Disease: Congenital ear anomaly NOS (disorder)
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
PEX12 O00623 peroxisomal biogenesis factor 12 Transporter 9.5E-16 0.601 0.615
PEX16 Q9Y5Y5 peroxisomal biogenesis factor 16 8.3E-05 0.597 0.615
PEX26 Q7Z412 peroxisomal biogenesis factor 26 0.93 0.584 0.615
ERF P50548 ETS2 repressor factor Transcription factor 0.99 0.572 0.654
PEX10 O60683 peroxisomal biogenesis factor 10 5.4E-04 0.584 0.654
PEX13 Q92968 peroxisomal biogenesis factor 13 5.9E-05 0.597 0.654
PEX2 P28328 peroxisomal biogenesis factor 2 2.6E-04 0.582 0.654
PEX11B O96011 peroxisomal biogenesis factor 11 beta 1.3E-04 0.612 0.654
PEX14 O75381 peroxisomal biogenesis factor 14 Receptor 0.23 0.592 0.692
RAD51C O43502 RAD51 paralog C 6.2E-14 0.533 0.692
FANCA O15360 FA complementation group A 1.6E-68 0.505 0.731
FANCF Q9NPI8 FA complementation group F 0.46 0.535 0.731
PEX6 Q13608 peroxisomal biogenesis factor 6 6.3E-06 0.547 0.731
PEX19 P40855 peroxisomal biogenesis factor 19 Storage 3.2E-04 0.585 0.731
PEX5 P50542 peroxisomal biogenesis factor 5 Transporter 5.6E-05 0.561 0.731
XRCC2 O43543 X-ray repair cross complementing 2 4.0E-07 0.512 0.731
PEX3 P56589 peroxisomal biogenesis factor 3 1.6E-02 0.595 0.731
MAD2L2 Q9UI95 mitotic arrest deficient 2 like 2 8.2E-02 0.547 0.731
UBE2T Q9NPD8 ubiquitin conjugating enzyme E2 T 1.1E-05 0.550 0.731
FANCL Q9NW38 FA complementation group L Enzyme 5.9E-23 0.551 0.731
RFWD3 Q6PCD5 ring finger and WD repeat domain 3 Enzyme 3.5E-10 0.569 0.731
FANCI Q9NVI1 FA complementation group I 8.9E-37 0.543 0.731
FANCM Q8IYD8 FA complementation group M Enzyme 2.4E-15 0.543 0.731
BRIP1 Q9BX63 BRCA1 interacting protein C-terminal helicase 1 Enzyme 6.2E-17 0.507 0.731
SLX4 Q8IY92 SLX4 structure-specific endonuclease subunit 1.6E-22 0.565 0.731