small basisphenoid bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone (Mammalian Phenotype Ontology, MP_0004462)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004462
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Genes

14 gene mutations causing the small basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
CDON cell adhesion associated, oncogene regulated
FGFRL1 fibroblast growth factor receptor-like 1
FOXC1 forkhead box C1
FOXC2 forkhead box C2
GLI3 GLI family zinc finger 3
LTBP1 latent transforming growth factor beta binding protein 1
MIR140 microRNA 140
MN1 meningioma (disrupted in balanced translocation) 1
NKX3-2 NK3 homeobox 2
PTCH1 patched 1
RUNX2 runt-related transcription factor 2
SKI SKI proto-oncogene
TMEM107 transmembrane protein 107