Disease: Deglutition Disorders
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ACTB P60709 actin beta Cellular structure 0.99 0.325 0.923
ADAR P55265 adenosine deaminase RNA specific Enzyme 2.6E-02 0.501 0.808
ALS2 Q96Q42 alsin Rho guanine nucleotide exchange factor ALS2 8.7E-12 0.647 0.423
APOE P02649 apolipoprotein E 1.9E-03 0.338 0.962
ARX Q96QS3 aristaless related homeobox 0.91 0.516 0.654
ATP13A2 Q9NQ11 ATPase cation transporting 13A2 9.0E-09 0.566 0.577
ATP1A3 P13637 ATPase Na+/K+ transporting subunit alpha 3 Transporter 1.00 0.544 0.615
ATP7B P35670 ATPase copper transporting beta Transporter 4.8E-30 0.529 0.654
ATXN1 P54253 ataxin 1 0.97 0.534 0.769
ATXN2 Q99700 ataxin 2 Nucleic acid binding 0.85 0.482 0.808
ATXN3 P54252 ataxin 3 Enzyme 0.11 0.521 0.808
ATXN7 O15265 ataxin 7 0.96 0.581 0.654
BDNF P23560 brain derived neurotrophic factor Signaling 0.66 0.345 0.923
C19orf12 Q9NSK7 chromosome 19 open reading frame 12 0.34 0.641 0.615
CACNA1A O00555 calcium voltage-gated channel subunit alpha1 A Ion channel 1.00 0.489 0.769
FA2H Q7L5A8 fatty acid 2-hydroxylase Enzyme 0.15 0.573 0.654
FBXO7 Q9Y3I1 F-box protein 7 5.8E-07 0.650 0.769
GCH1 P30793 GTP cyclohydrolase 1 Enzyme 0.90 0.511 0.846
HLA-B P01889 major histocompatibility complex, class I, B 3.9E-05 0.379 0.885
HPCA P84074 hippocalcin 0.68 0.760 0.385
KCND3 Q9UK17 potassium voltage-gated channel subfamily D member 3 Ion channel 0.99 0.619 0.615
KMT2B Q9UMN6 lysine methyltransferase 2B 1.00 0.529 0.808
LRRK2 Q5S007 leucine rich repeat kinase 2 Kinase 2.6E-30 0.510 0.808
LY6E Q16553 lymphocyte antigen 6 family member E 0.32 0.563 0.808
MECP2 P51608 methyl-CpG binding protein 2 Epigenetic regulator 0.89 0.414 0.846