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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking Slc26a4 and Deafness in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Wangemann P, etal., Am J Physiol Renal Physiol. 2007 May;292(5):F1345-53. Epub 2007 Feb 13.
  • The annotation has been inferred from sequence orthology with Slc26a4 (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Wangemann P, etal., Am J Physiol Renal Physiol. 2007 May;292(5):F1345-53. Epub 2007 Feb 13.
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4


  • An association has been curated linking Slc26a4 and Deafness in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Park HJ, etal., J Med Genet. 2003 Apr;40(4):242-8.
  • The annotation has been inferred from sequence orthology with SLC26A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Park HJ, etal., J Med Genet. 2003 Apr;40(4):242-8.
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4
  • Curation Notes: DNA:mutations:multiple (human)


  • An association has been curated linking Slc26a4 and Deafness in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Tekin M, etal., Clin Genet. 2003 Oct;64(4):371-4.
  • The annotation has been inferred from sequence orthology with SLC26A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Tekin M, etal., Clin Genet. 2003 Oct;64(4):371-4.
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4
  • Curation Notes: DNA:deletion, missense mutation:cds:c.1341delG, p.H723R (human)


  • An association has been curated linking Slc26a4 and Deafness in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Albert S, etal., Eur J Hum Genet. 2006 Jun;14(6):773-9.
  • The annotation has been inferred from sequence orthology with SLC26A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Albert S, etal., Eur J Hum Genet. 2006 Jun;14(6):773-9.
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4
  • Curation Notes: DNA:mutations:multiple (human)


  • An association has been curated linking Slc26a4 and Deafness in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Rebeh IB, etal., Clin Genet. 2010 Jul;78(1):74-80. doi: 10.1111/j.1399-0004.2009.01360.x. Epub 2009 Dec 2.
  • The annotation has been inferred from sequence orthology with SLC26A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Rebeh IB, etal., Clin Genet. 2010 Jul;78(1):74-80. doi: 10.1111/j.1399-0004.2009.01360.x. Epub 2009 Dec 2.
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4
  • Curation Notes: DNA:missense mutation:cds:p.L445W (human)


  • An association has been curated linking Slc26a4 and Deafness in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Li X, etal., PLoS Genet. 2013 Jul;9(7):e1003641. doi: 10.1371/journal.pgen.1003641. Epub 2013 Jul 11.
  • The annotation has been inferred from sequence orthology with SLC26A4 (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Li X, etal., PLoS Genet. 2013 Jul;9(7):e1003641. doi: 10.1371/journal.pgen.1003641. Epub 2013 Jul 11.
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4
  • Curation Notes: human gene in mouse model


  • An association has been curated linking Slc26a4 and Deafness 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 SLC26A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 364 RGD objects have been annotated to Deafness  (DOID:9008681)
  • 33 papers in RGD have been used to annotate Slc26a4
  • Curation Notes: ClinVar Annotator: match by term: Deafness
  • Original References(s): PMID:11317356 PMID:28492532 PMID:29372807 PMID:30303587 PMID:34170635


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