delayed intramembranous bone ossification Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description late onset of bone formation in bones that form without a cartilaginous intermediate including the cranium and clavicle (Mammalian Phenotype Ontology, MP_0003420)
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18 gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
AMER1 APC membrane recruitment protein 1
DLX5 distal-less homeobox 5
FGF18 fibroblast growth factor 18
FGFR2 fibroblast growth factor receptor 2
FGFRL1 fibroblast growth factor receptor-like 1
FUZ fuzzy planar cell polarity protein
GJA1 gap junction protein, alpha 1, 43kDa
LRP6 low density lipoprotein receptor-related protein 6
NIPBL Nipped-B homolog (Drosophila)
PKD1 polycystic kidney disease 1 (autosomal dominant)
RUNX2 runt-related transcription factor 2
SIK3 SIK family kinase 3
SP3 Sp3 transcription factor
STAG1 stromal antigen 1
SUCO SUN domain containing ossification factor
THRA thyroid hormone receptor, alpha
TMEM107 transmembrane protein 107