wide cranial sutures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally increased width of the cranial sutures for age-related norms (generally resulting from delayed closure). (Human Phenotype Ontology, HP_0010537)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010537
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Genes

17 genes associated with the wide cranial 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
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ALPL alkaline phosphatase, liver/bone/kidney
BANF1 barrier to autointegration factor 1
CRTAP cartilage associated protein
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
DCHS1 dachsous cadherin-related 1
FAT4 FAT atypical cadherin 4
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