abnormal sagittal suture morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the dense, fibrous connective tissue joint between the parietal bones (Mammalian Phenotype Ontology, MP_0003843)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003843
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13 gene mutations causing the abnormal sagittal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANXA1 annexin A1
CASP3 caspase 3, apoptosis-related cysteine peptidase
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
GLI3 GLI family zinc finger 3
ITGB1BP1 integrin beta 1 binding protein 1
LMNA lamin A/C
LMNB1 lamin B1
MMP2 matrix metallopeptidase 2
PSEN1 presenilin 1
SH3PXD2B SH3 and PX domains 2B
SP3 Sp3 transcription factor
WNT9A wingless-type MMTV integration site family, member 9A