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:2340
Term:	craniosynostosis
Definition:	A synostosis that results_in premature fusion located_in skull. (DO)
Definition Source(s):	http://en.wikipedia.org/wiki/Craniosynostosis "DO" "DO", http://www.mayoclinic.com/health/craniosynostosis/DS00959 "DO" "DO", http://www.ninds.nih.gov/disorders/craniosynostosis/craniosynostosis.htm "DO" "DO", http://www.nlm.nih.gov/medlineplus/ency/article/001590.htm "DO" "DO"

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		1600491	RGD	craniosynostosis type 2, OMIM:604757, DNA:point mutation:exon:P148H

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