tetraplegia Gene Set
Genes
13 genes associated with the tetraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AIFM1
|
apoptosis-inducing factor, mitochondrion-associated, 1
|
|
ALS2
|
amyotrophic lateral sclerosis 2 (juvenile)
|
|
ARSA
|
arylsulfatase A
|
|
ARX
|
aristaless related homeobox
|
|
ATP1A2
|
ATPase, Na+/K+ transporting, alpha 2 polypeptide
|
|
ATP1A3
|
ATPase, Na+/K+ transporting, alpha 3 polypeptide
|
|
BCAP31
|
B-cell receptor-associated protein 31
|
|
DPYD
|
dihydropyrimidine dehydrogenase
|
|
KCNT1
|
potassium channel, sodium activated subfamily T, member 1
|
|
PRF1
|
perforin 1 (pore forming protein)
|
|
PRPS1
|
phosphoribosyl pyrophosphate synthetase 1
|
|
RANBP2
|
RAN binding protein 2
|
|
TFG
|
TRK-fused gene
|
