axonal dystrophy Gene Set
Genes
13 gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ATP8A2
|
ATPase, aminophospholipid transporter, class I, type 8A, member 2
|
|
CACNA2D2
|
calcium channel, voltage-dependent, alpha 2/delta subunit 2
|
|
CHP1
|
calcineurin-like EF-hand protein 1
|
|
DOCK3
|
dedicator of cytokinesis 3
|
|
DST
|
dystonin
|
|
KLC1
|
kinesin light chain 1
|
|
PLA2G6
|
phospholipase A2, group VI (cytosolic, calcium-independent)
|
|
SLC12A6
|
solute carrier family 12 (potassium/chloride transporter), member 6
|
|
SPTBN4
|
spectrin, beta, non-erythrocytic 4
|
|
UBE4B
|
ubiquitination factor E4B
|
|
UCHL1
|
ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
|
|
UCHL3
|
ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase)
|
|
USP14
|
ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)
|
