Disease: Congenital Abnormality
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
HSPA6 P17066 heat shock protein family A (Hsp70) member 6 6.8E-06 0.743 0.423
MED13L Q71F56 mediator complex subunit 13L 1.00 0.617 0.538
ARF6 P62330 ADP ribosylation factor 6 0.72 0.631 0.577
FGFR1OP O95684 FGFR1 oncogene partner 6.3E-04 0.656 0.577
FNDC3A Q9Y2H6 fibronectin type III domain containing 3A 1.00 0.674 0.577
AXL P30530 AXL receptor tyrosine kinase Kinase 1.3E-02 0.489 0.615
TCN2 P20062 transcobalamin 2 1.0E-06 0.578 0.615
WNT2B Q93097 Wnt family member 2B Signaling 3.8E-02 0.644 0.615
TRAF4 Q9BUZ4 TNF receptor associated factor 4 Signaling 0.94 0.626 0.615
KIF3A Q9Y496 kinesin family member 3A Cellular structure 0.90 0.612 0.615
ZMIZ1 Q9ULJ6 zinc finger MIZ-type containing 1 1.00 0.588 0.615
GPR35 Q9HC97 G protein-coupled receptor 35 G-protein coupled receptor 4.9E-03 0.587 0.654
PDX1 P52945 pancreatic and duodenal homeobox 1 1.8E-02 0.530 0.654
LAMB1 P07942 laminin subunit beta 1 Enzyme modulator 5.1E-22 0.615 0.654
SLCO2A1 Q92959 solute carrier organic anion transporter family member 2A1 Transporter 2.3E-13 0.578 0.654
ZNF148 Q9UQR1 zinc finger protein 148 Transcription factor 1.00 0.615 0.654
TAB2 Q9NYJ8 TGF-beta activated kinase 1 (MAP3K7) binding protein 2 1.00 0.617 0.654
DNTT P04053 DNA nucleotidylexotransferase Enzyme 3.0E-10 0.606 0.692
RPGR Q92834 retinitis pigmentosa GTPase regulator 1.00 0.536 0.692
YWHAE P62258 tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon Chaperone 0.98 0.530 0.692
NT5C3A Q9H0P0 5'-nucleotidase, cytosolic IIIA Enzyme 1.5E-02 0.593 0.692
ACP1 P24666 acid phosphatase 1 1.8E-08 0.566 0.731
CHUK O15111 component of inhibitor of nuclear factor kappa B kinase complex Kinase 0.99 0.556 0.731
ETS1 P14921 ETS proto-oncogene 1, transcription factor Transcription factor 0.78 0.444 0.731
FUT2 Q10981 fucosyltransferase 2 Enzyme 5.3E-14 0.552 0.731