dysdiadochokinesis Gene Set
Genes
19 genes associated with the dysdiadochokinesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCB7
|
ATP-binding cassette, sub-family B (MDR/TAP), member 7
|
|
AFG3L2
|
AFG3-like AAA ATPase 2
|
|
ATXN1
|
ataxin 1
|
|
ATXN10
|
ataxin 10
|
|
ATXN2
|
ataxin 2
|
|
ELOVL4
|
ELOVL fatty acid elongase 4
|
|
FMR1
|
fragile X mental retardation 1
|
|
GRM1
|
glutamate receptor, metabotropic 1
|
|
ITPR1
|
inositol 1,4,5-trisphosphate receptor, type 1
|
|
KCNJ10
|
potassium channel, inwardly rectifying subfamily J, member 10
|
|
MRE11A
|
MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
|
|
PDE8B
|
phosphodiesterase 8B
|
|
PLA2G6
|
phospholipase A2, group VI (cytosolic, calcium-independent)
|
|
PPP2R2B
|
protein phosphatase 2, regulatory subunit B, beta
|
|
SLC20A2
|
solute carrier family 20 (phosphate transporter), member 2
|
|
SPTBN2
|
spectrin, beta, non-erythrocytic 2
|
|
TTC19
|
tetratricopeptide repeat domain 19
|
|
VLDLR
|
very low density lipoprotein receptor
|
|
WDR81
|
WD repeat domain 81
|
