Coronal Craniosynostosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Premature closure of the coronal suture of skull. (Human Phenotype Ontology, HP_0004440)
External Link https://www.disgenet.org/browser/0/1/0/C1856266
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Genes

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

Symbol Name
ALX4 ALX homeobox 4
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
BPNT2 3'(2'), 5'-bisphosphate nucleotidase 2
CCBE1 collagen and calcium binding EGF domains 1
EFNB1 ephrin-B1
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GTF2E2 general transcription factor IIE, polypeptide 2, beta 34kDa
IL11RA interleukin 11 receptor, alpha
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
P4HB prolyl 4-hydroxylase, beta polypeptide
POR P450 (cytochrome) oxidoreductase
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
SEC24D SEC24 family member D
SLC25A24 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 24
TCF12 transcription factor 12
TWIST1 twist family bHLH transcription factor 1
ZIC1 Zic family member 1