Source: GENOMICS_ENGLAND

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: 57178
Gene Symbol: ZMIZ1
ZMIZ1 		zinc finger MIZ-type containing 1 0.588 0.615 1.00
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 None 1.000 2 0 2015 2016
Entrez Id: 10297
Gene Symbol: APC2
APC2 		APC regulator of WNT signaling pathway 2 0.582 0.654 1.00
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 None 1.000 1 0 2012 2012
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292 		zinc finger protein 292 0.695 0.423 1.00
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 moderate 1.000 1 0 2018 2018
Entrez Id: 23512
Gene Symbol: SUZ12
SUZ12 		SUZ12 polycomb repressive complex 2 subunit 0.529 0.577 1.00
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 None 1.000 1 0 2019 2019
Entrez Id: 26173
Gene Symbol: INTS1
INTS1 		integrator complex subunit 1 0.666 0.500 7.1E-11
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 strong 1.000 1 0 2007 2007
Entrez Id: 54499
Gene Symbol: TMCO1
TMCO1 		transmembrane and coiled-coil domains 1 0.588 0.654 9.4E-10
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 strong 1.000 1 0 2014 2014
Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2 		polycomb group ring finger 2 0.579 0.615 0.86
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 strong 1.000 1 0 2018 2018