delayed closure of the anterior fontanelle Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A delay in closure (ossification) of the anterior fontanelle, which generally undergoes closure around the 18th month of life. (Human Phenotype Ontology, HP_0001476)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0001476
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Genes

16 genes associated with the delayed closure of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ADAMTS2	ADAM metallopeptidase with thrombospondin type 1 motif, 2
AMER1	APC membrane recruitment protein 1
ASPA	aspartoacylase
ATP7A	ATPase, Cu++ transporting, alpha polypeptide
BANF1	barrier to autointegration factor 1
CTSK	cathepsin K
FAM111A	family with sequence similarity 111, member A
FLNA	filamin A, alpha
MED12	mediator complex subunit 12
MMP2	matrix metallopeptidase 2
PEX14	peroxisomal biogenesis factor 14
PEX19	peroxisomal biogenesis factor 19
RPS6KA3	ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2	runt-related transcription factor 2
SEC23A	Sec23 homolog A (S. cerevisiae)
TBCE	tubulin folding cofactor E