Gene Term Annotation Report - Rat Genome Database

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GENE - TERM ANNOTATION REPORT

RGD ID:	1310497
Species:	Rattus norvegicus
RGD Object:	Gene
Symbol:	Six6
Name:	SIX homeobox 6

Acc ID:	DOID:0050569
Term:	Seckel syndrome
Definition:	A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. (DO)
Definition Source(s):	http://en.wikipedia.org/wiki/Seckel_syndrome "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

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.