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GENE - TERM ANNOTATION REPORT

RGD ID: 1549987
Species: Mus musculus
RGD Object: Gene
Symbol: Wdr19
Name: WD repeat domain 19
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)
Wdr19 ISOWDR19 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Jeune thoracic dystrophyPMID:16199547 PMID:22019273 PMID:23559409 PMID:23683095 PMID:24504730 PMID:25726036 PMID:25741868 PMID:26275793 PMID:26489029 PMID:27241786 PMID:28492532 PMID:28973083 PMID:29068549 PMID:33875766
Wdr19 ISOWDR19 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Jeune thoracic dystrophy | ClinVar Annotator: match by term: Jeune's syndromePMID:16199547 PMID:22019273 PMID:23559409 PMID:23683095 PMID:24504730 PMID:25726036 PMID:25741868 PMID:26275793 PMID:26489029 PMID:27241786 PMID:28492532 PMID:28973083 PMID:29068549 PMID:31216405 PMID:33875766
Wdr19 ISOWDR19 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Jeune thoracic dystrophy | ClinVar Annotator: match by term: Jeune's syndrome | ClinVar Annotator: match by term: Short rib-polydactyly syndromePMID:16199547 PMID:22019273 PMID:23559409 PMID:23683095 PMID:25741868 PMID:26275793 PMID:26489029 PMID:27241786 PMID:28492532 PMID:28973083 PMID:29068549
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