Mental Retardation, X-Linked Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D038901
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Genes

22 genes/proteins associated with the disease Mental Retardation, X-Linked from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SYP synaptophysin 2.88009
OPHN1 oligophrenin 1 2.88009
ZNF711 zinc finger protein 711 2.88009
ZNF41 zinc finger protein 41 2.88009
PQBP1 polyglutamine binding protein 1 2.88009
FGD1 FYVE, RhoGEF and PH domain containing 1 2.88009
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8 2.88009
AGTR2 angiotensin II receptor, type 2 2.88009
IL1RAPL1 interleukin 1 receptor accessory protein-like 1 2.88009
CXORF36 chromosome X open reading frame 36 2.88009
UPF3B UPF3 regulator of nonsense transcripts homolog B (yeast) 2.88009
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family) 2.88009
GDI1 GDP dissociation inhibitor 1 2.88009
MAOA monoamine oxidase A 2.88009
RAB40AL RAB40A, member RAS oncogene family-like 2.88009
PCDH19 protocadherin 19 2.88009
ATRX alpha thalassemia/mental retardation syndrome X-linked 2.88009
RAB39B RAB39B, member RAS oncogene family 2.88009
ZNF674 zinc finger protein 674 2.88009
ARHGEF9 Cdc42 guanine nucleotide exchange factor (GEF) 9 2.88009
DLG3 discs, large homolog 3 (Drosophila) 2.88009
PTCHD1 patched domain containing 1 2.88009