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GENE - TERM ANNOTATION REPORT

RGD ID: 1308761
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Smarcb1
Name: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
Acc ID: DOID:0070045
Term: Coffin-Siris syndrome 3
Definition: A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the SMARCB1 gene on chromosome 22q11.23. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/22426308 "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.
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