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GENE - TERM ANNOTATION REPORT

RGD ID: 1315323
Species: Homo sapiens
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 IAGP 7240710OMIM  
OTOG EXP 11554173CTDCTD Direct Evidence: marker/mechanism 
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:24033266
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b | ClinVar Annotator: match by term: OTOG-related conditionPMID:24033266 PMID:25741868 PMID:28492532
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b | ClinVar Annotator: match by term: OTOG-related conditionPMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532
OTOG IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:17576681 PMID:24033266 PMID:25741868 PMID:28492532 PMID:9536098
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:24033266 PMID:25741868
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b | ClinVar Annotator: match by term: OTOG-related conditionPMID:25741868 PMID:28492532
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b | ClinVar Annotator: match by term: OTOG-related conditionPMID:25741868
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b 
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:10655058 PMID:23122587 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29907799
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:24033266 PMID:28492532 PMID:30311386 PMID:32048449
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:24033266 PMID:25741868 PMID:28050010 PMID:28492532
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:10655058 PMID:16199547 PMID:23122587 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29196752
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:23122587 PMID:24033266 PMID:25741868 PMID:28492532
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:23122587 PMID:28492532 PMID:30139988
OTOG IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:28492532
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:23122587 PMID:25741868 PMID:28492532
OTOG IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18b | ClinVar Annotator: match by term: OTOG-related conditionPMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098
OTOG IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:35802133 PMID:36633841
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: OTOG-related conditionPMID:23122587 PMID:25741868 PMID:28492532 PMID:31152317 PMID:31827275
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:25741868 PMID:33223529
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:23122587 PMID:25741868 PMID:31645975
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:23122587
OTOG IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal recessive 18bPMID:23122587 PMID:24378291 PMID:28492532
OTOG ISSOtog (Mus musculus)13592920MouseDOOMIM:614945 
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