wide anterior fontanel Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Enlargement of the anterior fontanelle with respect to age-dependent norms. (Human Phenotype Ontology, HP_0000260)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000260
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30 genes associated with the wide anterior fontanel 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
ANTXR1 anthrax toxin receptor 1
ARX aristaless related homeobox
ATP6V0A2 ATPase, H+ transporting, lysosomal V0 subunit a2
B3GALTL beta 1,3-galactosyltransferase-like
COL11A1 collagen, type XI, alpha 1
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
CREBBP CREB binding protein
CRTAP cartilage associated protein
DCHS1 dachsous cadherin-related 1
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
FAT4 FAT atypical cadherin 4
FGFR2 fibroblast growth factor receptor 2
FLNA filamin A, alpha
HRAS Harvey rat sarcoma viral oncogene homolog
KIF7 kinesin family member 7
LRP2 low density lipoprotein receptor-related protein 2
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MED12 mediator complex subunit 12
P3H1 prolyl 3-hydroxylase 1
PIEZO2 piezo-type mechanosensitive ion channel component 2
ROR2 receptor tyrosine kinase-like orphan receptor 2
SEC23A Sec23 homolog A (S. cerevisiae)
SKI SKI proto-oncogene
SOX9 SRY (sex determining region Y)-box 9
TSHB thyroid stimulating hormone, beta
WNT5A wingless-type MMTV integration site family, member 5A