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)
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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