paresis Gene Set
Genes
19 gene mutations causing the paresis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ATP7A
|
ATPase, Cu++ transporting, alpha polypeptide
|
|
CCR10
|
chemokine (C-C motif) receptor 10
|
|
CD86
|
CD86 molecule
|
|
CLN6
|
ceroid-lipofuscinosis, neuronal 6, late infantile, variant
|
|
CLN8
|
ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
|
|
CNTNAP1
|
contactin associated protein 1
|
|
CX3CR1
|
chemokine (C-X3-C motif) receptor 1
|
|
DBNL
|
drebrin-like
|
|
DNM3OS
|
DNM3 opposite strand/antisense RNA
|
|
DST
|
dystonin
|
|
GALC
|
galactosylceramidase
|
|
LAMA2
|
laminin, alpha 2
|
|
NCOR2
|
nuclear receptor corepressor 2
|
|
NOTCH3
|
notch 3
|
|
PTPN9
|
protein tyrosine phosphatase, non-receptor type 9
|
|
SPG20
|
spastic paraplegia 20 (Troyer syndrome)
|
|
SPTBN4
|
spectrin, beta, non-erythrocytic 4
|
|
TTPA
|
tocopherol (alpha) transfer protein
|
|
VEGFA
|
vascular endothelial growth factor A
|
