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GENE - TERM ANNOTATION REPORT

RGD ID: 2513
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Dnm2
Name: dynamin 2
Acc ID: DOID:0111217
Term: autosomal dominant centronuclear myopathy
Definition: A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/30103348 "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)
Dnm2 ISODNM2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant centronuclear myopathyPMID:16199547 PMID:16227997 PMID:17008356 PMID:17825552 PMID:17932957 PMID:18414213 PMID:19130742 PMID:19623537 PMID:19932619 PMID:20227276 PMID:20529869 PMID:20700106 PMID:20817456 PMID:20858595 PMID:20927630 PMID:21221624 PMID:21762456 PMID:22096584 PMID:22369075 PMID:22396310 PMID:22613877 PMID:23338057 PMID:23374900 PMID:23394783 PMID:24016602 PMID:24033266 PMID:24088041 PMID:24135484 PMID:24366529 PMID:24465259 PMID:24728327 PMID:25214167 PMID:25262827 PMID:25326635 PMID:25492887 PMID:25501959 PMID:25741868 PMID:25957634 PMID:26199319 PMID:26273216 PMID:26467025 PMID:26503427 PMID:26633545 PMID:26842864 PMID:26908122 PMID:2734399 PMID:27343996 PMID:27572814 PMID:27698851 PMID:27854218 PMID:28492532 PMID:28676641 PMID:30103202 PMID:32860008 PMID:34008892 PMID:34354735 PMID:34837441
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