Disease: Neurodevelopmental Disorders
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
FRAXE fragile site, folic acid type, rare, fra(X)(q28) E 0.636 0.462
HTC2 hypertrichosis 2 (generalized, congenital) 0.392 0.808
SRY Q05066 sex determining region Y Transcription factor 0.456 0.808
CBLL2 Q8N7E2 Cbl proto-oncogene like 2 Enzyme 0.476 0.808
MIR137 microRNA 137 0.513 0.846
MDD1 Major depressive disorder 0.682 0.308
BDNF-AS BDNF antisense RNA 0.638 0.538
PTLS Potocki-Lupski syndrome 0.780 0.308
PTCHD1-AS PTCHD1 antisense RNA (head to head) 0.839 0.308
ERICD E2F1-regulated inhibitor of cell death 0.691 0.654
VPS13B Q7Z7G8 vacuolar protein sorting 13 homolog B 2.5E-45 0.579 0.769
CNTN6 Q9UQ52 contactin 6 Receptor 9.0E-31 0.678 0.462
MCPH1 Q8NEM0 microcephalin 1 Nucleic acid binding 7.8E-30 0.540 0.846
AHI1 Q8N157 Abelson helper integration site 1 1.1E-25 0.513 0.846
CAPS2 Q9BXY5 calcyphosine 2 6.1E-24 0.839 0.077
WDR62 O43379 WD repeat domain 62 2.4E-23 0.597 0.615
LAMB1 P07942 laminin subunit beta 1 Enzyme modulator 5.1E-22 0.615 0.654
CYP2C19 P33261 cytochrome P450 family 2 subfamily C member 19 6.5E-20 0.467 0.846
KANK1 Q14678 KN motif and ankyrin repeat domains 1 8.0E-18 0.641 0.538
WWOX Q9NZC7 WW domain containing oxidoreductase Enzyme 1.2E-15 0.453 0.808
KDM5B Q9UGL1 lysine demethylase 5B Epigenetic regulator 7.9E-15 0.532 0.731
MTRR Q9UBK8 5-methyltetrahydrofolate-homocysteine methyltransferase reductase 2.2E-14 0.502 0.808
SSTR4 P31391 somatostatin receptor 4 G-protein coupled receptor 3.7E-13 0.469 0.846
COL9A3 Q14050 collagen type IX alpha 3 chain 3.3E-12 0.569 0.769
ATG7 O95352 autophagy related 7 Enzyme 7.4E-12 0.505 0.769