Disease: Congenital Abnormality
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
EMILIN1 Q9Y6C2 elastin microfibril interfacer 1 4.4E-03 0.743 0.269
MIR876 microRNA 876 0.666 0.385
FBXW11 Q9UKB1 F-box and WD repeat domain containing 11 0.98 0.626 0.462
CALML3 P27482 calmodulin like 3 Calcium-binding protein 9.1E-04 0.621 0.500
EPHA7 Q15375 EPH receptor A7 Kinase 1.00 0.619 0.500
CRADD P78560 CASP2 and RIPK1 domain containing adaptor with death domain 0.88 0.619 0.500
EIF4A3 P38919 eukaryotic translation initiation factor 4A3 1.00 0.608 0.500
KIF26B Q2KJY2 kinesin family member 26B Cellular structure 1.00 0.670 0.500
FOXN3 O00409 forkhead box N3 0.93 0.686 0.538
HMGN1 P05114 high mobility group nucleosome binding domain 1 Nucleic acid binding 0.21 0.711 0.538
HOXB1 P14653 homeobox B1 8.2E-02 0.633 0.538
PAX7 P23759 paired box 7 0.14 0.597 0.538
COTL1 Q14019 coactosin like F-actin binding protein 1 Cellular structure 3.9E-02 0.615 0.538
MIR873 microRNA 873 0.601 0.538
H3P47 H3 histone pseudogene 47 0.603 0.538
SLC31A1 O15431 solute carrier family 31 member 1 Transporter 6.5E-02 0.612 0.577
GLDC P23378 glycine decarboxylase Enzyme 6.6E-28 0.628 0.577
SLC20A1 Q8WUM9 solute carrier family 20 member 1 Transporter 6.7E-02 0.582 0.577
AXL P30530 AXL receptor tyrosine kinase Kinase 1.3E-02 0.489 0.615
AKR1C1 Q04828 aldo-keto reductase family 1 member C1 Enzyme 3.5E-15 0.593 0.615
WNT2B Q93097 Wnt family member 2B Signaling 3.8E-02 0.644 0.615
LHX2 P50458 LIM homeobox 2 Nucleic acid binding 0.99 0.678 0.615
AKAP12 Q02952 A-kinase anchoring protein 12 3.6E-02 0.566 0.615
TRAF4 Q9BUZ4 TNF receptor associated factor 4 Signaling 0.94 0.626 0.615
EFS O43281 embryonal Fyn-associated substrate 1.8E-08 0.597 0.615