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GENE - TERM ANNOTATION REPORT

RGD ID: 2611
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Fgfr2
Name: fibroblast growth factor receptor 2
Acc ID: DOID:9008731
Term: Craniofacial Abnormalities
Definition: Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
Definition Source(s): MESH:D019465
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)
Fgfr2 ISOFgfr2 (Mus musculus)11251832RGDDNA:missense mutation:exon:p.S250W (mouse) 
Fgfr2 ISOFGFR2 (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanismPMID:10631169 PMID:16465081 PMID:18082115
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