abnormal alisphenoid bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of either of the broad curved wing like expanses on each side of the sphenoid bone in adults; may exist independently in the young (Mammalian Phenotype Ontology, MP_0003235)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003235
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19 gene mutations causing the abnormal alisphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
BMP7 bone morphogenetic protein 7
BNC2 basonuclin 2
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
FGFR1 fibroblast growth factor receptor 1
FOXC2 forkhead box C2
GJA1 gap junction protein, alpha 1, 43kDa
GSC goosecoid homeobox
MN1 meningioma (disrupted in balanced translocation) 1
OTX2 orthodenticle homeobox 2
PRRX1 paired related homeobox 1
PTCH1 patched 1
RARA retinoic acid receptor, alpha
SCUBE1 signal peptide, CUB domain, EGF-like 1
TGFB2 transforming growth factor, beta 2