confusion Gene Set
Genes
14 genes associated with the confusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADAMTS13
|
ADAM metallopeptidase with thrombospondin type 1 motif, 13
|
|
AMN
|
amnion associated transmembrane protein
|
|
ATP1A2
|
ATPase, Na+/K+ transporting, alpha 2 polypeptide
|
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
|
CPOX
|
coproporphyrinogen oxidase
|
|
CUBN
|
cubilin (intrinsic factor-cobalamin receptor)
|
|
MMACHC
|
methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
|
|
NAGS
|
N-acetylglutamate synthase
|
|
PRNP
|
prion protein
|
|
SLC19A3
|
solute carrier family 19 (thiamine transporter), member 3
|
|
SLC22A5
|
solute carrier family 22 (organic cation/carnitine transporter), member 5
|
|
SLC25A13
|
solute carrier family 25 (aspartate/glutamate carrier), member 13
|
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
|
TBP
|
TATA box binding protein
|
