small parietal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the curved bone forming part of the vault of the cranium (Mammalian Phenotype Ontology, MP_0004418)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004418
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Genes

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

Symbol Name
ALX4 ALX homeobox 4
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BMP1 bone morphogenetic protein 1
BNC2 basonuclin 2
CHUK conserved helix-loop-helix ubiquitous kinase
DKK1 dickkopf WNT signaling pathway inhibitor 1
DLX5 distal-less homeobox 5
FGFR2 fibroblast growth factor receptor 2
GAS1 growth arrest-specific 1
GJA1 gap junction protein, alpha 1, 43kDa
ITGB1BP1 integrin beta 1 binding protein 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2 runt-related transcription factor 2
SCUBE1 signal peptide, CUB domain, EGF-like 1
TGFB2 transforming growth factor, beta 2
WDR19 WD repeat domain 19