widely patent fontanelles and sutures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally increased width of the cranial fontanelles and sutures. (Human Phenotype Ontology, HP_0004492)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004492
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Genes

12 genes associated with the widely patent fontanelles and sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
ALPL alkaline phosphatase, liver/bone/kidney
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
MSX2 msh homeobox 2
PEX1 peroxisomal biogenesis factor 1
REN renin
SETBP1 SET binding protein 1
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor