Mirror Movements Disorder Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0454455
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Genes

38 genes associated with the disease Mirror Movements Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANOS1 anosmin 1
CASC5 cancer susceptibility candidate 5
CCDC141 coiled-coil domain containing 141
CDH2 cadherin 2, type 1, N-cadherin (neuronal)
CEP152 centrosomal protein 152kDa
CHD7 chromodomain helicase DNA binding protein 7
CREBBP CREB binding protein
DCC DCC netrin 1 receptor
DNAL4 dynein, axonemal, light chain 4
DUSP6 dual specificity phosphatase 6
EP300 E1A binding protein p300
FEZF1 FEZ family zinc finger 1
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLRT3 fibronectin leucine rich transmembrane protein 3
GDF6 growth differentiation factor 6
HESX1 HESX homeobox 1
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IL17RD interleukin 17 receptor D
KISS1R KISS1 receptor
MEF2C myocyte enhancer factor 2C
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
NTN1 netrin 1
NTNG1 netrin G1
POMK protein-O-mannose kinase
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
RAD51 RAD51 recombinase
RAD51B RAD51 paralog B
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SMN1 survival of motor neuron 1, telomeric
SMN2 survival of motor neuron 2, centromeric
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
TACR3 tachykinin receptor 3
WDR11 WD repeat domain 11