Disease: nervous system disorder
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ABO P16442 ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase Enzyme 0.427 0.885
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
HRES1 P13985 HTLV-1 related endogenous sequence 0.636 0.615
HTC2 hypertrichosis 2 (generalized, congenital) 0.392 0.808
NEFL P07196 neurofilament light 0.488 0.769
MRGPRX3 Q96LB0 MAS related GPR family member X3 G-protein coupled receptor 0.529 0.923
MRGPRX4 Q96LA9 MAS related GPR family member X4 G-protein coupled receptor 0.531 0.923
MRGPRX1 Q96LB2 MAS related GPR family member X1 G-protein coupled receptor 0.531 0.923
MIR132 microRNA 132 0.485 0.846
MIR155 microRNA 155 0.384 0.885
MIR21 microRNA 21 0.363 0.846
VN1R17P Q8TDU5 vomeronasal 1 receptor 17 pseudogene 0.529 0.923
GPR166P G protein-coupled receptor 166 pseudogene 0.531 0.923
BDNF-AS BDNF antisense RNA 0.638 0.538
C20orf181 chromosome 20 open reading frame 181 0.479 0.885
FMR1-IT1 FMR1 intronic transcript 1 0.716 0.385
ABCA13 Q86UQ4 ATP binding cassette subfamily A member 13 Transporter 8.8E-114 0.722 0.308
ATM Q13315 ATM serine/threonine kinase Kinase 5.6E-47 0.374 0.885
ACE P12821 angiotensin I converting enzyme Enzyme 1.0E-37 0.328 0.923
LRRK2 Q5S007 leucine rich repeat kinase 2 Kinase 2.6E-30 0.510 0.808
CYP2D6 P10635 cytochrome P450 family 2 subfamily D member 6 1.1E-25 0.437 0.885
BRCA2 P51587 BRCA2 DNA repair associated Nucleic acid binding 2.4E-25 0.379 0.846
SACS Q9NZJ4 sacsin molecular chaperone 1.1E-23 0.606 0.654
ABCB6 Q9NP58 ATP binding cassette subfamily B member 6 (Langereis blood group) Transporter 8.6E-19 0.431 0.885