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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred from direct assay (IDA)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 3 CRRD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in CRRD have been used to annotate MYO7A
  • Qualifier: treatment


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • The annotation has been inferred from sequence orthology with Myo7a (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 3 CRRD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in CRRD have been used to annotate MYO7A


  • An association has been curated linking Myo7a and Usher Syndrome Type 1B in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • The annotation has been inferred from sequence orthology with MYO7A (Homo sapiens) [(IDA) inferred from direct assay]
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 3 CRRD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 26 papers in CRRD have been used to annotate Myo7a
  • Qualifier: treatment


  • An association has been curated linking Myo7a and Usher Syndrome Type 1B in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • The annotation has been inferred from sequence orthology with Myo7a (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 3 CRRD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 26 papers in CRRD have been used to annotate Myo7a


  • An association has been curated linking Myo7a and Usher Syndrome Type 1B in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • The annotation has been inferred from sequence orthology with MYO7A (Homo sapiens) [(IDA) inferred from direct assay]
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 3 CRRD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 20 papers in CRRD have been used to annotate Myo7a
  • Qualifier: treatment


  • An association has been curated linking Myo7a and Usher Syndrome Type 1B in Mus musculus.        

  • The association was inferred from mutant phenotype (IMP)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 3 CRRD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 20 papers in CRRD have been used to annotate Myo7a


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.