Paraplegia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0030486
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Genes

63 genes associated with the disease Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ALB albumin
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
ANOS1 anosmin 1
AR androgen receptor
ATG7 autophagy related 7
ATL1 atlastin GTPase 1
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
BECN1 beclin 1, autophagy related
CCDC141 coiled-coil domain containing 141
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
CD38 CD38 molecule
CD6 CD6 molecule
CEACAM5 carcinoembryonic antigen-related cell adhesion molecule 5
CHD7 chromodomain helicase DNA binding protein 7
CKAP2L cytoskeleton associated protein 2-like
CTSL cathepsin L
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
DCC DCC netrin 1 receptor
DUSP6 dual specificity phosphatase 6
ERCC2 excision repair cross-complementation group 2
ERCC3 excision repair cross-complementation group 3
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
FOXO4 forkhead box O4
GTF2E2 general transcription factor IIE, polypeptide 2, beta 34kDa
GTF2H5 general transcription factor IIH, polypeptide 5
HESX1 HESX homeobox 1
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IL17RD interleukin 17 receptor D
KIF1A kinesin family member 1A
KISS1R KISS1 receptor
MBP myelin basic protein
MPLKIP M-phase specific PLK1 interacting protein
NAGS N-acetylglutamate synthase
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
NLN neurolysin (metallopeptidase M3 family)
NOS2 nitric oxide synthase 2, inducible
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
PAH phenylalanine hydroxylase
PLP1 proteolipid protein 1
PPP3R1 protein phosphatase 3, regulatory subunit B, alpha
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
PSAP prosaposin
RNF113A ring finger protein 113A
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SOST sclerostin
SOX10 SRY (sex determining region Y)-box 10
SP110 SP110 nuclear body protein
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG21 spastic paraplegia 21 (autosomal recessive, Mast syndrome)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
SPRY4 sprouty homolog 4 (Drosophila)
TACR3 tachykinin receptor 3
TP63 tumor protein p63
TTR transthyretin
WDR11 WD repeat domain 11
ZFYVE26 zinc finger, FYVE domain containing 26