Disease: Stereotypic Movement Disorder
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
AP4B1 Q9Y6B7 adaptor related protein complex 4 subunit beta 1 Transporter 1.3E-09 0.631 0.654
AP4E1 Q9UPM8 adaptor related protein complex 4 subunit epsilon 1 Receptor 2.8E-03 0.656 0.385
AP4M1 O00189 adaptor related protein complex 4 subunit mu 1 Extracellular structure 4.5E-17 0.638 0.500
CDKL5 O76039 cyclin dependent kinase like 5 Kinase 1.00 0.522 0.692
DEAF1 O75398 DEAF1 transcription factor 3.4E-04 0.575 0.615
ELP2 Q6IA86 elongator acetyltransferase complex subunit 2 4.2E-20 0.716 0.538
EZR P15311 ezrin Cellular structure 0.18 0.476 0.808
FGFR2 P21802 fibroblast growth factor receptor 2 Kinase 1.00 0.380 0.808
FOXG1 P55316 forkhead box G1 0.94 0.522 0.692
HDAC4 P56524 histone deacetylase 4 Epigenetic regulator 1.00 0.484 0.885
LETM1 O95202 leucine zipper and EF-hand containing transmembrane protein 1 Transporter 1.2E-06 0.545 0.692
LINS1 Q8NG48 lines homolog 1 2.4E-07 0.691 0.231
MAN1B1 Q9UKM7 mannosidase alpha class 1B member 1 Chaperone 1.2E-08 0.606 0.577
MECP2 P51608 methyl-CpG binding protein 2 Epigenetic regulator 0.89 0.414 0.846
MEF2C Q06413 myocyte enhancer factor 2C Transcription factor 1.7E-02 0.517 0.769
METTL23 Q86XA0 methyltransferase like 23 1.3E-07 0.682 0.231
NAA15 Q9BXJ9 N-alpha-acetyltransferase 15, NatA auxiliary subunit Enzyme 1.00 0.700 0.423
NDST1 P52848 N-deacetylase and N-sulfotransferase 1 1.00 0.608 0.692
NRXN1 P58400 Q9ULB1 neurexin 1 1.00 0.581 0.692
PRRT2 Q7Z6L0 proline rich transmembrane protein 2 0.58 0.448 0.808
RAB39B Q96DA2 RAB39B, member RAS oncogene family 0.83 0.619 0.615
RAI1 Q7Z5J4 retinoic acid induced 1 Transcription factor 1.00 0.545 0.731
SCN8A Q9UQD0 sodium voltage-gated channel alpha subunit 8 Ion channel 1.00 0.510 0.731
SLC9A6 Q92581 solute carrier family 9 member A6 Transporter 1.00 0.516 0.846
SNRPN P63162 Q9Y675 small nuclear ribonucleoprotein polypeptide N Nucleic acid binding 4.3E-02 0.538 0.731