Disease: Dysarthria
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ATCAY Q86WG3 ATCAY kinesin light chain interacting caytaxin 0.62 0.805 0.192
KCTD17 Q8N5Z5 potassium channel tetramerization domain containing 17 1.8E-02 0.743 0.308
HPCA P84074 hippocalcin 0.68 0.760 0.385
NDUFA9 Q16795 NADH:ubiquinone oxidoreductase subunit A9 Enzyme 4.8E-03 0.653 0.385
ALS2 Q96Q42 alsin Rho guanine nucleotide exchange factor ALS2 8.7E-12 0.647 0.423
NUBPL Q8TB37 nucleotide binding protein like 1.1E-05 0.670 0.423
THAP1 Q9NVV9 THAP domain containing 1 0.80 0.644 0.462
APTX Q7Z2E3 aprataxin Nucleic acid binding 4.0E-10 0.590 0.500
PDHA1 P08559 pyruvate dehydrogenase E1 subunit alpha 1 0.99 0.581 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
ATP13A2 Q9NQ11 ATPase cation transporting 13A2 9.0E-09 0.566 0.577
DCAF17 Q5H9S7 DDB1 and CUL4 associated factor 17 3.7E-07 0.653 0.577
ATP1A3 P13637 ATPase Na+/K+ transporting subunit alpha 3 Transporter 1.00 0.544 0.615
KCND3 Q9UK17 potassium voltage-gated channel subfamily D member 3 Ion channel 0.99 0.619 0.615
PRKRA O75569 protein activator of interferon induced protein kinase EIF2AK2 Kinase 0.42 0.579 0.615
TUBB4A P04350 tubulin beta 4A class IVa Cellular structure 0.11 0.608 0.615
PDE10A Q9Y233 phosphodiesterase 10A 1.00 0.619 0.615
PNKD Q8N490 PNKD metallo-beta-lactamase domain containing 4.1E-08 0.615 0.615
C19orf12 Q9NSK7 chromosome 19 open reading frame 12 0.34 0.641 0.615
NDUFAF6 Q330K2 NADH:ubiquinone oxidoreductase complex assembly factor 6 9.1E-08 0.659 0.615
ATP7B P35670 ATPase copper transporting beta Transporter 4.8E-30 0.529 0.654
ECHS1 P30084 enoyl-CoA hydratase, short chain 1 Enzyme 8.8E-04 0.601 0.654
ATXN7 O15265 ataxin 7 0.96 0.581 0.654
SLC30A10 Q6XR72 solute carrier family 30 member 10 Transporter 0.98 0.578 0.654