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GENE - TERM ANNOTATION REPORT

RGD ID: 18592252
Species: Chlorocebus sabaeus
RGD Object: Gene
Symbol: WHRN
Name: whirlin
Acc ID: DOID:0110490
Term: autosomal recessive nonsyndromic deafness 31
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32. (DO)
Definition Source(s): PMID:12833159 "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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