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GENE - TERM ANNOTATION REPORT

RGD ID: 1311915
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Flnb
Name: filamin B
Acc ID: DOID:2256
Term: osteochondrodysplasia
Definition: Abnormal development of cartilage and bone.
Definition Source(s): MESH:D010009, http://en.wikipedia.org/wiki/Osteochondrodysplasia, http://www.medcyclopaedia.com/library/topics/volume_iii_1/o/osteochondrodysplasia.aspx
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.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 ISORGD:13236211601168RGDatelosteogenesis type I, OMIM:108720, DNA:point mutation:exon:A173V

 
 ISORGD:132362112791027RGDDNA:missense, deletion mutations:exons:

 
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