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GENE - TERM ANNOTATION REPORT

RGD ID: 730954
Species: Mus musculus
RGD Object: Gene
Symbol: Tgfb2
Name: transforming growth factor, beta 2
Acc ID: DOID:0060468
Term: Holt-Oram syndrome
Definition: A syndrome characterized by congenital anomalies located_in heart and located_in upper limb. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/condition/holt-oram-syndrome "DO" "DO", https://en.wikipedia.org/wiki/Holt-Oram_syndrome "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/12223419 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/12436037 "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)
Tgfb2 ISOTGFB2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Holt-Oram syndromePMID:24465802 PMID:25741868 PMID:26017485 PMID:28492532 PMID:28633253 PMID:28655553
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