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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking C8H10orf105 and autosomal recessive nonsyndromic deafness 12 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 C10orf105 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 12  (DOID:0110467)
  • 0 papers in RGD have been used to annotate C8H10orf105
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 12
  • Original References(s): PMID:11138009 PMID:12075507 PMID:12522556 PMID:15537665 PMID:15660226 PMID:16199547 PMID:16679490 PMID:17850630 PMID:18273900 PMID:18429043 PMID:19683999 PMID:20146813 PMID:21228398 PMID:21569298 PMID:21940737 PMID:22135276 PMID:22899989 PMID:24033266 PMID:24875298 PMID:25468891 PMID:25741868 PMID:26467025 PMID:27610647 PMID:28492532 PMID:28847902 PMID:30303587 PMID:31445392 PMID:31541171 PMID:35020051


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