Sagittal Craniosynostosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A kind of craniosynostosis affecting the sagittal suture. (Human Phenotype Ontology, HP_0004442)
External Link https://www.disgenet.org/browser/0/1/0/C0432123
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Genes

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

Symbol Name
ALPP alkaline phosphatase, placental
ASRGL1 asparaginase like 1
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATRNL1 attractin-like 1
AXIN2 axin 2
BBS9 Bardet-Biedl syndrome 9
BMP2 bone morphogenetic protein 2
CCL27 chemokine (C-C motif) ligand 27
CDC45 cell division cycle 45
DPF2 D4, zinc and double PHD fingers family 2
ERF Ets2 repressor factor
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
GLI3 GLI family zinc finger 3
GNAS GNAS complex locus
H3F3A H3 histone, family 3A
HNRNPK heterogeneous nuclear ribonucleoprotein K
IFT122 intraflagellar transport 122
IL11RA interleukin 11 receptor, alpha
KRAS Kirsten rat sarcoma viral oncogene homolog
MSX2 msh homeobox 2
NAT10 N-acetyltransferase 10 (GCN5-related)
NELL1 NEL-like 1 (chicken)
PDLIM3 PDZ and LIM domain 3
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
SLPI secretory leukocyte peptidase inhibitor
SON SON DNA binding protein
TBC1D24 TBC1 domain family, member 24
TERT telomerase reverse transcriptase
TSPEAR thrombospondin-type laminin G domain and EAR repeats
TWIST1 twist family bHLH transcription factor 1
ZIC1 Zic family member 1