increased cranium width Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	having an increased side-to-side, or lateral distance of the cranium (Mammalian Phenotype Ontology, MP_0000441)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000441
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Genes

10 gene mutations causing the increased cranium width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
AMER1	APC membrane recruitment protein 1
ANKRD11	ankyrin repeat domain 11
ARSB	arylsulfatase B
CRKL	v-crk avian sarcoma virus CT10 oncogene homolog-like
FGFR3	fibroblast growth factor receptor 3
LAMA2	laminin, alpha 2
PLCB1	phospholipase C, beta 1 (phosphoinositide-specific)
RAF1	Raf-1 proto-oncogene, serine/threonine kinase
ROR2	receptor tyrosine kinase-like orphan receptor 2
RPL38	ribosomal protein L38