absent interparietal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the bone of the cranium that lies above and anterior to the occipital bone in some mammals (Mammalian Phenotype Ontology, MP_0004383)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004383
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Genes

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

Symbol Name
ALX1 ALX homeobox 1
APAF1 apoptotic peptidase activating factor 1
GTF2IRD1 GTF2I repeat domain containing 1
HECTD1 HECT domain containing E3 ubiquitin protein ligase 1
HHAT hedgehog acyltransferase
SCUBE1 signal peptide, CUB domain, EGF-like 1
SKI SKI proto-oncogene
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)