Roussy-Levy Syndrome (Disorder) Gene Set
Genes
26 genes associated with the disease Roussy-Levy Syndrome (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
COX6A1
|
cytochrome c oxidase subunit VIa polypeptide 1
|
|
DHTKD1
|
dehydrogenase E1 and transketolase domain containing 1
|
|
DYNC1H1
|
dynein, cytoplasmic 1, heavy chain 1
|
|
EGR2
|
early growth response 2
|
|
FGD4
|
FYVE, RhoGEF and PH domain containing 4
|
|
FIG4
|
FIG4 phosphoinositide 5-phosphatase
|
|
FXN
|
frataxin
|
|
GARS
|
glycyl-tRNA synthetase
|
|
GDAP1
|
ganglioside induced differentiation associated protein 1
|
|
GJB1
|
gap junction protein, beta 1, 32kDa
|
|
HOXD10
|
homeobox D10
|
|
KIF1B
|
kinesin family member 1B
|
|
LMNA
|
lamin A/C
|
|
LRSAM1
|
leucine rich repeat and sterile alpha motif containing 1
|
|
MFN2
|
mitofusin 2
|
|
MORC2
|
MORC family CW-type zinc finger 2
|
|
MPZ
|
myelin protein zero
|
|
MTMR2
|
myotubularin related protein 2
|
|
NDRG1
|
N-myc downstream regulated 1
|
|
NEFL
|
neurofilament, light polypeptide
|
|
PMP22
|
peripheral myelin protein 22
|
|
SBF2
|
SET binding factor 2
|
|
SH3TC2
|
SH3 domain and tetratricopeptide repeats 2
|
|
SLC12A6
|
solute carrier family 12 (potassium/chloride transporter), member 6
|
|
SLC25A46
|
solute carrier family 25, member 46
|
|
TRPV4
|
transient receptor potential cation channel, subfamily V, member 4
|
