Metopic Synostosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Premature fusion of the metopic suture. (Human Phenotype Ontology, HP_0011330)
External Link https://www.disgenet.org/browser/0/1/0/C1860819
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Genes

28 genes associated with the disease Metopic Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALX4 ALX homeobox 4
ASXL3 additional sex combs like transcriptional regulator 3
BBS9 Bardet-Biedl syndrome 9
BMP2 bone morphogenetic protein 2
CDON cell adhesion associated, oncogene regulated
CER1 cerberus 1, DAN family BMP antagonist
EFNB1 ephrin-B1
ERF Ets2 repressor factor
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FREM1 FRAS1 related extracellular matrix 1
GNAS GNAS complex locus
H3F3A H3 histone, family 3A
HUWE1 HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
IFT122 intraflagellar transport 122
NELL1 NEL-like 1 (chicken)
NFIA nuclear factor I/A
PTCH1 patched 1
RUNX2 runt-related transcription factor 2
SIX2 SIX homeobox 2
SMAD6 SMAD family member 6
SON SON DNA binding protein
TCF12 transcription factor 12
TWIST1 twist family bHLH transcription factor 1
WDR35 WD repeat domain 35
ZIC1 Zic family member 1
ZNF462 zinc finger protein 462