| Symbol |
Name |
|
APP
|
amyloid beta (A4) precursor protein
|
|
ARSA
|
arylsulfatase A
|
|
ATG4B
|
autophagy related 4B, cysteine peptidase
|
|
ATP2B2
|
ATPase, Ca++ transporting, plasma membrane 2
|
|
BLOC1S5
|
biogenesis of lysosomal organelles complex-1, subunit 5, muted
|
|
BLOC1S6
|
biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
|
|
CACNG2
|
calcium channel, voltage-dependent, gamma subunit 2
|
|
CDH23
|
cadherin-related 23
|
|
CHD7
|
chromodomain helicase DNA binding protein 7
|
|
CLIC5
|
chloride intracellular channel 5
|
|
CNTNAP1
|
contactin associated protein 1
|
|
CYBA
|
cytochrome b-245, alpha polypeptide
|
|
DBNL
|
drebrin-like
|
|
DFNB31
|
deafness, autosomal recessive 31
|
|
DFNB59
|
deafness, autosomal recessive 59
|
|
DOCK3
|
dedicator of cytokinesis 3
|
|
DSCAM
|
Down syndrome cell adhesion molecule
|
|
ESPN
|
espin
|
|
FOXI1
|
forkhead box I1
|
|
GABRB3
|
gamma-aminobutyric acid (GABA) A receptor, beta 3
|
|
GIT1
|
G protein-coupled receptor kinase interacting ArfGAP 1
|
|
GLRB
|
glycine receptor, beta
|
|
GRM8
|
glutamate receptor, metabotropic 8
|
|
GRXCR1
|
glutaredoxin, cysteine rich 1
|
|
HCN2
|
hyperpolarization activated cyclic nucleotide gated potassium channel 2
|
|
KCNA1
|
potassium channel, voltage gated shaker related subfamily A, member 1
|
|
KCNMA1
|
potassium channel, calcium activated large conductance subfamily M alpha, member 1
|
|
KCNQ1
|
potassium channel, voltage gated KQT-like subfamily Q, member 1
|
|
LAMA4
|
laminin, alpha 4
|
|
LHFPL5
|
lipoma HMGIC fusion partner-like 5
|
|
LOC102723475
|
putative uncharacterized protein LOC388820
|
|
LSAMP
|
limbic system-associated membrane protein
|
|
LYST
|
lysosomal trafficking regulator
|
|
MCOLN3
|
mucolipin 3
|
|
MPZ
|
myelin protein zero
|
|
MYO15A
|
myosin XVA
|
|
MYO6
|
myosin VI
|
|
MYO7A
|
myosin VIIA
|
|
NDUFS4
|
NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
|
|
NOX3
|
NADPH oxidase 3
|
|
NREP
|
neuronal regeneration related protein
|
|
OTOG
|
otogelin
|
|
OTOP1
|
otopetrin 1
|
|
PAH
|
phenylalanine hydroxylase
|
|
PCDH15
|
protocadherin-related 15
|
|
POU4F3
|
POU class 4 homeobox 3
|
|
PTPRD
|
protein tyrosine phosphatase, receptor type, D
|
|
S1PR2
|
sphingosine-1-phosphate receptor 2
|
|
SEZ6
|
seizure related 6 homolog (mouse)
|
|
SLC26A4
|
solute carrier family 26 (anion exchanger), member 4
|
|
SLC30A4
|
solute carrier family 30 (zinc transporter), member 4
|
|
SLC6A8
|
solute carrier family 6 (neurotransmitter transporter), member 8
|
|
SOX2
|
SRY (sex determining region Y)-box 2
|
|
SPRED1
|
sprouty-related, EVH1 domain containing 1
|
|
TBX10
|
T-box 10
|
|
TMIE
|
transmembrane inner ear
|
|
TMPRSS3
|
transmembrane protease, serine 3
|
|
TNC
|
tenascin C
|
|
USH1C
|
Usher syndrome 1C (autosomal recessive, severe)
|
|
USH1G
|
Usher syndrome 1G (autosomal recessive)
|
|
WFS1
|
Wolfram syndrome 1 (wolframin)
|
|
WNT1
|
wingless-type MMTV integration site family, member 1
|
|
ZDHHC17
|
zinc finger, DHHC-type containing 17
|
