Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 5125
Gene Symbol: PCSK5
PCSK5
proprotein convertase subtilisin/kexin type 5 0.659 0.538 2.5E-12
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.300 None 1.000 1 0 2008 2008
Entrez Id: 1139
Gene Symbol: CHRNA7
CHRNA7
cholinergic receptor nicotinic alpha 7 subunit 0.532 0.654 4.2E-04
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.300 None 1.000 1 0 2012 2012
Entrez Id: 4035
Gene Symbol: LRP1
LRP1
LDL receptor related protein 1 0.482 0.769 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.200 None 0 0
Entrez Id: 1028
Gene Symbol: CDKN1C
CDKN1C
cyclin dependent kinase inhibitor 1C 0.456 0.846 0.82
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.150 None 1.000 5 0 1999 2017
Entrez Id: 2316
Gene Symbol: FLNA
FLNA
filamin A 0.419 0.846 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.120 None 1.000 2 0 1982 2004
Entrez Id: 3481
Gene Symbol: IGF2
IGF2
insulin like growth factor 2 0.390 0.885 4.4E-02
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.110 None 1.000 1 0 1999 1999
Entrez Id: 10984
Gene Symbol: KCNQ1OT1
KCNQ1OT1
KCNQ1 opposite strand/antisense transcript 1 0.534 0.731
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.110 None 1.000 1 0 2017 2017
Entrez Id: 51339
Gene Symbol: DACT1
DACT1
dishevelled binding antagonist of beta catenin 1 0.547 0.692 0.40
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 51360
Gene Symbol: MBTPS2
MBTPS2
membrane bound transcription factor peptidase, site 2 0.513 0.769 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 51715
Gene Symbol: RAB23
RAB23
RAB23, member RAS oncogene family 0.541 0.654 5.6E-03
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 5351
Gene Symbol: PLOD1
PLOD1
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 0.579 0.731 1.5E-15
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 1
Entrez Id: 54903
Gene Symbol: MKS1
MKS1
MKS transition zone complex subunit 1 0.505 0.769 3.4E-16
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
platelet activating factor acetylhydrolase 1b regulatory subunit 1 0.504 0.769 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 4784
Gene Symbol: NFIX
NFIX
nuclear factor I X 0.547 0.769 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 4638
Gene Symbol: MYLK
MYLK
myosin light chain kinase 0.510 0.846 9.2E-12
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 4629
Gene Symbol: MYH11
MYH11
myosin heavy chain 11 0.528 0.731 0.77
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 4323
Gene Symbol: MMP14
MMP14
matrix metallopeptidase 14 0.447 0.769 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 4313
Gene Symbol: MMP2
MMP2
matrix metallopeptidase 2 0.333 0.923 0.84
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
LDL receptor related protein 2 0.491 0.846 1.00
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 72
Gene Symbol: ACTG2
ACTG2
actin gamma 2, smooth muscle 0.505 0.808 7.1E-02
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 3930
Gene Symbol: LBR
LBR
lamin B receptor 0.473 0.808 0.18
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 9723
Gene Symbol: SEMA3E
SEMA3E
semaphorin 3E 0.515 0.769 8.7E-09
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 55112
Gene Symbol: WDR60
WDR60
WD repeat domain 60 0.592 0.654 4.3E-12
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 91754
Gene Symbol: NEK9
NEK9
NIMA related kinase 9 0.623 0.500 8.2E-18
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0
Entrez Id: 89891
Gene Symbol: WDR34
WDR34
WD repeat domain 34 0.597 0.692 1.7E-07
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
disease 0.100 None 0 0