Nerve Degeneration Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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32 genes associated with the Nerve Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
APOE apolipoprotein E
APP amyloid beta (A4) precursor protein
ATXN2 ataxin 2
BACE1 beta-site APP-cleaving enzyme 1
CDKN2B-AS1 CDKN2B antisense RNA 1
CNR1 cannabinoid receptor 1 (brain)
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DHFR dihydrofolate reductase
GAPDH glyceraldehyde-3-phosphate dehydrogenase
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
GSK3A glycogen synthase kinase 3 alpha
HFE hemochromatosis
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
KIF5A kinesin family member 5A
MAPT microtubule-associated protein tau
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NINJ1 ninjurin 1
PARK2 parkin RBR E3 ubiquitin protein ligase
PITX3 paired-like homeodomain 3
SIX1 SIX homeobox 1
SIX6 SIX homeobox 6
SMN1 survival of motor neuron 1, telomeric
SMN2 survival of motor neuron 2, centromeric
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SOD1 superoxide dismutase 1, soluble
SORL1 sortilin-related receptor, L(DLR class) A repeats containing
UBQLN1 ubiquilin 1
WFS1 Wolfram syndrome 1 (wolframin)