Disease: Gait abnormality
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
PLEKHG4 Q58EX7 pleckstrin homology and RhoGEF domain containing G4 1.1E-16 0.769 0.154
MECR Q9BV79 mitochondrial trans-2-enoyl-CoA reductase 2.2E-05 0.736 0.385
MICOS13 Q5XKP0 mitochondrial contact site and cristae organizing system subunit 13 8.3E-04 0.736 0.346
EIF2B3 Q9NR50 eukaryotic translation initiation factor 2B subunit gamma 0.57 0.729 0.346
LYRM7 Q5U5X0 LYR motif containing 7 2.2E-02 0.716 0.346
SNORD118 small nucleolar RNA, C/D box 118 0.686 0.462
PABPN1 Q86U42 poly(A) binding protein nuclear 1 0.39 0.674 0.423
WDR81 Q562E7 WD repeat domain 81 6.7E-08 0.670 0.462
TANGO2 Q6ICL3 transport and golgi organization 2 homolog 1.5E-04 0.666 0.615
CCDC141 Q6ZP82 coiled-coil domain containing 141 1.6E-33 0.666 0.538
EIF2B1 Q14232 eukaryotic translation initiation factor 2B subunit alpha 7.6E-05 0.663 0.538
EIF2B4 Q9UI10 eukaryotic translation initiation factor 2B subunit delta 0.96 0.659 0.538
FLRT3 Q9NZU0 fibronectin leucine rich transmembrane protein 3 0.22 0.659 0.615
GLRX5 Q86SX6 glutaredoxin 5 Enzyme 0.75 0.659 0.538
ATP8A2 Q9NTI2 ATPase phospholipid transporting 8A2 Transporter 1.2E-12 0.659 0.577
NDUFAF6 Q330K2 NADH:ubiquinone oxidoreductase complex assembly factor 6 9.1E-08 0.659 0.615
NHLRC1 Q6VVB1 NHL repeat containing E3 ubiquitin protein ligase 1 9.4E-02 0.656 0.423
OPA3 Q9H6K4 outer mitochondrial membrane lipid metabolism regulator OPA3 0.57 0.653 0.385
VPS13A Q96RL7 vacuolar protein sorting 13 homolog A 9.3E-22 0.650 0.577
EIF2B2 P49770 eukaryotic translation initiation factor 2B subunit beta 2.1E-10 0.647 0.538
ALS2 Q96Q42 alsin Rho guanine nucleotide exchange factor ALS2 8.7E-12 0.647 0.423
B4GALNT1 Q00973 beta-1,4-N-acetyl-galactosaminyltransferase 1 3.9E-05 0.644 0.615
C19orf12 Q9NSK7 chromosome 19 open reading frame 12 0.34 0.641 0.615
SLC20A2 Q08357 solute carrier family 20 member 2 Transporter 0.97 0.638 0.577
PDE8B O95263 phosphodiesterase 8B 1.00 0.638 0.500