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
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
MICOS13 Q5XKP0 mitochondrial contact site and cristae organizing system subunit 13 8.3E-04 0.736 0.346
MECR Q9BV79 mitochondrial trans-2-enoyl-CoA reductase 2.2E-05 0.736 0.385
OPA3 Q9H6K4 outer mitochondrial membrane lipid metabolism regulator OPA3 0.57 0.653 0.385
PABPN1 Q86U42 poly(A) binding protein nuclear 1 0.39 0.674 0.423
ALS2 Q96Q42 alsin Rho guanine nucleotide exchange factor ALS2 8.7E-12 0.647 0.423
NHLRC1 Q6VVB1 NHL repeat containing E3 ubiquitin protein ligase 1 9.4E-02 0.656 0.423
TMEM106B Q9NUM4 transmembrane protein 106B 0.33 0.590 0.462
WDR81 Q562E7 WD repeat domain 81 6.7E-08 0.670 0.462
SNORD118 small nucleolar RNA, C/D box 118 0.686 0.462
PDE8B O95263 phosphodiesterase 8B 1.00 0.638 0.500
APTX Q7Z2E3 aprataxin Nucleic acid binding 4.0E-10 0.590 0.500
EIF2B1 Q14232 eukaryotic translation initiation factor 2B subunit alpha 7.6E-05 0.663 0.538
VAMP1 P23763 vesicle associated membrane protein 1 3.9E-03 0.628 0.538
EIF2B4 Q9UI10 eukaryotic translation initiation factor 2B subunit delta 0.96 0.659 0.538
EIF2B2 P49770 eukaryotic translation initiation factor 2B subunit beta 2.1E-10 0.647 0.538
MLH3 Q9UHC1 mutL homolog 3 Nucleic acid binding 4.9E-08 0.582 0.538
GLRX5 Q86SX6 glutaredoxin 5 Enzyme 0.75 0.659 0.538
JPH3 Q8WXH2 junctophilin 3 1.00 0.608 0.538
SPG11 Q96JI7 SPG11 vesicle trafficking associated, spatacsin 1.6E-39 0.576 0.538
CCDC141 Q6ZP82 coiled-coil domain containing 141 1.6E-33 0.666 0.538
ADCY5 O95622 adenylate cyclase 5 1.00 0.617 0.577
SLC20A2 Q08357 solute carrier family 20 member 2 Transporter 0.97 0.638 0.577