abnormal basisphenoid bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly 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_0000106)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000106
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Genes

33 gene mutations causing the abnormal basisphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
BMP7 bone morphogenetic protein 7
BMPER BMP binding endothelial regulator
CDON cell adhesion associated, oncogene regulated
CHRD chordin
DISP1 dispatched homolog 1 (Drosophila)
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
EDNRA endothelin receptor type A
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR2 fibroblast growth factor receptor 2
FGFRL1 fibroblast growth factor receptor-like 1
FOXC1 forkhead box C1
FOXC2 forkhead box C2
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
HOXA2 homeobox A2
LTBP1 latent transforming growth factor beta binding protein 1
LTBP3 latent transforming growth factor beta binding protein 3
MIR140 microRNA 140
MN1 meningioma (disrupted in balanced translocation) 1
NKX3-2 NK3 homeobox 2
OTX2 orthodenticle homeobox 2
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PKDCC protein kinase domain containing, cytoplasmic
PTCH1 patched 1
RUNX2 runt-related transcription factor 2
SKI SKI proto-oncogene
SP3 Sp3 transcription factor
TBX1 T-box 1
TMEM107 transmembrane protein 107
ZEB1 zinc finger E-box binding homeobox 1
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