Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   


CRRD ID: 8797424
Species: Chinchilla lanigera
CRRD Object: Gene
Symbol: Myh2
Name: myosin heavy chain 2
Acc ID: DOID:630
Term: genetic disease
Definition: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
Definition Source(s): "DO", MESH:D030342
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 ISORGD:104015919068941ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:11114175, PMID:11889243, PMID:15741996, PMID:20418530, PMID:22349865, PMID:22496423, PMID:22918376, PMID:23388406, PMID:23489661, PMID:28492532
Go Back to source page   Continue to Ontology report


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