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VARIANT - TERM ANNOTATION REPORT

RGD ID: 156317655
Species: Homo sapiens
RGD Object: Variant
Symbol: CV2018110
Name: NM_024753.5(TTC21B):c.3684+1G>A
Acc ID: DOID:0050592
Term: asphyxiating thoracic dystrophy
Definition: A bone development disease characterized by skeletal abnormalities and resulting in difficulty in breathing caused by mutations that result in ciliopathy. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/asphyxiating-thoracic-dystrophy "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)
CV2018110 IAGP 8554872ClinVarClinVar Annotator: match by term: Jeune thoracic dystrophyPMID:16199547 PMID:18327258 PMID:21068128 PMID:21258341 PMID:23559409 PMID:24876116 PMID:25492405 PMID:27491411 PMID:28492532 PMID:29068549
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