Disease: Mental Retardation
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
FMR1-IT1 FMR1 intronic transcript 1 0.716 0.385
FRAXA fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation) 0.641 0.462
FRAXE fragile site, folic acid type, rare, fra(X)(q28) E 0.636 0.462
WDR81 Q562E7 WD repeat domain 81 6.7E-08 0.670 0.462
ZMYND11 Q15326 zinc finger MYND-type containing 11 1.00 0.647 0.500
AFF2 P51816 AF4/FMR2 family member 2 Transcription factor 1.00 0.636 0.538
MED13L Q71F56 mediator complex subunit 13L 1.00 0.617 0.538
SYNGAP1 Q96PV0 synaptic Ras GTPase activating protein 1 Enzyme modulator 1.00 0.584 0.577
PCLO Q9Y6V0 piccolo presynaptic cytomatrix protein 1.00 0.656 0.577
NUFIP2 Q7Z417 nuclear FMR1 interacting protein 2 1.00 0.641 0.577
CNTN4 Q8IWV2 contactin 4 Receptor 3.3E-06 0.653 0.577
ADSL P30566 adenylosuccinate lyase Enzyme 8.9E-12 0.631 0.654
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
KCNQ2 O43526 potassium voltage-gated channel subfamily Q member 2 Ion channel 1.00 0.537 0.654
PQBP1 O60828 polyglutamine binding protein 1 Transcription factor 0.79 0.570 0.654
TMCO1 Q9UM00 transmembrane and coiled-coil domains 1 9.4E-10 0.588 0.654
ARX Q96QS3 aristaless related homeobox 0.91 0.516 0.654
KIF1A Q12756 kinesin family member 1A Cellular structure 1.00 0.559 0.692
FOXL2 P58012 forkhead box L2 Transcription factor 0.88 0.542 0.692
FOXG1 P55316 forkhead box G1 0.94 0.522 0.692
GRIN2B Q13224 glutamate ionotropic receptor NMDA type subunit 2B Ion channel 1.00 0.510 0.692
KCNJ6 P48051 potassium inwardly rectifying channel subfamily J member 6 Ion channel 0.54 0.615 0.692
CDKL5 O76039 cyclin dependent kinase like 5 Kinase 1.00 0.522 0.692
UBE3A Q05086 ubiquitin protein ligase E3A 1.00 0.561 0.692
SLC4A4 Q9Y6R1 solute carrier family 4 member 4 Transporter 1.00 0.644 0.692