Disease: Stereotypic Movement Disorder
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
LINS1 Q8NG48 lines homolog 1 2.4E-07 0.691 0.231
LMAN2L Q9H0V9 lectin, mannose binding 2 like Transporter 2.0E-11 0.641 0.385
MAN1B1 Q9UKM7 mannosidase alpha class 1B member 1 Chaperone 1.2E-08 0.606 0.577
MAPT P10636 microtubule associated protein tau 6.0E-03 0.446 0.923
MBD5 Q9P267 methyl-CpG binding domain protein 5 1.00 0.581 0.808
MBOAT7 Q96N66 membrane bound O-acyltransferase domain containing 7 Enzyme 0.11 0.612 0.500
MECP2 P51608 methyl-CpG binding protein 2 Epigenetic regulator 0.89 0.414 0.846
MED23 Q9ULK4 mediator complex subunit 23 3.1E-08 0.612 0.654
MED25 Q71SY5 mediator complex subunit 25 Transcription factor 8.4E-07 0.582 0.654
METTL23 Q86XA0 methyltransferase like 23 1.3E-07 0.682 0.231
NDP Q00604 norrin cystine knot growth factor NDP 0.65 0.566 0.692
NDST1 P52848 N-deacetylase and N-sulfotransferase 1 1.00 0.608 0.692
NSUN2 Q08J23 NOP2/Sun RNA methyltransferase 2 Enzyme 2.6E-04 0.559 0.846
PGAP1 Q75T13 post-GPI attachment to proteins inositol deacylase 1 Transporter 3.2E-08 0.650 0.423
PIGC Q92535 phosphatidylinositol glycan anchor biosynthesis class C Enzyme 5.5E-03 0.691 0.346
PRSS12 P56730 serine protease 12 Enzyme 8.4E-29 0.682 0.308
RAI1 Q7Z5J4 retinoic acid induced 1 Transcription factor 1.00 0.545 0.731
REM1 O75628 RRAD and GEM like GTPase 1 5.3E-08 0.531 0.885
RSRC1 Q96IZ7 arginine and serine rich coiled-coil 1 7.5E-05 0.650 0.462
RTTN Q86VV8 rotatin 9.0E-34 0.619 0.654
SARS1 P49591 seryl-tRNA synthetase 1 Enzyme 1.00 0.558 0.769
SIK1 A0A0B4J2F2 P57059 salt inducible kinase 1 Kinase 0.94 0.544 0.731
SLC45A1 Q9Y2W3 solute carrier family 45 member 1 Transporter 2.5E-05 0.674 0.269
SLC9A6 Q92581 solute carrier family 9 member A6 Transporter 1.00 0.516 0.846
SMC1A Q14683 structural maintenance of chromosomes 1A 1.00 0.509 0.808