Congenital Abnormal Synostosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0039093
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Genes

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

Symbol Name
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
EFNA4 ephrin-A4
EFNB1 ephrin-B1
FGF9 fibroblast growth factor 9
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
GDF6 growth differentiation factor 6
HOXA11 homeobox A11
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF1R insulin-like growth factor 1 receptor
LRPAP1 low density lipoprotein receptor-related protein associated protein 1
MSX2 msh homeobox 2
NELL1 NEL-like 1 (chicken)
NOG noggin
PBX1 pre-B-cell leukemia homeobox 1
POR P450 (cytochrome) oxidoreductase
RUNX2 runt-related transcription factor 2
SMAD6 SMAD family member 6
TCF12 transcription factor 12
TGFB2 transforming growth factor, beta 2
TWIST1 twist family bHLH transcription factor 1
ZIC1 Zic family member 1