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GENE - TERM ANNOTATION REPORT

RGD ID: 1306610
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Otog
Name: otogelin
Acc ID: DOID:0110474
Term: autosomal recessive nonsyndromic deafness 18B
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/23122587 "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)
Otog ISOOTOG (Homo sapiens)7240710OMIM  
Otog ISOOTOG (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanism 
Otog ISOOTOG (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b | ClinVar Annotator: match by term: OTOG-related conditionPMID:10655058 PMID:16199547 PMID:17576681 PMID:23122587 PMID:24033266 PMID:24378291 PMID:25741868 PMID:26467025 PMID:28050010 PMID:28492532 PMID:29196752 PMID:29907799 PMID:30139988 PMID:30311386 PMID:31152317 PMID:31645975 PMID:31827275 PMID:32048449 PMID:33223529 PMID:35802133 PMID:36633841 PMID:9536098
Otog ISSOtog (Mus musculus)13592920MouseDOOMIM:614945 
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