Disease: Epilepsy
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
HTC2 hypertrichosis 2 (generalized, congenital) 0.392 0.808
COX2 P00403 cytochrome c oxidase subunit II Enzyme 0.352 0.962
COX3 P00414 cytochrome c oxidase III Enzyme 0.546 0.808
NANS Q9NR45 N-acetylneuraminate synthase Enzyme 0.545 0.692
RSS Russell Silver syndrome 0.578 0.692
MTCO2P12 MT-CO2 pseudogene 12 0.368 0.962
CNTN6 Q9UQ52 contactin 6 Receptor 9.0E-31 0.678 0.462
EMC1 Q8N766 ER membrane protein complex subunit 1 6.7E-26 0.700 0.462
CEP128 Q6ZU80 centrosomal protein 128 4.7E-23 0.780 0.423
ABCB6 Q9NP58 ATP binding cassette subfamily B member 6 (Langereis blood group) Transporter 8.6E-19 0.431 0.885
SCN7A Q01118 sodium voltage-gated channel alpha subunit 7 Ion channel 2.2E-17 0.585 0.692
TRPV1 Q8NER1 transient receptor potential cation channel subfamily V member 1 Ion channel 1.0E-16 0.446 0.885
BBS4 Q96RK4 Bardet-Biedl syndrome 4 1.5E-16 0.647 0.615
WWOX Q9NZC7 WW domain containing oxidoreductase Enzyme 1.2E-15 0.453 0.808
TSHR P16473 thyroid stimulating hormone receptor G-protein coupled receptor 3.0E-15 0.486 0.808
SZT2 Q5T011 SZT2 subunit of KICSTOR complex 2.3E-14 0.670 0.423
RARS2 Q5T160 arginyl-tRNA synthetase 2, mitochondrial 7.7E-14 0.663 0.462
QARS1 P47897 glutaminyl-tRNA synthetase 1 Enzyme 2.7E-13 0.716 0.231
TUBB3 Q13509 tubulin beta 3 class III Cellular structure 2.6E-10 0.486 0.808
MTHFR P42898 methylenetetrahydrofolate reductase 3.2E-10 0.337 0.885
CP P00450 ceruloplasmin Enzyme 4.2E-10 0.466 0.846
ALDH6A1 Q02252 aldehyde dehydrogenase 6 family member A1 Enzyme 7.6E-10 0.716 0.462
EPRS1 P07814 glutamyl-prolyl-tRNA synthetase 1 Enzyme 1.0E-09 0.644 0.538
WDR73 Q6P4I2 WD repeat domain 73 2.8E-09 0.610 0.500
UROD P06132 uroporphyrinogen decarboxylase 1.3E-08 0.521 0.769