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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking OTOA and autosomal recessive nonsyndromic deafness 22 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with OTOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 22  (DOID:0110480)
  • 0 papers in RGD have been used to annotate OTOA


    • An association has been curated linking OTOA and autosomal recessive nonsyndromic deafness 22 in Pan paniscus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with OTOA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 22  (DOID:0110480)
  • 0 papers in RGD have been used to annotate OTOA
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 22 | ClinVar Annotator: match by term: OTOA-related condition
  • Original References(s): PMID:11972037 PMID:16199547 PMID:17576681 PMID:19888295 PMID:23173898 PMID:23690975 PMID:24033266 PMID:24963352 PMID:25373420 PMID:25741868 PMID:26434960 PMID:26467025 PMID:26969326 PMID:27068579 PMID:28492532 PMID:29196752 PMID:30303587 PMID:30311386 PMID:30740825 PMID:30828794 PMID:31152317 PMID:31527525 PMID:31827275 PMID:33492714 PMID:33597575 PMID:33879512 PMID:34175691 PMID:34416374 PMID:35802133 PMID:36633841 PMID:37114731 PMID:9536098


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