Paraplegia Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Similar Terms
Downloads & Tools

Genes

72 genes involed in the disease Paraplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
ATP5MC3 ATP synthase membrane subunit c locus 3 4.0
RTN2 reticulon 2 4.0
ABHD16A abhydrolase domain containing 16A 4.0
DSTYK dual serine/threonine and tyrosine protein kinase 4.0
CPT1C carnitine palmitoyltransferase 1C 4.0
CYP2U1 cytochrome P450, family 2, subfamily U, polypeptide 1 4.0
TMEM63C transmembrane protein 63C 4.0
NT5C2 5'-nucleotidase, cytosolic II 4.0
PLP1 proteolipid protein 1 4.0
ERLIN2 ER lipid raft associated 2 4.0
ERLIN1 ER lipid raft associated 1 4.0
ZFYVE26 zinc finger, FYVE domain containing 26 4.0
ZFYVE27 zinc finger, FYVE domain containing 27 4.0
NFU1 NFU1 iron-sulfur cluster scaffold 4.0
SPTSSA serine palmitoyltransferase, small subunit A 4.0
FARS2 phenylalanyl-tRNA synthetase 2, mitochondrial 4.0
AMPD2 adenosine monophosphate deaminase 2 4.0
AP4S1 adaptor-related protein complex 4, sigma 1 subunit 4.0
HPDL 4-hydroxyphenylpyruvate dioxygenase-like 4.0
SELENOI selenoprotein I 4.0
MARS1 methionyl-tRNA synthetase 1 4.0
SPART spartin 4.0
WASHC5 WASH complex subunit 5 4.0
PI4KA phosphatidylinositol 4-kinase, catalytic, alpha 4.0
SPTAN1 spectrin, alpha, non-erythrocytic 1 4.0
CAPN1 calpain 1, (mu/I) large subunit 4.0
KIF5A kinesin family member 5A 4.0
PNPLA6 patatin-like phospholipase domain containing 6 4.0
L1CAM L1 cell adhesion molecule 4.0
MAG myelin associated glycoprotein 4.0
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1 4.0
UBAP1 ubiquitin associated protein 1 4.0
ATP13A2 ATPase type 13A2 4.0
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1 4.0
FA2H fatty acid 2-hydroxylase 4.0
KIF1A kinesin family member 1A 4.0
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase) 4.0
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin) 4.0
DDHD1 DDHD domain containing 1 4.0
PCYT2 phosphate cytidylyltransferase 2, ethanolamine 4.0
ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1 4.0
TECPR2 tectonin beta-propeller repeat containing 2 4.0
DDHD2 DDHD domain containing 2 4.0
AP5Z1 adaptor-related protein complex 5, zeta 1 subunit 4.0
HACE1 HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 4.0
B4GALNT1 beta-1,4-N-acetyl-galactosaminyl transferase 1 4.0
KLC2 kinesin light chain 2 4.0
HSPD1 heat shock 60kDa protein 1 (chaperonin) 4.0
SPAST spastin 4.0
RNF170 ring finger protein 170 4.0
KIDINS220 kinase D-interacting substrate, 220kDa 4.0
GJC2 gap junction protein, gamma 2, 47kDa 4.0
C19ORF12 chromosome 19 open reading frame 12 4.0
AP4B1 adaptor-related protein complex 4, beta 1 subunit 4.0
IBA57 IBA57, iron-sulfur cluster assembly homolog (S. cerevisiae) 4.0
VPS37A vacuolar protein sorting 37 homolog A (S. cerevisiae) 4.0
AP4M1 adaptor-related protein complex 4, mu 1 subunit 4.0
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1 4.0
ARL6IP1 ADP-ribosylation factor-like 6 interacting protein 1 4.0
REEP2 receptor accessory protein 2 4.0
REEP1 receptor accessory protein 1 4.0
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit 4.0
ATL1 atlastin GTPase 1 4.0
AMFR autocrine motility factor receptor, E3 ubiquitin protein ligase 4.0
KPNA3 karyopherin alpha 3 (importin alpha 4) 4.0
GBA2 glucosidase, beta (bile acid) 2 4.0
FICD FIC domain containing 4.0
ALDH18A1 aldehyde dehydrogenase 18 family, member A1 4.0
SPG11 spastic paraplegia 11 (autosomal recessive) 4.0
TFG TRK-fused gene 4.0
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive) 4.0
SPG21 spastic paraplegia 21 (autosomal recessive, Mast syndrome) 4.0