.25621e-06
SHH [NCBI] 9.12757e-06
HIST3H3 [NCBI] 9.10016e-06
RNF4 [NCBI] 9.10016e-06
CUGBP2 [NCBI] 8.95717e-06
GP1BB [NCBI] 8.82522e-06
HAND1 [NCBI] 8.10959e-06
FOXN1 [NCBI] 8.02807e-06
PCBD1 [NCBI] 7.95026e-06
RTN4R [NCBI] 7.95026e-06
SEMA3A [NCBI] 7.80456e-06
CHAF1A [NCBI] 7.54593e-06
LAMC1 [NCBI] 7.0771e-06
ISL1 [NCBI] 6.94576e-06
GATA4 [NCBI] 6.56956e-06
DTNBP1 [NCBI] 6.07596e-06
FOXA2 [NCBI] 6.07596e-06
FOXC1 [NCBI] 5.95462e-06
GATA3 [NCBI] 5.05392e-06
NRG1 [NCBI] 5.00028e-06
SMARCB1 [NCBI] 4.87336e-06
SNAI2 [NCBI] 3.89416e-06
TP63 [NCBI] 2.99008e-06
FOXP3 [NCBI] 2.39829e-06
MLL [NCBI] 2.34052e-06
FMR1 [NCBI] 2.00596e-06
BCL2L1 [NCBI] 1.4335e-06
FASLG [NCBI] 6.48567e-07



OMIM


 OMIM Link Information
gain		 01
DGS [NCBI] 0.0146745
digeorge syndrome/velocardiofacial syndrome spectrum of malformation 2 [NCBI] 0.00488959
velocardiofacial syndrome [NCBI] 0.00173865
TBX1 [NCBI] 0.0012827
acromegaloid facial appearance syndrome [NCBI] 0.000705355
cayler cardiofacial syndrome [NCBI] 0.000461483
HIRA [NCBI] 0.000419763
GSCL [NCBI] 0.000373262
DGCR14 [NCBI] 0.000346394
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000328262
kabuki syndrome [NCBI] 0.000322547
DGCR2 [NCBI] 0.000298358
CTHM [NCBI] 0.000266424
SLC25A1 [NCBI] 0.000223582
CRKL [NCBI] 0.000201227
GNB1L [NCBI] 0.000148931
DGCR6 [NCBI] 0.000129954
CDC45L [NCBI] 0.00012138
SCZD4 [NCBI] 0.000119086
SEPT5 [NCBI] 0.000115496
COMT [NCBI] 0.000111638
charcot-marie-tooth peroneal muscular atrophy and friedreich ataxia, combined [NCBI] 0.000101631
facial dysmorphism with multiple malformations [NCBI] 0.000101631
PRODH [NCBI] 9.04501e-05
neural tube defects [NCBI] 8.85477e-05
ZNF74 [NCBI] 7.44041e-05
TXNRD2 [NCBI] 7.44041e-05
DVL1L1 [NCBI] 7.44041e-05
LZTR1 [NCBI] 7.44041e-05
DGCR8 [NCBI] 7.44041e-05
ZNF160 [NCBI] 7.44041e-05
HIRIP3 [NCBI] 7.44041e-05
SLC7A4 [NCBI] 7.44041e-05
npl4, s. cerevisiae, homolog of [NCBI] 7.44041e-05
ARVCF [NCBI] 7.44041e-05
PCQAP [NCBI] 7.44041e-05
MLL2 [NCBI] 7.44041e-05
microduplication 22q11.2 [NCBI] 7.07375e-05
CES [NCBI] 6.74602e-05
coarctation of aorta [NCBI] 6.52598e-05
PTLS [NCBI] 6.52598e-05
subglottic bar [NCBI] 6.11944e-05
PTPLA [NCBI] 6.06289e-05
SYN2 [NCBI] 6.06289e-05
DGCR6L [NCBI] 6.06289e-05
CLTCL1 [NCBI] 5.5433e-05
chromosome 16p13.3 deletion syndrome [NCBI] 5.52772e-05
GP1BB [NCBI] 5.20607e-05
TBX19 [NCBI] 5.20607e-05
hypoparathyroidism, sensorineural deafness, and renal disease [NCBI] 4.76157e-05
TBX22 [NCBI] 4.75584e-05
RTN4R [NCBI] 4.75584e-05
chromosome 17q21.31 microdeletion syndrome [NCBI] 4.58994e-05
hyperprolinemia, type i [NCBI] 4.48488e-05
GP9 [NCBI] 4.448e-05
ALDH1A2 [NCBI] 4.32397e-05
SMMCI [NCBI] 3.8675e-05
TBX5 [NCBI] 3.73024e-05
IFNGR1 [NCBI] 3.66863e-05
lymphedema-distichiasis syndrome [NCBI] 3.63302e-05
FOXC2 [NCBI] 3.55598e-05
CPX [NCBI] 3.49494e-05
TIMP3 [NCBI] 3.32089e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 3.30934e-05
hyperglycerolemia [NCBI] 3.25235e-05
SOX9 [NCBI] 3.16684e-05
FGF8 [NCBI] 2.97396e-05
SHH [NCBI] 2.94512e-05
MLL [NCBI] 2.6346e-05
FOXP3 [NCBI] 2.61445e-05
TGFB1 [NCBI] 2.51968e-05
BPES [NCBI] 2.19978e-05
SCZD [NCBI] 2.07527e-05
TCOF [NCBI] 1.94038e-05
WHS [NCBI] 1.51442e-05
VEGF [NCBI] 8.18286e-06
WBS [NCBI] 5.7251e-06



Database Center for Life Science