spastic paraparesis Gene Set
Genes
13 genes associated with the spastic paraparesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AFG3L2
|
AFG3-like AAA ATPase 2
|
|
AIMP1
|
aminoacyl tRNA synthetase complex-interacting multifunctional protein 1
|
|
COASY
|
CoA synthase
|
|
EDNRB
|
endothelin receptor type B
|
|
GBA
|
glucosidase, beta, acid
|
|
GJC2
|
gap junction protein, gamma 2, 47kDa
|
|
MTPAP
|
mitochondrial poly(A) polymerase
|
|
SLC25A15
|
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
|
|
SLC30A10
|
solute carrier family 30, member 10
|
|
SOX10
|
SRY (sex determining region Y)-box 10
|
|
SPG21
|
spastic paraplegia 21 (autosomal recessive, Mast syndrome)
|
|
TTC19
|
tetratricopeptide repeat domain 19
|
|
WDR45
|
WD repeat domain 45
|
