absent parietal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the curved bone forming part of the vault of the cranium (Mammalian Phenotype Ontology, MP_0004419)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004419
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8 gene mutations causing the absent parietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
DISP1 dispatched homolog 1 (Drosophila)
GTF2IRD1 GTF2I repeat domain containing 1
HHAT hedgehog acyltransferase
HSPG2 heparan sulfate proteoglycan 2
SKI SKI proto-oncogene
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)