abnormality of skull ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the process of ossification of the skull. (Human Phenotype Ontology, HP_0002703)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002703
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28 genes associated with the abnormality of skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
ALX4 ALX homeobox 4
ANTXR1 anthrax toxin receptor 1
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
CRTAP cartilage associated protein
EXT2 exostosin glycosyltransferase 2
FAM111A family with sequence similarity 111, member A
FIG4 FIG4 phosphoinositide 5-phosphatase
HDAC6 histone deacetylase 6
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
LBR lamin B receptor
LMNA lamin A/C
MPL MPL proto-oncogene, thrombopoietin receptor
NAGLU N-acetylglucosaminidase, alpha
NOTCH2 notch 2
P3H1 prolyl 3-hydroxylase 1
PHF21A PHD finger protein 21A
RUNX2 runt-related transcription factor 2
SEC23A Sec23 homolog A (S. cerevisiae)
SETBP1 SET binding protein 1
SGSH N-sulfoglucosamine sulfohydrolase
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
TBCE tubulin folding cofactor E
TRIP11 thyroid hormone receptor interactor 11
WNT7A wingless-type MMTV integration site family, member 7A
ZMPSTE24 zinc metallopeptidase STE24