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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Myh14 and Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss in Rattus norvegicus.        

  • 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  (DOID:9002779)
  • 8 papers in CRRD have been used to annotate Myh14


  • An association has been curated linking Myh14 and Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss in Rattus norvegicus.        

  • 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  (DOID:9002779)
  • 8 papers in CRRD have been used to annotate Myh14
  • Curation Notes: ClinVar Annotator: match by OMIM:614369
  • Original References(s): PMID:21480433, PMID:23806086, PMID:24088041, PMID:26257172


  • An association has been curated linking Myh14 and Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss in Rattus norvegicus.        

  • 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  (DOID:9002779)
  • 8 papers in CRRD have been used to annotate Myh14
  • Curation Notes: ClinVar Annotator: match by term: Peripheral neuropathy, myopathy, hoarseness, and hearing loss
  • Original References(s): PMID:25741868


  • An association has been curated linking Myh14 and Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss in Rattus norvegicus.        

  • 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  (DOID:9002779)
  • 8 papers in CRRD have been used to annotate Myh14
  • Curation Notes: ClinVar Annotator: match by term: Peripheral neuropathy, myopathy, hoarseness, and hearing loss
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Myh14 and Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss in Rattus norvegicus.        

  • 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 MYH14 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  (DOID:9002779)
  • 8 papers in CRRD have been used to annotate Myh14
  • Curation Notes: ClinVar Annotator: match by term: Peripheral neuropathy, myopathy, hoarseness, and hearing loss
  • Original References(s): PMID:26752647


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