paraplegia Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
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Genes

46 genes co-occuring with the biological term paraplegia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
AP4B1 adaptor-related protein complex 4, beta 1 subunit
AP5B1 adaptor-related protein complex 5, beta 1 subunit
ATL1 atlastin GTPase 1
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
C12ORF65 chromosome 12 open reading frame 65
C19ORF12 chromosome 19 open reading frame 12
C9ORF72 chromosome 9 open reading frame 72
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
DDHD2 DDHD domain containing 2
DPY30 dpy-30 homolog (C. elegans)
ERLIN2 ER lipid raft associated 2
F12 coagulation factor XII (Hageman factor)
FA2H fatty acid 2-hydroxylase
GBA2 glucosidase, beta (bile acid) 2
GBE1 glucan (1,4-alpha-), branching enzyme 1
GLRX5 glutaredoxin 5
HSPD1 heat shock 60kDa protein 1 (chaperonin)
HSPE1 heat shock 10kDa protein 1
IBA57 IBA57, iron-sulfur cluster assembly homolog (S. cerevisiae)
KIAA0196 KIAA0196
KIF1C kinesin family member 1C
KIF5A kinesin family member 5A
L1CAM L1 cell adhesion molecule
LOC647275 purine nucleoside phosphorylase pseudogene
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
PI4K2A phosphatidylinositol 4-kinase type 2 alpha
PLP1 proteolipid protein 1
REEP1 receptor accessory protein 1
REEP2 receptor accessory protein 2
RTN2 reticulon 2
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG19 spastic paraplegia 19 (autosomal dominant)
SPG20 spastic paraplegia 20 (Troyer syndrome)
SPG21 spastic paraplegia 21 (autosomal recessive, Mast syndrome)
SPG34 spastic paraplegia 34 (autosomal dominant)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TH tyrosine hydroxylase
ZFYVE26 zinc finger, FYVE domain containing 26
ZFYVE27 zinc finger, FYVE domain containing 27