Disease: Dystonia
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ACOX1 Q15067 acyl-CoA oxidase 1 Enzyme 6.2E-02 0.610 0.731
ACTB P60709 actin beta Cellular structure 0.99 0.325 0.923
AFG3L2 Q9Y4W6 AFG3 like matrix AAA peptidase subunit 2 Enzyme 5.3E-09 0.588 0.462
APTX Q7Z2E3 aprataxin Nucleic acid binding 4.0E-10 0.590 0.500
ARSA P15289 arylsulfatase A Enzyme 1.1E-11 0.448 0.923
ATP6 P00846 ATP synthase F0 subunit 6 Transporter 0.541 0.731
BCS1L Q9Y276 BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone 4.7E-13 0.534 0.808
CACNA1A O00555 calcium voltage-gated channel subunit alpha1 A Ion channel 1.00 0.489 0.769
CASP3 P42574 caspase 3 Enzyme 0.10 0.351 0.923
COQ8A Q8NI60 coenzyme Q8A Kinase 9.3E-11 0.674 0.385
COQ9 O75208 coenzyme Q9 5.5E-06 0.700 0.423
COX10 Q12887 cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 Enzyme 8.4E-02 0.623 0.654
COX15 Q7KZN9 cytochrome c oxidase assembly homolog COX15 1.1E-13 0.638 0.538
COX2 P00403 cytochrome c oxidase subunit II Enzyme 0.352 0.962
CYTB P00156 cytochrome b 0.529 0.808
FASTKD2 Q9NYY8 FAST kinase domains 2 2.9E-06 0.659 0.731
FOXRED1 Q96CU9 FAD dependent oxidoreductase domain containing 1 Enzyme 2.0E-16 0.633 0.462
FXN Q16595 frataxin Enzyme 0.34 0.510 0.654
GFM2 Q969S9 G elongation factor mitochondrial 2 Enzyme 1.5E-18 0.736 0.269
MPV17 P39210 mitochondrial inner membrane protein MPV17 Receptor 9.7E-11 0.595 0.577
ND1 P03886 NADH dehydrogenase, subunit 1 (complex I) Enzyme 0.522 0.769
ND3 P03897 NADH dehydrogenase, subunit 3 (complex I) 0.604 0.654
ND4 P03905 NADH dehydrogenase, subunit 4 (complex I) Enzyme 0.546 0.769
ND5 P03915 NADH dehydrogenase, subunit 5 (complex I) Enzyme 0.531 0.769
NDUFA10 O95299 NADH:ubiquinone oxidoreductase subunit A10 Enzyme 6.2E-08 0.678 0.385