Prieto X-Linked Mental Retardation Syndrome Gene Set
Genes
15 genes associated with the disease Prieto X-Linked Mental Retardation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
BMP2
|
bone morphogenetic protein 2
|
|
BMPR1B
|
bone morphogenetic protein receptor, type IB
|
|
DLX5
|
distal-less homeobox 5
|
|
DLX6
|
distal-less homeobox 6
|
|
FBN2
|
fibrillin 2
|
|
GRM4
|
glutamate receptor, metabotropic 4
|
|
IRF6
|
interferon regulatory factor 6
|
|
KCNJ16
|
potassium channel, inwardly rectifying subfamily J, member 16
|
|
KCNJ2
|
potassium channel, inwardly rectifying subfamily J, member 2
|
|
KIF15
|
kinesin family member 15
|
|
MED13L
|
mediator complex subunit 13-like
|
|
PAX2
|
paired box 2
|
|
PHAX
|
phosphorylated adaptor for RNA export
|
|
SOX9
|
SRY (sex determining region Y)-box 9
|
|
WNT1
|
wingless-type MMTV integration site family, member 1
|
