Apert Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0001193
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Genes

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

Symbol Name
BMP2 bone morphogenetic protein 2
CCND1 cyclin D1
COL2A1 collagen, type II, alpha 1
ERF Ets2 repressor factor
FGF10 fibroblast growth factor 10
FGF13 fibroblast growth factor 13
FGF19 fibroblast growth factor 19
FGF2 fibroblast growth factor 2 (basic)
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FN1 fibronectin 1
MAPK8 mitogen-activated protein kinase 8
PIN1 peptidylprolyl cis/trans isomerase, NIMA-interacting 1
RAB18 RAB18, member RAS oncogene family
RET ret proto-oncogene
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TBC1D20 TBC1 domain family, member 20
TWIST1 twist family bHLH transcription factor 1