small interparietal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the bone of the cranium that lies above and anterior to the occipital bone in some mammals (Mammalian Phenotype Ontology, MP_0004384)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004384
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Genes

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

Symbol Name
BMP1 bone morphogenetic protein 1
BMPER BMP binding endothelial regulator
CHUK conserved helix-loop-helix ubiquitous kinase
DKK1 dickkopf WNT signaling pathway inhibitor 1
DLX5 distal-less homeobox 5
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
GJA1 gap junction protein, alpha 1, 43kDa
MNT MAX network transcriptional repressor
MSX2 msh homeobox 2
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PSIP1 PC4 and SFRS1 interacting protein 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2 runt-related transcription factor 2
SC5D sterol-C5-desaturase
TGFB2 transforming growth factor, beta 2
WDR19 WD repeat domain 19