Gene Term Annotation Report - Rat Genome Database

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GENE - TERM ANNOTATION REPORT

RGD ID:	735997
Species:	Homo sapiens
RGD Object:	Gene
Symbol:	MSX2
Name:	msh homeobox 2

Acc ID:	DOID:9008731
Term:	Craniofacial Abnormalities
Definition:	Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
Definition Source(s):	MESH:D019465

Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.

Object Symbol	Qualifier	Evidence	With	Reference	Source	Notes	Original Reference(s)
MSX2		IAGP		1600492	RGD	parietal foramina, OMIM:168500, DNA:point mutation:exon: R172H, DNA:deletions
MSX2		EXP		11554173	CTD	CTD Direct Evidence: marker/mechanism	PMID:9147639

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