Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking MYO15A and autosomal recessive nonsyndromic deafness 3 in Chlorocebus sabaeus.        

  • 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 MYO15A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 3  (DOID:0110488)
  • 0 papers in RGD have been used to annotate MYO15A
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive nonsyndromic hearing loss 3 | ClinVar Annotator: match by term: Deafness, autosomal recessive 3 | ClinVar Annotator: match by term: MYO15A-related condition | ClinVar Annotator: match by term: NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 3
  • Original References(s): PMID:10552926 PMID:11735029 PMID:16199547 PMID:17546645 PMID:17576681 PMID:17851452 PMID:17853461 PMID:19274735 PMID:19888295 PMID:20505086 PMID:20642360 PMID:21917145 PMID:22245518 PMID:22736430 PMID:22903915 PMID:23208854 PMID:23767834 PMID:23804846 PMID:23865914 PMID:23967202 PMID:24033266 PMID:24105371 PMID:24123792 PMID:24130743 PMID:24206587 PMID:24498627 PMID:24853665 PMID:24875298 PMID:24949729 PMID:25262649 PMID:25373420 PMID:2574186 PMID:25741868 PMID:25788563 PMID:25792667 PMID:26011067 PMID:26075876 PMID:26226137 PMID:26242193 PMID:26302205 PMID:26399936 PMID:26445815 PMID:26467025 PMID:26561413 PMID:26633542 PMID:26763877 PMID:26810297 PMID:26915297 PMID:26969326 PMID:27068579 PMID:27344577 PMID:27375115 PMID:27436265 PMID:27573290 PMID:27635202 PMID:27734841 PMID:27870113 PMID:28000701 PMID:28390610 PMID:28492532 PMID:29196752 PMID:29482514 PMID:29907799 PMID:29986705 PMID:30096381 PMID:30139988 PMID:30303587 PMID:30311386 PMID:30622556 PMID:30682115 PMID:30733538 PMID:30828794 PMID:30896630 PMID:30953472 PMID:31053783 PMID:31130284 PMID:31379920 PMID:31389194 PMID:31581539 PMID:31827275 PMID:31980526 PMID:32279305 PMID:32617096 PMID:32623615 PMID:32658404 PMID:32747562 PMID:32802042 PMID:32860223 PMID:33095980 PMID:33111345 PMID:33187236 PMID:33208113 PMID:33297549 PMID:33398081 PMID:33524517 PMID:33597575 PMID:33879512 PMID:34265623 PMID:34325055 PMID:34374074 PMID:34416374 PMID:34599368 PMID:34733312 PMID:34974475 PMID:35062939 PMID:35346193 PMID:35440622 PMID:35580552 PMID:35802133 PMID:35939872 PMID:35982127 PMID:36217262 PMID:36401330 PMID:36633841 PMID:7616538 PMID:7704031 PMID:9536098 PMID:9603736


  • An association has been curated linking MYO15A and autosomal recessive nonsyndromic deafness 3 in Chlorocebus sabaeus.        

  • 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 MYO15A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 3  (DOID:0110488)
  • 0 papers in RGD have been used to annotate MYO15A


  • Go Back to source page   Continue to Ontology report