abnormal squamosal bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the thin, plate-like part of the temporal bone (Mammalian Phenotype Ontology, MP_0004423)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004423
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20 gene mutations causing the abnormal squamosal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
BMPER BMP binding endothelial regulator
CHRD chordin
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
FOXI3 forkhead box I3
HMX1 H6 family homeobox 1
HOXA2 homeobox A2
MN1 meningioma (disrupted in balanced translocation) 1
POU3F3 POU class 3 homeobox 3
PRRX1 paired related homeobox 1
RARA retinoic acid receptor, alpha
RSPO2 R-spondin 2
SCUBE1 signal peptide, CUB domain, EGF-like 1
SIX1 SIX homeobox 1
TWIST1 twist family bHLH transcription factor 1