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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking HSPA1A and Sudden Hearing Loss in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 30 papers in RGD have been used to annotate HSPA1A
  • Curation Notes: DNA:SNP, haplotype: :rs1043618 (human)


  • An association has been curated linking HSPA1B and Sudden Hearing Loss in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 23 papers in RGD have been used to annotate HSPA1B
  • Curation Notes: DNA:SNP, haplotype: :rs2763979 (human)


  • An association has been curated linking HSPA1L and Sudden Hearing Loss in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 12 papers in RGD have been used to annotate HSPA1L
  • Curation Notes: DNA:SNP, haplotype: :rs2075800 (human)


  • An association has been curated linking Hspa1a and Sudden Hearing Loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • The annotation has been inferred from sequence orthology with HSPA1A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 32 papers in RGD have been used to annotate Hspa1a
  • Curation Notes: DNA:SNP, haplotype: :rs1043618 (human)


  • An association has been curated linking Hspa1a and Sudden Hearing Loss in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • The annotation has been inferred from sequence orthology with HSPA1A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 39 papers in RGD have been used to annotate Hspa1a
  • Curation Notes: DNA:SNP, haplotype: :rs1043618 (human)


  • An association has been curated linking Hspa1b and Sudden Hearing Loss in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • The annotation has been inferred from sequence orthology with HSPA1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 41 papers in RGD have been used to annotate Hspa1b
  • Curation Notes: DNA:SNP, haplotype: :rs2763979 (human)


  • An association has been curated linking Hspa1b and Sudden Hearing Loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • The annotation has been inferred from sequence orthology with HSPA1B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 24 papers in RGD have been used to annotate Hspa1b
  • Curation Notes: DNA:SNP, haplotype: :rs2763979 (human)


  • An association has been curated linking Hspa1l and Sudden Hearing Loss in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • The annotation has been inferred from sequence orthology with HSPA1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 15 papers in RGD have been used to annotate Hspa1l
  • Curation Notes: DNA:SNP, haplotype: :rs2075800 (human)


  • An association has been curated linking Hspa1l and Sudden Hearing Loss in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • The annotation has been inferred from sequence orthology with HSPA1L (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Chien CY, etal., Audiol Neurootol. 2012;17(6):381-5. doi: 10.1159/000341815. Epub 2012 Aug 22.
  • 16 RGD objects have been annotated to Sudden Hearing Loss  (DOID:9003817)
  • 16 papers in RGD have been used to annotate Hspa1l
  • Curation Notes: DNA:SNP, haplotype: :rs2075800 (human)


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