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GENE - TERM ANNOTATION REPORT

RGD ID: 1616843
Species: Mus musculus
RGD Object: Gene
Symbol: Myh2
Name: myosin, heavy polypeptide 2, skeletal muscle, adult
Acc ID: DOID:3429
Term: inclusion body myositis
Definition: A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Inclusion_body_myositis "DO" "DO", https://ghr.nlm.nih.gov/condition/idiopathic-inflammatory-myopathy "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 SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Myh2 ISOMYH2 (Homo sapiens)9068941RGDIBM3, OMIM:605637, DNA:point mutation:exon:E706KPMID:11114175 REF_RGD_ID:1600532
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