Gene Term Annotation Report - Rat Genome Database

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GENE - TERM ANNOTATION REPORT

RGD ID:	2025
Species:	Rattus norvegicus
RGD Object:	Gene
Symbol:	Acta1
Name:	actin, alpha 1, skeletal muscle

Acc ID:	DOID:0080100
Term:	congenital myopathy
Definition:	A myopathy that is characterized by the lack of muscle tone or floppiness at birth. (DO)
Definition Source(s):	https://rarediseases.org/rare-diseases/myopathy-congenital-batten-turner-type/ "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.

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