| Symbol |
Name |
|
ABCD1
|
ATP-binding cassette, sub-family D (ALD), member 1
|
|
ABCD2
|
ATP-binding cassette, sub-family D (ALD), member 2
|
|
AFG3L2
|
AFG3-like AAA ATPase 2
|
|
ALS2
|
amyotrophic lateral sclerosis 2 (juvenile)
|
|
ASPA
|
aspartoacylase
|
|
ATP8A2
|
ATPase, aminophospholipid transporter, class I, type 8A, member 2
|
|
CACNA2D2
|
calcium channel, voltage-dependent, alpha 2/delta subunit 2
|
|
CHP1
|
calcineurin-like EF-hand protein 1
|
|
CISD2
|
CDGSH iron sulfur domain 2
|
|
CLCN1
|
chloride channel, voltage-sensitive 1
|
|
CLCN2
|
chloride channel, voltage-sensitive 2
|
|
CLN6
|
ceroid-lipofuscinosis, neuronal 6, late infantile, variant
|
|
CLN8
|
ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
|
|
CLP1
|
cleavage and polyadenylation factor I subunit 1
|
|
CNP
|
2',3'-cyclic nucleotide 3' phosphodiesterase
|
|
CNTF
|
ciliary neurotrophic factor
|
|
DOCK3
|
dedicator of cytokinesis 3
|
|
DST
|
dystonin
|
|
EPG5
|
ectopic P-granules autophagy protein 5 homolog (C. elegans)
|
|
EPM2A
|
epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
|
|
GALC
|
galactosylceramidase
|
|
GARS
|
glycyl-tRNA synthetase
|
|
HSD17B4
|
hydroxysteroid (17-beta) dehydrogenase 4
|
|
KCNJ10
|
potassium channel, inwardly rectifying subfamily J, member 10
|
|
KIF1A
|
kinesin family member 1A
|
|
KLC1
|
kinesin light chain 1
|
|
LPIN1
|
lipin 1
|
|
LRSAM1
|
leucine rich repeat and sterile alpha motif containing 1
|
|
LYNX1
|
Ly6/neurotoxin 1
|
|
MAG
|
myelin associated glycoprotein
|
|
MTMR2
|
myotubularin related protein 2
|
|
NDUFS4
|
NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
|
|
NEFH
|
neurofilament, heavy polypeptide
|
|
NEFM
|
neurofilament, medium polypeptide
|
|
NKX6-2
|
NK6 homeobox 2
|
|
NMNAT2
|
nicotinamide nucleotide adenylyltransferase 2
|
|
OPA3
|
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
|
|
PLA2G6
|
phospholipase A2, group VI (cytosolic, calcium-independent)
|
|
PLP1
|
proteolipid protein 1
|
|
PMP22
|
peripheral myelin protein 22
|
|
PSAP
|
prosaposin
|
|
REEP1
|
receptor accessory protein 1
|
|
SCN8A
|
sodium channel, voltage gated, type VIII alpha subunit
|
|
SLC12A6
|
solute carrier family 12 (potassium/chloride transporter), member 6
|
|
SLC9A1
|
solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
|
|
SOD2
|
superoxide dismutase 2, mitochondrial
|
|
SPG7
|
spastic paraplegia 7 (pure and complicated autosomal recessive)
|
|
SPTBN4
|
spectrin, beta, non-erythrocytic 4
|
|
STMN1
|
stathmin 1
|
|
STXBP1
|
syntaxin binding protein 1
|
|
TBCE
|
tubulin folding cofactor E
|
|
UBE4B
|
ubiquitination factor E4B
|
|
UCHL1
|
ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
|
|
UCHL3
|
ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase)
|
|
USP14
|
ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)
|
|
VEGFA
|
vascular endothelial growth factor A
|
