argininosuccinic aciduria Gene Set
Genes
28 genes co-occuring with the disease argininosuccinic aciduria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
| Symbol |
Name |
Standardized Value |
|
ASL
|
argininosuccinate lyase
|
3.10608
|
|
OTC
|
ornithine carbamoyltransferase
|
1.50316
|
|
NAGS
|
N-acetylglutamate synthase
|
1.42323
|
|
MID1
|
midline 1
|
1.22649
|
|
ASS1
|
argininosuccinate synthase 1
|
1.21955
|
|
PEX2
|
peroxisomal biogenesis factor 2
|
1.01216
|
|
HMGCL
|
3-hydroxymethyl-3-methylglutaryl-CoA lyase
|
0.942443
|
|
MYO5A
|
myosin VA (heavy chain 12, myoxin)
|
0.850354
|
|
SLC25A13
|
solute carrier family 25 (aspartate/glutamate carrier), member 13
|
0.740299
|
|
ATP1A2
|
ATPase, Na+/K+ transporting, alpha 2 polypeptide
|
0.691495
|
|
MMD
|
monocyte to macrophage differentiation-associated
|
0.658026
|
|
PEPD
|
peptidase D
|
0.654067
|
|
ASPA
|
aspartoacylase
|
0.65288
|
|
GAN
|
gigaxonin
|
0.631991
|
|
GNE
|
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
|
0.60069
|
|
RPS19
|
ribosomal protein S19
|
0.557509
|
|
ARG1
|
arginase 1
|
0.555568
|
|
ADSL
|
adenylosuccinate lyase
|
0.548971
|
|
BBS2
|
Bardet-Biedl syndrome 2
|
0.528449
|
|
HPX
|
hemopexin
|
0.517265
|
|
MDH2
|
malate dehydrogenase 2, NAD (mitochondrial)
|
0.513802
|
|
MDH1
|
malate dehydrogenase 1, NAD (soluble)
|
0.498467
|
|
GHR
|
growth hormone receptor
|
0.42664
|
|
APOC3
|
apolipoprotein C-III
|
0.379997
|
|
PTER
|
phosphotriesterase related
|
0.360764
|
|
ATP7A
|
ATPase, Cu++ transporting, alpha polypeptide
|
0.32993
|
|
DLL1
|
delta-like 1 (Drosophila)
|
0.325552
|
|
LPL
|
lipoprotein lipase
|
0.173832
|
