decreased skull ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A reduction in the magnitude or amount of ossification of the skull. (Human Phenotype Ontology, HP_0004331)
External Link
Similar Terms
Downloads & Tools


25 genes associated with the decreased 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
LBR lamin B receptor
LMNA lamin A/C
MPL MPL proto-oncogene, thrombopoietin receptor
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
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