Fg Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An X-linked disease characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern. (Human Disease Ontology, DOID_14711)
External Link https://www.disgenet.org/browser/0/1/0/C1845546
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Genes

14 genes associated with the disease Fg Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AGO2 argonaute RISC catalytic component 2
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
FLNA filamin A, alpha
FMR1 fragile X mental retardation 1
GLI3 GLI family zinc finger 3
HPD 4-hydroxyphenylpyruvate dioxygenase
IGBP1 immunoglobulin (CD79A) binding protein 1
KIF22 kinesin family member 22
MED12 mediator complex subunit 12
MID2 midline 2
OBP2A odorant binding protein 2A
RCOR1 REST corepressor 1
VSX1 visual system homeobox 1
WISP3 WNT1 inducible signaling pathway protein 3